Publications:

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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: rs7819412

PubMed Link: 37223289

Variant Present in the following documents:

• Main text
• cjim-14-249.pdf

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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: rs7819412

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.

Journal Of The American Heart Association

Shi, Mengyao M; Kelly, Tanika N TN; Zhu, Zhengbao Z; Li, Changwei C; Shen, Chong C; Sun, Yingxian Y; Wang, Aili A; Shan, Guangliang G; Bu, Xiaoqing X; Guo, Daoxia D; Zhao, Jingbo J; Xu, Tan T; Peng, Hao H; Xu, Tian T; Zhong, Chongke C; Sun, Xiao X; Chen, Jing J; Zhang, Yonghong Y; He, Jiang J

Publication Date: 2022-10-04

Variant appearance in text: rs7819412

PubMed Link: 36193932

Variant Present in the following documents:

• JAH3-11-e025245.pdf

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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight

Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL

Publication Date: 2020-09-03

Variant appearance in text: rs7819412

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

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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: rs7819412

PubMed Link: 32821703

Variant Present in the following documents:

• Main text
• jla-8-132.pdf

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Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.

Bmc Medical Genomics

Dron, Jacqueline S JS; Wang, Jian J; McIntyre, Adam D AD; Iacocca, Michael A MA; Robinson, John F JF; Ban, Matthew R MR; Cao, Henian H; Hegele, Robert A RA

Publication Date: 2020-02-10

Variant appearance in text: XKR6: 764+12924C>T

PubMed Link: 32041611

Variant Present in the following documents:

• 12920_2020_669_MOESM1_ESM.xlsx, sheet 3

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XKR6 rs7014968 SNP Increases Serum Total Cholesterol Levels and the Risk of Coronary Heart Disease and Ischemic Stroke.

Clinical And Applied Thrombosis/Hemostasis : Official Journal Of The International Academy Of Clinical And Applied Thrombosis/Hemostasis

Li, Kai-Guang KG; Yin, Rui-Xing RX; Huang, Feng F; Chen, Wu-Xian WX; Wu, Jin-Zhen JZ; Cao, Xiao-Li XL

Publication Date: 2020

Variant appearance in text: rs7819412

PubMed Link: 32024373

Variant Present in the following documents:

• Main text
• 10.1177_1076029620902844.pdf

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Association between the XKR6 rs7819412 SNP and serum lipid levels and the risk of coronary artery disease and ischemic stroke.

Bmc Cardiovascular Disorders

Zheng, Peng-Fei PF; Yin, Rui-Xing RX; Deng, Guo-Xiong GX; Guan, Yao-Zong YZ; Wei, Bi-Liu BL; Liu, Chun-Xiao CX

Publication Date: 2019-08-20

Variant appearance in text: rs7819412

PubMed Link: 31429711

Variant Present in the following documents:

• Main text
• 12872_2019_Article_1179.pdf

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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: rs7819412

PubMed Link: 30652019

Variant Present in the following documents:

• Main text
• fsoa-05-350.pdf

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Multiple signals at the extended 8p23 locus are associated with susceptibility to systemic lupus erythematosus.

Journal Of Medical Genetics

Demirci, F Yesim FY; Wang, Xingbin X; Morris, David L DL; Feingold, Eleanor E; Bernatsky, Sasha S; Pineau, Christian C; Clarke, Ann A; Ramsey-Goldman, Rosalind R; Manzi, Susan S; Vyse, Timothy J TJ; Kamboh, M I MI

Publication Date: 2017-06

Variant appearance in text: rs7819412

PubMed Link: 28289186

Variant Present in the following documents:

• Main text

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Signatures of natural selection on genetic variants affecting complex human traits.

Applied & Translational Genomics

Zhang, Ge G; Muglia, Louis J LJ; Chakraborty, Ranajit R; Akey, Joshua M JM; Williams, Scott M SM

Publication Date: 2013-12-01

Variant appearance in text: rs7819412

PubMed Link: 27896059

Variant Present in the following documents:

• Main text
• main.pdf

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Mendelian randomization studies of biomarkers and type 2 diabetes.

Endocrine Connections

Abbasi, Ali A

Publication Date: 2015-12

Variant appearance in text: rs7819412

PubMed Link: 26446360

Variant Present in the following documents:

• Main text
• ec-04-249.pdf

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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: rs7819412

PubMed Link: 25249548

Variant Present in the following documents:

• Main text

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

Frontiers In Genetics

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: rs7819412

PubMed Link: 25147553

Variant Present in the following documents:

• Main text
• fgene-05-00222.pdf

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LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias.

Journal Of Lipid Research

Johansen, Christopher T CT; Dubé, Joseph B JB; Loyzer, Melissa N MN; MacDonald, Austin A; Carter, David E DE; McIntyre, Adam D AD; Cao, Henian H; Wang, Jian J; Robinson, John F JF; Hegele, Robert A RA

Publication Date: 2014-04

Variant appearance in text: rs7819412

PubMed Link: 24503134

Variant Present in the following documents:

• supp_D045963_jlr.D045963-1.pdf

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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: rs7819412

PubMed Link: 23555584

Variant Present in the following documents:

• Main text

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

Bmc Medical Genetics

Huhn, Stefanie S; Bevier, Melanie M; Rudolph, Anja A; Pardini, Barbara B; Naccarati, Alessio A; Hein, Rebecca R; Hoffmeister, Michael M; Vodickova, Ludmila L; Novotny, Jan J; Brenner, Hermann H; Chang-Claude, Jenny J; Hemminki, Kari K; Vodicka, Pavel P; Försti, Asta A

Publication Date: 2012-10-05

Variant appearance in text: rs7819412

PubMed Link: 23036011

Variant Present in the following documents:

• 1471-2350-13-94-S1.pdf

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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: rs7819412

PubMed Link: 21860704

Variant Present in the following documents:

• Main text

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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: rs7819412

PubMed Link: 21282362

Variant Present in the following documents:

• Main text

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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: rs7819412

PubMed Link: 20839009

Variant Present in the following documents:

• Main text

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Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.

Plos Genetics

Smith, Erin N EN; Chen, Wei W; Kähönen, Mika M; Kettunen, Johannes J; Lehtimäki, Terho T; Peltonen, Leena L; Raitakari, Olli T OT; Salem, Rany M RM; Schork, Nicholas J NJ; Shaw, Marian M; Srinivasan, Sathanur R SR; Topol, Eric J EJ; Viikari, Jorma S JS; Berenson, Gerald S GS; Murray, Sarah S SS

Publication Date: 2010-09-09

Variant appearance in text: rs7819412

PubMed Link: 20838585

Variant Present in the following documents:

• Main text
• pgen.1001094.pdf

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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: rs7819412

PubMed Link: 20657596

Variant Present in the following documents:

• Main text

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Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.

Plos Genetics

Scherag, André A; Dina, Christian C; Hinney, Anke A; Vatin, Vincent V; Scherag, Susann S; Vogel, Carla I G CI; Müller, Timo D TD; Grallert, Harald H; Wichmann, H-Erich HE; Balkau, Beverley B; Heude, Barbara B; Jarvelin, Marjo-Riitta MR; Hartikainen, Anna-Liisa AL; Levy-Marchal, Claire C; Weill, Jacques J; Delplanque, Jérôme J; Körner, Antje A; Kiess, Wieland W; Kovacs, Peter P; Rayner, Nigel W NW; Prokopenko, Inga I; McCarthy, Mark I MI; Schäfer, Helmut H; Jarick, Ivonne I; Boeing, Heiner H; Fisher, Eva E; Reinehr, Thomas T; Heinrich, Joachim J; Rzehak, Peter P; Berdel, Dietrich D; Borte, Michael M; Biebermann, Heike H; Krude, Heiko H; Rosskopf, Dieter D; Rimmbach, Christian C; Rief, Winfried W; Fromme, Tobias T; Klingenspor, Martin M; Schürmann, Annette A; Schulz, Nadja N; Nöthen, Markus M MM; Mühleisen, Thomas W TW; Erbel, Raimund R; Jöckel, Karl-Heinz KH; Moebus, Susanne S; Boes, Tanja T; Illig, Thomas T; Froguel, Philippe P; Hebebrand, Johannes J; Meyre, David D

Publication Date: 2010-04-22

Variant appearance in text: rs7819412

PubMed Link: 20421936

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: rs7819412

PubMed Link: 20406164

Variant Present in the following documents:

• Main text

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Genetics of lipid disorders.

Current Opinion In Cardiology

Pirruccello, James J; Kathiresan, Sekar S

Publication Date: 2010-05

Variant appearance in text: rs7819412

PubMed Link: 20224388

Variant Present in the following documents:

• Main text

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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: rs7819412

PubMed Link: 20160193

Variant Present in the following documents:

• Main text

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Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.

Plos Genetics

Chasman, Daniel I DI; Paré, Guillaume G; Mora, Samia S; Hopewell, Jemma C JC; Peloso, Gina G; Clarke, Robert R; Cupples, L Adrienne LA; Hamsten, Anders A; Kathiresan, Sekar S; Mälarstig, Anders A; Ordovas, José M JM; Ripatti, Samuli S; Parker, Alex N AN; Miletich, Joseph P JP; Ridker, Paul M PM

Publication Date: 2009-11

Variant appearance in text: rs7819412

PubMed Link: 19936222

Variant Present in the following documents:

• Main text
• pgen.1000730.pdf

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The effect of a novel intergenic polymorphism (rs11774572) on HDL-cholesterol concentrations depends on TaqIB polymorphism in the cholesterol ester transfer protein gene.

Nutrition, Metabolism, And Cardiovascular Diseases : Nmcd

Junyent, M M; Lee, Y-C YC; Smith, C E CE; Arnett, D K DK; Tsai, M Y MY; Kabagambe, E K EK; Straka, R J RJ; Province, M M; An, P P; Lai, C-Q CQ; Parnell, L D LD; Shen, J J; Borecki, I I; Ordovas, J M JM

Publication Date: 2010-01

Variant appearance in text: rs7819412

PubMed Link: 19364639

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: rs7819412

PubMed Link: 19060906

Variant Present in the following documents:

• Main text

View BVdb publication page

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