PCIF1 c.*108T>C

Variant ID: 20-44576502-T-C

NM_022104.3(PCIF1):c.*108T>C

This variant was identified in 45 publications

View GRCh38 version.




Publications:


Genetic markers of the risk of coronary heart disease and coronary artery thrombosis developing in the Kazakh population.

Caspian Journal Of Internal Medicine
Taizhanova, Dana D; Toleuova, Aliya A; Babenko, Dmitry D; Turmuhambetova, Anar A; Bodaubay, Roza R; Visternichan, Olga O; Kalimbetova, Akerke A; Ahmaltdinova, Ludmila L; Kurmanova, Aigul A
Publication Date: 2023

Variant appearance in text: rs7679
PubMed Link: 37223289
Variant Present in the following documents:
  • Main text
  • cjim-14-249.pdf
View BVdb publication page



Multivariate Genome-wide Association Analysis by Iterative Hard Thresholding.

Bioinformatics (Oxford, England)
Chu, Benjamin B BB; Ko, Seyoon S; Zhou, Jin J JJ; Jensen, Aubrey A; Zhou, Hua H; Sinsheimer, Janet S JS; Lange, Kenneth K
Publication Date: 2023-04-17

Variant appearance in text: rs7679
PubMed Link: 37067496
Variant Present in the following documents:
  • Main text
  • btad193.pdf
View BVdb publication page



Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-29

Variant appearance in text: rs7679
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs7679
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs7679
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs7679
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



A Mendelian randomization study of the role of lipoprotein subfractions in coronary artery disease.

Elife
Zhao, Qingyuan Q; Wang, Jingshu J; Miao, Zhen Z; Zhang, Nancy R NR; Hennessy, Sean S; Small, Dylan S DS; Rader, Daniel J DJ
Publication Date: 2021-04-26

Variant appearance in text: rs7679
PubMed Link: 33899735
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetically Mediated Lipid Metabolism and Risk of Insulin Resistance: Insights from Mendelian Randomization Studies.

Journal Of Lipid And Atherosclerosis
Bu, So Young SY
Publication Date: 2019-09

Variant appearance in text: rs7679
PubMed Link: 32821703
Variant Present in the following documents:
  • Main text
  • jla-8-132.pdf
View BVdb publication page



The regulation of glucose and lipid homeostasis via PLTP as a mediator of BAT-liver communication.

Embo Reports
Sponton, Carlos H CH; Hosono, Takashi T; Taura, Junki J; Jedrychowski, Mark P MP; Yoneshiro, Takeshi T; Wang, Qiang Q; Takahashi, Makoto M; Matsui, Yumi Y; Ikeda, Kenji K; Oguri, Yasuo Y; Tajima, Kazuki K; Shinoda, Kosaku K; Pradhan, Rachana N RN; Chen, Yong Y; Brown, Zachary Z; Roberts, Lindsay S LS; Ward, Carl C CC; Taoka, Hiroki H; Yokoyama, Yoko Y; Watanabe, Mitsuhiro M; Karasawa, Hiroshi H; Nomura, Daniel K DK; Kajimura, Shingo S
Publication Date: 2020-09-03

Variant appearance in text: rs7679
PubMed Link: 32672883
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of Monogenic vs Polygenic Hypercholesterolemia With Risk of Atherosclerotic Cardiovascular Disease.

Jama Cardiology
Trinder, Mark M; Francis, Gordon A GA; Brunham, Liam R LR
Publication Date: 2020-04-01

Variant appearance in text: rs7679
PubMed Link: 32049305
Variant Present in the following documents:
  • jamacardiol-5-390-s001.pdf
View BVdb publication page



Causal Inference for Genetically Determined Levels of High-Density Lipoprotein Cholesterol and Risk of Infectious Disease.

Arteriosclerosis, Thrombosis, And Vascular Biology
Trinder, Mark M; Walley, Keith R KR; Boyd, John H JH; Brunham, Liam R LR
Publication Date: 2020-01

Variant appearance in text: rs7679
PubMed Link: 31694394
Variant Present in the following documents:
  • atv-40-267-s002.pdf
View BVdb publication page



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

Nature Communications
Kuchenbaecker, Karoline K; Telkar, Nikita N; Reiker, Theresa T; Walters, Robin G RG; Lin, Kuang K; Eriksson, Anders A; Gurdasani, Deepti D; Gilly, Arthur A; Southam, Lorraine L; Tsafantakis, Emmanouil E; Karaleftheri, Maria M; Seeley, Janet J; Kamali, Anatoli A; Asiki, Gershim G; Millwood, Iona Y IY; Holmes, Michael M; Du, Huaidong H; Guo, Yu Y; Kumari, Meena M; Dedoussis, George G; Li, Liming L; Chen, Zhengming Z; Sandhu, Manjinder S MS; Zeggini, Eleftheria E; ,
Publication Date: 2019-09-24

Variant appearance in text: rs7679
PubMed Link: 31551420
Variant Present in the following documents:
  • 41467_2019_12026_MOESM1_ESM.pdf
View BVdb publication page



Identifying genetic markers associated with susceptibility to cardiovascular diseases.

Future Science Oa
Shukla, Hitesh H; Mason, Jessica Louise JL; Sabyah, Abdullah A
Publication Date: 2019-01

Variant appearance in text: rs7679
PubMed Link: 30652019
Variant Present in the following documents:
  • Main text
  • fsoa-05-350.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: rs7679
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



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: rs7679
PubMed Link: 28577571
Variant Present in the following documents:
  • Main text
  • 12944_2017_Article_488.pdf
View BVdb publication page



Mendelian randomization studies of biomarkers and type 2 diabetes.

Endocrine Connections
Abbasi, Ali A
Publication Date: 2015-12

Variant appearance in text: rs7679
PubMed Link: 26446360
Variant Present in the following documents:
  • Main text
  • ec-04-249.pdf
View BVdb publication page



PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity.

Journal Of Lipid Research
Kim, Daniel Seung DS; Burt, Amber A AA; Ranchalis, Jane E JE; Vuletic, Simona S; Vaisar, Tomas T; Li, Wan-Fen WF; Rosenthal, Elisabeth A EA; Dong, Weijiang W; Eintracht, Jason F JF; Motulsky, Arno G AG; Brunzell, John D JD; Albers, John J JJ; Furlong, Clement E CE; Jarvik, Gail P GP
Publication Date: 2015-07

Variant appearance in text: rs7679
PubMed Link: 26009633
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mendelian randomization provides no evidence for a causal role of serum urate in increasing serum triglyceride levels.

Circulation. Cardiovascular Genetics
Rasheed, Humaira H; Hughes, Kim K; Flynn, Tanya J TJ; Merriman, Tony R TR
Publication Date: 2014-12

Variant appearance in text: rs7679
PubMed Link: 25249548
Variant Present in the following documents:
  • Main text
View BVdb publication page



Clinical outcomes and genome-wide association for a brain methylation site in an antidepressant pharmacogenetics study in Mexican Americans.

The American Journal Of Psychiatry
Wong, Ma-Li ML; Dong, Chuanhui C; Flores, Deborah L DL; Ehrhart-Bornstein, Monika M; Bornstein, Stefan S; Arcos-Burgos, Mauricio M; Licinio, Julio J
Publication Date: 2014-12-01

Variant appearance in text: rs7679
PubMed Link: 25220861
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Frontiers In Genetics
Parihar, Ankita A; Wood, G Craig GC; Chu, Xin X; Jin, Qunjan Q; Argyropoulos, George G; Still, Christopher D CD; Shuldiner, Alan R AR; Mitchell, Braxton D BD; Gerhard, Glenn S GS
Publication Date: 2014

Variant appearance in text: rs7679
PubMed Link: 25147553
Variant Present in the following documents:
  • Main text
  • fgene-05-00222.pdf
View BVdb publication page



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

British Journal Of Medicine And Medical Research
Vaidya, Dhananjay D; Yanek, Lisa R LR; Mathias, Rasika A RA; Moy, Taryn F TF; Becker, Diane M DM; Becker, Lewis C LC
Publication Date: 2014-03

Variant appearance in text: rs7679
PubMed Link: 24688980
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
Kocarnik, Jonathan M JM; Pendergrass, Sarah A SA; Carty, Cara L CL; Pankow, James S JS; Schumacher, Fredrick R FR; Cheng, Iona I; Durda, Peter P; Ambite, José Luis JL; Deelman, Ewa E; Cook, Nancy R NR; Liu, Simin S; Wactawski-Wende, Jean J; Hutter, Carolyn C; Brown-Gentry, Kristin K; Wilson, Sarah S; Best, Lyle G LG; Pankratz, Nathan N; Hong, Ching-Ping CP; Cole, Shelley A SA; Voruganti, V Saroja VS; Bůžkova, Petra P; Jorgensen, Neal W NW; Jenny, Nancy S NS; Wilkens, Lynne R LR; Haiman, Christopher A CA; Kolonel, Laurence N LN; Lacroix, Andrea A; North, Kari K; Jackson, Rebecca R; Le Marchand, Loic L; Hindorff, Lucia A LA; Crawford, Dana C DC; Gross, Myron M; Peters, Ulrike U
Publication Date: 2014-04

Variant appearance in text: rs7679
PubMed Link: 24622110
Variant Present in the following documents:
  • Main text
View BVdb publication page



Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III).

Bmc Medical Genetics
Goodloe, Robert R; Brown-Gentry, Kristin K; Gillani, Niloufar B NB; Jin, Hailing H; Mayo, Ping P; Allen, Melissa M; McClellan, Bob B; Boston, Jonathan J; Sutcliffe, Cara C; Schnetz-Boutaud, Nathalie N; Dilks, Holli H HH; Crawford, Dana C DC
Publication Date: 2013-11-21

Variant appearance in text: rs7679
PubMed Link: 24256507
Variant Present in the following documents:
  • Main text
  • 1471-2350-14-120.pdf
View BVdb publication page



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

Bmc Genetics
Taylor, Kira C KC; Carty, Cara L CL; Dumitrescu, Logan L; Bůžková, Petra P; Cole, Shelley A SA; Hindorff, Lucia L; Schumacher, Fred R FR; Wilkens, Lynne R LR; Shohet, Ralph V RV; Quibrera, P Miguel PM; Johnson, Karen C KC; Henderson, Brian E BE; Haessler, Jeff J; Franceschini, Nora N; Eaton, Charles B CB; Duggan, David J DJ; Cochran, Barbara B; Cheng, Iona I; Carlson, Chris S CS; Brown-Gentry, Kristin K; Anderson, Garnet G; Ambite, Jose Luis JL; Haiman, Christopher C; Le Marchand, Loïc L; Kooperberg, Charles C; Crawford, Dana C DC; Buyske, Steven S; North, Kari E KE; Fornage, Myriam M; ,
Publication Date: 2013-05-01

Variant appearance in text: rs7679
PubMed Link: 23634756
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association analysis of dyslipidemia-related genes in diabetic nephropathy.

Plos One
McKay, Gareth J GJ; Savage, David A DA; Patterson, Christopher C CC; Lewis, Gareth G; McKnight, Amy Jayne AJ; Maxwell, Alexander P AP; ,
Publication Date: 2013

Variant appearance in text: rs7679
PubMed Link: 23555584
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide analysis of LXRα activation reveals new transcriptional networks in human atherosclerotic foam cells.

Nucleic Acids Research
Feldmann, Radmila R; Fischer, Cornelius C; Kodelja, Vitam V; Behrens, Sarah S; Haas, Stefan S; Vingron, Martin M; Timmermann, Bernd B; Geikowski, Anne A; Sauer, Sascha S
Publication Date: 2013-04-01

Variant appearance in text: rs7679
PubMed Link: 23393188
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs7679
PubMed Link: 23101478
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic modulation of lipid profiles following lifestyle modification or metformin treatment: the Diabetes Prevention Program.

Plos Genetics
Pollin, Toni I TI; Isakova, Tamara T; Jablonski, Kathleen A KA; de Bakker, Paul I W PI; Taylor, Andrew A; McAteer, Jarred J; Pan, Qing Q; Horton, Edward S ES; Delahanty, Linda M LM; Altshuler, David D; Shuldiner, Alan R AR; Goldberg, Ronald B RB; Florez, Jose C JC; Franks, Paul W PW; ,
Publication Date: 2012

Variant appearance in text: rs7679
PubMed Link: 22951888
Variant Present in the following documents:
  • Main text
  • pgen.1002895.pdf
View BVdb publication page



Hepatic ABCA1 and VLDL triglyceride production.

Biochimica Et Biophysica Acta
Liu, Mingxia M; Chung, Soonkyu S; Shelness, Gregory S GS; Parks, John S JS
Publication Date: 2012-05

Variant appearance in text: rs7679
PubMed Link: 22001232
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs7679
PubMed Link: 21860704
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs7679
PubMed Link: 21738485
Variant Present in the following documents:
  • Main text
  • pgen.1002138.pdf
View BVdb publication page



Role of plasma phospholipid transfer protein in lipid and lipoprotein metabolism.

Biochimica Et Biophysica Acta
Albers, John J JJ; Vuletic, Simona S; Cheung, Marian C MC
Publication Date: 2012-03

Variant appearance in text: rs7679
PubMed Link: 21736953
Variant Present in the following documents:
  • Main text
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
Lettre, Guillaume G; Palmer, Cameron D CD; Young, Taylor T; Ejebe, Kenechi G KG; Allayee, Hooman H; Benjamin, Emelia J EJ; Bennett, Franklyn F; Bowden, Donald W DW; Chakravarti, Aravinda A; Dreisbach, Al A; Farlow, Deborah N DN; Folsom, Aaron R AR; Fornage, Myriam M; Forrester, Terrence T; Fox, Ervin E; Haiman, Christopher A CA; Hartiala, Jaana J; Harris, Tamara B TB; Hazen, Stanley L SL; Heckbert, Susan R SR; Henderson, Brian E BE; Hirschhorn, Joel N JN; Keating, Brendan J BJ; Kritchevsky, Stephen B SB; Larkin, Emma E; Li, Mingyao M; Rudock, Megan E ME; McKenzie, Colin A CA; Meigs, James B JB; Meng, Yang A YA; Mosley, Tom H TH; Newman, Anne B AB; Newton-Cheh, Christopher H CH; Paltoo, Dina N DN; Papanicolaou, George J GJ; Patterson, Nick N; Post, Wendy S WS; Psaty, Bruce M BM; Qasim, Atif N AN; Qu, Liming L; Rader, Daniel J DJ; Redline, Susan S; Reilly, Muredach P MP; Reiner, Alexander P AP; Rich, Stephen S SS; Rotter, Jerome I JI; Liu, Yongmei Y; Shrader, Peter P; Siscovick, David S DS; Tang, W H Wilson WH; Taylor, Herman A HA; Tracy, Russell P RP; Vasan, Ramachandran S RS; Waters, Kevin M KM; Wilks, Rainford R; Wilson, James G JG; Fabsitz, Richard R RR; Gabriel, Stacey B SB; Kathiresan, Sekar S; Boerwinkle, Eric E
Publication Date: 2011-02-10

Variant appearance in text: rs7679
PubMed Link: 21347282
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mendelian randomization studies do not support a role for raised circulating triglyceride levels influencing type 2 diabetes, glucose levels, or insulin resistance.

Diabetes
De Silva, N Maneka G NM; Freathy, Rachel M RM; Palmer, Tom M TM; Donnelly, Louise A LA; Luan, Jian'an J; Gaunt, Tom T; Langenberg, Claudia C; Weedon, Michael N MN; Shields, Beverley B; Knight, Beatrice A BA; Ward, Kirsten J KJ; Sandhu, Manjinder S MS; Harbord, Roger M RM; McCarthy, Mark I MI; Smith, George Davey GD; Ebrahim, Shah S; Hattersley, Andrew T AT; Wareham, Nicholas N; Lawlor, Debbie A DA; Morris, Andrew D AD; Palmer, Colin N A CN; Frayling, Timothy M TM
Publication Date: 2011-03

Variant appearance in text: rs7679
PubMed Link: 21282362
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of common DNA sequence variants at 33 genetic loci with blood lipids in individuals of African ancestry from Jamaica.

Human Genetics
Gupta, R R; Ejebe, K K; Butler, J J; Lettre, G G; Lyon, H H; Guiducci, C C; Wilks, R R; Bennett, F F; Forrester, T T; Tayo, B B; Musunuru, K K; Hirschhorn, J J; Kathiresan, S S; Cooper, R S RS; McKenzie, C A CA
Publication Date: 2010-11

Variant appearance in text: rs7679
PubMed Link: 20839009
Variant Present in the following documents:
  • Main text
View BVdb publication page



Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.

Nature Genetics
Johansen, Christopher T CT; Wang, Jian J; Lanktree, Matthew B MB; Cao, Henian H; McIntyre, Adam D AD; Ban, Matthew R MR; Martins, Rebecca A RA; Kennedy, Brooke A BA; Hassell, Reina G RG; Visser, Maartje E ME; Schwartz, Stephen M SM; Voight, Benjamin F BF; Elosua, Roberto R; Salomaa, Veikko V; O'Donnell, Christopher J CJ; Dallinga-Thie, Geesje M GM; Anand, Sonia S SS; Yusuf, Salim S; Huff, Murray W MW; Kathiresan, Sekar S; Hegele, Robert A RA
Publication Date: 2010-08

Variant appearance in text: rs7679
PubMed Link: 20657596
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs7679
PubMed Link: 20571754
Variant Present in the following documents:
  • 125_2010_Article_1792.pdf
View BVdb publication page



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: rs7679
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
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: rs7679
PubMed Link: 20406164
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).

Proceedings Of The National Academy Of Sciences Of The United States Of America
Neale, Benjamin M BM; Fagerness, Jesen J; Reynolds, Robyn R; Sobrin, Lucia L; Parker, Margaret M; Raychaudhuri, Soumya S; Tan, Perciliz L PL; Oh, Edwin C EC; Merriam, Joanna E JE; Souied, Eric E; Bernstein, Paul S PS; Li, Binxing B; Frederick, Jeanne M JM; Zhang, Kang K; Brantley, Milam A MA; Lee, Aaron Y AY; Zack, Donald J DJ; Campochiaro, Betsy B; Campochiaro, Peter P; Ripke, Stephan S; Smith, R Theodore RT; Barile, Gaetano R GR; Katsanis, Nicholas N; Allikmets, Rando R; Daly, Mark J MJ; Seddon, Johanna M JM
Publication Date: 2010-04-20

Variant appearance in text: rs7679
PubMed Link: 20385826
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of lipid disorders.

Current Opinion In Cardiology
Pirruccello, James J; Kathiresan, Sekar S
Publication Date: 2010-05

Variant appearance in text: rs7679
PubMed Link: 20224388
Variant Present in the following documents:
  • Main text
View BVdb publication page



Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.

Circulation. Cardiovascular Genetics
Weissglas-Volkov, Daphna D; Aguilar-Salinas, Carlos A CA; Sinsheimer, Janet S JS; Riba, Laura L; Huertas-Vazquez, Adriana A; Ordoñez-Sánchez, Maria L ML; Rodriguez-Guillen, Rosario R; Cantor, Rita M RM; Tusie-Luna, Teresa T; Pajukanta, Päivi P
Publication Date: 2010-02

Variant appearance in text: rs7679
PubMed Link: 20160193
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic and nongenetic sources of variation in phospholipid transfer protein activity.

Journal Of Lipid Research
Jarvik, Gail P GP; Rajagopalan, Ramakrishnan R; Rosenthal, Elisabeth A EA; Wolfbauer, Gertrud G; McKinstry, Laura L; Vaze, Aditya A; Brunzell, John J; Motulsky, Arno G AG; Nickerson, Deborah A DA; Heagerty, Patrick J PJ; Wijsman, Ellen M EM; Albers, John J JJ
Publication Date: 2010-05

Variant appearance in text: rs7679
PubMed Link: 19965587
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs7679
PubMed Link: 19951432
Variant Present in the following documents:
  • Main text
  • 1476-511X-8-52.pdf
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Common variants at 30 loci contribute to polygenic dyslipidemia.

Nature Genetics
Kathiresan, Sekar S; Willer, Cristen J CJ; Peloso, Gina M GM; Demissie, Serkalem S; Musunuru, Kiran K; Schadt, Eric E EE; Kaplan, Lee L; Bennett, Derrick D; Li, Yun Y; Tanaka, Toshiko T; Voight, Benjamin F BF; Bonnycastle, Lori L LL; Jackson, Anne U AU; Crawford, Gabriel G; Surti, Aarti A; Guiducci, Candace C; Burtt, Noel P NP; Parish, Sarah S; Clarke, Robert R; Zelenika, Diana D; Kubalanza, Kari A KA; Morken, Mario A MA; Scott, Laura J LJ; Stringham, Heather M HM; Galan, Pilar P; Swift, Amy J AJ; Kuusisto, Johanna J; Bergman, Richard N RN; Sundvall, Jouko J; Laakso, Markku M; Ferrucci, Luigi L; Scheet, Paul P; Sanna, Serena S; Uda, Manuela M; Yang, Qiong Q; Lunetta, Kathryn L KL; Dupuis, Josée J; de Bakker, Paul I W PI; O'Donnell, Christopher J CJ; Chambers, John C JC; Kooner, Jaspal S JS; Hercberg, Serge S; Meneton, Pierre P; Lakatta, Edward G EG; Scuteri, Angelo A; Schlessinger, David D; Tuomilehto, Jaakko J; Collins, Francis S FS; Groop, Leif L; Altshuler, David D; Collins, Rory R; Lathrop, G Mark GM; Melander, Olle O; Salomaa, Veikko V; Peltonen, Leena L; Orho-Melander, Marju M; Ordovas, Jose M JM; Boehnke, Michael M; Abecasis, Gonçalo R GR; Mohlke, Karen L KL; Cupples, L Adrienne LA
Publication Date: 2009-01

Variant appearance in text: rs7679
PubMed Link: 19060906
Variant Present in the following documents:
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