Publications:

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Risk factors for progression of age-related macular degeneration.

Ophthalmic & Physiological Optics : The Journal Of The British College Of Ophthalmic Opticians (Optometrists)

TJ Heesterbeek, L Lorés-Motta, CB Hoyng, YTE Lechanteur, AI den Hollander

Publication Date: 2020-03

Variant appearance in text: rs1864163

PubMed Link: 32100327

Variant Present in the following documents:

• Main text

View BVdb publication page

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Do age-related macular degeneration genes show association with keratoconus?

Eye And Vision (London, England)

K Cao, S Sahebjada, AJ Richardson, PN Baird

Publication Date: 2019

Variant appearance in text: rs1864163

PubMed Link: 31819893

Variant Present in the following documents:

• 40662_2019_Article_164.pdf
• aaaaaMain text

View BVdb publication page

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A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.

Nature Communications

A Gallois, J Mefford, A Ko, A Vaysse, H Julienne, M Ala-Korpela, M Laakso, N Zaitlen, P Pajukanta, H Aschard

Publication Date: 2019-10-21

Variant appearance in text: rs1864163

PubMed Link: 31636271

Variant Present in the following documents:

• 41467_2019_12703_MOESM3_ESM.xlsx

View BVdb publication page

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Association of age-related macular degeneration with complement activation products, smoking, and single nucleotide polymorphisms in South Carolinians of European and African descent.

Molecular Vision

B Rohrer, A Frazer-Abel, A Leonard, R Ratnapriya, T Ward, A Pietraszkiewicz, E O'Quinn, K Adams, A Swaroop, BJ Wolf

Publication Date: 2019

Variant appearance in text: rs1864163

PubMed Link: 30820144

Variant Present in the following documents:

• Main text

View BVdb publication page

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A Perception on Genome-Wide Genetic Analysis of Metabolic Traits in Arab Populations.

Frontiers In Endocrinology

P Hebbar, JA Abubaker, M Abu-Farha, J Tuomilehto, F Al-Mulla, TA Thanaraj

Publication Date: 2019

Variant appearance in text: rs1864163

PubMed Link: 30761081

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Identification for Non-Communicable Disease: Findings from 20 Years of the Tehran Lipid and Glucose Study.

International Journal Of Endocrinology And Metabolism

MS Daneshpour, M Hedayati, B Sedaghati-Khayat, K Guity, M Zarkesh, M Akbarzadeh, N Javanrooh, A Zadeh-Vakili, F Azizi

Publication Date: 2018-10

Variant appearance in text: rs1864163

PubMed Link: 30584432

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.

Journal Of Lipid Research

P Hebbar, R Nizam, M Melhem, F Alkayal, N Elkum, SE John, J Tuomilehto, O Alsmadi, TA Thanaraj

Publication Date: 2018-10

Variant appearance in text: rs1864163

PubMed Link: 30108155

Variant Present in the following documents:

• 10.1194_P080218_jlr.P080218-1.pdf
• 10.1194_P080218_jlr.P080218-2.xlsx
• aaaaaMain text

View BVdb publication page

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Association of Genes in the High-Density Lipoprotein Metabolic Pathway with Polypoidal Choroidal Vasculopathy in Asian Population: A Systematic Review and Meta-Analysis.

Journal Of Ophthalmology

MZ Yuan, RA Han, CX Zhang, YX Chen

Publication Date: 2018

Variant appearance in text: rs1864163

PubMed Link: 29977615

Variant Present in the following documents:

• 9538671.f1.docx
• aaaaaMain text

View BVdb publication page

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The role of genetic variation of human metabolism for BMI, mental traits and mental disorders.

Molecular Metabolism

J Hebebrand, T Peters, D Schijven, M Hebebrand, C Grasemann, TW Winkler, IM Heid, J Antel, M Föcker, L Tegeler, L Brauner, RAH Adan, JJ Luykx, CU Correll, IR König, A Hinney, L Libuda

Publication Date: 2018-06

Variant appearance in text: rs1864163

PubMed Link: 29673576

Variant Present in the following documents:

• mmc1.xlsx

View BVdb publication page

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Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants.

Oncotarget

R Cascella, C Strafella, G Longo, M Ragazzo, L Manzo, C De Felici, V Errichiello, V Caputo, F Viola, CM Eandi, G Staurenghi, A Cusumano, S Mauriello, LT Marsella, C Ciccacci, P Borgiani, F Sangiuolo, G Novelli, F Ricci, E Giardina

Publication Date: 2018-01-30

Variant appearance in text: rs1864163

PubMed Link: 29487693

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variations of cholesteryl ester transfer protein and diet interactions in relation to lipid profiles and coronary heart disease: a systematic review.

Nutrition & Metabolism

P Mirmiran, Z Esfandiar, F Hosseini-Esfahani, G Koochakpoor, MS Daneshpour, B Sedaghati-Khayat, F Azizi

Publication Date: 2017

Variant appearance in text: rs1864163

PubMed Link: 29234452

Variant Present in the following documents:

• 12986_2017_231_MOESM1_ESM.docx
• aaaaaMain 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: rs1864163

PubMed Link: 29084231

Variant Present in the following documents:

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

View BVdb publication page

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Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.

Biodata Mining

ER Holzinger, SS Verma, CB Moore, M Hall, R De, D Gilbert-Diamond, MB Lanktree, N Pankratz, A Amuzu, A Burt, C Dale, S Dudek, CE Furlong, TR Gaunt, DS Kim, H Riess, S Sivapalaratnam, V Tragante, EPA van Iperen, A Brautbar, DS Carrell, DR Crosslin, GP Jarvik, H Kuivaniemi, IJ Kullo, EB Larson, LJ Rasmussen-Torvik, G Tromp, J Baumert, KJ Cruickshanks, M Farrall, AD Hingorani, GK Hovingh, ME Kleber, BE Klein, R Klein, W Koenig, LA Lange, W Mӓrz, KE North, N Charlotte Onland-Moret, AP Reiner, PJ Talmud, YT van der Schouw, JG Wilson, M Kivimaki, M Kumari, JH Moore, F Drenos, FW Asselbergs, BJ Keating, MD Ritchie

Publication Date: 2017

Variant appearance in text: rs1864163

PubMed Link: 28770004

Variant Present in the following documents:

• Main text

View BVdb publication page

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Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C.

Npj Aging And Mechanisms Of Disease

EM van Leeuwen, JE Huffman, JC Bis, A Isaacs, M Mulder, A Sabo, AV Smith, S Demissie, A Manichaikul, JA Brody, MF Feitosa, Q Duan, KE Schraut, P Navarro, JV van Vliet-Ostaptchouk, G Zhu, H Mbarek, S Trompet, N Verweij, LP Lyytikäinen, J Deelen, IM Nolte, SW van der Laan, G Davies, AJ Vermeij-Verdoold, AA van Oosterhout, JM Vergeer-Drop, DE Arking, H Trochet, , C Medina-Gomez, F Rivadeneira, AG Uitterlinden, A Dehghan, OH Franco, EJ Sijbrands, A Hofman, CC White, JC Mychaleckyj, GM Peloso, MA Swertz, , G Willemsen, EJ de Geus, Y Milaneschi, BW Penninx, I Ford, BM Buckley, AJ de Craen, JM Starr, IJ Deary, G Pasterkamp, AJ Oldehinkel, H Snieder, PE Slagboom, K Nikus, M Kähönen, T Lehtimäki, JS Viikari, OT Raitakari, P van der Harst, JW Jukema, JJ Hottenga, DI Boomsma, JB Whitfield, G Montgomery, NG Martin, , O Polasek, V Vitart, C Hayward, I Kolcic, AF Wright, I Rudan, PK Joshi, JF Wilson, LA Lange, JG Wilson, V Gudnason, TB Harris, AC Morrison, IB Borecki, SS Rich, S Padmanabhan, BM Psaty, JI Rotter, BH Smith, E Boerwinkle, LA Cupples, C van Duijn

Publication Date: 2015

Variant appearance in text: rs1864163

PubMed Link: 28721259

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: rs1864163

PubMed Link: 28577571

Variant Present in the following documents:

• 12944_2017_488_MOESM1_ESM.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: rs1864163

PubMed Link: 28371326

Variant Present in the following documents:

• JCMM-21-1106-s002.xlsx

View BVdb publication page

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Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).

Human Genetics

Z Wang, A Manichukal, DC Goff, S Mora, JM Ordovas, NM Pajewski, WS Post, JI Rotter, MM Sale, SA Santorico, D Siscovick, MY Tsai, DK Arnett, S Rich, AC Frazier-Wood

Publication Date: 2017-06

Variant appearance in text: rs1864163

PubMed Link: 28352986

Variant Present in the following documents:

• 439_2017_1782_MOESM1_ESM.docx

View BVdb publication page

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Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.

Genome Medicine

R Nagy, TS Boutin, J Marten, JE Huffman, SM Kerr, A Campbell, L Evenden, J Gibson, C Amador, DM Howard, P Navarro, A Morris, IJ Deary, LJ Hocking, S Padmanabhan, BH Smith, P Joshi, JF Wilson, ND Hastie, AF Wright, AM McIntosh, DJ Porteous, CS Haley, V Vitart, C Hayward

Publication Date: 2017-03-07

Variant appearance in text: rs1864163

PubMed Link: 28270201

Variant Present in the following documents:

• 13073_2017_414_MOESM9_ESM.xlsx

View BVdb publication page

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Association and interaction of APOA5, BUD13, CETP, LIPA and health-related behavior with metabolic syndrome in a Taiwanese population.

Scientific Reports

E Lin, PH Kuo, YL Liu, AC Yang, CF Kao, SJ Tsai

Publication Date: 2016-11-09

Variant appearance in text: rs1864163

PubMed Link: 27827461

Variant Present in the following documents:

• srep36830-s1.pdf

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: rs1864163

PubMed Link: 27784733

Variant Present in the following documents:

• NIHMS825913-supplement-001457_-_Supplemental_Material.pdf

View BVdb publication page

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c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Plos One

M Ganesan, S Nizamuddin, SK Katkam, K Kumaraswami, UK Hosad, LL Lobo, VK Kutala, K Thangaraj

Publication Date: 2016

Variant appearance in text: rs1864163

PubMed Link: 27768712

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genome-wide compendium and functional assessment of in vivo heart enhancers.

Nature Communications

DE Dickel, I Barozzi, Y Zhu, Y Fukuda-Yuzawa, M Osterwalder, BJ Mannion, D May, CH Spurrell, I Plajzer-Frick, CS Pickle, E Lee, TH Garvin, M Kato, JA Akiyama, V Afzal, AY Lee, DU Gorkin, B Ren, EM Rubin, A Visel, LA Pennacchio

Publication Date: 2016-10-05

Variant appearance in text: rs1864163

PubMed Link: 27703156

Variant Present in the following documents:

• ncomms12923-s2.xlsx

View BVdb publication page

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CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration.

Advances In Medicine

R Sakiene, A Vilkeviciute, L Kriauciuniene, VJ Balciuniene, D Buteikiene, G Miniauskiene, R Liutkeviciene

Publication Date: 2016

Variant appearance in text: rs1864163

PubMed Link: 27652291

Variant Present in the following documents:

• Main text

View BVdb publication page

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Whole exome sequencing of extreme age-related macular degeneration phenotypes.

Molecular Vision

RJ Sardell, JN Bailey, MD Courtenay, P Whitehead, RA Laux, LD Adams, JA Fortun, MA Brantley, JL Kovach, SG Schwartz, A Agarwal, WK Scott, JL Haines, MA Pericak-Vance

Publication Date: 2016

Variant appearance in text: rs1864163

PubMed Link: 27625572

Variant Present in the following documents:

• mv-v22-1062-app-1.docx

View BVdb publication page

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Oxidative stress, innate immunity, and age-related macular degeneration.

Aims Molecular Science

PX Shaw, T Stiles, C Douglas, D Ho, W Fan, H Du, X Xiao

Publication Date: 2016

Variant appearance in text: rs1864163

PubMed Link: 27239555

Variant Present in the following documents:

• Main text

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: rs1864163

PubMed Link: 26780889

Variant Present in the following documents:

• srep19429-s5.xls

View BVdb publication page

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INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing

A Verma, JB Leader, SS Verma, A Frase, J Wallace, S Dudek, DR Lavage, CV Van Hout, FE Dewey, J Penn, A Lopez, JD Overton, DJ Carey, DH Ledbetter, HL Kirchner, MD Ritchie, SA Pendergrass

Publication Date: 2016

Variant appearance in text: rs1864163

PubMed Link: 26776183

Variant Present in the following documents:

• NIHMS742521-supplement-2.pdf

View BVdb publication page

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Privacy-preserving genomic testing in the clinic: a model using HIV treatment.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics

PJ McLaren, JL Raisaro, M Aouri, M Rotger, E Ayday, I Bartha, MB Delgado, Y Vallet, HF Günthard, M Cavassini, H Furrer, T Doco-Lecompte, C Marzolini, P Schmid, C Di Benedetto, LA Decosterd, J Fellay, JP Hubaux, A Telenti

Publication Date: 2016-08

Variant appearance in text: rs1864163

PubMed Link: 26765343

Variant Present in the following documents:

• gim2015167x5.doc
• gim2015167x8.doc

View BVdb publication page

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A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.

Nature Genetics

LG Fritsche, W Igl, JN Bailey, F Grassmann, S Sengupta, JL Bragg-Gresham, KP Burdon, SJ Hebbring, C Wen, M Gorski, IK Kim, D Cho, D Zack, E Souied, HP Scholl, E Bala, KE Lee, DJ Hunter, RJ Sardell, P Mitchell, JE Merriam, V Cipriani, JD Hoffman, T Schick, YT Lechanteur, RH Guymer, MP Johnson, Y Jiang, CM Stanton, GH Buitendijk, X Zhan, AM Kwong, A Boleda, M Brooks, L Gieser, R Ratnapriya, KE Branham, JR Foerster, JR Heckenlively, MI Othman, BJ Vote, HH Liang, E Souzeau, IL McAllister, T Isaacs, J Hall, S Lake, DA Mackey, IJ Constable, JE Craig, TE Kitchner, Z Yang, Z Su, H Luo, D Chen, H Ouyang, K Flagg, D Lin, G Mao, H Ferreyra, K Stark, CN von Strachwitz, A Wolf, C Brandl, G Rudolph, M Olden, MA Morrison, DJ Morgan, M Schu, J Ahn, G Silvestri, EE Tsironi, KH Park, LA Farrer, A Orlin, A Brucker, M Li, CA Curcio, S Mohand-Saïd, JA Sahel, I Audo, M Benchaboune, AJ Cree, CA Rennie, SV Goverdhan, M Grunin, S Hagbi-Levi, P Campochiaro, N Katsanis, FG Holz, F Blond, H Blanché, JF Deleuze, RP Igo, B Truitt, NS Peachey, SM Meuer, CE Myers, EL Moore, R Klein, MA Hauser, EA Postel, MD Courtenay, SG Schwartz, JL Kovach, WK Scott, G Liew, AG Tan, B Gopinath, JC Merriam, RT Smith, JC Khan, H Shahid, AT Moore, JA McGrath, R Laux, MA Brantley, A Agarwal, L Ersoy, A Caramoy, T Langmann, NT Saksens, EK de Jong, CB Hoyng, MS Cain, AJ Richardson, TM Martin, J Blangero, DE Weeks, B Dhillon, CM van Duijn, KF Doheny, J Romm, CC Klaver, C Hayward, MB Gorin, ML Klein, PN Baird, AI den Hollander, S Fauser, JR Yates, R Allikmets, JJ Wang, DA Schaumberg, BE Klein, SA Hagstrom, I Chowers, AJ Lotery, T Léveillard, K Zhang, MH Brilliant, AW Hewitt, A Swaroop, EY Chew, MA Pericak-Vance, M DeAngelis, D Stambolian, JL Haines, SK Iyengar, BH Weber, GR Abecasis, IM Heid

Publication Date: 2016-02

Variant appearance in text: rs1864163

PubMed Link: 26691988

Variant Present in the following documents:

• NIHMS733253-supplement-1.docx
• NIHMS733253-supplement-2.docx

View BVdb publication page

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Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels.

Metabolism: Clinical And Experimental

D Pirim, X Wang, V Niemsiri, ZH Radwan, CH Bunker, JE Hokanson, RF Hamman, MM Barmada, FY Demirci, MI Kamboh

Publication Date: 2016-01

Variant appearance in text: rs1864163

PubMed Link: 26683795

Variant Present in the following documents:

• Main text

View BVdb publication page

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The UK10K project identifies rare variants in health and disease.

Nature

, K Walter, JL Min, J Huang, L Crooks, Y Memari, S McCarthy, JR Perry, C Xu, M Futema, D Lawson, V Iotchkova, S Schiffels, AE Hendricks, P Danecek, R Li, J Floyd, LV Wain, I Barroso, SE Humphries, ME Hurles, E Zeggini, JC Barrett, V Plagnol, JB Richards, CM Greenwood, NJ Timpson, R Durbin, N Soranzo

Publication Date: 2015-10-01

Variant appearance in text: rs1864163

PubMed Link: 26367797

Variant Present in the following documents:

• NIHMS64288-supplement-Tables_S1-S19.xlsx

View BVdb publication page

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Proinflammatory genotype is associated with the frailty phenotype in the English Longitudinal Study of Ageing.

Aging Clinical And Experimental Research

K Mekli, JY Nazroo, AD Marshall, M Kumari, N Pendleton

Publication Date: 2016-06

Variant appearance in text: rs1864163

PubMed Link: 26248682

Variant Present in the following documents:

• 40520_2015_419_MOESM2_ESM.xlsx

View BVdb publication page

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Differences in the Genetic Susceptibility to Age-Related Macular Degeneration Clinical Subtypes.

Investigative Ophthalmology & Visual Science

L Shen, TJ Hoffmann, RB Melles, LC Sakoda, MN Kvale, Y Banda, C Schaefer, N Risch, E Jorgenson

Publication Date: 2015-07

Variant appearance in text: rs1864163

PubMed Link: 26176866

Variant Present in the following documents:

• Main text

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: rs1864163

PubMed Link: 26130488

Variant Present in the following documents:

• ejhg2015150x4.xls

View BVdb publication page

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Transcriptome of the human retina, retinal pigmented epithelium and choroid.

Genomics

L Tian, KL Kazmierkiewicz, AS Bowman, M Li, CA Curcio, DE Stambolian

Publication Date: 2015-05

Variant appearance in text: rs1864163

PubMed Link: 25645700

Variant Present in the following documents:

• Main text

View BVdb publication page

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New loci and coding variants confer risk for age-related macular degeneration in East Asians.

Nature Communications

CY Cheng, K Yamashiro, LJ Chen, J Ahn, L Huang, L Huang, CM Cheung, M Miyake, PD Cackett, IY Yeo, A Laude, R Mathur, J Pang, KS Sim, AH Koh, P Chen, SY Lee, D Wong, CM Chan, BK Loh, Y Sun, S Davila, I Nakata, H Nakanishi, Y Akagi-Kurashige, N Gotoh, A Tsujikawa, F Matsuda, K Mori, S Yoneya, Y Sakurada, H Iijima, T Iida, S Honda, TY Lai, PO Tam, H Chen, S Tang, X Ding, F Wen, F Lu, X Zhang, Y Shi, P Zhao, B Zhao, J Sang, B Gong, R Dorajoo, JM Yuan, WP Koh, RM van Dam, Y Friedlander, Y Lin, ML Hibberd, JN Foo, N Wang, CH Wong, GS Tan, SJ Park, M Bhargava, L Gopal, T Naing, J Liao, PG Ong, P Mitchell, P Zhou, X Xie, J Liang, J Mei, X Jin, SM Saw, M Ozaki, T Mizoguchi, Y Kurimoto, SJ Woo, H Chung, HG Yu, JY Shin, DH Park, IT Kim, W Chang, M Sagong, SJ Lee, HW Kim, JE Lee, Y Li, J Liu, YY Teo, CK Heng, TH Lim, SK Yang, K Song, EN Vithana, T Aung, JX Bei, YX Zeng, ES Tai, XX Li, Z Yang, KH Park, CP Pang, N Yoshimura, TY Wong, CC Khor

Publication Date: 2015-01-28

Variant appearance in text: rs1864163

PubMed Link: 25629512

Variant Present in the following documents:

• ncomms7063-s1.pdf

View BVdb publication page

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The reduction of vascular disease risk mutations contributes to longevity in the Chinese population.

Meta Gene

YH He, X Lu, MX Bi, LQ Yang, LY Xu, QP Kong

Publication Date: 2014-12

Variant appearance in text: rs1864163

PubMed Link: 25606459

Variant Present in the following documents:

• Main text
• mmc1.docx
• mmc2.xlsx
• mmc3.xlsx

View BVdb publication page

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Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population.

Meta Gene

I Radovica, D Fridmanis, I Silamikelis, L Nikitina-Zake, J Klovins

Publication Date: 2014-12

Variant appearance in text: rs1864163

PubMed Link: 25606439

Variant Present in the following documents:

• Main text
• mmc1.docx

View BVdb publication page

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Endophenotypes for Age-Related Macular Degeneration: Extending Our Reach into the Preclinical Stages of Disease.

Journal Of Clinical Medicine

MB Gorin, DE Weeks, RV Baron, YP Conley, MC Ortube, S Nusinowitz

Publication Date: 2014-11-28

Variant appearance in text: rs1864163

PubMed Link: 25568804

Variant Present in the following documents:

• Main text

View BVdb publication page

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Age-related macular degeneration: insights into inflammatory genes.

Journal Of Ophthalmology

R Cascella, M Ragazzo, C Strafella, F Missiroli, P Borgiani, F Angelucci, LT Marsella, A Cusumano, G Novelli, F Ricci, E Giardina

Publication Date: 2014

Variant appearance in text: rs1864163

PubMed Link: 25478207

Variant Present in the following documents:

• Main text

View BVdb publication page

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Lipids, lipid genes, and incident age-related macular degeneration: the three continent age-related macular degeneration consortium.

American Journal Of Ophthalmology

R Klein, CE Myers, GH Buitendijk, E Rochtchina, X Gao, PT de Jong, TA Sivakumaran, G Burlutsky, R McKean-Cowdin, A Hofman, SK Iyengar, KE Lee, BH Stricker, JR Vingerling, P Mitchell, BE Klein, CC Klaver, JJ Wang

Publication Date: 2014-09

Variant appearance in text: rs1864163

PubMed Link: 24879949

Variant Present in the following documents:

• Main text

View BVdb publication page

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Macular xanthophylls, lipoprotein-related genes, and age-related macular degeneration.

The American Journal Of Clinical Nutrition

E Koo, M Neuringer, JP SanGiovanni

Publication Date: 2014-07

Variant appearance in text: rs1864163

PubMed Link: 24829491

Variant Present in the following documents:

• Main text

View BVdb publication page

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The role of the complement system in age-related macular degeneration.

Deutsches Arzteblatt International

BH Weber, P Charbel Issa, D Pauly, P Herrmann, F Grassmann, FG Holz

Publication Date: 2014-02-21

Variant appearance in text: rs1864163

PubMed Link: 24622760

Variant Present in the following documents:

• Main text

View BVdb publication page

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Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study.

Circulation. Cardiovascular Genetics

JM Kocarnik, SA Pendergrass, CL Carty, JS Pankow, FR Schumacher, I Cheng, P Durda, JL Ambite, E Deelman, NR Cook, S Liu, J Wactawski-Wende, C Hutter, K Brown-Gentry, S Wilson, LG Best, N Pankratz, CP Hong, SA Cole, VS Voruganti, P Bůžkova, NW Jorgensen, NS Jenny, LR Wilkens, CA Haiman, LN Kolonel, A Lacroix, K North, R Jackson, L Le Marchand, LA Hindorff, DC Crawford, M Gross, U Peters

Publication Date: 2014-04

Variant appearance in text: rs1864163

PubMed Link: 24622110

Variant Present in the following documents:

• NIHMS575195-supplement-000173_-_Supplemental_Material.pdf

View BVdb publication page

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Search for age-related macular degeneration risk variants in Alzheimer disease genes and pathways.

Neurobiology Of Aging

MW Logue, M Schu, BN Vardarajan, J Farrell, KL Lunetta, G Jun, CT Baldwin, MM Deangelis, LA Farrer

Publication Date: 2014-06

Variant appearance in text: rs1864163

PubMed Link: 24439028

Variant Present in the following documents:

• Main text

View BVdb publication page

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CETP gene polymorphisms and risk of coronary atherosclerosis in a Chinese population.

Lipids In Health And Disease

J Wang, LJ Wang, Y Zhong, P Gu, JQ Shao, SS Jiang, JB Gong

Publication Date: 2013-11-27

Variant appearance in text: rs1864163

PubMed Link: 24283500

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations.

Cerebrovascular Diseases (Basel, Switzerland)

SY Chou, JM Shulman, BT Keenan, EA Secor, AS Buchman, J Schneider, DA Bennett, PL De Jager

Publication Date: 2013

Variant appearance in text: rs1864163

PubMed Link: 24135527

Variant Present in the following documents:

• Main text
• NIHMS527173-supplement-01.pdf

View BVdb publication page

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Prediction of age-related macular degeneration in the general population: the Three Continent AMD Consortium.

Ophthalmology

GHS Buitendijk, E Rochtchina, C Myers, CM van Duijn, KE Lee, BEK Klein, SM Meuer, PTVM de Jong, EG Holliday, AG Tan, AG Uitterlinden, TS Sivakumaran, J Attia, A Hofman, P Mitchell, JR Vingerling, SK Iyengar, ACJW Janssens, JJ Wang, R Klein, CCW Klaver

Publication Date: 2013-12

Variant appearance in text: rs1864163

PubMed Link: 24120328

Variant Present in the following documents:

• NIHMS513526-supplement-03.pdf

View BVdb publication page

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No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.

Human Genetics

L Dumitrescu, CL Carty, N Franceschini, LA Hindorff, SA Cole, P Bůžková, FR Schumacher, CB Eaton, RJ Goodloe, DJ Duggan, J Haessler, B Cochran, BE Henderson, I Cheng, KC Johnson, CS Carlson, SA Love, K Brown-Gentry, AQ Nato, M Quibrera, RV Shohet, JL Ambite, LR Wilkens, L Le Marchand, CA Haiman, S Buyske, C Kooperberg, KE North, M Fornage, DC Crawford

Publication Date: 2013-12

Variant appearance in text: rs1864163

PubMed Link: 24100633

Variant Present in the following documents:

• NIHMS530028-supplement-439_2013_1375_MOESM1_ESM.docx

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: rs1864163

PubMed Link: 24097068

Variant Present in the following documents:

• NIHMS524703-supplement-1.pdf

View BVdb publication page

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Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study.

Plos Biology

CS Carlson, TC Matise, KE North, CA Haiman, MD Fesinmeyer, S Buyske, FR Schumacher, U Peters, N Franceschini, MD Ritchie, DJ Duggan, KL Spencer, L Dumitrescu, CB Eaton, F Thomas, A Young, C Carty, G Heiss, L Le Marchand, DC Crawford, LA Hindorff, CL Kooperberg,

Publication Date: 2013-09

Variant appearance in text: rs1864163

PubMed Link: 24068893

Variant Present in the following documents:

• pbio.1001661.s003.xlsx
• pbio.1001661.s004.xlsx

View BVdb publication page

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Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.

Nature Genetics

JM Seddon, Y Yu, EC Miller, R Reynolds, PL Tan, S Gowrisankar, JI Goldstein, M Triebwasser, HE Anderson, J Zerbib, D Kavanagh, E Souied, N Katsanis, MJ Daly, JP Atkinson, S Raychaudhuri

Publication Date: 2013-11

Variant appearance in text: rs1864163

PubMed Link: 24036952

Variant Present in the following documents:

• NIHMS512112-supplement-1.pdf

View BVdb publication page

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The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population.

Plos One

I Radovica, D Fridmanis, I Vaivade, L Nikitina-Zake, J Klovins

Publication Date: 2013

Variant appearance in text: rs1864163

PubMed Link: 23675527

Variant Present in the following documents:

• Main text
• pone.0064191.s002.docx

View BVdb publication page

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Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study.

Bmc Genetics

KC Taylor, CL Carty, L Dumitrescu, P Bůžková, SA Cole, L Hindorff, FR Schumacher, LR Wilkens, RV Shohet, PM Quibrera, KC Johnson, BE Henderson, J Haessler, N Franceschini, CB Eaton, DJ Duggan, B Cochran, I Cheng, CS Carlson, K Brown-Gentry, G Anderson, JL Ambite, C Haiman, L Le Marchand, C Kooperberg, DC Crawford, S Buyske, KE North, M Fornage,

Publication Date: 2013-05-01

Variant appearance in text: rs1864163

PubMed Link: 23634756

Variant Present in the following documents:

• 1471-2156-14-33-S1.pdf
• aaaaaMain text

View BVdb publication page

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Genetic variants from lipid-related pathways and risk for incident myocardial infarction.

Plos One

C Song, NL Pedersen, CA Reynolds, M Sabater-Lleal, S Kanoni, C Willenborg, , AC Syvänen, H Watkins, A Hamsten, JA Prince, E Ingelsson

Publication Date: 2013

Variant appearance in text: rs1864163

PubMed Link: 23555974

Variant Present in the following documents:

• pone.0060454.s001.pdf

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: rs1864163

PubMed Link: 23505323

Variant Present in the following documents:

• NIHMS454100-supplement-Supplementary_Table6.xls

View BVdb publication page

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Seven new loci associated with age-related macular degeneration.

Nature Genetics

LG Fritsche, W Chen, M Schu, BL Yaspan, Y Yu, G Thorleifsson, DJ Zack, S Arakawa, V Cipriani, S Ripke, RP Igo, GH Buitendijk, X Sim, DE Weeks, RH Guymer, JE Merriam, PJ Francis, G Hannum, A Agarwal, AM Armbrecht, I Audo, T Aung, GR Barile, M Benchaboune, AC Bird, PN Bishop, KE Branham, M Brooks, AJ Brucker, WH Cade, MS Cain, PA Campochiaro, CC Chan, CY Cheng, EY Chew, KA Chin, I Chowers, DG Clayton, R Cojocaru, YP Conley, BK Cornes, MJ Daly, B Dhillon, AO Edwards, E Evangelou, J Fagerness, HA Ferreyra, JS Friedman, A Geirsdottir, RJ George, C Gieger, N Gupta, SA Hagstrom, SP Harding, C Haritoglou, JR Heckenlively, FG Holz, G Hughes, JP Ioannidis, T Ishibashi, P Joseph, G Jun, Y Kamatani, N Katsanis, C N Keilhauer, JC Khan, IK Kim, Y Kiyohara, BE Klein, R Klein, JL Kovach, I Kozak, CJ Lee, KE Lee, P Lichtner, AJ Lotery, T Meitinger, P Mitchell, S Mohand-Saïd, AT Moore, DJ Morgan, MA Morrison, CE Myers, AC Naj, Y Nakamura, Y Okada, A Orlin, MC Ortube, MI Othman, C Pappas, KH Park, GJ Pauer, NS Peachey, O Poch, RR Priya, R Reynolds, AJ Richardson, R Ripp, G Rudolph, E Ryu, JA Sahel, DA Schaumberg, HP Scholl, SG Schwartz, WK Scott, H Shahid, H Sigurdsson, G Silvestri, TA Sivakumaran, RT Smith, L Sobrin, EH Souied, DE Stambolian, H Stefansson, GM Sturgill-Short, A Takahashi, N Tosakulwong, BJ Truitt, EE Tsironi, AG Uitterlinden, CM van Duijn, L Vijaya, JR Vingerling, EN Vithana, AR Webster, HE Wichmann, TW Winkler, TY Wong, AF Wright, D Zelenika, M Zhang, L Zhao, K Zhang, ML Klein, GS Hageman, GM Lathrop, K Stefansson, R Allikmets, PN Baird, MB Gorin, JJ Wang, CC Klaver, JM Seddon, MA Pericak-Vance, SK Iyengar, JR Yates, A Swaroop, BH Weber, M Kubo, MM Deangelis, T Léveillard, U Thorsteinsdottir, JL Haines, LA Farrer, IM Heid, GR Abecasis,

Publication Date: 2013-04

Variant appearance in text: rs1864163

PubMed Link: 23455636

Variant Present in the following documents:

• Main text
• NIHMS474886-supplement-1.pdf

View BVdb publication page

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Association of cardiovascular and metabolic disease genes with psoriasis.

The Journal Of Investigative Dermatology

Y Lu, H Chen, P Nikamo, H Qi Low, C Helms, M Seielstad, J Liu, AM Bowcock, M Stahle, W Liao

Publication Date: 2013-03

Variant appearance in text: rs1864163

PubMed Link: 23190900

Variant Present in the following documents:

• NIHMS404713-supplement-01.pdf

View BVdb publication page

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Evaluation of seven common lipid associated loci in a large Indian sib pair study.

Lipids In Health And Disease

S Rafiq, KK Venkata, V Gupta, DG Vinay, CJ Spurgeon, S Parameshwaran, SN Madana, S Kinra, L Bowen, NJ Timpson, GD Smith, F Dudbridge, D Prabhakaran, Y Ben-Shlomo, KS Reddy, S Ebrahim, GR Chandak,

Publication Date: 2012-11-14

Variant appearance in text: rs1864163

PubMed Link: 23150898

Variant Present in the following documents:

• Main text

View BVdb publication page

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Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

American Journal Of Human Genetics

FW Asselbergs, Y Guo, EP van Iperen, S Sivapalaratnam, V Tragante, MB Lanktree, LA Lange, B Almoguera, YE Appelman, J Barnard, J Baumert, AL Beitelshees, TR Bhangale, YD Chen, TR Gaunt, Y Gong, JC Hopewell, T Johnson, ME Kleber, TY Langaee, M Li, YR Li, K Liu, CW McDonough, MF Meijs, RP Middelberg, K Musunuru, CP Nelson, JR O'Connell, S Padmanabhan, JS Pankow, N Pankratz, S Rafelt, R Rajagopalan, SP Romaine, NJ Schork, J Shaffer, H Shen, EN Smith, SE Tischfield, PJ van der Most, JV van Vliet-Ostaptchouk, N Verweij, KA Volcik, L Zhang, KR Bailey, KM Bailey, F Bauer, JM Boer, PS Braund, A Burt, PR Burton, SG Buxbaum, W Chen, RM Cooper-Dehoff, LA Cupples, JS deJong, C Delles, D Duggan, M Fornage, CE Furlong, N Glazer, JG Gums, C Hastie, MV Holmes, T Illig, SA Kirkland, M Kivimaki, R Klein, BE Klein, C Kooperberg, K Kottke-Marchant, M Kumari, AZ LaCroix, L Mallela, G Murugesan, J Ordovas, WH Ouwehand, WS Post, R Saxena, H Scharnagl, PJ Schreiner, T Shah, DC Shields, D Shimbo, SR Srinivasan, RP Stolk, DI Swerdlow, HA Taylor, EJ Topol, E Toskala, JL van Pelt, J van Setten, S Yusuf, JC Whittaker, AH Zwinderman, , SS Anand, AJ Balmforth, GS Berenson, CR Bezzina, BO Boehm, E Boerwinkle, JP Casas, MJ Caulfield, R Clarke, JM Connell, KJ Cruickshanks, KW Davidson, IN Day, PI de Bakker, PA Doevendans, AF Dominiczak, AS Hall, CA Hartman, C Hengstenberg, HL Hillege, MH Hofker, SE Humphries, GP Jarvik, JA Johnson, BM Kaess, S Kathiresan, W Koenig, DA Lawlor, W März, O Melander, BD Mitchell, GW Montgomery, PB Munroe, SS Murray, SJ Newhouse, NC Onland-Moret, N Poulter, B Psaty, S Redline, SS Rich, JI Rotter, H Schunkert, P Sever, AR Shuldiner, RL Silverstein, A Stanton, B Thorand, MD Trip, MY Tsai, P van der Harst, E van der Schoot, YT van der Schouw, WM Verschuren, H Watkins, AA Wilde, BH Wolffenbuttel, JB Whitfield, GK Hovingh, CM Ballantyne, C Wijmenga, MP Reilly, NG Martin, JG Wilson, DJ Rader, NJ Samani, AP Reiner, RA Hegele, JJ Kastelein, AD Hingorani, PJ Talmud, H Hakonarson, CC Elbers, BJ Keating, F Drenos

Publication Date: 2012-11-02

Variant appearance in text: rs1864163

PubMed Link: 23063622

Variant Present in the following documents:

• mmc4.xls
• mmc7.xls

View BVdb publication page

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Association of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals.

Plos One

F Takeuchi, M Isono, T Katsuya, M Yokota, K Yamamoto, T Nabika, K Shimokawa, E Nakashima, T Sugiyama, H Rakugi, S Yamaguchi, T Ogihara, Y Yamori, N Kato

Publication Date: 2012

Variant appearance in text: rs1864163

PubMed Link: 23050023

Variant Present in the following documents:

• pone.0046385.s002.xls

View BVdb publication page

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Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

Bmc Medical Genetics

S Huhn, M Bevier, A Rudolph, B Pardini, A Naccarati, R Hein, M Hoffmeister, L Vodickova, J Novotny, H Brenner, J Chang-Claude, K Hemminki, P Vodicka, A Försti

Publication Date: 2012-10-05

Variant appearance in text: rs1864163

PubMed Link: 23036011

Variant Present in the following documents:

• 1471-2350-13-94-S1.pdf

View BVdb publication page

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Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain.

Neurobiology Of Disease

DG Hernandez, MA Nalls, M Moore, S Chong, A Dillman, D Trabzuni, JR Gibbs, M Ryten, S Arepalli, ME Weale, AB Zonderman, J Troncoso, R O'Brien, R Walker, C Smith, S Bandinelli, BJ Traynor, J Hardy, AB Singleton, MR Cookson

Publication Date: 2012-07

Variant appearance in text: rs1864163

PubMed Link: 22433082

Variant Present in the following documents:

• mmc1.xls

View BVdb publication page

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Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk.

Plos One

AC Papp, JK Pinsonneault, D Wang, LC Newman, Y Gong, JA Johnson, CJ Pepine, M Kumari, AD Hingorani, PJ Talmud, S Shah, SE Humphries, W Sadee

Publication Date: 2012

Variant appearance in text: rs1864163

PubMed Link: 22403620

Variant Present in the following documents:

• pone.0031930.s009.docx

View BVdb publication page

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Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

Plos Genetics

A Demirkan, CM van Duijn, P Ugocsai, A Isaacs, PP Pramstaller, G Liebisch, JF Wilson, Å Johansson, I Rudan, YS Aulchenko, AV Kirichenko, AC Janssens, RC Jansen, C Gnewuch, FS Domingues, C Pattaro, SH Wild, I Jonasson, O Polasek, IV Zorkoltseva, A Hofman, LC Karssen, M Struchalin, J Floyd, W Igl, Z Biloglav, L Broer, A Pfeufer, I Pichler, S Campbell, G Zaboli, I Kolcic, F Rivadeneira, J Huffman, ND Hastie, A Uitterlinden, L Franke, CS Franklin, V Vitart, , CP Nelson, M Preuss, , JC Bis, CJ O'Donnell, N Franceschini, , JC Witteman, T Axenovich, BA Oostra, T Meitinger, AA Hicks, C Hayward, AF Wright, U Gyllensten, H Campbell, G Schmitz,

Publication Date: 2012

Variant appearance in text: rs1864163

PubMed Link: 22359512

Variant Present in the following documents:

• pgen.1002490.s009.pdf

View BVdb publication page

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Genome-wide association study identifies multiple loci influencing human serum metabolite levels.

Nature Genetics

J Kettunen, T Tukiainen, AP Sarin, A Ortega-Alonso, E Tikkanen, LP Lyytikäinen, AJ Kangas, P Soininen, P Würtz, K Silander, DM Dick, RJ Rose, MJ Savolainen, J Viikari, M Kähönen, T Lehtimäki, KH Pietiläinen, M Inouye, MI McCarthy, A Jula, J Eriksson, OT Raitakari, V Salomaa, J Kaprio, MR Järvelin, L Peltonen, M Perola, NB Freimer, M Ala-Korpela, A Palotie, S Ripatti

Publication Date: 2012-01-29

Variant appearance in text: rs1864163

PubMed Link: 22286219

Variant Present in the following documents:

• NIHMS444574-supplement-supplementary_table_2.xlsx

View BVdb publication page

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A genome-wide scan for common variants affecting the rate of age-related cognitive decline.

Neurobiology Of Aging

PL De Jager, JM Shulman, LB Chibnik, BT Keenan, T Raj, RS Wilson, L Yu, SE Leurgans, D Tran, C Aubin, CD Anderson, A Biffi, JJ Corneveaux, MJ Huentelman, , J Rosand, MJ Daly, AJ Myers, EM Reiman, DA Bennett, DA Evans

Publication Date: 2012-05

Variant appearance in text: rs1864163

PubMed Link: 22054870

Variant Present in the following documents:

• NIHMS328602-supplement-01.doc

View BVdb publication page

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Validation of candidate genes associated with cardiovascular risk factors in psychiatric patients.

Progress In Neuro-Psychopharmacology & Biological Psychiatry

A Windemuth, J de Leon, JW Goethe, HI Schwartz, S Woolley, M Susce, M Kocherla, K Bogaard, TR Holford, RL Seip, G Ruaño

Publication Date: 2012-03-30

Variant appearance in text: rs1864163

PubMed Link: 21851846

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI.

Atherosclerosis

BJ Peters, H Pett, OH Klungel, BH Stricker, BM Psaty, NL Glazer, KL Wiggins, JC Bis, A de Boer, AH Maitland-van der Zee

Publication Date: 2011-08

Variant appearance in text: rs1864163

PubMed Link: 21741043

Variant Present in the following documents:

• NIHMS310676-supplement-01.doc

View BVdb publication page

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Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study.

Plos Genetics

L Dumitrescu, CL Carty, K Taylor, FR Schumacher, LA Hindorff, JL Ambite, G Anderson, LG Best, K Brown-Gentry, P Bůžková, CS Carlson, B Cochran, SA Cole, RB Devereux, D Duggan, CB Eaton, M Fornage, N Franceschini, J Haessler, BV Howard, KC Johnson, S Laston, LN Kolonel, ET Lee, JW MacCluer, TA Manolio, SA Pendergrass, M Quibrera, RV Shohet, LR Wilkens, CA Haiman, L Le Marchand, S Buyske, C Kooperberg, KE North, DC Crawford

Publication Date: 2011-06

Variant appearance in text: rs1864163

PubMed Link: 21738485

Variant Present in the following documents:

• Main text
• pgen.1002138.s015.doc

View BVdb publication page

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An assessment of CETP sequence variation in relation to cognitive decline and dementia risk.

International Journal Of Molecular Epidemiology And Genetics

CA Reynolds, M Gatz, NL Pedersen, JA Prince

Publication Date: 2011

Variant appearance in text: rs1864163

PubMed Link: 21686126

Variant Present in the following documents:

• Main text

View BVdb publication page

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GENIE: a software package for gene-gene interaction analysis in genetic association studies using multiple GPU or CPU cores.

Bmc Research Notes

S Chikkagoudar, K Wang, M Li

Publication Date: 2011-05-26

Variant appearance in text: rs1864163

PubMed Link: 21615923

Variant Present in the following documents:

• Main text

View BVdb publication page

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Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

Plos One

SD Turner, RL Berg, JG Linneman, PL Peissig, DC Crawford, JC Denny, DM Roden, CA McCarty, MD Ritchie, RA Wilke

Publication Date: 2011-05-11

Variant appearance in text: rs1864163

PubMed Link: 21589926

Variant Present in the following documents:

• pone.0019586.s004.pdf

View BVdb publication page

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Genetic architecture of circulating lipid levels.

European Journal Of Human Genetics : Ejhg

A Demirkan, N Amin, A Isaacs, MR Jarvelin, JB Whitfield, HE Wichmann, KO Kyvik, I Rudan, C Gieger, AA Hicks, Å Johansson, JJ Hottenga, JJ Smith, SH Wild, NL Pedersen, G Willemsen, M Mangino, C Hayward, AG Uitterlinden, A Hofman, J Witteman, GW Montgomery, KH Pietiläinen, T Rantanen, J Kaprio, A Döring, PP Pramstaller, U Gyllensten, EJ de Geus, BW Penninx, JF Wilson, F Rivadeneria, PK Magnusson, DI Boomsma, T Spector, H Campbell, B Hoehne, NG Martin, BA Oostra, M McCarthy, L Peltonen-Palotie, Y Aulchenko, PM Visscher, S Ripatti, AC Janssens, CM van Duijn,

Publication Date: 2011-07

Variant appearance in text: rs1864163

PubMed Link: 21448234

Variant Present in the following documents:

• ejhg201121x5.doc

View BVdb publication page

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Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

Plos Genetics

G Lettre, CD Palmer, T Young, KG Ejebe, H Allayee, EJ Benjamin, F Bennett, DW Bowden, A Chakravarti, A Dreisbach, DN Farlow, AR Folsom, M Fornage, T Forrester, E Fox, CA Haiman, J Hartiala, TB Harris, SL Hazen, SR Heckbert, BE Henderson, JN Hirschhorn, BJ Keating, SB Kritchevsky, E Larkin, M Li, ME Rudock, CA McKenzie, JB Meigs, YA Meng, TH Mosley, AB Newman, CH Newton-Cheh, DN Paltoo, GJ Papanicolaou, N Patterson, WS Post, BM Psaty, AN Qasim, L Qu, DJ Rader, S Redline, MP Reilly, AP Reiner, SS Rich, JI Rotter, Y Liu, P Shrader, DS Siscovick, WH Tang, HA Taylor, RP Tracy, RS Vasan, KM Waters, R Wilks, JG Wilson, RR Fabsitz, SB Gabriel, S Kathiresan, E Boerwinkle

Publication Date: 2011-02-10

Variant appearance in text: rs1864163

PubMed Link: 21347282

Variant Present in the following documents:

• pgen.1001300.s016.doc
• pgen.1001300.s017.doc

View BVdb publication page

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Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.

Circulation. Cardiovascular Genetics

AC Edmondson, PS Braund, IM Stylianou, AV Khera, CP Nelson, ML Wolfe, SL Derohannessian, BJ Keating, L Qu, J He, MD Tobin, M Tomaszewski, J Baumert, N Klopp, A Döring, B Thorand, M Li, MP Reilly, W Koenig, NJ Samani, DJ Rader

Publication Date: 2011-04

Variant appearance in text: rs1864163

PubMed Link: 21303902

Variant Present in the following documents:

• NIHMS280051-supplement-1.pdf

View BVdb publication page

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Physical activity modifies the effect of LPL, LIPC, and CETP polymorphisms on HDL-C levels and the risk of myocardial infarction in women of European ancestry.

Circulation. Cardiovascular Genetics

T Ahmad, DI Chasman, JE Buring, IM Lee, PM Ridker, BM Everett

Publication Date: 2011-02

Variant appearance in text: rs1864163

PubMed Link: 21252145

Variant Present in the following documents:

• NIHMS260598-supplement-Supplemental.doc

View BVdb publication page

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Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis.

Biodata Mining

SA Pendergrass, SM Dudek, DC Crawford, MD Ritchie

Publication Date: 2010-12-16

Variant appearance in text: rs1864163

PubMed Link: 21162740

Variant Present in the following documents:

• Main text

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Genetic causes of high and low serum HDL-cholesterol.

Journal Of Lipid Research

D Weissglas-Volkov, P Pajukanta

Publication Date: 2010-08

Variant appearance in text: rs1864163

PubMed Link: 20421590

Variant Present in the following documents:

• Main text

View BVdb publication page

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The genetics of obesity and the metabolic syndrome.

Endocrine, Metabolic & Immune Disorders Drug Targets

KL Monda, KE North, SC Hunt, DC Rao, MA Province, AT Kraja

Publication Date: 2010-06

Variant appearance in text: rs1864163

PubMed Link: 20406164

Variant Present in the following documents:

• Main text

View BVdb publication page

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Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000200676.3	c.233+197G>A	-	intron_variant	-	2/15
ENST00000379780.2	c.233+197G>A	-	intron_variant	-	2/14
ENST00000566128.1	c.38+197G>A	-	intron_variant	-	2/15
ENST00000569082.1	n.231+197G>A	-	intron_variant,non_coding_transcript_variant	-	2/8
NM_000078.3	c.233+197G>A	-	intron_variant	-	2/15
NM_001286085.2	c.233+197G>A	-	intron_variant	-	2/14