ABCA1 c.161-806C>A

Variant ID: 9-107647655-G-T

NM_005502.3(ABCA1):c.161-806C>A

This variant was identified in 44 publications

View GRCh38 version.




Publications:


Personalized Dietary Recommendations Based on Lipid-Related Genetic Variants: A Systematic Review.

Frontiers In Nutrition
Pérez-Beltrán, Yolanda E YE; Rivera-Iñiguez, Ingrid I; Gonzalez-Becerra, Karina K; Pérez-Naitoh, Naomi N; Tovar, Juscelino J; Sáyago-Ayerdi, Sonia G SG; Mendivil, Edgar J EJ
Publication Date: 2022

Variant appearance in text: rs3890182
PubMed Link: 35387194
Variant Present in the following documents:
  • Main text
  • fnut-09-830283.pdf
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Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults.

Jama Cardiology
Björnsson, Eythór E; Thorleifsson, Guðmar G; Helgadóttir, Anna A; Guðnason, Thórarinn T; Guðbjartsson, Tómas T; Andersen, Karl K; Grétarsdóttir, Sólveig S; Ólafsson, Ísleifur Í; Tragante, Vinicius V; Ólafsson, Ólafur Hreiðar ÓH; Jónsdóttir, Birna B; Eyjólfsson, Guðmundur I GI; Sigurðardóttir, Ólöf Ó; Thorgeirsson, Guðmundur G; Guðbjartsson, Daníel F DF; Thorsteinsdóttir, Unnur U; Hólm, Hilma H; Stefánsson, Kári K
Publication Date: 2020-01-01

Variant appearance in text: rs3890182
PubMed Link: 31746962
Variant Present in the following documents:
  • jamacardiol-5-13-s001.pdf
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Quantitative and Qualitative Role of Antagonistic Heterogeneity in Genetics of Blood Lipids.

The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences
Kulminski, Alexander M AM; Loika, Yury Y; Nazarian, Alireza A; Culminskaya, Irina I
Publication Date: 2020-09-25

Variant appearance in text: rs3890182
PubMed Link: 31566214
Variant Present in the following documents:
  • Main text
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A Birth Cohort Study on the Genetic Modification of the Association of Prenatal Methylmercury With Child Cognitive Development.

American Journal Of Epidemiology
Julvez, Jordi J; Davey Smith, George G; Ring, Susan S; Grandjean, Philippe P
Publication Date: 2019-10-01

Variant appearance in text: rs3890182
PubMed Link: 31241132
Variant Present in the following documents:
  • Main text
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Allele-specific enhancers mediate associations between LCAT and ABCA1 polymorphisms and HDL metabolism.

Plos One
Howard, Alicia D AD; Wang, Xiaochun X; Prasad, Megana M; Sahu, Avinash Das AD; Aniba, Radhouane R; Miller, Michael M; Hannenhalli, Sridhar S; Chang, Yen-Pei Christy YC
Publication Date: 2019

Variant appearance in text: rs3890182
PubMed Link: 31039173
Variant Present in the following documents:
  • Main text
  • pone.0215911.pdf
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Vitamin E Metabolic Effects and Genetic Variants: A Challenge for Precision Nutrition in Obesity and Associated Disturbances.

Nutrients
Galmés, Sebastià S; Serra, Francisca F; Palou, Andreu A
Publication Date: 2018-12-04

Variant appearance in text: rs3890182
PubMed Link: 30518135
Variant Present in the following documents:
  • Main text
  • nutrients-10-01919.pdf
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Genetic and secondary causes of severe HDL deficiency and cardiovascular disease.

Journal Of Lipid Research
Geller, Andrew S AS; Polisecki, Eliana Y EY; Diffenderfer, Margaret R MR; Asztalos, Bela F BF; Karathanasis, Sotirios K SK; Hegele, Robert A RA; Schaefer, Ernst J EJ
Publication Date: 2018-12

Variant appearance in text: rs3890182
PubMed Link: 30333156
Variant Present in the following documents:
  • Main text
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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
Davis, James P JP; Huyghe, Jeroen R JR; Locke, Adam E AE; Jackson, Anne U AU; Sim, Xueling X; Stringham, Heather M HM; Teslovich, Tanya M TM; Welch, Ryan P RP; Fuchsberger, Christian C; Narisu, Narisu N; Chines, Peter S PS; Kangas, Antti J AJ; Soininen, Pasi P; Ala-Korpela, Mika M; Kuusisto, Johanna J; Collins, Francis S FS; Laakso, Markku M; Boehnke, Michael M; Mohlke, Karen L KL
Publication Date: 2017-10

Variant appearance in text: rs3890182
PubMed Link: 29084231
Variant Present in the following documents:
  • Main text
  • pgen.1007079.pdf
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Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.

Lipids In Health And Disease
Paththinige, C S CS; Sirisena, N D ND; Dissanayake, Vhw V
Publication Date: 2017-06-02

Variant appearance in text: rs3890182
PubMed Link: 28577571
Variant Present in the following documents:
  • Main text
  • 12944_2017_Article_488.pdf
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Association between Polymorphisms and Haplotype in the ABCA1 Gene and Overweight/Obesity Patients in the Uyghur Population of China.

International Journal Of Environmental Research And Public Health
Yao, Ming-Hong MH; He, Jia J; Ma, Ru-Lin RL; Ding, Yu-Song YS; Guo, Heng H; Yan, Yi-Zhong YZ; Zhang, Jing-Yu JY; Liu, Jia-Ming JM; Zhang, Mei M; Rui, Dong-Shen DS; Niu, Qiang Q; Guo, Shu-Xia SX
Publication Date: 2016-02-15

Variant appearance in text: rs3890182
PubMed Link: 26891315
Variant Present in the following documents:
  • Main text
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Interactions of Six SNPs in ABCA1gene and Obesity in Low HDL-C Disease in Kazakh of China.

International Journal Of Environmental Research And Public Health
Yao, Ming-hong MH; Guo, Heng H; He, Jia J; Yan, Yi-zhong YZ; Ma, Ru-lin RL; Ding, Yu-song YS; Zhang, Jing-yu JY; Liu, Jia-ming JM; Zhang, Mei M; Li, Shu-gang SG; Xu, Shang-zhi SZ; Niu, Qiang Q; Ma, Jiao-long JL; Guo, Shu-xia SX
Publication Date: 2016-01-28

Variant appearance in text: rs3890182
PubMed Link: 26828509
Variant Present in the following documents:
  • Main text
  • ijerph-13-00176.pdf
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Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes.

Plos One
Kong, Xiaomu X; Zhao, Qi Q; Xing, Xiaoyan X; Zhang, Bo B; Zhang, Xuelian X; Hong, Jing J; Yang, Wenying W
Publication Date: 2015

Variant appearance in text: rs3890182
PubMed Link: 26252223
Variant Present in the following documents:
  • Main text
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Multivariable Mendelian randomization: the use of pleiotropic genetic variants to estimate causal effects.

American Journal Of Epidemiology
Burgess, Stephen S; Thompson, Simon G SG
Publication Date: 2015-02-15

Variant appearance in text: rs3890182
PubMed Link: 25632051
Variant Present in the following documents:
  • supp_kwu283_kwu283supp.pdf
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A comparative encyclopedia of DNA elements in the mouse genome.

Nature
Yue, Feng F; Cheng, Yong Y; Breschi, Alessandra A; Vierstra, Jeff J; Wu, Weisheng W; Ryba, Tyrone T; Sandstrom, Richard R; Ma, Zhihai Z; Davis, Carrie C; Pope, Benjamin D BD; Shen, Yin Y; Pervouchine, Dmitri D DD; Djebali, Sarah S; Thurman, Robert E RE; Kaul, Rajinder R; Rynes, Eric E; Kirilusha, Anthony A; Marinov, Georgi K GK; Williams, Brian A BA; Trout, Diane D; Amrhein, Henry H; Fisher-Aylor, Katherine K; Antoshechkin, Igor I; DeSalvo, Gilberto G; See, Lei-Hoon LH; Fastuca, Meagan M; Drenkow, Jorg J; Zaleski, Chris C; Dobin, Alex A; Prieto, Pablo P; Lagarde, Julien J; Bussotti, Giovanni G; Tanzer, Andrea A; Denas, Olgert O; Li, Kanwei K; Bender, M A MA; Zhang, Miaohua M; Byron, Rachel R; Groudine, Mark T MT; McCleary, David D; Pham, Long L; Ye, Zhen Z; Kuan, Samantha S; Edsall, Lee L; Wu, Yi-Chieh YC; Rasmussen, Matthew D MD; Bansal, Mukul S MS; Kellis, Manolis M; Keller, Cheryl A CA; Morrissey, Christapher S CS; Mishra, Tejaswini T; Jain, Deepti D; Dogan, Nergiz N; Harris, Robert S RS; Cayting, Philip P; Kawli, Trupti T; Boyle, Alan P AP; Euskirchen, Ghia G; Kundaje, Anshul A; Lin, Shin S; Lin, Yiing Y; Jansen, Camden C; Malladi, Venkat S VS; Cline, Melissa S MS; Erickson, Drew T DT; Kirkup, Vanessa M VM; Learned, Katrina K; Sloan, Cricket A CA; Rosenbloom, Kate R KR; Lacerda de Sousa, Beatriz B; Beal, Kathryn K; Pignatelli, Miguel M; Flicek, Paul P; Lian, Jin J; Kahveci, Tamer T; Lee, Dongwon D; Kent, W James WJ; Ramalho Santos, Miguel M; Herrero, Javier J; Notredame, Cedric C; Johnson, Audra A; Vong, Shinny S; Lee, Kristen K; Bates, Daniel D; Neri, Fidencio F; Diegel, Morgan M; Canfield, Theresa T; Sabo, Peter J PJ; Wilken, Matthew S MS; Reh, Thomas A TA; Giste, Erika E; Shafer, Anthony A; Kutyavin, Tanya T; Haugen, Eric E; Dunn, Douglas D; Reynolds, Alex P AP; Neph, Shane S; Humbert, Richard R; Hansen, R Scott RS; De Bruijn, Marella M; Selleri, Licia L; Rudensky, Alexander A; Josefowicz, Steven S; Samstein, Robert R; Eichler, Evan E EE; Orkin, Stuart H SH; Levasseur, Dana D; Papayannopoulou, Thalia T; Chang, Kai-Hsin KH; Skoultchi, Arthur A; Gosh, Srikanta S; Disteche, Christine C; Treuting, Piper P; Wang, Yanli Y; Weiss, Mitchell J MJ; Blobel, Gerd A GA; Cao, Xiaoyi X; Zhong, Sheng S; Wang, Ting T; Good, Peter J PJ; Lowdon, Rebecca F RF; Adams, Leslie B LB; Zhou, Xiao-Qiao XQ; Pazin, Michael J MJ; Feingold, Elise A EA; Wold, Barbara B; Taylor, James J; Mortazavi, Ali A; Weissman, Sherman M SM; Stamatoyannopoulos, John A JA; Snyder, Michael P MP; Guigo, Roderic R; Gingeras, Thomas R TR; Gilbert, David M DM; Hardison, Ross C RC; Beer, Michael A MA; Ren, Bing B; ,
Publication Date: 2014-11-20

Variant appearance in text: rs3890182
PubMed Link: 25409824
Variant Present in the following documents:
  • Main text
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Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study.

Investigative Ophthalmology & Visual Science
Restrepo, Nicole A NA; Spencer, Kylee L KL; Goodloe, Robert R; Garrett, Tiana A TA; Heiss, Gerardo G; Bůžková, Petra P; Jorgensen, Neal N; Jensen, Richard A RA; Matise, Tara C TC; Hindorff, Lucia A LA; Klein, Barbara E K BE; Klein, Ronald R; Wong, Tien Y TY; Cheng, Ching-Yu CY; Cornes, Belinda K BK; Tai, E-Shyong ES; Ritchie, Marylyn D MD; Haines, Jonathan L JL; Crawford, Dana C DC
Publication Date: 2014-09-09

Variant appearance in text: rs3890182
PubMed Link: 25205864
Variant Present in the following documents:
  • Main text
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An in-silico model of lipoprotein metabolism and kinetics for the evaluation of targets and biomarkers in the reverse cholesterol transport pathway.

Plos Computational Biology
Lu, James J; Hübner, Katrin K; Nanjee, M Nazeem MN; Brinton, Eliot A EA; Mazer, Norman A NA
Publication Date: 2014-03

Variant appearance in text: rs3890182
PubMed Link: 24625468
Variant Present in the following documents:
  • Main text
  • pcbi.1003509.pdf
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Impact of HDL genetic risk scores on coronary artery calcified plaque and mortality in individuals with type 2 diabetes from the Diabetes Heart Study.

Cardiovascular Diabetology
Raffield, Laura M LM; Cox, Amanda J AJ; Hsu, Fang-Chi FC; Ng, Maggie C-Y MC; Langefeld, Carl D CD; Carr, J Jeffrey JJ; Freedman, Barry I BI; Bowden, Donald W DW
Publication Date: 2013-06-25

Variant appearance in text: rs3890182
PubMed Link: 23799899
Variant Present in the following documents:
  • Main text
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Linear regression in genetic association studies.

Plos One
Bůžková, Petra P
Publication Date: 2013

Variant appearance in text: rs3890182
PubMed Link: 23437286
Variant Present in the following documents:
  • Main text
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Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study.

Cardiovascular Diabetology
Povel, Cécile M CM; Boer, Jolanda M A JM; Onland-Moret, N Charlotte NC; Dollé, Martijn E T ME; Feskens, Edith J M EJ; van der Schouw, Yvonne T YT
Publication Date: 2012-10-29

Variant appearance in text: rs3890182
PubMed Link: 23101478
Variant Present in the following documents:
  • Main text
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Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population.

Journal Of Perinatology : Official Journal Of The California Perinatal Association
Mann, P C PC; Cooper, M E ME; Ryckman, K K KK; Comas, B B; Gili, J J; Crumley, S S; Bream, E N A EN; Byers, H M HM; Piester, T T; Schaefer, A A; Christine, P J PJ; Lawrence, A A; Schaa, K L KL; Kelsey, K J P KJ; Berends, S K SK; Momany, A M AM; Gadow, E E; Cosentino, V V; Castilla, E E EE; López Camelo, J J; Saleme, C C; Day, L J LJ; England, S K SK; Marazita, M L ML; Dagle, J M JM; Murray, J C JC
Publication Date: 2013-05

Variant appearance in text: rs3890182
PubMed Link: 23018797
Variant Present in the following documents:
  • Main text
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Linking disease associations with regulatory information in the human genome.

Genome Research
Schaub, Marc A MA; Boyle, Alan P AP; Kundaje, Anshul A; Batzoglou, Serafim S; Snyder, Michael M
Publication Date: 2012-09

Variant appearance in text: rs3890182
PubMed Link: 22955986
Variant Present in the following documents:
  • 1748.pdf
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Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.

Lancet (London, England)
Voight, Benjamin F BF; Peloso, Gina M GM; Orho-Melander, Marju M; Frikke-Schmidt, Ruth R; Barbalic, Maja M; Jensen, Majken K MK; Hindy, George G; Hólm, Hilma H; Ding, Eric L EL; Johnson, Toby T; Schunkert, Heribert H; Samani, Nilesh J NJ; Clarke, Robert R; Hopewell, Jemma C JC; Thompson, John F JF; Li, Mingyao M; Thorleifsson, Gudmar G; Newton-Cheh, Christopher C; Musunuru, Kiran K; Pirruccello, James P JP; Saleheen, Danish D; Chen, Li L; Stewart, Alexandre F R A; Schillert, Arne A; Thorsteinsdottir, Unnur U; Thorgeirsson, Gudmundur G; Anand, Sonia S; Engert, James C JC; Morgan, Thomas T; Spertus, John J; Stoll, Monika M; Berger, Klaus K; Martinelli, Nicola N; Girelli, Domenico D; McKeown, Pascal P PP; Patterson, Christopher C CC; Epstein, Stephen E SE; Devaney, Joseph J; Burnett, Mary-Susan MS; Mooser, Vincent V; Ripatti, Samuli S; Surakka, Ida I; Nieminen, Markku S MS; Sinisalo, Juha J; Lokki, Marja-Liisa ML; Perola, Markus M; Havulinna, Aki A; de Faire, Ulf U; Gigante, Bruna B; Ingelsson, Erik E; Zeller, Tanja T; Wild, Philipp P; de Bakker, Paul I W PI; Klungel, Olaf H OH; Maitland-van der Zee, Anke-Hilse AH; Peters, Bas J M BJ; de Boer, Anthonius A; Grobbee, Diederick E DE; Kamphuisen, Pieter W PW; Deneer, Vera H M VH; Elbers, Clara C CC; Onland-Moret, N Charlotte NC; Hofker, Marten H MH; Wijmenga, Cisca C; Verschuren, W M Monique WM; Boer, Jolanda M A JM; van der Schouw, Yvonne T YT; Rasheed, Asif A; Frossard, Philippe P; Demissie, Serkalem S; Willer, Cristen C; Do, Ron R; Ordovas, Jose M JM; Abecasis, Gonçalo R GR; Boehnke, Michael M; Mohlke, Karen L KL; Daly, Mark J MJ; Guiducci, Candace C; Burtt, Noël P NP; Surti, Aarti A; Gonzalez, Elena E; Purcell, Shaun S; Gabriel, Stacey S; Marrugat, Jaume J; Peden, John J; Erdmann, Jeanette J; Diemert, Patrick P; Willenborg, Christina C; König, Inke R IR; Fischer, Marcus M; Hengstenberg, Christian C; Ziegler, Andreas A; Buysschaert, Ian I; Lambrechts, Diether D; Van de Werf, Frans F; Fox, Keith A KA; El Mokhtari, Nour Eddine NE; Rubin, Diana D; Schrezenmeir, Jürgen J; Schreiber, Stefan S; Schäfer, Arne A; Danesh, John J; Blankenberg, Stefan S; Roberts, Robert R; McPherson, Ruth R; Watkins, Hugh H; Hall, Alistair S AS; Overvad, Kim K; Rimm, Eric E; Boerwinkle, Eric E; Tybjaerg-Hansen, Anne A; Cupples, L Adrienne LA; Reilly, Muredach P MP; Melander, Olle O; Mannucci, Pier M PM; Ardissino, Diego D; Siscovick, David D; Elosua, Roberto R; Stefansson, Kari K; O'Donnell, Christopher J CJ; Salomaa, Veikko V; Rader, Daniel J DJ; Peltonen, Leena L; Schwartz, Stephen M SM; Altshuler, David D; Kathiresan, Sekar S
Publication Date: 2012-08-11

Variant appearance in text: rs3890182
PubMed Link: 22607825
Variant Present in the following documents:
  • Main text
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Implications of discoveries from genome-wide association studies in current cardiovascular practice.

World Journal Of Cardiology
Jeemon, Panniyammakal P; Pettigrew, Kerry K; Sainsbury, Christopher C; Prabhakaran, Dorairaj D; Padmanabhan, Sandosh S
Publication Date: 2011-07-26

Variant appearance in text: rs3890182
PubMed Link: 21860704
Variant Present in the following documents:
  • Main text
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Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.

European Heart Journal
Angelakopoulou, Aspasia A; Shah, Tina T; Sofat, Reecha R; Shah, Sonia S; Berry, Diane J DJ; Cooper, Jackie J; Palmen, Jutta J; Tzoulaki, Ioanna I; Wong, Andrew A; Jefferis, Barbara J BJ; Maniatis, Nikolas N; Drenos, Fotios F; Gigante, Bruna B; Hardy, Rebecca R; Laxton, Ross C RC; Leander, Karin K; Motterle, Anna A; Simpson, Iain A IA; Smeeth, Liam L; Thomson, Andy A; Verzilli, Claudio C; Kuh, Diana D; Ireland, Helen H; Deanfield, John J; Caulfield, Mark M; Wallace, Chris C; Samani, Nilesh N; Munroe, Patricia B PB; Lathrop, Mark M; Fowkes, F Gerry R FG; Marmot, Michael M; Whincup, Peter H PH; Whittaker, John C JC; de Faire, Ulf U; Kivimaki, Mika M; Kumari, Meena M; Hypponen, Elina E; Power, Chris C; Humphries, Steve E SE; Talmud, Philippa J PJ; Price, Jackie J; Morris, Richard W RW; Ye, Shu S; Casas, Juan P JP; Hingorani, Aroon D AD
Publication Date: 2012-02

Variant appearance in text: rs3890182
PubMed Link: 21804106
Variant Present in the following documents:
  • Main text
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Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study.

Plos Genetics
Dumitrescu, Logan L; Carty, Cara L CL; Taylor, Kira K; Schumacher, Fredrick R FR; Hindorff, Lucia A LA; Ambite, José L JL; Anderson, Garnet G; Best, Lyle G LG; Brown-Gentry, Kristin K; Bůžková, Petra P; Carlson, Christopher S CS; Cochran, Barbara B; Cole, Shelley A SA; Devereux, Richard B RB; Duggan, Dave D; Eaton, Charles B CB; Fornage, Myriam M; Franceschini, Nora N; Haessler, Jeff J; Howard, Barbara V BV; Johnson, Karen C KC; Laston, Sandra S; Kolonel, Laurence N LN; Lee, Elisa T ET; MacCluer, Jean W JW; Manolio, Teri A TA; Pendergrass, Sarah A SA; Quibrera, Miguel M; Shohet, Ralph V RV; Wilkens, Lynne R LR; Haiman, Christopher A CA; Le Marchand, Loïc L; Buyske, Steven S; Kooperberg, Charles C; North, Kari E KE; Crawford, Dana C DC
Publication Date: 2011-06

Variant appearance in text: rs3890182
PubMed Link: 21738485
Variant Present in the following documents:
  • Main text
  • pgen.1002138.pdf
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Genetic variants and their interactions in the prediction of increased pre-clinical carotid atherosclerosis: the cardiovascular risk in young Finns study.

Plos Genetics
Okser, Sebastian S; Lehtimäki, Terho T; Elo, Laura L LL; Mononen, Nina N; Peltonen, Nina N; Kähönen, Mika M; Juonala, Markus M; Fan, Yue-Mei YM; Hernesniemi, Jussi A JA; Laitinen, Tomi T; Lyytikäinen, Leo-Pekka LP; Rontu, Riikka R; Eklund, Carita C; Hutri-Kähönen, Nina N; Taittonen, Leena L; Hurme, Mikko M; Viikari, Jorma S A JS; Raitakari, Olli T OT; Aittokallio, Tero T
Publication Date: 2010-09-30

Variant appearance in text: rs3890182
PubMed Link: 20941391
Variant Present in the following documents:
  • Main text
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Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology
Panagiotou, Orestis A OA; Evangelou, Evangelos E; Ioannidis, John P A JP
Publication Date: 2010-10-15

Variant appearance in text: rs3890182
PubMed Link: 20876667
Variant Present in the following documents:
  • Main text
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Genetic variants influencing circulating lipid levels and risk of coronary artery disease.

Arteriosclerosis, Thrombosis, And Vascular Biology
Waterworth, Dawn M DM; Ricketts, Sally L SL; Song, Kijoung K; Chen, Li L; Zhao, Jing Hua JH; Ripatti, Samuli S; Aulchenko, Yurii S YS; Zhang, Weihua W; Yuan, Xin X; Lim, Noha N; Luan, Jian'an J; Ashford, Sofie S; Wheeler, Eleanor E; Young, Elizabeth H EH; Hadley, David D; Thompson, John R JR; Braund, Peter S PS; Johnson, Toby T; Struchalin, Maksim M; Surakka, Ida I; Luben, Robert R; Khaw, Kay-Tee KT; Rodwell, Sheila A SA; Loos, Ruth J F RJ; Boekholdt, S Matthijs SM; Inouye, Michael M; Deloukas, Panagiotis P; Elliott, Paul P; Schlessinger, David D; Sanna, Serena S; Scuteri, Angelo A; Jackson, Anne A; Mohlke, Karen L KL; Tuomilehto, Jaako J; Roberts, Robert R; Stewart, Alexandre A; Kesäniemi, Y Antero YA; Mahley, Robert W RW; Grundy, Scott M SM; , ; McArdle, Wendy W; Cardon, Lon L; Waeber, Gérard G; Vollenweider, Peter P; Chambers, John C JC; Boehnke, Michael M; Abecasis, Gonçalo R GR; Salomaa, Veikko V; Järvelin, Marjo-Riitta MR; Ruokonen, Aimo A; Barroso, Inês I; Epstein, Stephen E SE; Hakonarson, Hakon H HH; Rader, Daniel J DJ; Reilly, Muredach P MP; Witteman, Jacqueline C M JC; Hall, Alistair S AS; Samani, Nilesh J NJ; Strachan, David P DP; Barter, Philip P; van Duijn, Cornelia M CM; Kooner, Jaspal S JS; Peltonen, Leena L; Wareham, Nicholas J NJ; McPherson, Ruth R; Mooser, Vincent V; Sandhu, Manjinder S MS
Publication Date: 2010-11

Variant appearance in text: rs3890182
PubMed Link: 20864672
Variant Present in the following documents:
  • Main text
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Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.

Diabetologia
Fontaine-Bisson, B B; Renström, F F; Rolandsson, O O; , ; Payne, F F; Hallmans, G G; Barroso, I I; Franks, P W PW
Publication Date: 2010-10

Variant appearance in text: rs3890182
PubMed Link: 20571754
Variant Present in the following documents:
  • 125_2010_Article_1792.pdf
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Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.

Plos One
Zeller, Tanja T; Wild, Philipp P; Szymczak, Silke S; Rotival, Maxime M; Schillert, Arne A; Castagne, Raphaele R; Maouche, Seraya S; Germain, Marine M; Lackner, Karl K; Rossmann, Heidi H; Eleftheriadis, Medea M; Sinning, Christoph R CR; Schnabel, Renate B RB; Lubos, Edith E; Mennerich, Detlev D; Rust, Werner W; Perret, Claire C; Proust, Carole C; Nicaud, Viviane V; Loscalzo, Joseph J; Hübner, Norbert N; Tregouet, David D; Münzel, Thomas T; Ziegler, Andreas A; Tiret, Laurence L; Blankenberg, Stefan S; Cambien, François F
Publication Date: 2010-05-18

Variant appearance in text: rs3890182
PubMed Link: 20502693
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
Weissglas-Volkov, Daphna D; Pajukanta, Päivi P
Publication Date: 2010-08

Variant appearance in text: rs3890182
PubMed Link: 20421590
Variant Present in the following documents:
  • Main text
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The genetics of obesity and the metabolic syndrome.

Endocrine, Metabolic & Immune Disorders Drug Targets
Monda, Keri L KL; North, Kari E KE; Hunt, Steven C SC; Rao, D C DC; Province, Michael A MA; Kraja, Aldi T AT
Publication Date: 2010-06

Variant appearance in text: rs3890182
PubMed Link: 20406164
Variant Present in the following documents:
  • Main text
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Association of blood lipids with common DNA sequence variants at 19 genetic loci in the multiethnic United States National Health and Nutrition Examination Survey III.

Circulation. Cardiovascular Genetics
Keebler, Mary E ME; Sanders, Christopher L CL; Surti, Aarti A; Guiducci, Candace C; Burtt, Noel P NP; Kathiresan, Sekar S
Publication Date: 2009-06

Variant appearance in text: rs3890182
PubMed Link: 20031591
Variant Present in the following documents:
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Using a latent growth curve model for an integrative assessment of the effects of genetic and environmental factors on multiple phenotypes.

Bmc Proceedings
Hamid, Jemila S JS; Roslin, Nicole M NM; Paterson, Andrew D AD; Beyene, Joseph J
Publication Date: 2009-12-15

Variant appearance in text: rs3890182
PubMed Link: 20018036
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Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.

Lipids In Health And Disease
Ronald, James J; Rajagopalan, Ramakrishnan R; Ranchalis, Jane E JE; Marshall, Julieann K JK; Hatsukami, Thomas S TS; Heagerty, Patrick J PJ; Jarvik, Gail P GP
Publication Date: 2009-12-01

Variant appearance in text: rs3890182
PubMed Link: 19951432
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A gene score of nine LDL and HDL regulating genes is associated with fluvastatin-induced cholesterol changes in women.

Journal Of Lipid Research
Hamrefors, Viktor V; Orho-Melander, Marju M; Krauss, Ronald M RM; Hedblad, Bo B; Almgren, Peter P; Berglund, Göran G; Melander, Olle O
Publication Date: 2010-03

Variant appearance in text: rs3890182
PubMed Link: 19773416
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A survey of ABCA1 sequence variation confirms association with dementia.

Human Mutation
Reynolds, Chandra A CA; Hong, Mun-Gwan MG; Eriksson, Ulrika K UK; Blennow, Kaj K; Bennet, Anna M AM; Johansson, Boo B; Malmberg, Bo B; Berg, Stig S; Wiklund, Fredrik F; Gatz, Margaret M; Pedersen, Nancy L NL; Prince, Jonathan A JA
Publication Date: 2009-09

Variant appearance in text: rs3890182
PubMed Link: 19606474
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Genome-wide linkage scan for plasma high density lipoprotein cholesterol, apolipoprotein A-1 and triglyceride variation among American Indian populations: the Strong Heart Family Study.

Journal Of Medical Genetics
Li, X X; Monda, K L KL; Göring, H H H HH; Haack, K K; Cole, S A SA; Diego, V P VP; Almasy, L L; Laston, S S; Howard, B V BV; Shara, N M NM; Lee, E T ET; Best, L G LG; Fabsitz, R R RR; MacCluer, J W JW; North, Kari E KE
Publication Date: 2009-07

Variant appearance in text: rs3890182
PubMed Link: 19429595
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Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.

Plos Genetics
Lowe, Jennifer K JK; Maller, Julian B JB; Pe'er, Itsik I; Neale, Benjamin M BM; Salit, Jacqueline J; Kenny, Eimear E EE; Shea, Jessica L JL; Burkhardt, Ralph R; Smith, J Gustav JG; Ji, Weizhen W; Noel, Martha M; Foo, Jia Nee JN; Blundell, Maude L ML; Skilling, Vita V; Garcia, Laura L; Sullivan, Marcia L ML; Lee, Heather E HE; Labek, Anna A; Ferdowsian, Hope H; Auerbach, Steven B SB; Lifton, Richard P RP; Newton-Cheh, Christopher C; Breslow, Jan L JL; Stoffel, Markus M; Daly, Mark J MJ; Altshuler, David M DM; Friedman, Jeffrey M JM
Publication Date: 2009-02

Variant appearance in text: rs3890182
PubMed Link: 19197348
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Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study.

Plos Genetics
Deo, Rahul C RC; Reich, David D; Tandon, Arti A; Akylbekova, Ermeg E; Patterson, Nick N; Waliszewska, Alicja A; Kathiresan, Sekar S; Sarpong, Daniel D; Taylor, Herman A HA; Wilson, James G JG
Publication Date: 2009-01

Variant appearance in text: rs3890182
PubMed Link: 19148283
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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

Nature Genetics
Sabatti, Chiara C; Service, Susan K SK; Hartikainen, Anna-Liisa AL; Pouta, Anneli A; Ripatti, Samuli S; Brodsky, Jae J; Jones, Chris G CG; Zaitlen, Noah A NA; Varilo, Teppo T; Kaakinen, Marika M; Sovio, Ulla U; Ruokonen, Aimo A; Laitinen, Jaana J; Jakkula, Eveliina E; Coin, Lachlan L; Hoggart, Clive C; Collins, Andrew A; Turunen, Hannu H; Gabriel, Stacey S; Elliot, Paul P; McCarthy, Mark I MI; Daly, Mark J MJ; Järvelin, Marjo-Riitta MR; Freimer, Nelson B NB; Peltonen, Leena L
Publication Date: 2009-01

Variant appearance in text: rs3890182
PubMed Link: 19060910
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Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

Experimental Gerontology
Boes, Eva E; Coassin, Stefan S; Kollerits, Barbara B; Heid, Iris M IM; Kronenberg, Florian F
Publication Date: 2009-03

Variant appearance in text: rs3890182
PubMed Link: 19041386
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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.

Nature Genetics
Kathiresan, Sekar S; Melander, Olle O; Guiducci, Candace C; Surti, Aarti A; Burtt, Noël P NP; Rieder, Mark J MJ; Cooper, Gregory M GM; Roos, Charlotta C; Voight, Benjamin F BF; Havulinna, Aki S AS; Wahlstrand, Björn B; Hedner, Thomas T; Corella, Dolores D; Tai, E Shyong ES; Ordovas, Jose M JM; Berglund, Göran G; Vartiainen, Erkki E; Jousilahti, Pekka P; Hedblad, Bo B; Taskinen, Marja-Riitta MR; Newton-Cheh, Christopher C; Salomaa, Veikko V; Peltonen, Leena L; Groop, Leif L; Altshuler, David M DM; Orho-Melander, Marju M
Publication Date: 2008-02

Variant appearance in text: rs3890182
PubMed Link: 18193044
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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.

American Journal Of Human Genetics
Wallace, Chris C; Newhouse, Stephen J SJ; Braund, Peter P; Zhang, Feng F; Tobin, Martin M; Falchi, Mario M; Ahmadi, Kourosh K; Dobson, Richard J RJ; Marçano, Ana Carolina B AC; Hajat, Cother C; Burton, Paul P; Deloukas, Panagiotis P; Brown, Morris M; Connell, John M JM; Dominiczak, Anna A; Lathrop, G Mark GM; Webster, John J; Farrall, Martin M; Spector, Tim T; Samani, Nilesh J NJ; Caulfield, Mark J MJ; Munroe, Patricia B PB
Publication Date: 2008-01

Variant appearance in text: rs3890182
PubMed Link: 18179892
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