Publications:

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Genetic determinants of blood lipids and cerebral small vessel disease: role of high-density lipoprotein cholesterol.

Brain : A Journal Of Neurology

MK Georgakis, R Malik, CD Anderson, KG Parhofer, JC Hopewell, M Dichgans

Publication Date: 2020-02-01

Variant appearance in text: rs4660293

PubMed Link: 31968102

PubMed Central Link

Variant Present in the following documents:

• Main text
• Supplemental file

View BVdb publication page

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A Mendelian Randomization Study Provides Evidence That Adiposity and Dyslipidemia Lead to Lower Urinary Albumin-to-Creatinine Ratio, a Marker of Microvascular Function.

Diabetes

F Casanova, AR Wood, H Yaghootkar, RN Beaumont, SE Jones, KM Gooding, K Aizawa, WD Strain, AT Hattersley, F Khan, AC Shore, TM Frayling, J Tyrrell

Publication Date: 2020-05

Variant appearance in text: rs4660293

PubMed Link: 31915152

PubMed Central Link

Variant Present in the following documents:

• Supplemental file

View BVdb publication page

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Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

Nature Communications

R Noordam, MM Bos, H Wang, TW Winkler, AR Bentley, TO Kilpeläinen, PS de Vries, YJ Sung, K Schwander, BE Cade, A Manning, H Aschard, MR Brown, H Chen, N Franceschini, SK Musani, M Richard, D Vojinovic, S Aslibekyan, TM Bartz, L de Las Fuentes, M Feitosa, AR Horimoto, M Ilkov, M Kho, A Kraja, C Li, E Lim, Y Liu, DO Mook-Kanamori, T Rankinen, SM Tajuddin, A van der Spek, Z Wang, J Marten, V Laville, M Alver, E Evangelou, ME Graff, M He, B Kühnel, LP Lyytikäinen, P Marques-Vidal, IM Nolte, ND Palmer, R Rauramaa, XO Shu, H Snieder, S Weiss, W Wen, LR Yanek, C Adolfo, C Ballantyne, L Bielak, NR Biermasz, E Boerwinkle, N Dimou, G Eiriksdottir, C Gao, SA Gharib, DJ Gottlieb, J Haba-Rubio, TB Harris, S Heikkinen, R Heinzer, JE Hixson, G Homuth, MA Ikram, P Komulainen, JE Krieger, J Lee, J Liu, KK Lohman, AI Luik, R Mägi, LW Martin, T Meitinger, A Metspalu, Y Milaneschi, MA Nalls, J O'Connell, A Peters, P Peyser, OT Raitakari, AP Reiner, PCN Rensen, TK Rice, SS Rich, T Roenneberg, JI Rotter, PJ Schreiner, J Shikany, SS Sidney, M Sims, CM Sitlani, T Sofer, K Strauch, MA Swertz, KD Taylor, AG Uitterlinden, CM van Duijn, H Völzke, M Waldenberger, RB Wallance, KW van Dijk, C Yu, AB Zonderman, DM Becker, P Elliott, T Esko, C Gieger, HJ Grabe, TA Lakka, T Lehtimäki, KE North, BWJH Penninx, P Vollenweider, LE Wagenknecht, T Wu, YB Xiang, W Zheng, DK Arnett, C Bouchard, MK Evans, V Gudnason, S Kardia, TN Kelly, SB Kritchevsky, RJF Loos, AC Pereira, M Province, BM Psaty, C Rotimi, X Zhu, N Amin, LA Cupples, M Fornage, EF Fox, X Guo, WJ Gauderman, K Rice, C Kooperberg, PB Munroe, CT Liu, AC Morrison, DC Rao, D van Heemst, S Redline

Publication Date: 2019-11-12

Variant appearance in text: rs4660293

PubMed Link: 31719535

PubMed Central Link

Variant Present in the following documents:

• 41467_2019_12958_MOESM7_ESM.xlsx

View BVdb publication page

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Bayesian multivariate reanalysis of large genetic studies identifies many new associations.

Plos Genetics

MC Turchin, M Stephens

Publication Date: 2019-10

Variant appearance in text: rs4660293

PubMed Link: 31596850

PubMed Central Link

Variant Present in the following documents:

• pgen.1008431.s007.xls
• pgen.1008431.s006.xls

View BVdb publication page

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Genetic architecture of human plasma lipidome and its link to cardiovascular disease.

Nature Communications

R Tabassum, JT Rämö, P Ripatti, JT Koskela, M Kurki, J Karjalainen, P Palta, S Hassan, J Nunez-Fontarnau, TTJ Kiiskinen, S Söderlund, N Matikainen, MJ Gerl, MA Surma, C Klose, NO Stitziel, H Laivuori, AS Havulinna, SK Service, V Salomaa, M Pirinen, , M Jauhiainen, MJ Daly, NB Freimer, A Palotie, MR Taskinen, K Simons, S Ripatti

Publication Date: 2019-09-24

Variant appearance in text: rs4660293

PubMed Link: 31551469

PubMed Central Link

Variant Present in the following documents:

• 41467_2019_11954_MOESM13_ESM.xlsx
• 41467_2019_11954_MOESM14_ESM.xlsx

View BVdb publication page

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The transferability of lipid loci across African, Asian and European cohorts.

Nature Communications

K Kuchenbaecker, N Telkar, T Reiker, RG Walters, K Lin, A Eriksson, D Gurdasani, A Gilly, L Southam, E Tsafantakis, M Karaleftheri, J Seeley, A Kamali, G Asiki, IY Millwood, M Holmes, H Du, Y Guo, M Kumari, G Dedoussis, L Li, Z Chen, MS Sandhu, E Zeggini,

Publication Date: 2019-09-24

Variant appearance in text: rs4660293

PubMed Link: 31551420

PubMed Central Link

Variant Present in the following documents:

• 41467_2019_12026_MOESM1_ESM.pdf

View BVdb publication page

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Mendelian randomization analysis rules out disylipidaemia as colorectal cancer cause.

Scientific Reports

G Ibáñez-Sanz, A Díez-Villanueva, M Riera-Ponsati, T Fernández-Villa, P Fernández Navarro, M Bustamante, J Llorca, P Amiano, N Ascunce, G Fernández-Tardón, I Salcedo Bellido, D Salas, R Capelo Álvarez, M Crous-Bou, L Ortega-Valín, B Pérez-Gómez, G Castaño-Vinyals, C Palazuelos, JM Altzibar, E Ardanaz, A Tardón, JJ Jiménez Moleón, V Olmos Juste, N Aragonés, M Pollán, M Kogevinas, V Moreno

Publication Date: 2019-09-16

Variant appearance in text: rs4660293

PubMed Link: 31527690

PubMed Central Link

Variant Present in the following documents:

• 41598_2019_49880_MOESM1_ESM.doc

View BVdb publication page

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Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene.

Genome Biology

S Lalonde, VA Codina-Fauteux, SM de Bellefon, F Leblanc, M Beaudoin, MM Simon, R Dali, T Kwan, KS Lo, T Pastinen, G Lettre

Publication Date: 2019-07-08

Variant appearance in text: rs4660293

PubMed Link: 31287004

PubMed Central Link

Variant Present in the following documents:

• 13059_2019_1749_MOESM11_ESM.xlsx

View BVdb publication page

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Discovery of Allele-Specific Protein-RNA Interactions in Human Transcriptomes.

American Journal Of Human Genetics

E Bahrami-Samani, Y Xing

Publication Date: 2019-03-07

Variant appearance in text: rs4660293

PubMed Link: 30827501

PubMed Central Link

Variant Present in the following documents:

• mmc7.xlsx

View BVdb publication page

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Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations.

Nature Genetics

P Sakornsakolpat, D Prokopenko, M Lamontagne, NF Reeve, AL Guyatt, VE Jackson, N Shrine, D Qiao, TM Bartz, DK Kim, MK Lee, JC Latourelle, X Li, JD Morrow, M Obeidat, AB Wyss, P Bakke, RG Barr, TH Beaty, SA Belinsky, GG Brusselle, JD Crapo, K de Jong, DL DeMeo, TE Fingerlin, SA Gharib, A Gulsvik, IP Hall, JE Hokanson, WJ Kim, DA Lomas, SJ London, DA Meyers, GT O'Connor, SI Rennard, DA Schwartz, P Sliwinski, D Sparrow, DP Strachan, R Tal-Singer, Y Tesfaigzi, J Vestbo, JM Vonk, JJ Yim, X Zhou, Y Bossé, A Manichaikul, L Lahousse, EK Silverman, HM Boezen, LV Wain, MD Tobin, BD Hobbs, MH Cho, ,

Publication Date: 2019-03

Variant appearance in text: rs4660293

PubMed Link: 30804561

PubMed Central Link

Variant Present in the following documents:

• NIHMS1517255-supplement-Sup_Tables.xlsx

View BVdb publication page

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Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.

Nature Communications

TO Kilpeläinen, AR Bentley, R Noordam, YJ Sung, K Schwander, TW Winkler, H Jakupović, DI Chasman, A Manning, I Ntalla, H Aschard, MR Brown, L de Las Fuentes, N Franceschini, X Guo, D Vojinovic, S Aslibekyan, MF Feitosa, M Kho, SK Musani, M Richard, H Wang, Z Wang, TM Bartz, LF Bielak, A Campbell, R Dorajoo, V Fisher, FP Hartwig, ARVR Horimoto, C Li, KK Lohman, J Marten, X Sim, AV Smith, SM Tajuddin, M Alver, M Amini, M Boissel, JF Chai, X Chen, J Divers, E Evangelou, C Gao, M Graff, SE Harris, M He, FC Hsu, AU Jackson, JH Zhao, AT Kraja, B Kühnel, F Laguzzi, LP Lyytikäinen, IM Nolte, R Rauramaa, M Riaz, A Robino, R Rueedi, HM Stringham, F Takeuchi, PJ van der Most, TV Varga, N Verweij, EB Ware, W Wen, X Li, LR Yanek, N Amin, DK Arnett, E Boerwinkle, M Brumat, B Cade, M Canouil, YI Chen, MP Concas, J Connell, R de Mutsert, HJ de Silva, PS de Vries, A Demirkan, J Ding, CB Eaton, JD Faul, Y Friedlander, KP Gabriel, M Ghanbari, F Giulianini, CC Gu, D Gu, TB Harris, J He, S Heikkinen, CK Heng, SC Hunt, MA Ikram, JB Jonas, WP Koh, P Komulainen, JE Krieger, SB Kritchevsky, Z Kutalik, J Kuusisto, CD Langefeld, C Langenberg, LJ Launer, K Leander, RN Lemaitre, CE Lewis, J Liang, , J Liu, R Mägi, A Manichaikul, T Meitinger, A Metspalu, Y Milaneschi, KL Mohlke, TH Mosley, AD Murray, MA Nalls, EK Nang, CP Nelson, S Nona, JM Norris, CV Nwuba, J O'Connell, ND Palmer, GJ Papanicolau, R Pazoki, NL Pedersen, A Peters, PA Peyser, O Polasek, DJ Porteous, A Poveda, OT Raitakari, SS Rich, N Risch, JG Robinson, LM Rose, I Rudan, PJ Schreiner, RA Scott, SS Sidney, M Sims, JA Smith, H Snieder, T Sofer, JM Starr, B Sternfeld, K Strauch, H Tang, KD Taylor, MY Tsai, J Tuomilehto, AG Uitterlinden, MY van der Ende, D van Heemst, T Voortman, M Waldenberger, P Wennberg, G Wilson, YB Xiang, J Yao, C Yu, JM Yuan, W Zhao, AB Zonderman, DM Becker, M Boehnke, DW Bowden, U de Faire, IJ Deary, P Elliott, T Esko, BI Freedman, P Froguel, P Gasparini, C Gieger, N Kato, M Laakso, TA Lakka, T Lehtimäki, PKE Magnusson, AJ Oldehinkel, BWJH Penninx, NJ Samani, XO Shu, P van der Harst, JV Van Vliet-Ostaptchouk, P Vollenweider, LE Wagenknecht, YX Wang, NJ Wareham, DR Weir, T Wu, W Zheng, X Zhu, MK Evans, PW Franks, V Gudnason, C Hayward, BL Horta, TN Kelly, Y Liu, KE North, AC Pereira, PM Ridker, ES Tai, RM van Dam, ER Fox, SLR Kardia, CT Liu, DO Mook-Kanamori, MA Province, S Redline, CM van Duijn, JI Rotter, CB Kooperberg, WJ Gauderman, BM Psaty, K Rice, PB Munroe, M Fornage, LA Cupples, CN Rotimi, AC Morrison, DC Rao, RJF Loos

Publication Date: 2019-01-22

Variant appearance in text: rs4660293

PubMed Link: 30670697

PubMed Central Link

Variant Present in the following documents:

• 41467_2018_8008_MOESM7_ESM.xlsx
• 41467_2018_8008_MOESM10_ESM.xlsx

View BVdb publication page

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Type 2 Diabetes and Hypertension.

Circulation Research

D Sun, T Zhou, Y Heianza, X Li, M Fan, VA Fonseca, L Qi

Publication Date: 2019-03-15

Variant appearance in text: rs4660293

PubMed Link: 30646822

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Gene-Based Elevated Triglycerides and Type 2 Diabetes Mellitus Risk in the Women's Genome Health Study.

Arteriosclerosis, Thrombosis, And Vascular Biology

S Ahmad, S Mora, PM Ridker, FB Hu, DI Chasman

Publication Date: 2019-01

Variant appearance in text: rs4660293

PubMed Link: 30565958

PubMed Central Link

Variant Present in the following documents:

• NIHMS1512616-supplement-Supplemental_Material.pdf

View BVdb publication page

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Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.

Nature Communications

E Ferkingstad, A Oddsson, S Gretarsdottir, S Benonisdottir, G Thorleifsson, AM Deaton, S Jonsson, OA Stefansson, GL Norddahl, F Zink, GA Arnadottir, B Gunnarsson, GH Halldorsson, A Helgadottir, BO Jensson, RP Kristjansson, G Sveinbjornsson, DA Sverrisson, G Masson, I Olafsson, GI Eyjolfsson, O Sigurdardottir, H Holm, I Jonsdottir, S Olafsson, T Steingrimsdottir, T Rafnar, ES Bjornsson, U Thorsteinsdottir, DF Gudbjartsson, P Sulem, K Stefansson

Publication Date: 2018-11-30

Variant appearance in text: rs4660293

PubMed Link: 30504769

PubMed Central Link

Variant Present in the following documents:

• 41467_2018_7460_MOESM12_ESM.xlsx

View BVdb publication page

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Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.

American Journal Of Human Genetics

S Ligthart, A Vaez, U Võsa, MG Stathopoulou, PS de Vries, BP Prins, PJ Van der Most, T Tanaka, E Naderi, LM Rose, Y Wu, R Karlsson, M Barbalic, H Lin, R Pool, G Zhu, A Macé, C Sidore, S Trompet, M Mangino, M Sabater-Lleal, JP Kemp, A Abbasi, T Kacprowski, N Verweij, AV Smith, T Huang, C Marzi, MF Feitosa, KK Lohman, ME Kleber, Y Milaneschi, C Mueller, M Huq, E Vlachopoulou, LP Lyytikäinen, C Oldmeadow, J Deelen, M Perola, JH Zhao, B Feenstra, , M Amini, , J Lahti, KE Schraut, M Fornage, B Suktitipat, WM Chen, X Li, T Nutile, G Malerba, J Luan, T Bak, N Schork, F Del Greco M, E Thiering, A Mahajan, RE Marioni, E Mihailov, J Eriksson, AB Ozel, W Zhang, M Nethander, YC Cheng, S Aslibekyan, W Ang, I Gandin, L Yengo, L Portas, C Kooperberg, E Hofer, KB Rajan, C Schurmann, W den Hollander, TS Ahluwalia, J Zhao, HHM Draisma, I Ford, N Timpson, A Teumer, H Huang, S Wahl, Y Liu, J Huang, HW Uh, F Geller, PK Joshi, LR Yanek, E Trabetti, B Lehne, D Vozzi, M Verbanck, G Biino, Y Saba, I Meulenbelt, JR O'Connell, M Laakso, F Giulianini, PKE Magnusson, CM Ballantyne, JJ Hottenga, GW Montgomery, F Rivadineira, R Rueedi, M Steri, KH Herzig, DJ Stott, C Menni, M Frånberg, B St Pourcain, SB Felix, TH Pers, SJL Bakker, P Kraft, A Peters, D Vaidya, G Delgado, JH Smit, V Großmann, J Sinisalo, I Seppälä, SR Williams, EG Holliday, M Moed, C Langenberg, K Räikkönen, J Ding, H Campbell, MM Sale, YI Chen, AL James, D Ruggiero, N Soranzo, CA Hartman, EN Smith, GS Berenson, C Fuchsberger, D Hernandez, CMT Tiesler, V Giedraitis, D Liewald, K Fischer, D Mellström, A Larsson, Y Wang, WR Scott, M Lorentzon, J Beilby, KA Ryan, CE Pennell, D Vuckovic, B Balkau, MP Concas, R Schmidt, CF Mendes de Leon, EP Bottinger, M Kloppenburg, L Paternoster, M Boehnke, AW Musk, G Willemsen, DM Evans, PAF Madden, M Kähönen, Z Kutalik, M Zoledziewska, V Karhunen, SB Kritchevsky, N Sattar, G Lachance, R Clarke, TB Harris, OT Raitakari, JR Attia, D van Heemst, E Kajantie, R Sorice, G Gambaro, RA Scott, AA Hicks, L Ferrucci, M Standl, CM Lindgren, JM Starr, M Karlsson, L Lind, JZ Li, JC Chambers, TA Mori, EJCN de Geus, AC Heath, NG Martin, J Auvinen, BM Buckley, AJM de Craen, M Waldenberger, K Strauch, T Meitinger, RJ Scott, M McEvoy, M Beekman, C Bombieri, PM Ridker, KL Mohlke, NL Pedersen, AC Morrison, DI Boomsma, JB Whitfield, DP Strachan, A Hofman, P Vollenweider, F Cucca, MR Jarvelin, JW Jukema, TD Spector, A Hamsten, T Zeller, AG Uitterlinden, M Nauck, V Gudnason, L Qi, H Grallert, IB Borecki, JI Rotter, W März, PS Wild, ML Lokki, M Boyle, V Salomaa, M Melbye, JG Eriksson, JF Wilson, BWJH Penninx, DM Becker, BB Worrall, G Gibson, RM Krauss, M Ciullo, G Zaza, NJ Wareham, AJ Oldehinkel, LJ Palmer, SS Murray, PP Pramstaller, S Bandinelli, J Heinrich, E Ingelsson, IJ Deary, R Mägi, L Vandenput, P van der Harst, KC Desch, JS Kooner, C Ohlsson, C Hayward, T Lehtimäki, AR Shuldiner, DK Arnett, LJ Beilin, A Robino, P Froguel, M Pirastu, T Jess, W Koenig, RJF Loos, DA Evans, H Schmidt, GD Smith, PE Slagboom, G Eiriksdottir, AP Morris, BM Psaty, RP Tracy, IM Nolte, E Boerwinkle, S Visvikis-Siest, AP Reiner, M Gross, JC Bis, L Franke, OH Franco, EJ Benjamin, DI Chasman, J Dupuis, H Snieder, A Dehghan, BZ Alizadeh

Publication Date: 2018-11-01

Variant appearance in text: rs4660293

PubMed Link: 30388399

PubMed Central Link

Variant Present in the following documents:

• mmc2.xlsx

View BVdb publication page

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Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin.

Journal Of The American Heart Association

S Tuteja, L Qu, M Vujkovic, RL Dunbar, J Chen, S DerOhannessian, DJ Rader

Publication Date: 2018-10-02

Variant appearance in text: rs4660293

PubMed Link: 30371334

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.

Nature Communications

A Xue, Y Wu, Z Zhu, F Zhang, KE Kemper, Z Zheng, L Yengo, LR Lloyd-Jones, J Sidorenko, Y Wu, , AF McRae, PM Visscher, J Zeng, J Yang

Publication Date: 2018-07-27

Variant appearance in text: rs4660293

PubMed Link: 30054458

PubMed Central Link

Variant Present in the following documents:

• 41467_2018_4951_MOESM15_ESM.xlsx

View BVdb publication page

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Risk of Neuropsychiatric Adverse Effects of Lipid-Lowering Drugs: A Mendelian Randomization Study.

The International Journal Of Neuropsychopharmacology

J Alghamdi, S Matou-Nasri, F Alghamdi, S Alghamdi, M Alfadhel, S Padmanabhan

Publication Date: 2018-12-01

Variant appearance in text: rs4660293

PubMed Link: 29986042

PubMed Central Link

Variant Present in the following documents:

• pyy060_suppl_supplementary_tables.xlsx

View BVdb publication page

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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

Nature Communications

SM Zekavat, S Ruotsalainen, RE Handsaker, M Alver, J Bloom, T Poterba, C Seed, J Ernst, M Chaffin, J Engreitz, GM Peloso, A Manichaikul, C Yang, KA Ryan, M Fu, WC Johnson, M Tsai, M Budoff, RS Vasan, LA Cupples, JI Rotter, SS Rich, W Post, BD Mitchell, A Correa, A Metspalu, JG Wilson, V Salomaa, M Kellis, MJ Daly, BM Neale, S McCarroll, I Surakka, T Esko, A Ganna, S Ripatti, S Kathiresan, P Natarajan,

Publication Date: 2018-07-04

Variant appearance in text: rs4660293

PubMed Link: 29973585

PubMed Central Link

Variant Present in the following documents:

• 41467_2018_4668_MOESM9_ESM.xlsx
• 41467_2018_4668_MOESM18_ESM.xlsx
• 41467_2018_4668_MOESM13_ESM.xlsx
• 41467_2018_4668_MOESM10_ESM.xlsx
• 41467_2018_4668_MOESM15_ESM.xlsx
• 41467_2018_4668_MOESM14_ESM.xlsx
• 41467_2018_4668_MOESM11_ESM.xlsx
• 41467_2018_4668_MOESM12_ESM.xlsx
• 41467_2018_4668_MOESM16_ESM.xlsx

View BVdb publication page

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Brief Overview of a Decade of Genome-Wide Association Studies on Primary Hypertension.

International Journal Of Endocrinology

AB Azam, EAB Azizan

Publication Date: 2018

Variant appearance in text: rs4660293

PubMed Link: 29666641

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.

Aging

AM Kulminski, J Huang, Y Loika, KG Arbeev, O Bagley, A Yashkin, M Duan, I Culminskaya

Publication Date: 2018-03-29

Variant appearance in text: rs4660293

PubMed Link: 29615537

PubMed Central Link

Variant Present in the following documents:

• aging-10-101407-s003.xlsx

View BVdb publication page

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.

Nature Genetics

R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, L Rutten-Jacobs, AK Giese, SW van der Laan, S Gretarsdottir, CD Anderson, M Chong, HHH Adams, T Ago, P Almgren, P Amouyel, H Ay, TM Bartz, OR Benavente, S Bevan, GB Boncoraglio, RD Brown, AS Butterworth, C Carrera, CL Carty, DI Chasman, WM Chen, JW Cole, A Correa, I Cotlarciuc, C Cruchaga, J Danesh, PIW de Bakker, AL DeStefano, M den Hoed, Q Duan, ST Engelter, GJ Falcone, RF Gottesman, RP Grewal, V Gudnason, S Gustafsson, J Haessler, TB Harris, A Hassan, AS Havulinna, SR Heckbert, EG Holliday, G Howard, FC Hsu, HI Hyacinth, MA Ikram, E Ingelsson, MR Irvin, X Jian, J Jiménez-Conde, JA Johnson, JW Jukema, M Kanai, KL Keene, BM Kissela, DO Kleindorfer, C Kooperberg, M Kubo, LA Lange, CD Langefeld, C Langenberg, LJ Launer, JM Lee, R Lemmens, D Leys, CM Lewis, WY Lin, AG Lindgren, E Lorentzen, PK Magnusson, J Maguire, A Manichaikul, PF McArdle, JF Meschia, BD Mitchell, TH Mosley, MA Nalls, T Ninomiya, MJ O'Donnell, BM Psaty, SL Pulit, K Rannikmäe, AP Reiner, KM Rexrode, K Rice, SS Rich, PM Ridker, NS Rost, PM Rothwell, JI Rotter, T Rundek, RL Sacco, S Sakaue, MM Sale, V Salomaa, BR Sapkota, R Schmidt, CO Schmidt, U Schminke, P Sharma, A Slowik, CLM Sudlow, C Tanislav, T Tatlisumak, KD Taylor, VNS Thijs, G Thorleifsson, U Thorsteinsdottir, S Tiedt, S Trompet, C Tzourio, CM van Duijn, M Walters, NJ Wareham, S Wassertheil-Smoller, JG Wilson, KL Wiggins, Q Yang, S Yusuf, , , , , , JC Bis, T Pastinen, A Ruusalepp, EE Schadt, S Koplev, JLM Björkegren, V Codoni, M Civelek, NL Smith, DA Trégouët, IE Christophersen, C Roselli, SA Lubitz, PT Ellinor, ES Tai, JS Kooner, N Kato, J He, P van der Harst, P Elliott, JC Chambers, F Takeuchi, AD Johnson, , , , , , , , , , , DK Sanghera, O Melander, C Jern, D Strbian, I Fernandez-Cadenas, WT Longstreth, A Rolfs, J Hata, D Woo, J Rosand, G Pare, JC Hopewell, D Saleheen, K Stefansson, BB Worrall, SJ Kittner, S Seshadri, M Fornage, HS Markus, JMM Howson, Y Kamatani, S Debette, M Dichgans

Publication Date: 2018-04

Variant appearance in text: rs4660293

PubMed Link: 29531354

PubMed Central Link

Variant Present in the following documents:

• NIHMS959658-supplement-Supplementary_Table_27.xlsx

View BVdb publication page

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Influence of obesity-related risk factors in the aetiology of glioma.

British Journal Of Cancer

L Disney-Hogg, A Sud, PJ Law, AJ Cornish, B Kinnersley, QT Ostrom, K Labreche, JE Eckel-Passow, GN Armstrong, EB Claus, D Il'yasova, J Schildkraut, JS Barnholtz-Sloan, SH Olson, JL Bernstein, RK Lai, AJ Swerdlow, M Simon, P Hoffmann, MM Nöthen, KH Jöckel, S Chanock, P Rajaraman, C Johansen, RB Jenkins, BS Melin, MR Wrensch, M Sanson, ML Bondy, RS Houlston

Publication Date: 2018-04

Variant appearance in text: rs4660293

PubMed Link: 29531326

PubMed Central Link

Variant Present in the following documents:

• 41416_2018_9_MOESM1_ESM.docx
• 41416_2018_9_MOESM2_ESM.xlsx

View BVdb publication page

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Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits.

Nature Communications

Y Wu, J Zeng, F Zhang, Z Zhu, T Qi, Z Zheng, LR Lloyd-Jones, RE Marioni, NG Martin, GW Montgomery, IJ Deary, NR Wray, PM Visscher, AF McRae, J Yang

Publication Date: 2018-03-02

Variant appearance in text: rs4660293

PubMed Link: 29500431

PubMed Central Link

Variant Present in the following documents:

• 41467_2018_3371_MOESM7_ESM.xlsx

View BVdb publication page

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Visit-to-visit lipid variability: Clinical significance, effects of lipid-lowering treatment, and (pharmaco) genetics.

Journal Of Clinical Lipidology

RAJ Smit, JW Jukema, I Postmus, I Ford, PE Slagboom, BT Heijmans, S Le Cessie, S Trompet

Publication Date: 2018

Variant appearance in text: rs4660293

PubMed Link: 29422286

PubMed Central Link

Variant Present in the following documents:

• Supplemental file

View BVdb publication page

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Interactions between Genetics and Sugar-Sweetened Beverage Consumption on Health Outcomes: A Review of Gene-Diet Interaction Studies.

Frontiers In Endocrinology

DE Haslam, NM McKeown, MA Herman, AH Lichtenstein, HS Dashti

Publication Date: 2017

Variant appearance in text: rs4660293

PubMed Link: 29375475

PubMed Central Link

Variant Present in the following documents:

• Main text

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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.

Nature Communications

S Bonàs-Guarch, M Guindo-Martínez, I Miguel-Escalada, N Grarup, D Sebastian, E Rodriguez-Fos, F Sánchez, M Planas-Fèlix, P Cortes-Sánchez, S González, P Timshel, TH Pers, CC Morgan, I Moran, G Atla, JR González, M Puiggros, J Martí, EA Andersson, C Díaz, RM Badia, M Udler, A Leong, V Kaur, J Flannick, T Jørgensen, A Linneberg, ME Jørgensen, DR Witte, C Christensen, I Brandslund, EV Appel, RA Scott, J Luan, C Langenberg, NJ Wareham, O Pedersen, A Zorzano, JC Florez, T Hansen, J Ferrer, JM Mercader, D Torrents

Publication Date: 2018-01-22

Variant appearance in text: rs4660293

PubMed Link: 29358691

PubMed Central Link

Variant Present in the following documents:

• 41467_2017_2380_MOESM11_ESM.xlsx

View BVdb publication page

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Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

Plos Genetics

JP Davis, JR Huyghe, AE Locke, AU Jackson, X Sim, HM Stringham, TM Teslovich, RP Welch, C Fuchsberger, N Narisu, PS Chines, AJ Kangas, P Soininen, M Ala-Korpela, J Kuusisto, FS Collins, M Laakso, M Boehnke, KL Mohlke

Publication Date: 2017-10

Variant appearance in text: rs4660293

PubMed Link: 29084231

PubMed Central Link

Variant Present in the following documents:

• pgen.1007079.s011.xlsx
• pgen.1007079.s010.xlsx

View BVdb publication page

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Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.

Nature Genetics

X Lu, GM Peloso, DJ Liu, Y Wu, H Zhang, W Zhou, J Li, CS Tang, R Dorajoo, H Li, J Long, X Guo, M Xu, CN Spracklen, Y Chen, X Liu, Y Zhang, CC Khor, J Liu, L Sun, L Wang, YT Gao, Y Hu, K Yu, Y Wang, CYY Cheung, F Wang, J Huang, Q Fan, Q Cai, S Chen, J Shi, X Yang, W Zhao, WH Sheu, SS Cherny, M He, AB Feranil, LS Adair, P Gordon-Larsen, S Du, R Varma, YI Chen, XO Shu, KSL Lam, TY Wong, SK Ganesh, Z Mo, K Hveem, LG Fritsche, JB Nielsen, HF Tse, Y Huo, CY Cheng, YE Chen, W Zheng, ES Tai, W Gao, X Lin, W Huang, G Abecasis, , S Kathiresan, KL Mohlke, T Wu, PC Sham, D Gu, CJ Willer

Publication Date: 2017-12

Variant appearance in text: rs4660293

PubMed Link: 29083407

PubMed Central Link

Variant Present in the following documents:

• NIHMS909133-supplement-2.xlsx

View BVdb publication page

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Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

Plos One

LC Pilling, JL Atkins, MO Duff, RN Beaumont, SE Jones, J Tyrrell, CL Kuo, KS Ruth, MA Tuke, H Yaghootkar, AR Wood, A Murray, MN Weedon, LW Harries, GA Kuchel, L Ferrucci, TM Frayling, D Melzer

Publication Date: 2017

Variant appearance in text: rs4660293

PubMed Link: 28957414

PubMed Central Link

Variant Present in the following documents:

• pone.0185083.s004.xlsx

View BVdb publication page

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Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study.

Diabetes

L Sobrin, YH Chong, Q Fan, A Gan, LK Stanwyck, G Kaidonis, JE Craig, J Kim, WL Liao, YC Huang, WJ Lee, YJ Hung, X Guo, Y Hai, E Ipp, S Pollack, H Hancock, A Price, A Penman, P Mitchell, G Liew, AV Smith, V Gudnason, G Tan, BEK Klein, J Kuo, X Li, MW Christiansen, BM Psaty, K Sandow, , RA Jensen, R Klein, MF Cotch, JJ Wang, Y Jia, CJ Chen, YI Chen, JI Rotter, FJ Tsai, CL Hanis, KP Burdon, TY Wong, CY Cheng

Publication Date: 2017-12

Variant appearance in text: rs4660293

PubMed Link: 28951389

PubMed Central Link

Variant Present in the following documents:

• DB170398SupplementaryData.pdf

View BVdb publication page

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Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.

Scientific Reports

T Sofer, Q Wong, FP Hartwig, K Taylor, HR Warren, E Evangelou, CP Cabrera, D Levy, H Kramer, LA Lange, BL Horta, , KF Kerr, AP Reiner, N Franceschini

Publication Date: 2017-09-04

Variant appearance in text: rs4660293

PubMed Link: 28871152

PubMed Central Link

Variant Present in the following documents:

• 41598_2017_9019_MOESM1_ESM.pdf

View BVdb publication page

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Evaluating the Causal Relation of ApoA-IV with Disease-Related Traits - A Bidirectional Two-sample Mendelian Randomization Study.

Scientific Reports

S Mack, S Coassin, J Vaucher, F Kronenberg, C Lamina,

Publication Date: 2017-08-18

Variant appearance in text: rs4660293

PubMed Link: 28821713

PubMed Central Link

Variant Present in the following documents:

• 41598_2017_7213_MOESM1_ESM.pdf

View BVdb publication page

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Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.

Hypertension (Dallas, Tex. : 1979)

LV Wain, A Vaez, R Jansen, R Joehanes, PJ van der Most, AM Erzurumluoglu, PF O'Reilly, CP Cabrera, HR Warren, LM Rose, GC Verwoert, JJ Hottenga, RJ Strawbridge, T Esko, DE Arking, SJ Hwang, X Guo, Z Kutalik, S Trompet, N Shrine, A Teumer, JS Ried, JC Bis, AV Smith, N Amin, IM Nolte, LP Lyytikäinen, A Mahajan, NJ Wareham, E Hofer, PK Joshi, K Kristiansson, M Traglia, AS Havulinna, A Goel, MA Nalls, S Sõber, D Vuckovic, J Luan, F Del Greco M, KL Ayers, J Marrugat, D Ruggiero, LM Lopez, T Niiranen, S Enroth, AU Jackson, CP Nelson, JE Huffman, W Zhang, J Marten, I Gandin, SE Harris, T Zemunik, Y Lu, E Evangelou, N Shah, MH de Borst, M Mangino, BP Prins, A Campbell, R Li-Gao, G Chauhan, C Oldmeadow, G Abecasis, M Abedi, CM Barbieri, MR Barnes, C Batini, J Beilby, T Blake, M Boehnke, EP Bottinger, PS Braund, M Brown, M Brumat, H Campbell, JC Chambers, M Cocca, F Collins, J Connell, HJ Cordell, JJ Damman, G Davies, EJ de Geus, R de Mutsert, J Deelen, Y Demirkale, ASF Doney, M Dörr, M Farrall, T Ferreira, M Frånberg, H Gao, V Giedraitis, C Gieger, F Giulianini, AJ Gow, A Hamsten, TB Harris, A Hofman, EG Holliday, J Hui, MR Jarvelin, Å Johansson, AD Johnson, P Jousilahti, A Jula, M Kähönen, S Kathiresan, KT Khaw, I Kolcic, S Koskinen, C Langenberg, M Larson, LJ Launer, B Lehne, DCM Liewald, L Lin, L Lind, F Mach, C Mamasoula, C Menni, B Mifsud, Y Milaneschi, A Morgan, AD Morris, AC Morrison, PJ Munson, P Nandakumar, QT Nguyen, T Nutile, AJ Oldehinkel, BA Oostra, E Org, S Padmanabhan, A Palotie, G Paré, A Pattie, BWJH Penninx, N Poulter, PP Pramstaller, OT Raitakari, M Ren, K Rice, PM Ridker, H Riese, S Ripatti, A Robino, JI Rotter, I Rudan, Y Saba, A Saint Pierre, CF Sala, AP Sarin, R Schmidt, R Scott, MA Seelen, DC Shields, D Siscovick, R Sorice, A Stanton, DJ Stott, J Sundström, M Swertz, KD Taylor, S Thom, I Tzoulaki, C Tzourio, AG Uitterlinden, U Völker, P Vollenweider, S Wild, G Willemsen, AF Wright, J Yao, S Thériault, D Conen, J Attia, P Sever, S Debette, DO Mook-Kanamori, E Zeggini, TD Spector, P van der Harst, CNA Palmer, AC Vergnaud, RJF Loos, O Polasek, JM Starr, G Girotto, C Hayward, JS Kooner, CM Lindgren, V Vitart, NJ Samani, J Tuomilehto, U Gyllensten, P Knekt, IJ Deary, M Ciullo, R Elosua, BD Keavney, AA Hicks, RA Scott, P Gasparini, M Laan, Y Liu, H Watkins, CA Hartman, V Salomaa, D Toniolo, M Perola, JF Wilson, H Schmidt, JH Zhao, T Lehtimäki, CM van Duijn, V Gudnason, BM Psaty, A Peters, R Rettig, A James, JW Jukema, DP Strachan, W Palmas, A Metspalu, E Ingelsson, DI Boomsma, OH Franco, M Bochud, C Newton-Cheh, PB Munroe, P Elliott, DI Chasman, A Chakravarti, J Knight, AP Morris, D Levy, MD Tobin, H Snieder, MJ Caulfield, GB Ehret

Publication Date: 2017-07-24

Variant appearance in text: rs4660293

PubMed Link: 28739976

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.

Lipids In Health And Disease

CS Paththinige, ND Sirisena, V Dissanayake

Publication Date: 2017-06-02

Variant appearance in text: rs4660293

PubMed Link: 28577571

PubMed Central Link

Variant Present in the following documents:

• 12944_2017_488_MOESM2_ESM.xlsx

View BVdb publication page

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Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.

International Journal Of Molecular Medicine

Y Yamada, J Sakuma, I Takeuchi, Y Yasukochi, K Kato, M Oguri, T Fujimaki, H Horibe, M Muramatsu, M Sawabe, Y Fujiwara, Y Taniguchi, S Obuchi, H Kawai, S Shinkai, S Mori, T Arai, M Tanaka

Publication Date: 2017-06

Variant appearance in text: rs4660293

PubMed Link: 28487959

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Common and rare genetic markers of lipid variation in subjects with type 2 diabetes from the ACCORD clinical trial.

Peerj

SW Marvel, DM Rotroff, MJ Wagner, JB Buse, TM Havener, HL McLeod, AA Motsinger-Reif,

Publication Date: 2017

Variant appearance in text: rs4660293

PubMed Link: 28480134

PubMed Central Link

Variant Present in the following documents:

• peerj-05-3187-s002.xlsx

View BVdb publication page

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Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.

Journal Of Cellular And Molecular Medicine

Y Zhu, D Zhang, D Zhou, Z Li, Z Li, L Fang, M Yang, Z Shan, H Li, J Chen, X Zhou, W Ye, S Yu, H Li, L Cai, C Liu, J Zhang, L Wang, Y Lai, L Ruan, Z Sun, S Zhang, H Wang, Y Liu, Y Xu, J Ling, C Xu, Y Zhang, D Lv, Z Yuan, J Zhang, Y Zhang, Y Shi, M Lai

Publication Date: 2017-06

Variant appearance in text: rs4660293

PubMed Link: 28371326

PubMed Central Link

Variant Present in the following documents:

• JCMM-21-1106-s002.xlsx

View BVdb publication page

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Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.

International Journal Of Cancer

H Rodriguez-Broadbent, PJ Law, A Sud, K Palin, S Tuupanen, A Gylfe, UA Hänninen, T Cajuso, T Tanskanen, J Kondelin, E Kaasinen, AP Sarin, S Ripatti, JG Eriksson, H Rissanen, P Knekt, E Pukkala, P Jousilahti, V Salomaa, A Palotie, L Renkonen-Sinisalo, A Lepistö, J Böhm, JP Mecklin, NA Al-Tassan, C Palles, L Martin, E Barclay, SM Farrington, MN Timofeeva, BF Meyer, SM Wakil, H Campbell, CG Smith, S Idziaszczyk, TS Maughan, R Kaplan, R Kerr, D Kerr, MN Passarelli, JC Figueiredo, DD Buchanan, AK Win, JL Hopper, MA Jenkins, NM Lindor, PA Newcomb, S Gallinger, D Conti, F Schumacher, G Casey, LA Aaltonen, JP Cheadle, IP Tomlinson, MG Dunlop, RS Houlston

Publication Date: 2017-06-15

Variant appearance in text: rs4660293

PubMed Link: 28340513

PubMed Central Link

Variant Present in the following documents:

• NIHMS79344-supplement-Supplementary_Data.pdf
• NIHMS79344-supplement-Supplementary_Material.pdf

View BVdb publication page

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Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.

American Journal Of Human Genetics

M Civelek, Y Wu, C Pan, CK Raulerson, A Ko, A He, C Tilford, NK Saleem, A Stančáková, LJ Scott, C Fuchsberger, HM Stringham, AU Jackson, N Narisu, PS Chines, KS Small, J Kuusisto, BW Parks, P Pajukanta, T Kirchgessner, FS Collins, PS Gargalovic, M Boehnke, M Laakso, KL Mohlke, AJ Lusis

Publication Date: 2017-03-02

Variant appearance in text: rs4660293

PubMed Link: 28257690

PubMed Central Link

Variant Present in the following documents:

• mmc3.xlsx

View BVdb publication page

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Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY study.

Scientific Reports

S Christie, S Robiou-du-Pont, SS Anand, KM Morrison, SD McDonald, G Paré, SA Atkinson, KK Teo, D Meyre

Publication Date: 2017-03-06

Variant appearance in text: rs4660293

PubMed Link: 28250428

PubMed Central Link

Variant Present in the following documents:

• 41598_2017_102_MOESM1_ESM.pdf

View BVdb publication page

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Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.

Nature Genetics

LV Wain, N Shrine, MS Artigas, AM Erzurumluoglu, B Noyvert, L Bossini-Castillo, M Obeidat, AP Henry, MA Portelli, RJ Hall, CK Billington, TL Rimington, AG Fenech, C John, T Blake, VE Jackson, RJ Allen, BP Prins, , A Campbell, DJ Porteous, MR Jarvelin, M Wielscher, AL James, J Hui, NJ Wareham, JH Zhao, JF Wilson, PK Joshi, B Stubbe, R Rawal, H Schulz, M Imboden, NM Probst-Hensch, S Karrasch, C Gieger, IJ Deary, SE Harris, J Marten, I Rudan, S Enroth, U Gyllensten, SM Kerr, O Polasek, M Kähönen, I Surakka, V Vitart, C Hayward, T Lehtimäki, OT Raitakari, DM Evans, AJ Henderson, CE Pennell, CA Wang, PD Sly, ES Wan, R Busch, BD Hobbs, AA Litonjua, DW Sparrow, A Gulsvik, PS Bakke, JD Crapo, TH Beaty, NN Hansel, RA Mathias, I Ruczinski, KC Barnes, Y Bossé, P Joubert, M van den Berge, CA Brandsma, PD Paré, DD Sin, DC Nickle, K Hao, O Gottesman, FE Dewey, SE Bruse, DJ Carey, HL Kirchner, , S Jonsson, G Thorleifsson, I Jonsdottir, T Gislason, K Stefansson, C Schurmann, G Nadkarni, EP Bottinger, RJ Loos, RG Walters, Z Chen, IY Millwood, J Vaucher, OP Kurmi, L Li, AL Hansell, C Brightling, E Zeggini, MH Cho, EK Silverman, I Sayers, G Trynka, AP Morris, DP Strachan, IP Hall, MD Tobin

Publication Date: 2017-03

Variant appearance in text: rs4660293

PubMed Link: 28166213

PubMed Central Link

Variant Present in the following documents:

• NIHMS71102-supplement-Supplementary_Tables_3__4__10_and_12.xlsx

View BVdb publication page

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Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention Program.

Circulation. Cardiovascular Genetics

TV Varga, AH Winters, KA Jablonski, ES Horton, P Khare-Ranade, WC Knowler, SM Marcovina, F Renström, KE Watson, R Goldberg, JC Florez, TI Pollin, PW Franks

Publication Date: 2016-12

Variant appearance in text: rs4660293

PubMed Link: 27784733

PubMed Central Link

Variant Present in the following documents:

• NIHMS825913-supplement-001457_-_Supplemental_Material.pdf

View BVdb publication page

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Is High-Density Lipoprotein Cholesterol Causally Related to Kidney Function? Evidence From Genetic Epidemiological Studies.

Arteriosclerosis, Thrombosis, And Vascular Biology

S Coassin, S Friedel, A Köttgen, C Lamina, F Kronenberg

Publication Date: 2016-11

Variant appearance in text: rs4660293

PubMed Link: 27687604

PubMed Central Link

Variant Present in the following documents:

• atv-36-2252-s002.pdf

View BVdb publication page

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Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.

Nature Genetics

C Liu, AT Kraja, JA Smith, JA Brody, N Franceschini, JC Bis, K Rice, AC Morrison, Y Lu, S Weiss, X Guo, W Palmas, LW Martin, YD Chen, P Surendran, F Drenos, JP Cook, PL Auer, AY Chu, A Giri, W Zhao, J Jakobsdottir, LA Lin, JM Stafford, N Amin, H Mei, J Yao, A Voorman, , , , , MG Larson, ML Grove, AV Smith, SJ Hwang, H Chen, T Huan, G Kosova, NO Stitziel, S Kathiresan, N Samani, H Schunkert, P Deloukas, , M Li, C Fuchsberger, C Pattaro, M Gorski, , C Kooperberg, GJ Papanicolaou, JE Rossouw, JD Faul, SL Kardia, C Bouchard, LJ Raffel, AG Uitterlinden, OH Franco, RS Vasan, CJ O'Donnell, KD Taylor, K Liu, EP Bottinger, O Gottesman, EW Daw, F Giulianini, S Ganesh, E Salfati, TB Harris, LJ Launer, M Dörr, SB Felix, R Rettig, H Völzke, E Kim, WJ Lee, IT Lee, WH Sheu, KS Tsosie, DR Edwards, Y Liu, A Correa, DR Weir, U Völker, PM Ridker, E Boerwinkle, V Gudnason, AP Reiner, CM van Duijn, IB Borecki, TL Edwards, A Chakravarti, JI Rotter, BM Psaty, RJ Loos, M Fornage, GB Ehret, C Newton-Cheh, D Levy, DI Chasman

Publication Date: 2016-10

Variant appearance in text: rs4660293

PubMed Link: 27618448

PubMed Central Link

Variant Present in the following documents:

• NIHMS845220-supplement-Supplementary_Figures__Tables__and_Notes.docx
• Main text

View BVdb publication page

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Genetic susceptibility to dyslipidemia and incidence of cardiovascular disease depending on a diet quality index in the Malmö Diet and Cancer cohort.

Genes & Nutrition

S Hellstrand, U Ericson, CA Schulz, I Drake, B Gullberg, B Hedblad, G Engström, M Orho-Melander, E Sonestedt

Publication Date: 2016

Variant appearance in text: rs4660293

PubMed Link: 27551321

PubMed Central Link

Variant Present in the following documents:

• 12263_2016_536_MOESM1_ESM.docx

View BVdb publication page

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Cardiometabolic risk loci share downstream cis- and trans-gene regulation across tissues and diseases.

Science (New York, N.Y.)

O Franzén, R Ermel, A Cohain, NK Akers, A Di Narzo, HA Talukdar, H Foroughi-Asl, C Giambartolomei, JF Fullard, K Sukhavasi, S Köks, LM Gan, C Giannarelli, JC Kovacic, C Betsholtz, B Losic, T Michoel, K Hao, P Roussos, J Skogsberg, A Ruusalepp, EE Schadt, JL Björkegren

Publication Date: 2016-08-19

Variant appearance in text: rs4660293

PubMed Link: 27540175

PubMed Central Link

Variant Present in the following documents:

• NIHMS865440-supplement-Figure_S41.pdf

View BVdb publication page

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Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study.

Plos Medicine

BP Prins, A Abbasi, A Wong, A Vaez, I Nolte, N Franceschini, PE Stuart, J Guterriez Achury, V Mistry, JP Bradfield, AM Valdes, J Bras, A Shatunov, , , , , , , , , , , , , , , C Lu, B Han, S Raychaudhuri, S Bevan, MD Mayes, LC Tsoi, E Evangelou, RP Nair, SF Grant, C Polychronakos, TR Radstake, DA van Heel, ML Dunstan, NW Wood, A Al-Chalabi, A Dehghan, H Hakonarson, HS Markus, JT Elder, J Knight, DE Arking, TD Spector, BP Koeleman, CM van Duijn, J Martin, AP Morris, RK Weersma, C Wijmenga, PB Munroe, JR Perry, JG Pouget, Y Jamshidi, H Snieder, BZ Alizadeh

Publication Date: 2016-06

Variant appearance in text: rs4660293

PubMed Link: 27327646

PubMed Central Link

Variant Present in the following documents:

• pmed.1001976.s002.xlsx
• pmed.1001976.s012.xlsx

View BVdb publication page

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A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits.

Plos One

P Volkov, AH Olsson, L Gillberg, SW Jørgensen, C Brøns, KF Eriksson, L Groop, PA Jansson, E Nilsson, T Rönn, A Vaag, C Ling

Publication Date: 2016

Variant appearance in text: rs4660293

PubMed Link: 27322064

PubMed Central Link

Variant Present in the following documents:

• pone.0157776.s004.xlsx

View BVdb publication page

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Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.

Bmc Genomics

S Ligthart, A Vaez, YH Hsu, , , , R Stolk, AG Uitterlinden, A Hofman, BZ Alizadeh, OH Franco, A Dehghan

Publication Date: 2016-06-10

Variant appearance in text: rs4660293

PubMed Link: 27286809

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution.

Atherosclerosis

AP Patel, GM Peloso, JP Pirruccello, CT Johansen, JB Dubé, DB Larach, MR Ban, GM Dallinge-Thie, N Gupta, M Boehnke, GR Abecasis, JJ Kastelein, GK Hovingh, RA Hegele, DJ Rader, S Kathiresan

Publication Date: 2016-07

Variant appearance in text: rs4660293

PubMed Link: 27182959

PubMed Central Link

Variant Present in the following documents:

• NIHMS787201-supplement.pdf

View BVdb publication page

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Diet Quality and Change in Blood Lipids during 16 Years of Follow-up and Their Interaction with Genetic Risk for Dyslipidemia.

Nutrients

E Sonestedt, S Hellstrand, I Drake, CA Schulz, U Ericson, J Hlebowicz, MM Persson, B Gullberg, B Hedblad, G Engström, M Orho-Melander

Publication Date: 2016-05-09

Variant appearance in text: rs4660293

PubMed Link: 27171109

PubMed Central Link

Variant Present in the following documents:

• nutrients-08-00274-s001.doc

View BVdb publication page

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Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants.

Aging

LC Pilling, JL Atkins, K Bowman, SE Jones, J Tyrrell, RN Beaumont, KS Ruth, MA Tuke, H Yaghootkar, AR Wood, RM Freathy, A Murray, MN Weedon, L Xue, K Lunetta, JM Murabito, LW Harries, JM Robine, C Brayne, GA Kuchel, L Ferrucci, TM Frayling, D Melzer

Publication Date: 2016-03

Variant appearance in text: rs4660293

PubMed Link: 27015805

PubMed Central Link

Variant Present in the following documents:

• aging-08-547-s003.docx

View BVdb publication page

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Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.

Scientific Reports

JE Below, EJ Parra, ER Gamazon, J Torres, S Krithika, S Candille, Y Lu, A Manichakul, J Peralta-Romero, Q Duan, Y Li, AP Morris, O Gottesman, E Bottinger, XQ Wang, KD Taylor, YD Ida Chen, JI Rotter, SS Rich, RJ Loos, H Tang, NJ Cox, M Cruz, CL Hanis, A Valladares-Salgado

Publication Date: 2016-01-19

Variant appearance in text: rs4660293

PubMed Link: 26780889

PubMed Central Link

Variant Present in the following documents:

• srep19429-s2.xls

View BVdb publication page

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Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.

Nature Communications

CS Tang, H Zhang, CY Cheung, M Xu, JC Ho, W Zhou, SS Cherny, Y Zhang, O Holmen, KW Au, H Yu, L Xu, J Jia, RM Porsch, L Sun, W Xu, H Zheng, LY Wong, Y Mu, J Dou, CH Fong, S Wang, X Hong, L Dong, Y Liao, J Wang, LS Lam, X Su, H Yan, ML Yang, J Chen, CW Siu, G Xie, YC Woo, Y Wu, KC Tan, K Hveem, BM Cheung, S Zöllner, A Xu, Y Eugene Chen, CQ Jiang, Y Zhang, TH Lam, SK Ganesh, Y Huo, PC Sham, KS Lam, CJ Willer, HF Tse, W Gao

Publication Date: 2015-12-22

Variant appearance in text: rs4660293

PubMed Link: 26690388

PubMed Central Link

Variant Present in the following documents:

• ncomms10206-s1.pdf

View BVdb publication page

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Assessment of established HDL-C loci for association with HDL-C levels and type 2 diabetes in Pima Indians.

Diabetologia

AK Nair, P Piaggi, NA McLean, M Kaur, S Kobes, WC Knowler, C Bogardus, RL Hanson, LJ Baier

Publication Date: 2016-03

Variant appearance in text: rs4660293

PubMed Link: 26670163

PubMed Central Link

Variant Present in the following documents:

• NIHMS745539-supplement-125_2015_3835_MOESM1_ESM.pdf

View BVdb publication page

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Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.

Nature Communications

FR Day, DA Hinds, JY Tung, L Stolk, U Styrkarsdottir, R Saxena, A Bjonnes, L Broer, DB Dunger, BV Halldorsson, DA Lawlor, G Laval, I Mathieson, WL McCardle, Y Louwers, C Meun, S Ring, RA Scott, P Sulem, AG Uitterlinden, NJ Wareham, U Thorsteinsdottir, C Welt, K Stefansson, JSE Laven, KK Ong, JRB Perry

Publication Date: 2015-09-29

Variant appearance in text: rs4660293

PubMed Link: 26416764

PubMed Central Link

Variant Present in the following documents:

• ncomms9464-s2.xlsx

View BVdb publication page

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The Gut Microbiome Contributes to a Substantial Proportion of the Variation in Blood Lipids.

Circulation Research

J Fu, MJ Bonder, MC Cenit, EF Tigchelaar, A Maatman, JA Dekens, E Brandsma, J Marczynska, F Imhann, RK Weersma, L Franke, TW Poon, RJ Xavier, D Gevers, MH Hofker, C Wijmenga, A Zhernakova

Publication Date: 2015-10-09

Variant appearance in text: rs4660293

PubMed Link: 26358192

PubMed Central Link

Variant Present in the following documents:

• res-117-817-s002.pdf

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Differential Genetic Effects on Statin-Induced Changes Across Low-Density Lipoprotein-Related Measures.

Circulation. Cardiovascular Genetics

AY Chu, F Giulianini, BJ Barratt, B Ding, F Nyberg, S Mora, PM Ridker, DI Chasman

Publication Date: 2015-10

Variant appearance in text: rs4660293

PubMed Link: 26273092

PubMed Central Link

Variant Present in the following documents:

• NIHMS717334-supplement-000962_-_Supplemental_Material.pdf
• Main text
• NIHMS717334-supplement-000962_-_PAP.pdf

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Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.

European Journal Of Human Genetics : Ejhg

X Wang, CY Cheng, J Liao, X Sim, J Liu, KS Chia, ES Tai, P Little, CC Khor, T Aung, TY Wong, YY Teo

Publication Date: 2016-04

Variant appearance in text: rs4660293

PubMed Link: 26130488

PubMed Central Link

Variant Present in the following documents:

• ejhg2015150x4.xls

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Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization Study.

Plos Medicine

SD Østergaard, S Mukherjee, SJ Sharp, P Proitsi, LA Lotta, F Day, JR Perry, KL Boehme, S Walter, JS Kauwe, LE Gibbons, , , , EB Larson, JF Powell, C Langenberg, PK Crane, NJ Wareham, RA Scott

Publication Date: 2015-06

Variant appearance in text: rs4660293

PubMed Link: 26079503

PubMed Central Link

Variant Present in the following documents:

• pmed.1001841.s014.xlsx

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Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease.

Human Genetics

X Zhang, W Zhang, SL Saraf, M Nouraie, J Han, M Gowhari, J Hassan, G Miasnikova, A Sergueeva, S Nekhai, R Kittles, RF Machado, JG Garcia, MT Gladwin, MH Steinberg, P Sebastiani, DA McClain, VR Gordeuk

Publication Date: 2015-08

Variant appearance in text: rs4660293

PubMed Link: 26025476

PubMed Central Link

Variant Present in the following documents:

• NIHMS729106-supplement-Supplemental_Tables.xls

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Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

Human Molecular Genetics

H Kirsten, H Al-Hasani, L Holdt, A Gross, F Beutner, K Krohn, K Horn, P Ahnert, R Burkhardt, K Reiche, J Hackermüller, M Löffler, D Teupser, J Thiery, M Scholz

Publication Date: 2015-08-15

Variant appearance in text: rs4660293

PubMed Link: 26019233

PubMed Central Link

Variant Present in the following documents:

• Main text

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Gender-specific association between the cytoplasmic poly(A) binding protein 4 rs4660293 single nucleotide polymorphism and serum lipid levels.

Molecular Medicine Reports

J Wu, RX Yin, T Guo, QZ Lin, SW Shen, JQ Sun, GY Shi, JZ Wu, DZ Yang, WX Lin

Publication Date: 2015-09

Variant appearance in text: rs4660293

PubMed Link: 26005159

PubMed Central Link

Variant Present in the following documents:

• Main text

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The impact of low-frequency and rare variants on lipid levels.

Nature Genetics

I Surakka, M Horikoshi, R Mägi, AP Sarin, A Mahajan, V Lagou, L Marullo, T Ferreira, B Miraglio, S Timonen, J Kettunen, M Pirinen, J Karjalainen, G Thorleifsson, S Hägg, JJ Hottenga, A Isaacs, C Ladenvall, M Beekman, T Esko, JS Ried, CP Nelson, C Willenborg, S Gustafsson, HJ Westra, M Blades, AJ de Craen, EJ de Geus, J Deelen, H Grallert, A Hamsten, AS Havulinna, C Hengstenberg, JJ Houwing-Duistermaat, E Hyppönen, LC Karssen, T Lehtimäki, V Lyssenko, PK Magnusson, E Mihailov, M Müller-Nurasyid, JP Mpindi, NL Pedersen, BW Penninx, M Perola, TH Pers, A Peters, J Rung, JH Smit, V Steinthorsdottir, MD Tobin, N Tsernikova, EM van Leeuwen, JS Viikari, SM Willems, G Willemsen, H Schunkert, J Erdmann, NJ Samani, J Kaprio, L Lind, C Gieger, A Metspalu, PE Slagboom, L Groop, CM van Duijn, JG Eriksson, A Jula, V Salomaa, DI Boomsma, C Power, OT Raitakari, E Ingelsson, MR Järvelin, U Thorsteinsdottir, L Franke, E Ikonen, O Kallioniemi, V Pietiäinen, CM Lindgren, K Stefansson, A Palotie, MI McCarthy, AP Morris, I Prokopenko, S Ripatti,

Publication Date: 2015-06

Variant appearance in text: rs4660293

PubMed Link: 25961943

PubMed Central Link

Variant Present in the following documents:

• NIHMS67068-supplement-Supplementary_tables_1-7__9-14.docx

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The association between carbohydrate-rich foods and risk of cardiovascular disease is not modified by genetic susceptibility to dyslipidemia as determined by 80 validated variants.

Plos One

E Sonestedt, S Hellstrand, CA Schulz, P Wallström, I Drake, U Ericson, B Gullberg, B Hedblad, M Orho-Melander

Publication Date: 2015

Variant appearance in text: rs4660293

PubMed Link: 25898210

PubMed Central Link

Variant Present in the following documents:

• pone.0126104.s004.doc

View BVdb publication page

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Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein.

Plos One

S Ligthart, PS de Vries, AG Uitterlinden, A Hofman, , OH Franco, DI Chasman, A Dehghan

Publication Date: 2015

Variant appearance in text: rs4660293

PubMed Link: 25768928

PubMed Central Link

Variant Present in the following documents:

• Main text
• pone.0118859.s004.docx
• pone.0118859.s003.docx

View BVdb publication page

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Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.

Nature Communications

B Benyamin, T Esko, JS Ried, A Radhakrishnan, SH Vermeulen, M Traglia, M Gögele, D Anderson, L Broer, C Podmore, J Luan, Z Kutalik, S Sanna, P van der Meer, T Tanaka, F Wang, HJ Westra, L Franke, E Mihailov, L Milani, J Hälldin, J Häldin, J Winkelmann, T Meitinger, J Thiery, A Peters, M Waldenberger, A Rendon, J Jolley, J Sambrook, LA Kiemeney, FC Sweep, CF Sala, C Schwienbacher, I Pichler, J Hui, A Demirkan, A Isaacs, N Amin, M Steri, G Waeber, N Verweij, JE Powell, DR Nyholt, AC Heath, PA Madden, PM Visscher, MJ Wright, GW Montgomery, NG Martin, D Hernandez, S Bandinelli, P van der Harst, M Uda, P Vollenweider, RA Scott, C Langenberg, NJ Wareham, , C van Duijn, J Beilby, PP Pramstaller, AA Hicks, WH Ouwehand, K Oexle, C Gieger, A Metspalu, C Camaschella, D Toniolo, DW Swinkels, JB Whitfield

Publication Date: 2014-10-29

Variant appearance in text: rs4660293

PubMed Link: 25352340

PubMed Central Link

Variant Present in the following documents:

• NIHMS619770-supplement-1.pdf

View BVdb publication page

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Using multivariable Mendelian randomization to disentangle the causal effects of lipid fractions.

Plos One

S Burgess, DF Freitag, H Khan, DN Gorman, SG Thompson

Publication Date: 2014

Variant appearance in text: rs4660293

PubMed Link: 25302496

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a Mendelian randomization analysis.

Plos Medicine

P Proitsi, MK Lupton, L Velayudhan, S Newhouse, I Fogh, M Tsolaki, M Daniilidou, M Pritchard, I Kloszewska, H Soininen, P Mecocci, B Vellas, , J Williams, , R Stewart, P Sham, S Lovestone, JF Powell

Publication Date: 2014-09

Variant appearance in text: rs4660293

PubMed Link: 25226301

PubMed Central Link

Variant Present in the following documents:

• pmed.1001713.s003.xlsx

View BVdb publication page

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Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study.

Plos Genetics

TV Varga, E Sonestedt, D Shungin, RW Koivula, G Hallmans, SA Escher, I Barroso, P Nilsson, O Melander, M Orho-Melander, F Renström, PW Franks

Publication Date: 2014-06

Variant appearance in text: rs4660293

PubMed Link: 24922540

PubMed Central Link

Variant Present in the following documents:

• pgen.1004388.s003.xlsx
• pgen.1004388.s005.pdf

View BVdb publication page

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Mapping the genetic architecture of gene regulation in whole blood.

Plos One

K Schramm, C Marzi, C Schurmann, M Carstensen, E Reinmaa, R Biffar, G Eckstein, C Gieger, HJ Grabe, G Homuth, G Kastenmüller, R Mägi, A Metspalu, E Mihailov, A Peters, A Petersmann, M Roden, K Strauch, K Suhre, A Teumer, U Völker, H Völzke, R Wang-Sattler, M Waldenberger, T Meitinger, T Illig, C Herder, H Grallert, H Prokisch

Publication Date: 2014

Variant appearance in text: rs4660293

PubMed Link: 24740359

PubMed Central Link

Variant Present in the following documents:

• pone.0093844.s005.xls

View BVdb publication page

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Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids.

Genome Medicine

SY Shin, AK Petersen, S Wahl, G Zhai, W Römisch-Margl, KS Small, A Döring, BS Kato, A Peters, E Grundberg, C Prehn, R Wang-Sattler, HE Wichmann, MH de Angelis, T Illig, J Adamski, P Deloukas, TD Spector, K Suhre, C Gieger, N Soranzo

Publication Date: 2014

Variant appearance in text: rs4660293

PubMed Link: 24678845

PubMed Central Link

Variant Present in the following documents:

• gm542-S1.xlsx

View BVdb publication page

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Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants.

The Application Of Clinical Genetics

S Sayols-Baixeras, C Lluís-Ganella, G Lucas, R Elosua

Publication Date: 2014

Variant appearance in text: rs4660293

PubMed Link: 24520200

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Discovery and refinement of loci associated with lipid levels.

Nature Genetics

CJ Willer, EM Schmidt, S Sengupta, GM Peloso, S Gustafsson, S Kanoni, A Ganna, J Chen, ML Buchkovich, S Mora, JS Beckmann, JL Bragg-Gresham, HY Chang, A Demirkan, HM Den Hertog, R Do, LA Donnelly, GB Ehret, T Esko, MF Feitosa, T Ferreira, K Fischer, P Fontanillas, RM Fraser, DF Freitag, D Gurdasani, K Heikkilä, E Hyppönen, A Isaacs, AU Jackson, Å Johansson, T Johnson, M Kaakinen, J Kettunen, ME Kleber, X Li, J Luan, LP Lyytikäinen, PKE Magnusson, M Mangino, E Mihailov, ME Montasser, M Müller-Nurasyid, IM Nolte, JR O'Connell, CD Palmer, M Perola, AK Petersen, S Sanna, R Saxena, SK Service, S Shah, D Shungin, C Sidore, C Song, RJ Strawbridge, I Surakka, T Tanaka, TM Teslovich, G Thorleifsson, EG Van den Herik, BF Voight, KA Volcik, LL Waite, A Wong, Y Wu, W Zhang, D Absher, G Asiki, I Barroso, LF Been, JL Bolton, LL Bonnycastle, P Brambilla, MS Burnett, G Cesana, M Dimitriou, ASF Doney, A Döring, P Elliott, SE Epstein, G Ingi Eyjolfsson, B Gigante, MO Goodarzi, H Grallert, ML Gravito, CJ Groves, G Hallmans, AL Hartikainen, C Hayward, D Hernandez, AA Hicks, H Holm, YJ Hung, T Illig, MR Jones, P Kaleebu, JJP Kastelein, KT Khaw, E Kim, N Klopp, P Komulainen, M Kumari, C Langenberg, T Lehtimäki, SY Lin, J Lindström, RJF Loos, F Mach, WL McArdle, C Meisinger, BD Mitchell, G Müller, R Nagaraja, N Narisu, TVM Nieminen, RN Nsubuga, I Olafsson, KK Ong, A Palotie, T Papamarkou, C Pomilla, A Pouta, DJ Rader, MP Reilly, PM Ridker, F Rivadeneira, I Rudan, A Ruokonen, N Samani, H Scharnagl, J Seeley, K Silander, A Stančáková, K Stirrups, AJ Swift, L Tiret, AG Uitterlinden, LJ van Pelt, S Vedantam, N Wainwright, C Wijmenga, SH Wild, G Willemsen, T Wilsgaard, JF Wilson, EH Young, JH Zhao, LS Adair, D Arveiler, TL Assimes, S Bandinelli, F Bennett, M Bochud, BO Boehm, DI Boomsma, IB Borecki, SR Bornstein, P Bovet, M Burnier, H Campbell, A Chakravarti, JC Chambers, YI Chen, FS Collins, RS Cooper, J Danesh, G Dedoussis, U de Faire, AB Feranil, J Ferrières, L Ferrucci, NB Freimer, C Gieger, LC Groop, V Gudnason, U Gyllensten, A Hamsten, TB Harris, A Hingorani, JN Hirschhorn, A Hofman, GK Hovingh, CA Hsiung, SE Humphries, SC Hunt, K Hveem, C Iribarren, MR Järvelin, A Jula, M Kähönen, J Kaprio, A Kesäniemi, M Kivimaki, JS Kooner, PJ Koudstaal, RM Krauss, D Kuh, J Kuusisto, KO Kyvik, M Laakso, TA Lakka, L Lind, CM Lindgren, NG Martin, W März, MI McCarthy, CA McKenzie, P Meneton, A Metspalu, L Moilanen, AD Morris, PB Munroe, I Njølstad, NL Pedersen, C Power, PP Pramstaller, JF Price, BM Psaty, T Quertermous, R Rauramaa, D Saleheen, V Salomaa, DK Sanghera, J Saramies, PEH Schwarz, WH Sheu, AR Shuldiner, A Siegbahn, TD Spector, K Stefansson, DP Strachan, BO Tayo, E Tremoli, J Tuomilehto, M Uusitupa, CM van Duijn, P Vollenweider, L Wallentin, NJ Wareham, JB Whitfield, BHR Wolffenbuttel, JM Ordovas, E Boerwinkle, CNA Palmer, U Thorsteinsdottir, DI Chasman, JI Rotter, PW Franks, S Ripatti, LA Cupples, MS Sandhu, SS Rich, M Boehnke, P Deloukas, S Kathiresan, KL Mohlke, E Ingelsson, GR Abecasis,

Publication Date: 2013-11

Variant appearance in text: rs4660293

PubMed Link: 24097068

PubMed Central Link

Variant Present in the following documents:

• NIHMS524703-supplement-1.pdf

View BVdb publication page

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Common variants associated with plasma triglycerides and risk for coronary artery disease.

Nature Genetics

R Do, CJ Willer, EM Schmidt, S Sengupta, C Gao, GM Peloso, S Gustafsson, S Kanoni, A Ganna, J Chen, ML Buchkovich, S Mora, JS Beckmann, JL Bragg-Gresham, HY Chang, A Demirkan, HM Den Hertog, LA Donnelly, GB Ehret, T Esko, MF Feitosa, T Ferreira, K Fischer, P Fontanillas, RM Fraser, DF Freitag, D Gurdasani, K Heikkilä, E Hyppönen, A Isaacs, AU Jackson, A Johansson, T Johnson, M Kaakinen, J Kettunen, ME Kleber, X Li, J Luan, LP Lyytikäinen, PK Magnusson, M Mangino, E Mihailov, ME Montasser, M Müller-Nurasyid, IM Nolte, JR O'Connell, CD Palmer, M Perola, AK Petersen, S Sanna, R Saxena, SK Service, S Shah, D Shungin, C Sidore, C Song, RJ Strawbridge, I Surakka, T Tanaka, TM Teslovich, G Thorleifsson, EG Van den Herik, BF Voight, KA Volcik, LL Waite, A Wong, Y Wu, W Zhang, D Absher, G Asiki, I Barroso, LF Been, JL Bolton, LL Bonnycastle, P Brambilla, MS Burnett, G Cesana, M Dimitriou, AS Doney, A Döring, P Elliott, SE Epstein, GI Eyjolfsson, B Gigante, MO Goodarzi, H Grallert, ML Gravito, CJ Groves, G Hallmans, AL Hartikainen, C Hayward, D Hernandez, AA Hicks, H Holm, YJ Hung, T Illig, MR Jones, P Kaleebu, JJ Kastelein, KT Khaw, E Kim, N Klopp, P Komulainen, M Kumari, C Langenberg, T Lehtimäki, SY Lin, J Lindström, RJ Loos, F Mach, WL McArdle, C Meisinger, BD Mitchell, G Müller, R Nagaraja, N Narisu, TV Nieminen, RN Nsubuga, I Olafsson, KK Ong, A Palotie, T Papamarkou, C Pomilla, A Pouta, DJ Rader, MP Reilly, PM Ridker, F Rivadeneira, I Rudan, A Ruokonen, N Samani, H Scharnagl, J Seeley, K Silander, A Stančáková, K Stirrups, AJ Swift, L Tiret, AG Uitterlinden, LJ van Pelt, S Vedantam, N Wainwright, C Wijmenga, SH Wild, G Willemsen, T Wilsgaard, JF Wilson, EH Young, JH Zhao, LS Adair, D Arveiler, TL Assimes, S Bandinelli, F Bennett, M Bochud, BO Boehm, DI Boomsma, IB Borecki, SR Bornstein, P Bovet, M Burnier, H Campbell, A Chakravarti, JC Chambers, YD Chen, FS Collins, RS Cooper, J Danesh, G Dedoussis, U de Faire, AB Feranil, J Ferrières, L Ferrucci, NB Freimer, C Gieger, LC Groop, V Gudnason, U Gyllensten, A Hamsten, TB Harris, A Hingorani, JN Hirschhorn, A Hofman, GK Hovingh, CA Hsiung, SE Humphries, SC Hunt, K Hveem, C Iribarren, MR Järvelin, A Jula, M Kähönen, J Kaprio, A Kesäniemi, M Kivimaki, JS Kooner, PJ Koudstaal, RM Krauss, D Kuh, J Kuusisto, KO Kyvik, M Laakso, TA Lakka, L Lind, CM Lindgren, NG Martin, W März, MI McCarthy, CA McKenzie, P Meneton, A Metspalu, L Moilanen, AD Morris, PB Munroe, I Njølstad, NL Pedersen, C Power, PP Pramstaller, JF Price, BM Psaty, T Quertermous, R Rauramaa, D Saleheen, V Salomaa, DK Sanghera, J Saramies, PE Schwarz, WH Sheu, AR Shuldiner, A Siegbahn, TD Spector, K Stefansson, DP Strachan, BO Tayo, E Tremoli, J Tuomilehto, M Uusitupa, CM van Duijn, P Vollenweider, L Wallentin, NJ Wareham, JB Whitfield, BH Wolffenbuttel, D Altshuler, JM Ordovas, E Boerwinkle, CN Palmer, U Thorsteinsdottir, DI Chasman, JI Rotter, PW Franks, S Ripatti, LA Cupples, MS Sandhu, SS Rich, M Boehnke, P Deloukas, KL Mohlke, E Ingelsson, GR Abecasis, MJ Daly, BM Neale, S Kathiresan

Publication Date: 2013-11

Variant appearance in text: rs4660293

PubMed Link: 24097064

PubMed Central Link

Variant Present in the following documents:

• NIHMS524704-supplement-1.pdf

View BVdb publication page

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A multiethnic replication study of plasma lipoprotein levels-associated SNPs identified in recent GWAS.

Plos One

EK Bryant, AS Dressen, CH Bunker, JE Hokanson, RF Hamman, MI Kamboh, FY Demirci

Publication Date: 2013

Variant appearance in text: rs4660293

PubMed Link: 23717430

PubMed Central Link

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.

Journal Of Medical Genetics

D Weissglas-Volkov, CA Aguilar-Salinas, E Nikkola, KA Deere, I Cruz-Bautista, O Arellano-Campos, LL Muñoz-Hernandez, L Gomez-Munguia, ML Ordoñez-Sánchez, PM Reddy, AJ Lusis, N Matikainen, MR Taskinen, L Riba, RM Cantor, JS Sinsheimer, T Tusie-Luna, P Pajukanta

Publication Date: 2013-05

Variant appearance in text: rs4660293

PubMed Link: 23505323

PubMed Central Link

Variant Present in the following documents:

• NIHMS454100-supplement-Supplementary_Table6.xls

View BVdb publication page

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Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000372856.3	c.1582-92T>C	-	intron_variant	-	11/14
ENST00000372857.3	c.1621-92T>C	-	intron_variant	-	12/15
ENST00000372858.3	c.1669-92T>C	-	intron_variant	-	12/15
ENST00000372862.3	c.1534-92T>C	-	intron_variant	-	11/14
ENST00000421687.2	c.1374-128T>C	-	intron_variant	-	11/13
ENST00000437136.1	c.285-92T>C	-	intron_variant	-	3/6
ENST00000468476.1	n.2019T>C	-	non_coding_transcript_exon_variant	1/2	-
ENST00000484555.1	n.418-92T>C	-	intron_variant,non_coding_transcript_variant	-	2/2
ENST00000492468.1	n.1531T>C	-	non_coding_transcript_exon_variant	1/4	-
NM_001135653.2	c.1669-92T>C	-	intron_variant	-	12/15
NM_001135654.2	c.1582-92T>C	-	intron_variant	-	11/14
NM_003819.4	c.1621-92T>C	-	intron_variant	-	12/15