Publications:

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A bi-directional Mendelian randomization study of sarcopenia-related traits and type 2 diabetes mellitus.

Frontiers In Endocrinology

Chen, Simin S; Yan, Shikang S; Aiheti, Nuerbiyamu N; Kuribanjiang, Kaidiriyan K; Yao, Xuemei X; Wang, Qian Q; Zhou, Tao T; Yang, Lei L

Publication Date: 2023

Variant appearance in text: rs16926246

PubMed Link: 36967750

Variant Present in the following documents:

• Main text
• fendo-14-1109800.pdf

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Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits.

Plos Genetics

Chun, Sung S; Akle, Sebastian S; Teodosiadis, Athanasios A; Cade, Brian E BE; Wang, Heming H; Sofer, Tamar T; Evans, Daniel S DS; Stone, Katie L KL; Gharib, Sina A SA; Mukherjee, Sutapa S; Palmer, Lyle J LJ; Hillman, David D; Rotter, Jerome I JI; Hanis, Craig L CL; Stamatoyannopoulos, John A JA; Redline, Susan S; Cotsapas, Chris C; Sunyaev, Shamil R SR

Publication Date: 2022-12-27

Variant appearance in text: rs16926246

PubMed Link: 36574455

Variant Present in the following documents:

• Main text
• pgen.1010557.pdf

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Genetic associations for two biological age measures point to distinct aging phenotypes.

Aging Cell

Kuo, Chia-Ling CL; Pilling, Luke C LC; Liu, Zuyun Z; Atkins, Janice L JL; Levine, Morgan E ME

Publication Date: 2021-06

Variant appearance in text: rs16926246

PubMed Link: 34038024

Variant Present in the following documents:

• Main text
• ACEL-20-e13376.pdf

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Searching for causal relationships of glioma: a phenome-wide Mendelian randomisation study.

British Journal Of Cancer

Saunders, Charlie N CN; Cornish, Alex J AJ; Kinnersley, Ben B; Law, Philip J PJ; Houlston, Richard S RS; ,

Publication Date: 2021-01

Variant appearance in text: rs16926246

PubMed Link: 33020596

Variant Present in the following documents:

• Main text
• 41416_2020_Article_1083.pdf

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Mitochondrial pathways in human health and aging.

Mitochondrion

Bornstein, Rebecca R; Gonzalez, Brenda B; Johnson, Simon C SC

Publication Date: 2020-09

Variant appearance in text: rs16926246

PubMed Link: 32738358

Variant Present in the following documents:

• Main text

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Polygenic Hyperlipidemias and Coronary Artery Disease Risk.

Circulation. Genomic And Precision Medicine

Ripatti, Pietari P; Rämö, Joel T JT; Mars, Nina J NJ; Fu, Yu Y; Lin, Jake J; Söderlund, Sanni S; Benner, Christian C; Surakka, Ida I; Kiiskinen, Tuomo T; Havulinna, Aki S AS; Palta, Priit P; Freimer, Nelson B NB; Widén, Elisabeth E; Salomaa, Veikko V; Tukiainen, Taru T; Pirinen, Matti M; Palotie, Aarno A; Taskinen, Marja-Riitta MR; Ripatti, Samuli S; ,

Publication Date: 2020-04

Variant appearance in text: rs16926246

PubMed Link: 32154731

Variant Present in the following documents:

• hcg-13-e002725-s001.pdf

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Lack of association between modifiable exposures and glioma risk: a Mendelian randomization analysis.

Neuro-Oncology

Saunders, Charlie N CN; Cornish, Alex J AJ; Kinnersley, Ben B; Law, Philip J PJ; Claus, Elizabeth B EB; Il'yasova, Dora D; Schildkraut, Joellen J; Barnholtz-Sloan, Jill S JS; Olson, Sara H SH; Bernstein, Jonine L JL; Lai, Rose K RK; Chanock, Stephen S; Rajaraman, Preetha P; Johansen, Christoffer C; Jenkins, Robert B RB; Melin, Beatrice S BS; Wrensch, Margaret R MR; Sanson, Marc M; Bondy, Melissa L ML; Houlston, Richard S RS

Publication Date: 2020-02-20

Variant appearance in text: rs16926246

PubMed Link: 31665421

Variant Present in the following documents:

• Main text
• noz209.pdf

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Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep.

Plos Genetics

Cade, Brian E BE; Chen, Han H; Stilp, Adrienne M AM; Louie, Tin T; Ancoli-Israel, Sonia S; Arens, Raanan R; Barfield, Richard R; Below, Jennifer E JE; Cai, Jianwen J; Conomos, Matthew P MP; Evans, Daniel S DS; Frazier-Wood, Alexis C AC; Gharib, Sina A SA; Gleason, Kevin J KJ; Gottlieb, Daniel J DJ; Hillman, David R DR; Johnson, W Craig WC; Lederer, David J DJ; Lee, Jiwon J; Loredo, Jose S JS; Mei, Hao H; Mukherjee, Sutapa S; Patel, Sanjay R SR; Post, Wendy S WS; Purcell, Shaun M SM; Ramos, Alberto R AR; Reid, Kathryn J KJ; Rice, Ken K; Shah, Neomi A NA; Sofer, Tamar T; Taylor, Kent D KD; Thornton, Timothy A TA; Wang, Heming H; Yaffe, Kristine K; Zee, Phyllis C PC; Hanis, Craig L CL; Palmer, Lyle J LJ; Rotter, Jerome I JI; Stone, Katie L KL; Tranah, Gregory J GJ; Wilson, James G JG; Sunyaev, Shamil R SR; Laurie, Cathy C CC; Zhu, Xiaofeng X; Saxena, Richa R; Lin, Xihong X; Redline, Susan S

Publication Date: 2019-04

Variant appearance in text: rs16926246

PubMed Link: 30990817

Variant Present in the following documents:

• Main text
• pgen.1007739.pdf

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Genetic Ancestry Markers and Difference in A1c Between African American and White in the Diabetes Prevention Program.

The Journal Of Clinical Endocrinology And Metabolism

Hivert, Marie-France MF; Christophi, Costas A CA; Jablonski, Kathleen A KA; Edelstein, Sharon L SL; Kahn, Steven E SE; Golden, Sherita Hill SH; Dagogo-Jack, Samuel S; Mather, Kieren J KJ; Luchsinger, José A JA; Caballero, A Enrique AE; Barrett-Connor, Elizabeth E; Knowler, William C WC; Florez, Jose C JC; Herman, William H WH

Publication Date: 2019-02-01

Variant appearance in text: rs16926246

PubMed Link: 30358859

Variant Present in the following documents:

• Main text

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Generalization and fine mapping of red blood cell trait genetic associations to multi-ethnic populations: The PAGE Study.

American Journal Of Hematology

Jo Hodonsky, Chani C; Schurmann, Claudia C; Schick, Ursula M UM; Kocarnik, Jonathan J; Tao, Ran R; van Rooij, Frank Ja FJ; Wassel, Christina C; Buyske, Steve S; Fornage, Myriam M; Hindorff, Lucia A LA; Floyd, James S JS; Ganesh, Santhi K SK; Lin, Dan-Yu DY; North, Kari E KE; Reiner, Alex P AP; Loos, Ruth Jf RJ; Kooperberg, Charles C; Avery, Christy L CL

Publication Date: 2018-06-15

Variant appearance in text: rs16926246

PubMed Link: 29905378

Variant Present in the following documents:

• Main text

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Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population.

European Journal Of Human Genetics : Ejhg

Appel, Emil V R EVR; Moltke, Ida I; Jørgensen, Marit E ME; Bjerregaard, Peter P; Linneberg, Allan A; Pedersen, Oluf O; Albrechtsen, Anders A; Hansen, Torben T; Grarup, Niels N

Publication Date: 2018-06

Variant appearance in text: rs16926246

PubMed Link: 29483669

Variant Present in the following documents:

• Main text

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Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c.

Scientific Reports

Hachiya, Tsuyoshi T; Komaki, Shohei S; Hasegawa, Yutaka Y; Ohmomo, Hideki H; Tanno, Kozo K; Hozawa, Atsushi A; Tamiya, Gen G; Yamamoto, Masayuki M; Ogasawara, Kuniaki K; Nakamura, Motoyuki M; Hitomi, Jiro J; Ishigaki, Yasushi Y; Sasaki, Makoto M; Shimizu, Atsushi A

Publication Date: 2017-11-23

Variant appearance in text: rs16926246

PubMed Link: 29170429

Variant Present in the following documents:

• Main text
• 41598_2017_Article_16493.pdf

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Genetic aetiology of glycaemic traits: approaches and insights.

Human Molecular Genetics

Wheeler, Eleanor E; Marenne, Gaëlle G; Barroso, Inês I

Publication Date: 2017-10-01

Variant appearance in text: rs16926246

PubMed Link: 28977447

Variant Present in the following documents:

• Main text
• ddx293.pdf

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Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism.

Scientific Reports

Li, Man M; Maruthur, Nisa M NM; Loomis, Stephanie J SJ; Pietzner, Maik M; North, Kari E KE; Mei, Hao H; Morrison, Alanna C AC; Friedrich, Nele N; Pankow, James S JS; Nauck, Matthias M; Boerwinkle, Eric E; Teumer, Alexander A; Selvin, Elizabeth E; Köttgen, Anna A

Publication Date: 2017-06-06

Variant appearance in text: rs16926246

PubMed Link: 28588231

Variant Present in the following documents:

• 41598_2017_2287_MOESM1_ESM.pdf

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Type 2 Diabetes Prevention: Implications of Hemoglobin A1c Genetics.

The Review Of Diabetic Studies : Rds

Leong, Aaron A; Meigs, James B JB

Publication Date: 2015

Variant appearance in text: rs16926246

PubMed Link: 27111120

Variant Present in the following documents:

• Main text

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Update on genetics and diabetic retinopathy.

Clinical Ophthalmology (Auckland, N.Z.)

Hampton, Blake M BM; Schwartz, Stephen G SG; Brantley, Milam A MA; Flynn, Harry W HW

Publication Date: 2015

Variant appearance in text: rs16926246

PubMed Link: 26648684

Variant Present in the following documents:

• Main text
• opth-9-2175.pdf

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Recent advances in understanding the genetic architecture of type 2 diabetes.

Human Molecular Genetics

Mohlke, Karen L KL; Boehnke, Michael M

Publication Date: 2015-10-15

Variant appearance in text: rs16926246

PubMed Link: 26160912

Variant Present in the following documents:

• Main text

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Heritability and genomics of gene expression in peripheral blood.

Nature Genetics

Wright, Fred A FA; Sullivan, Patrick F PF; Brooks, Andrew I AI; Zou, Fei F; Sun, Wei W; Xia, Kai K; Madar, Vered V; Jansen, Rick R; Chung, Wonil W; Zhou, Yi-Hui YH; Abdellaoui, Abdel A; Batista, Sandra S; Butler, Casey C; Chen, Guanhua G; Chen, Ting-Huei TH; D'Ambrosio, David D; Gallins, Paul P; Ha, Min Jin MJ; Hottenga, Jouke Jan JJ; Huang, Shunping S; Kattenberg, Mathijs M; Kochar, Jaspreet J; Middeldorp, Christel M CM; Qu, Ani A; Shabalin, Andrey A; Tischfield, Jay J; Todd, Laura L; Tzeng, Jung-Ying JY; van Grootheest, Gerard G; Vink, Jacqueline M JM; Wang, Qi Q; Wang, Wei W; Wang, Weibo W; Willemsen, Gonneke G; Smit, Johannes H JH; de Geus, Eco J EJ; Yin, Zhaoyu Z; Penninx, Brenda W J H BW; Boomsma, Dorret I DI

Publication Date: 2014-05

Variant appearance in text: rs16926246

PubMed Link: 24728292

Variant Present in the following documents:

• NIHMS576016-supplement-1.pdf

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Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.

Diabetes

Chen, Peng P; Takeuchi, Fumihiko F; Lee, Jong-Young JY; Li, Huaixing H; Wu, Jer-Yuarn JY; Liang, Jun J; Long, Jirong J; Tabara, Yasuharu Y; Goodarzi, Mark O MO; Pereira, Mark A MA; Kim, Young Jin YJ; Go, Min Jin MJ; Stram, Daniel O DO; Vithana, Eranga E; Khor, Chiea-Chuen CC; Liu, Jianjun J; Liao, Jiemin J; Ye, Xingwang X; Wang, Yiqin Y; Lu, Ling L; Young, Terri L TL; Lee, Jeannette J; Thai, Ah Chuan AC; Cheng, Ching-Yu CY; van Dam, Rob M RM; Friedlander, Yechiel Y; Heng, Chew-Kiat CK; Koh, Woon-Puay WP; Chen, Chien-Hsiun CH; Chang, Li-Ching LC; Pan, Wen-Harn WH; Qi, Qibin Q; Isono, Masato M; Zheng, Wei W; Cai, Qiuyin Q; Gao, Yutang Y; Yamamoto, Ken K; Ohnaka, Keizo K; Takayanagi, Ryoichi R; Kita, Yoshikuni Y; Ueshima, Hirotsugu H; Hsiung, Chao A CA; Cui, Jinrui J; Sheu, Wayne H-H WH; Rotter, Jerome I JI; Chen, Yii-Der I YD; Hsu, Chris C; Okada, Yukinori Y; Kubo, Michiaki M; Takahashi, Atsushi A; Tanaka, Toshihiro T; van Rooij, Frank J A FJ; Ganesh, Santhi K SK; Huang, Jinyan J; Huang, Tao T; Yuan, Jianmin J; Hwang, Joo-Yeon JY; , ; Gross, Myron D MD; Assimes, Themistocles L TL; Miki, Tetsuro T; Shu, Xiao-Ou XO; Qi, Lu L; Chen, Yuan-Tson YT; Lin, Xu X; Aung, Tin T; Wong, Tien-Yin TY; Teo, Yik-Ying YY; Kim, Bong-Jo BJ; Kato, Norihiro N; Tai, E-Shyong ES

Publication Date: 2014-07

Variant appearance in text: rs16926246

PubMed Link: 24647736

Variant Present in the following documents:

• Main text

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A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry.

Plos One

Chen, Peng P; Ong, Rick Twee-Hee RT; Tay, Wan-Ting WT; Sim, Xueling X; Ali, Mohammad M; Xu, Haiyan H; Suo, Chen C; Liu, Jianjun J; Chia, Kee-Seng KS; Vithana, Eranga E; Young, Terri L TL; Aung, Tin T; Lim, Wei-Yen WY; Khor, Chiea-Chuen CC; Cheng, Ching-Yu CY; Wong, Tien-Yin TY; Teo, Yik-Ying YY; Tai, E-Shyong ES

Publication Date: 2013

Variant appearance in text: rs16926246

PubMed Link: 24244560

Variant Present in the following documents:

• Main text
• pone.0079767.pdf

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Family-based association study between SLC2A1, HK1, and LEPR polymorphisms with myelomeningocele in Chile.

Reproductive Sciences (Thousand Oaks, Calif.)

Suazo, José J; Pardo, Rosa R; Castillo, Silvia S; Martin, Luz Maria LM; Rojas, Francisca F; Santos, José Luis JL; Rotter, Karin K; Solar, Margarita M; Tapia, Eva E

Publication Date: 2013-10

Variant appearance in text: rs16926246

PubMed Link: 23427181

Variant Present in the following documents:

• Main text

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Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination Survey (NHANES III).

Bmc Medical Genetics

Grimsby, Jonna L JL; Porneala, Bianca C BC; Vassy, Jason L JL; Yang, Quanhe Q; Florez, José C JC; Dupuis, Josée J; Liu, Tiebin T; Yesupriya, Ajay A; Chang, Man-Huei MH; Ned, Renee M RM; Dowling, Nicole F NF; Khoury, Muin J MJ; Meigs, James B JB; ,

Publication Date: 2012-04-27

Variant appearance in text: rs16926246

PubMed Link: 22540250

Variant Present in the following documents:

• Main text

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Genetic determinants of variability in glycated hemoglobin (HbA(1c)) in humans: review of recent progress and prospects for use in diabetes care.

Current Diabetes Reports

Soranzo, Nicole N

Publication Date: 2011-12

Variant appearance in text: rs16926246

PubMed Link: 21975967

Variant Present in the following documents:

• Main text

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Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes.

Bmc Medical Genetics

Gjesing, Anette P AP; Nielsen, Aneta A AA; Brandslund, Ivan I; Christensen, Cramer C; Sandbæk, Anneli A; Jørgensen, Torben T; Witte, Daniel D; Bonnefond, Amélie A; Froguel, Phillippe P; Hansen, Torben T; Pedersen, Oluf O

Publication Date: 2011-07-25

Variant appearance in text: rs16926246

PubMed Link: 21781351

Variant Present in the following documents:

• Main text
• 1471-2350-12-99.pdf

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Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.

Diabetes

Soranzo, Nicole N; Sanna, Serena S; Wheeler, Eleanor E; Gieger, Christian C; Radke, Dörte D; Dupuis, Josée J; Bouatia-Naji, Nabila N; Langenberg, Claudia C; Prokopenko, Inga I; Stolerman, Elliot E; Sandhu, Manjinder S MS; Heeney, Matthew M MM; Devaney, Joseph M JM; Reilly, Muredach P MP; Ricketts, Sally L SL; Stewart, Alexandre F R AF; Voight, Benjamin F BF; Willenborg, Christina C; Wright, Benjamin B; Altshuler, David D; Arking, Dan D; Balkau, Beverley B; Barnes, Daniel D; Boerwinkle, Eric E; Böhm, Bernhard B; Bonnefond, Amélie A; Bonnycastle, Lori L LL; Boomsma, Dorret I DI; Bornstein, Stefan R SR; Böttcher, Yvonne Y; Bumpstead, Suzannah S; Burnett-Miller, Mary Susan MS; Campbell, Harry H; Cao, Antonio A; Chambers, John J; Clark, Robert R; Collins, Francis S FS; Coresh, Josef J; de Geus, Eco J C EJ; Dei, Mariano M; Deloukas, Panos P; Döring, Angela A; Egan, Josephine M JM; Elosua, Roberto R; Ferrucci, Luigi L; Forouhi, Nita N; Fox, Caroline S CS; Franklin, Christopher C; Franzosi, Maria Grazia MG; Gallina, Sophie S; Goel, Anuj A; Graessler, Jürgen J; Grallert, Harald H; Greinacher, Andreas A; Hadley, David D; Hall, Alistair A; Hamsten, Anders A; Hayward, Caroline C; Heath, Simon S; Herder, Christian C; Homuth, Georg G; Hottenga, Jouke-Jan JJ; Hunter-Merrill, Rachel R; Illig, Thomas T; Jackson, Anne U AU; Jula, Antti A; Kleber, Marcus M; Knouff, Christopher W CW; Kong, Augustine A; Kooner, Jaspal J; Köttgen, Anna A; Kovacs, Peter P; Krohn, Knut K; Kühnel, Brigitte B; Kuusisto, Johanna J; Laakso, Markku M; Lathrop, Mark M; Lecoeur, Cécile C; Li, Man M; Li, Mingyao M; Loos, Ruth J F RJ; Luan, Jian'an J; Lyssenko, Valeriya V; Mägi, Reedik R; Magnusson, Patrik K E PK; Mälarstig, Anders A; Mangino, Massimo M; Martínez-Larrad, María Teresa MT; März, Winfried W; McArdle, Wendy L WL; McPherson, Ruth R; Meisinger, Christa C; Meitinger, Thomas T; Melander, Olle O; Mohlke, Karen L KL; Mooser, Vincent E VE; Morken, Mario A MA; Narisu, Narisu N; Nathan, David M DM; Nauck, Matthias M; O'Donnell, Chris C; Oexle, Konrad K; Olla, Nazario N; Pankow, James S JS; Payne, Felicity F; Peden, John F JF; Pedersen, Nancy L NL; Peltonen, Leena L; Perola, Markus M; Polasek, Ozren O; Porcu, Eleonora E; Rader, Daniel J DJ; Rathmann, Wolfgang W; Ripatti, Samuli S; Rocheleau, Ghislain G; Roden, Michael M; Rudan, Igor I; Salomaa, Veikko V; Saxena, Richa R; Schlessinger, David D; Schunkert, Heribert H; Schwarz, Peter P; Seedorf, Udo U; Selvin, Elizabeth E; Serrano-Ríos, Manuel M; Shrader, Peter P; Silveira, Angela A; Siscovick, David D; Song, Kjioung K; Spector, Timothy D TD; Stefansson, Kari K; Steinthorsdottir, Valgerdur V; Strachan, David P DP; Strawbridge, Rona R; Stumvoll, Michael M; Surakka, Ida I; Swift, Amy J AJ; Tanaka, Toshiko T; Teumer, Alexander A; Thorleifsson, Gudmar G; Thorsteinsdottir, Unnur U; Tönjes, Anke A; Usala, Gianluca G; Vitart, Veronique V; Völzke, Henry H; Wallaschofski, Henri H; Waterworth, Dawn M DM; Watkins, Hugh H; Wichmann, H-Erich HE; Wild, Sarah H SH; Willemsen, Gonneke G; Williams, Gordon H GH; Wilson, James F JF; Winkelmann, Juliane J; Wright, Alan F AF; , ; Zabena, Carina C; Zhao, Jing Hua JH; Epstein, Stephen E SE; Erdmann, Jeanette J; Hakonarson, Hakon H HH; Kathiresan, Sekar S; Khaw, Kay-Tee KT; Roberts, Robert R; Samani, Nilesh J NJ; Fleming, Mark D MD; Sladek, Robert R; Abecasis, Gonçalo G; Boehnke, Michael M; Froguel, Philippe P; Groop, Leif L; McCarthy, Mark I MI; Kao, W H Linda WH; Florez, Jose C JC; Uda, Manuela M; Wareham, Nicholas J NJ; Barroso, Inês I; Meigs, James B JB

Publication Date: 2010-12

Variant appearance in text: rs16926246

PubMed Link: 20858683

Variant Present in the following documents:

• Main text
• supp_db10-0502_db100502nlineappendix.pdf
• zdb3229.pdf

View BVdb publication page

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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

Nature Genetics

Ganesh, Santhi K SK; Zakai, Neil A NA; van Rooij, Frank J A FJ; Soranzo, Nicole N; Smith, Albert V AV; Nalls, Michael A MA; Chen, Ming-Huei MH; Kottgen, Anna A; Glazer, Nicole L NL; Dehghan, Abbas A; Kuhnel, Brigitte B; Aspelund, Thor T; Yang, Qiong Q; Tanaka, Toshiko T; Jaffe, Andrew A; Bis, Joshua C M JC; Verwoert, Germaine C GC; Teumer, Alexander A; Fox, Caroline S CS; Guralnik, Jack M JM; Ehret, Georg B GB; Rice, Kenneth K; Felix, Janine F JF; Rendon, Augusto A; Eiriksdottir, Gudny G; Levy, Daniel D; Patel, Kushang V KV; Boerwinkle, Eric E; Rotter, Jerome I JI; Hofman, Albert A; Sambrook, Jennifer G JG; Hernandez, Dena G DG; Zheng, Gang G; Bandinelli, Stefania S; Singleton, Andrew B AB; Coresh, Josef J; Lumley, Thomas T; Uitterlinden, André G AG; Vangils, Janine M JM; Launer, Lenore J LJ; Cupples, L Adrienne LA; Oostra, Ben A BA; Zwaginga, Jaap-Jan JJ; Ouwehand, Willem H WH; Thein, Swee-Lay SL; Meisinger, Christa C; Deloukas, Panos P; Nauck, Matthias M; Spector, Tim D TD; Gieger, Christian C; Gudnason, Vilmundur V; van Duijn, Cornelia M CM; Psaty, Bruce M BM; Ferrucci, Luigi L; Chakravarti, Aravinda A; Greinacher, Andreas A; O'Donnell, Christopher J CJ; Witteman, Jacqueline C M JC; Furth, Susan S; Cushman, Mary M; Harris, Tamara B TB; Lin, Jing-Ping JP

Publication Date: 2009-11

Variant appearance in text: rs16926246

PubMed Link: 19862010

Variant Present in the following documents:

• Main text
• nihms-145796.pdf
• NIHMS145796-supplement-1.pdf

View BVdb publication page

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