Publications:

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Genetics of Hypertriglyceridemia.

Frontiers In Endocrinology

JS Dron, RA Hegele

Publication Date: 2020

Variant appearance in text: rs4846914

PubMed Link: 32793115

Variant Present in the following documents:

• Main text

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: rs4846914

PubMed Link: 31719535

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: rs4846914

PubMed Link: 31596850

Variant Present in the following documents:

• pgen.1008431.s006.xls
• pgen.1008431.s007.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: rs4846914

PubMed Link: 31551469

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: rs4846914

PubMed Link: 31551420

Variant Present in the following documents:

• 41467_2019_12026_MOESM1_ESM.pdf

View BVdb publication page

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Allele-specific enhancers mediate associations between LCAT and ABCA1 polymorphisms and HDL metabolism.

Plos One

AD Howard, X Wang, M Prasad, AD Sahu, R Aniba, M Miller, S Hannenhalli, YC Chang

Publication Date: 2019

Variant appearance in text: rs4846914

PubMed Link: 31039173

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetics-driven discovery of novel regulators of lipid metabolism.

Current Opinion In Lipidology

EE Ha, AG Van Camp, RC Bauer

Publication Date: 2019-06

Variant appearance in text: rs4846914

PubMed Link: 30985365

Variant Present in the following documents:

• Main text

View BVdb publication page

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Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.

Nature Communications

F Allum, ÅK Hedman, X Shao, WA Cheung, J Vijay, F Guénard, T Kwan, MM Simon, B Ge, C Moura, E Boulier, L Rönnblom, S Bernatsky, M Lathrop, MI McCarthy, P Deloukas, A Tchernof, T Pastinen, MC Vohl, E Grundberg

Publication Date: 2019-03-14

Variant appearance in text: rs4846914

PubMed Link: 30872577

Variant Present in the following documents:

• Main text

View BVdb publication page

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Identifying genetic markers associated with susceptibility to cardiovascular diseases.

Future Science Oa

H Shukla, JL Mason, A Sabyah

Publication Date: 2019-01

Variant appearance in text: rs4846914

PubMed Link: 30652019

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: rs4846914

PubMed Link: 30565958

Variant Present in the following documents:

• Main text
• nihms-1512616.pdf
• 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: rs4846914

PubMed Link: 30504769

Variant Present in the following documents:

• 41467_2018_7460_MOESM12_ESM.xlsx

View BVdb publication page

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CETP genetic variant rs1800777 (allele A) is associated with abnormally low HDL-C levels and increased risk of AKI during sepsis.

Scientific Reports

KR Genga, M Trinder, HJ Kong, X Li, AKK Leung, T Shimada, KR Walley, JA Russell, GA Francis, LR Brunham, JH Boyd

Publication Date: 2018-11-13

Variant appearance in text: rs4846914

PubMed Link: 30425299

Variant Present in the following documents:

• 41598_2018_35261_MOESM1_ESM.doc

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: rs4846914

PubMed Link: 29986042

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: rs4846914

PubMed Link: 29973585

Variant Present in the following documents:

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

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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: rs4846914

PubMed Link: 29531354

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: rs4846914

PubMed Link: 29531326

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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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: rs4846914

PubMed Link: 29375475

Variant Present in the following documents:

• Main text

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: rs4846914

PubMed Link: 29084231

Variant Present in the following documents:

• 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: rs4846914

PubMed Link: 29083407

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: rs4846914

PubMed Link: 28957414

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: rs4846914

PubMed Link: 28951389

Variant Present in the following documents:

• DB170398SupplementaryData.pdf

View BVdb publication page

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Polygenic determinants in extremes of high-density lipoprotein cholesterol.

Journal Of Lipid Research

JS Dron, J Wang, C Low-Kam, SA Khetarpal, JF Robinson, AD McIntyre, MR Ban, H Cao, D Rhainds, MP Dubé, DJ Rader, G Lettre, JC Tardif, RA Hegele

Publication Date: 2017-11

Variant appearance in text: rs4846914

PubMed Link: 28870971

Variant Present in the following documents:

• Main text

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: rs4846914

PubMed Link: 28821713

Variant Present in the following documents:

• 41598_2017_7213_MOESM1_ESM.pdf

View BVdb publication page

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Data to genetic risk assessment on high-density cholesterol level associated polymorphisms in Hungarian general and Roma populations.

Data In Brief

P Pikó, S Fiatal, Z Kósa, J Sándor, R Ádány

Publication Date: 2017-10

Variant appearance in text: rs4846914

PubMed Link: 28795114

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: rs4846914

PubMed Link: 28577571

Variant Present in the following documents:

• 12944_2017_488_MOESM1_ESM.xlsx
• aaaaaMain 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: rs4846914

PubMed Link: 28480134

Variant Present in the following documents:

• peerj-05-3187-s002.xlsx

View BVdb publication page

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Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.

Human Molecular Genetics

N Zubair, M Graff, J Luis Ambite, WS Bush, G Kichaev, Y Lu, A Manichaikul, WH Sheu, D Absher, TL Assimes, SJ Bielinski, EP Bottinger, P Buzkova, LM Chuang, RH Chung, B Cochran, L Dumitrescu, O Gottesman, JW Haessler, C Haiman, G Heiss, CA Hsiung, YJ Hung, CM Hwu, JJ Juang, L Le Marchand, IT Lee, WJ Lee, LA Lin, D Lin, SY Lin, RH Mackey, LW Martin, B Pasaniuc, U Peters, I Predazzi, T Quertermous, AP Reiner, J Robinson, JI Rotter, KK Ryckman, PJ Schreiner, E Stahl, R Tao, MY Tsai, LL Waite, TD Wang, S Buyske, YD Ida Chen, I Cheng, DC Crawford, RJF Loos, SS Rich, M Fornage, KE North, C Kooperberg, CL Carty

Publication Date: 2016-12-15

Variant appearance in text: rs4846914

PubMed Link: 28426890

Variant Present in the following documents:

• ddw358_supp.docx

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: rs4846914

PubMed Link: 28371326

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: rs4846914

PubMed Link: 28340513

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: rs4846914

PubMed Link: 28257690

Variant Present in the following documents:

• Main text
• mmc3.xlsx
• mmc8.pdf

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: rs4846914

PubMed Link: 28250428

Variant Present in the following documents:

• 41598_2017_102_MOESM1_ESM.pdf

View BVdb publication page

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Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters.

Cell

BM Javierre, OS Burren, SP Wilder, R Kreuzhuber, SM Hill, S Sewitz, J Cairns, SW Wingett, C Várnai, MJ Thiecke, F Burden, S Farrow, AJ Cutler, K Rehnström, K Downes, L Grassi, M Kostadima, P Freire-Pritchett, F Wang, , HG Stunnenberg, JA Todd, DR Zerbino, O Stegle, WH Ouwehand, M Frontini, C Wallace, M Spivakov, P Fraser

Publication Date: 2016-11-17

Variant appearance in text: rs4846914

PubMed Link: 27863249

Variant Present in the following documents:

• mmc3.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: rs4846914

PubMed Link: 27784733

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: rs4846914

PubMed Link: 27687604

Variant Present in the following documents:

• atv-36-2252-s002.pdf

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: rs4846914

PubMed Link: 27551321

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: rs4846914

PubMed Link: 27540175

Variant Present in the following documents:

• NIHMS865440-supplement-Figure_S41.pdf

View BVdb publication page

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Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents.

Cell Metabolism

SA Khetarpal, KT Schjoldager, C Christoffersen, A Raghavan, AC Edmondson, HM Reutter, B Ahmed, R Ouazzani, GM Peloso, C Vitali, W Zhao, AV Somasundara, JS Millar, Y Park, G Fernando, V Livanov, S Choi, E Noé, P Patel, SP Ho, , TG Kirchgessner, HH Wandall, L Hansen, EP Bennett, SY Vakhrushev, D Saleheen, S Kathiresan, CD Brown, R Abou Jamra, E LeGuern, H Clausen, DJ Rader

Publication Date: 2016-08-09

Variant appearance in text: rs4846914

PubMed Link: 27508872

Variant Present in the following documents:

• Main text
• NIHMS807282-supplement-1.pdf

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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: rs4846914

PubMed Link: 27182959

Variant Present in the following documents:

• NIHMS787201-supplement.pdf

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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: rs4846914

PubMed Link: 27171109

Variant Present in the following documents:

• nutrients-08-00274-s001.doc

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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: rs4846914

PubMed Link: 27015805

Variant Present in the following documents:

• aging-08-547-s003.docx

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Interaction of Insulin Resistance and Related Genetic Variants With Triglyceride-Associated Genetic Variants.

Circulation. Cardiovascular Genetics

YC Klimentidis, A Arora

Publication Date: 2016-04

Variant appearance in text: rs4846914

PubMed Link: 26850992

Variant Present in the following documents:

• NIHMS758238-supplement-001246_-_Supplemental_Material.pdf

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Looking beyond GWAS: allele-specific transcription factor binding drives the association of GALNT2 to HDL-C plasma levels.

Lipids In Health And Disease

M Cavalli, G Pan, H Nord, C Wadelius

Publication Date: 2016-01-27

Variant appearance in text: rs4846914

PubMed Link: 26817450

Variant Present in the following documents:

• Main text

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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: rs4846914

PubMed Link: 26780889

Variant Present in the following documents:

• srep19429-s2.xls

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Association between the DOCK7, PCSK9 and GALNT2 Gene Polymorphisms and Serum Lipid levels.

Scientific Reports

T Guo, RX Yin, F Huang, LM Yao, WX Lin, SL Pan

Publication Date: 2016-01-08

Variant appearance in text: rs4846914

PubMed Link: 26744084

Variant Present in the following documents:

• Main text

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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: rs4846914

PubMed Link: 26690388

Variant Present in the following documents:

• ncomms10206-s1.pdf

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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: rs4846914

PubMed Link: 26670163

Variant Present in the following documents:

• NIHMS745539-supplement-125_2015_3835_MOESM1_ESM.pdf
• NIHMS745539-supplement-125_2015_3835_MOESM2_ESM.pdf

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Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol.

American Journal Of Human Genetics

TS Roman, AF Marvelle, MP Fogarty, S Vadlamudi, AJ Gonzalez, ML Buchkovich, JR Huyghe, C Fuchsberger, AU Jackson, Y Wu, M Civelek, AJ Lusis, KJ Gaulton, P Sethupathy, AJ Kangas, P Soininen, M Ala-Korpela, J Kuusisto, FS Collins, M Laakso, M Boehnke, KL Mohlke

Publication Date: 2015-12-03

Variant appearance in text: rs4846914

PubMed Link: 26637976

Variant Present in the following documents:

• Main text
• mmc1.pdf
• mmc2.pdf

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Discovery of phenotypic networks from genotypic association studies with application to obesity.

International Journal Of Data Mining And Bioinformatics

CW Duarte, YC Klimentidis, JJ Harris, M Cardel, JR Fernández

Publication Date: 2015

Variant appearance in text: rs4846914

PubMed Link: 26510299

Variant Present in the following documents:

• NIHMS738263-supplement-Supplemental_tables.docx

View BVdb publication page

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Association of the variants and haplotypes in the DOCK7, PCSK9 and GALNT2 genes and the risk of hyperlipidaemia.

Journal Of Cellular And Molecular Medicine

T Guo, RX Yin, WX Lin, W Wang, F Huang, SL Pan

Publication Date: 2016-02

Variant appearance in text: rs4846914

PubMed Link: 26493351

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genomic and transcriptomic predictors of triglyceride response to regular exercise.

British Journal Of Sports Medicine

MA Sarzynski, PK Davidsen, YJ Sung, MK Hesselink, P Schrauwen, TK Rice, DC Rao, F Falciani, C Bouchard

Publication Date: 2015-12

Variant appearance in text: rs4846914

PubMed Link: 26491034

Variant Present in the following documents:

• NIHMS735601-supplement-Supplementary_Material.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: rs4846914

PubMed Link: 26416764

Variant Present in the following documents:

• ncomms9464-s2.xlsx

View BVdb publication page

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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: rs4846914

PubMed Link: 26273092

Variant Present in the following documents:

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

View BVdb publication page

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The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data.

Plos One

A Ferrarini, L Xumerle, F Griggio, M Garonzi, C Cantaloni, C Centomo, SM Vargas, P Descombes, J Marquis, S Collino, C Franceschi, P Garagnani, BA Salisbury, JM Harvey, M Delledonne

Publication Date: 2015

Variant appearance in text: rs4846914

PubMed Link: 26147798

Variant Present in the following documents:

• pone.0132180.s006.xlsx

View BVdb publication page

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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: rs4846914

PubMed Link: 26130488

Variant Present in the following documents:

• ejhg2015150x4.xls

View BVdb publication page

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Apolipoprotein E and protection against hepatitis E viral infection in American non-Hispanic blacks.

Hepatology (Baltimore, Md.)

L Zhang, A Yesupriya, MH Chang, E Teshale, CG Teo

Publication Date: 2015-11

Variant appearance in text: rs4846914

PubMed Link: 26096528

Variant Present in the following documents:

• NIHMS1043972-supplement-Supplemental.pdf

View BVdb publication page

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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: rs4846914

PubMed Link: 26079503

Variant Present in the following documents:

• pmed.1001841.s014.xlsx

View BVdb publication page

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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: rs4846914

PubMed Link: 26025476

Variant Present in the following documents:

• NIHMS729106-supplement-Supplemental_Tables.xls

View BVdb publication page

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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: rs4846914

PubMed Link: 25961943

Variant Present in the following documents:

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

View BVdb publication page

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Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array.

European Journal Of Human Genetics : Ejhg

S Rodriguez, TR Gaunt, Y Guo, J Zheng, MR Barnes, W Tang, F Danish, A Johnson, BA Castillo, YR Li, H Hakonarson, SG Buxbaum, T Palmer, MY Tsai, LA Lange, S Ebrahim, G Davey Smith, DA Lawlor, AR Folsom, R Hoogeveen, A Reiner, B Keating, IN Day

Publication Date: 2016-01

Variant appearance in text: rs4846914

PubMed Link: 25920552

Variant Present in the following documents:

• ejhg201563x1.doc

View BVdb publication page

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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: rs4846914

PubMed Link: 25898210

Variant Present in the following documents:

• pone.0126104.s004.doc

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: rs4846914

PubMed Link: 25352340

Variant Present in the following documents:

• NIHMS619770-supplement-1.pdf

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: rs4846914

PubMed Link: 25226301

Variant Present in the following documents:

• pmed.1001713.s003.xlsx

View BVdb publication page

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Adiposity significantly modifies genetic risk for dyslipidemia.

Journal Of Lipid Research

CB Cole, M Nikpay, P Lau, AF Stewart, RW Davies, GA Wells, R Dent, R McPherson

Publication Date: 2014-11

Variant appearance in text: rs4846914

PubMed Link: 25225679

Variant Present in the following documents:

• Main text

View BVdb publication page

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Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease.

Circulation. Cardiovascular Genetics

H Tada, HH Won, O Melander, J Yang, GM Peloso, S Kathiresan

Publication Date: 2014-10

Variant appearance in text: rs4846914

PubMed Link: 25170055

Variant Present in the following documents:

• NIHMS664832-supplement-supplement.doc

View BVdb publication page

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Extension of GWAS results for lipid-related phenotypes to extreme obesity using electronic health record (EHR) data and the Metabochip.

Frontiers In Genetics

A Parihar, GC Wood, X Chu, Q Jin, G Argyropoulos, CD Still, AR Shuldiner, BD Mitchell, GS Gerhard

Publication Date: 2014

Variant appearance in text: rs4846914

PubMed Link: 25147553

Variant Present in the following documents:

• Main text

View BVdb publication page

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Strategies to fine-map genetic associations with lipid levels by combining epigenomic annotations and liver-specific transcription profiles.

Genomics

KS Lo, S Vadlamudi, MP Fogarty, KL Mohlke, G Lettre

Publication Date: 2014-08

Variant appearance in text: rs4846914

PubMed Link: 24997396

Variant Present in the following documents:

• Main text

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: rs4846914

PubMed Link: 24922540

Variant Present in the following documents:

• pgen.1004388.s001.xlsx
• pgen.1004388.s003.xlsx
• pgen.1004388.s005.pdf

View BVdb publication page

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Genetic predisposition scores for dyslipidaemia influence plasma lipid concentrations at baseline, but not the changes after controlled intake of n-3 polyunsaturated fatty acids.

Genes & Nutrition

A AlSaleh, Z Maniou, FJ Lewis, WL Hall, TA Sanders, SD O'Dell

Publication Date: 2014-07

Variant appearance in text: rs4846914

PubMed Link: 24890013

Variant Present in the following documents:

• 12263_2014_412_MOESM1_ESM.pdf
• 12263_2014_412_MOESM2_ESM.pdf
• 12263_2014_412_MOESM3_ESM.pdf
• 12263_2014_412_MOESM4_ESM.pdf

View BVdb publication page

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A Simple Scalable Association Hypothesis Test Combining Gene-wide Evidence From Multiple Polymorphisms.

British Journal Of Medicine And Medical Research

D Vaidya, LR Yanek, RA Mathias, TF Moy, DM Becker, LC Becker

Publication Date: 2014-03

Variant appearance in text: rs4846914

PubMed Link: 24688980

Variant Present in the following documents:

• Main text

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: rs4846914

PubMed Link: 24678845

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: rs4846914

PubMed Link: 24520200

Variant Present in the following documents:

• Main text

View BVdb publication page

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A genome wide association study identifies common variants associated with lipid levels in the Chinese population.

Plos One

L Zhou, M He, Z Mo, C Wu, H Yang, D Yu, X Yang, X Zhang, Y Wang, J Sun, Y Gao, A Tan, Y He, H Zhang, X Qin, J Zhu, H Li, X Lin, J Zhu, X Min, M Lang, D Li, K Zhai, J Chang, W Tan, J Yuan, W Chen, Y Wang, S Wei, X Miao, F Wang, W Fang, Y Liang, Q Deng, X Dai, D Lin, S Huang, H Guo, S Lilly Zheng, J Xu, D Lin, FB Hu, T Wu

Publication Date: 2013

Variant appearance in text: rs4846914

PubMed Link: 24386095

Variant Present in the following documents:

• pone.0082420.s002.doc

View BVdb publication page

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Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000366672.4	c.127-18273G>A	-	intron_variant	-	1/15
ENST00000494106.1	n.90-18273G>A	-	intron_variant,non_coding_transcript_variant	-	1/6
ENST00000541865.1	c.-50-43192G>A	-	intron_variant	-	1/12
ENST00000543760.1	c.13-18273G>A	-	intron_variant	-	1/15
NM_001291866.2	c.13-18273G>A	-	intron_variant	-	1/15
NM_004481.5	c.127-18273G>A	-	intron_variant	-	1/15