Variant ID: 16-56997233-G-A

NM_000078.2(CETP):c.233+197G>A

This variant was identified in 89 publications




Publications:


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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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
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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
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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
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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
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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
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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
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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
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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



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
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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
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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
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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
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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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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



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
View BVdb publication page



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



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



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