KCNQ1 c.1514+8189G>A

Variant ID: 11-2691500-G-A

NM_000218.2(KCNQ1):c.1514+8189G>A

This variant was identified in 30 publications

View GRCh38 version.




Publications:


The utility of a type 2 diabetes polygenic score in addition to clinical variables for prediction of type 2 diabetes incidence in birth, youth and adult cohorts in an Indigenous study population.

Diabetologia
Wedekind, Lauren E LE; Mahajan, Anubha A; Hsueh, Wen-Chi WC; Chen, Peng P; Olaiya, Muideen T MT; Kobes, Sayuko S; Sinha, Madhumita M; Baier, Leslie J LJ; Knowler, William C WC; McCarthy, Mark I MI; Hanson, Robert L RL
Publication Date: 2023-03-02

Variant appearance in text: rs231361
PubMed Link: 36862161
Variant Present in the following documents:
  • 125_2023_5870_MOESM1_ESM.pdf
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Mutation analysis of the WFS1 gene in a Chinese family with autosomal-dominant non-syndrome deafness.

Scientific Reports
Zhao, Jing J; Zhang, Siqi S; Jiang, Yuan Y; Liu, Yan Y; Wang, Jiantao J; Zhu, QingWen Q
Publication Date: 2022-12-23

Variant appearance in text: rs231361
PubMed Link: 36564540
Variant Present in the following documents:
  • 41598_2022_26850_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Mutation analysis of the GSDME gene in a Chinese family with non-syndromic hearing loss.

Plos One
Lei, Peiliang P; Zhu, Qingwen Q; Dong, Wenrong W; Zhang, Siqi S; Sun, Yanyan Y; Du, Xitong X; Geng, Meng M; Jiang, Yuan Y
Publication Date: 2022

Variant appearance in text: rs231361
PubMed Link: 36350814
Variant Present in the following documents:
  • pone.0276233.s004.xlsx, sheet 1
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A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese family.

Bmc Medical Genomics
Li, Qiong Q; Wang, Shujuan S; Liang, Pengfei P; Li, Wei W; Wang, Jian J; Fan, Bei B; Yang, Yang Y; An, Xiaogang X; Chen, Jun J; Zha, Dingjun D
Publication Date: 2022-07-21

Variant appearance in text: rs231361
PubMed Link: 35864542
Variant Present in the following documents:
  • 12920_2022_1315_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Associations Between Glycemic Traits and Colorectal Cancer: A Mendelian Randomization Analysis.

Journal Of The National Cancer Institute
Murphy, Neil N; Song, Mingyang M; Papadimitriou, Nikos N; Carreras-Torres, Robert R; Langenberg, Claudia C; Martin, Richard M RM; Tsilidis, Konstantinos K KK; Barroso, Inês I; Chen, Ji J; Frayling, Timothy M TM; Bull, Caroline J CJ; Vincent, Emma E EE; Cotterchio, Michelle M; Gruber, Stephen B SB; Pai, Rish K RK; Newcomb, Polly A PA; Perez-Cornago, Aurora A; van Duijnhoven, Franzel J B FJB; Van Guelpen, Bethany B; Vodicka, Pavel P; Wolk, Alicja A; Wu, Anna H AH; Peters, Ulrike U; Chan, Andrew T AT; Gunter, Marc J MJ
Publication Date: 2022-05-09

Variant appearance in text: rs231361
PubMed Link: 35048991
Variant Present in the following documents:
  • djac011_supplementary_data.pdf
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Epigenetic Regulation of β Cell Identity and Dysfunction.

Frontiers In Endocrinology
Sun, Xiaoqiang X; Wang, Liu L; Obayomi, S M Bukola SMB; Wei, Zong Z
Publication Date: 2021

Variant appearance in text: rs231361
PubMed Link: 34630329
Variant Present in the following documents:
  • Main text
  • fendo-12-725131.pdf
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Single-cell chromatin accessibility identifies pancreatic islet cell type- and state-specific regulatory programs of diabetes risk.

Nature Genetics
Chiou, Joshua J; Zeng, Chun C; Cheng, Zhang Z; Han, Jee Yun JY; Schlichting, Michael M; Miller, Michael M; Mendez, Robert R; Huang, Serina S; Wang, Jinzhao J; Sui, Yinghui Y; Deogaygay, Allison A; Okino, Mei-Lin ML; Qiu, Yunjiang Y; Sun, Ying Y; Kudtarkar, Parul P; Fang, Rongxin R; Preissl, Sebastian S; Sander, Maike M; Gorkin, David U DU; Gaulton, Kyle J KJ
Publication Date: 2021-04

Variant appearance in text: rs231361
PubMed Link: 33795864
Variant Present in the following documents:
  • Main text
  • nihms-1675458.pdf
  • NIHMS1675458-supplement-1675458_supp1.pdf
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Association study between KCNQ1 and KCNQ1OT1 genetic polymorphisms and gastric cancer susceptibility and survival in a Chinese Han population: a case-control study.

Annals Of Translational Medicine
Yang, Zhenyu Z; Yuan, Lijuan L; Yang, Lin L; Peng, Shujia S; Yang, Ping P; He, Xianli X; Bao, Guoqiang G
Publication Date: 2021-01

Variant appearance in text: rs231361
PubMed Link: 33569458
Variant Present in the following documents:
  • Main text
  • atm-09-02-156.pdf
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Genetics of 35 blood and urine biomarkers in the UK Biobank.

Nature Genetics
Sinnott-Armstrong, Nasa N; Tanigawa, Yosuke Y; Amar, David D; Mars, Nina N; Benner, Christian C; Aguirre, Matthew M; Venkataraman, Guhan Ram GR; Wainberg, Michael M; Ollila, Hanna M HM; Kiiskinen, Tuomo T; Havulinna, Aki S AS; Pirruccello, James P JP; Qian, Junyang J; Shcherbina, Anna A; , ; Rodriguez, Fatima F; Assimes, Themistocles L TL; Agarwala, Vineeta V; Tibshirani, Robert R; Hastie, Trevor T; Ripatti, Samuli S; Pritchard, Jonathan K JK; Daly, Mark J MJ; Rivas, Manuel A MA
Publication Date: 2021-02

Variant appearance in text: KCNQ1: 1514+8189G>A; rs231361
PubMed Link: 33462484
Variant Present in the following documents:
  • NIHMS1651539-supplement-2.xlsx, sheet 21
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A Multi-omic Integrative Scheme Characterizes Tissues of Action at Loci Associated with Type 2 Diabetes.

American Journal Of Human Genetics
Torres, Jason M JM; Abdalla, Moustafa M; Payne, Anthony A; Fernandez-Tajes, Juan J; Thurner, Matthias M; Nylander, Vibe V; Gloyn, Anna L AL; Mahajan, Anubha A; McCarthy, Mark I MI
Publication Date: 2020-12-03

Variant appearance in text: rs231361
PubMed Link: 33186544
Variant Present in the following documents:
  • mmc3.pdf
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Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.

Nature Genetics
Vujkovic, Marijana M; Keaton, Jacob M JM; Lynch, Julie A JA; Miller, Donald R DR; Zhou, Jin J; Tcheandjieu, Catherine C; Huffman, Jennifer E JE; Assimes, Themistocles L TL; Lorenz, Kimberly K; Zhu, Xiang X; Hilliard, Austin T AT; Judy, Renae L RL; Huang, Jie J; Lee, Kyung M KM; Klarin, Derek D; Pyarajan, Saiju S; Danesh, John J; Melander, Olle O; Rasheed, Asif A; Mallick, Nadeem H NH; Hameed, Shahid S; Qureshi, Irshad H IH; Afzal, Muhammad Naeem MN; Malik, Uzma U; Jalal, Anjum A; Abbas, Shahid S; Sheng, Xin X; Gao, Long L; Kaestner, Klaus H KH; Susztak, Katalin K; Sun, Yan V YV; DuVall, Scott L SL; Cho, Kelly K; Lee, Jennifer S JS; Gaziano, J Michael JM; Phillips, Lawrence S LS; Meigs, James B JB; Reaven, Peter D PD; Wilson, Peter W PW; Edwards, Todd L TL; Rader, Daniel J DJ; Damrauer, Scott M SM; O'Donnell, Christopher J CJ; Tsao, Philip S PS; , ; , ; , ; Chang, Kyong-Mi KM; Voight, Benjamin F BF; Saleheen, Danish D
Publication Date: 2020-07

Variant appearance in text: rs231361
PubMed Link: 32541925
Variant Present in the following documents:
  • Main text
  • nihms-1589535.pdf
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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11

Variant appearance in text: KCNQ1: 1514+8189G>A; rs231361
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



When drug treatments bias genetic studies: Mediation and interaction.

Plos One
Schmidt, Amand F AF; Heerspink, Hiddo J L HJL; Denig, Petra P; Finan, Chris C; Groenwold, Rolf H H RHH
Publication Date: 2019

Variant appearance in text: rs231361
PubMed Link: 31461463
Variant Present in the following documents:
  • pone.0221209.s001.pdf
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Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report.

Bmc Neurology
Zhang, Xiaoqian X; Zhang, Lei L; Wu, Yanqing Y; Li, Gang G; Chen, Shengcai S; Xia, Yuanpeng Y; Li, Hongge H
Publication Date: 2018-11-29

Variant appearance in text: rs231361
PubMed Link: 30497413
Variant Present in the following documents:
  • 12883_2018_1199_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Associations between the maternal circulating lipid profile in pregnancy and fetal imprinted gene alleles: a cohort study.

Reproductive Biology And Endocrinology : Rb&E
Petry, Clive J CJ; Koulman, Albert A; Lu, Liangjian L; Jenkins, Benjamin B; Furse, Samuel S; Prentice, Philippa P; Matthews, Lee L; Hughes, Ieuan A IA; Acerini, Carlo L CL; Ong, Ken K KK; Dunger, David B DB
Publication Date: 2018-08-29

Variant appearance in text: rs231361
PubMed Link: 30157874
Variant Present in the following documents:
  • Main text
View BVdb publication page



A variant in KCNQ1 gene predicts metabolic syndrome among northern urban Han Chinese women.

Bmc Medical Genetics
Liu, Yafei Y; Wang, Chunxia C; Chen, Yafei Y; Yuan, Zhongshang Z; Yu, Tao T; Zhang, Wenchao W; Tang, Fang F; Gu, Jianhua J; Xu, Qinqin Q; Chi, Xiaotong X; Ding, Lijie L; Xue, Fuzhong F; Zhang, Chengqi C
Publication Date: 2018-08-29

Variant appearance in text: rs231361
PubMed Link: 30157802
Variant Present in the following documents:
  • Main text
  • 12881_2018_Article_652.pdf
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A systematic analysis highlights multiple long non-coding RNAs associated with cardiometabolic disorders.

Journal Of Human Genetics
Ghanbari, Mohsen M; Peters, Marjolein J MJ; de Vries, Paul S PS; Boer, Cindy G CG; van Rooij, Jeroen G J JGJ; Lee, Yu-Chi YC; Kumar, Vinod V; Uitterlinden, André G AG; Ikram, M Arfan MA; Wijmenga, Cisca C; Ordovas, Jose M JM; Smith, Caren E CE; van Meurs, Joyce B J JBJ; Erkeland, Stefan J SJ; Franco, Oscar H OH; Dehghan, Abbas A
Publication Date: 2018-04

Variant appearance in text: rs231361
PubMed Link: 29382920
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between a fetal imprinted gene allele score and late pregnancy maternal glucose concentrations.

Diabetes & Metabolism
Petry, C J CJ; Mooslehner, K K; Prentice, P P; Hayes, M G MG; Nodzenski, M M; Scholtens, D M DM; Hughes, I A IA; Acerini, C L CL; Ong, K K KK; Lowe, W L WL; Dunger, D B DB
Publication Date: 2017-09

Variant appearance in text: rs231361
PubMed Link: 28392167
Variant Present in the following documents:
  • Main text
View BVdb publication page



THE DIABETES EPIDEMIC IN CHINA: AN INTEGRATED REVIEW OF NATIONAL SURVEYS.

Endocrine Practice : Official Journal Of The American College Of Endocrinology And The American Association Of Clinical Endocrinologists
Shen, Xiuhua X; Vaidya, Anand A; Wu, Shoulin S; Gao, Xiang X
Publication Date: 2016-09

Variant appearance in text: rs231361
PubMed Link: 27295015
Variant Present in the following documents:
  • Main text
View BVdb publication page



Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.

Human Molecular Genetics
Horikoshi, Momoko M; Pasquali, Lorenzo L; Wiltshire, Steven S; Huyghe, Jeroen R JR; Mahajan, Anubha A; Asimit, Jennifer L JL; Ferreira, Teresa T; Locke, Adam E AE; Robertson, Neil R NR; Wang, Xu X; Sim, Xueling X; Fujita, Hayato H; Hara, Kazuo K; Young, Robin R; Zhang, Weihua W; Choi, Sungkyoung S; Chen, Han H; Kaur, Ismeet I; Takeuchi, Fumihiko F; Fontanillas, Pierre P; Thuillier, Dorothée D; Yengo, Loic L; Below, Jennifer E JE; Tam, Claudia H T CH; Wu, Ying Y; Abecasis, Gonçalo G; Altshuler, David D; Bell, Graeme I GI; Blangero, John J; Burtt, Noél P NP; Duggirala, Ravindranath R; Florez, Jose C JC; Hanis, Craig L CL; Seielstad, Mark M; Atzmon, Gil G; Chan, Juliana C N JC; Ma, Ronald C W RC; Froguel, Philippe P; Wilson, James G JG; Bharadwaj, Dwaipayan D; Dupuis, Josee J; Meigs, James B JB; Cho, Yoon Shin YS; Park, Taesung T; Kooner, Jaspal S JS; Chambers, John C JC; Saleheen, Danish D; Kadowaki, Takashi T; Tai, E Shyong ES; Mohlke, Karen L KL; Cox, Nancy J NJ; Ferrer, Jorge J; Zeggini, Eleftheria E; Kato, Norihiro N; Teo, Yik Ying YY; Boehnke, Michael M; McCarthy, Mark I MI; Morris, Andrew P AP; ,
Publication Date: 2016-05-15

Variant appearance in text: rs231361
PubMed Link: 26911676
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.

Nature Genetics
Gaulton, Kyle J KJ; Ferreira, Teresa T; Lee, Yeji Y; Raimondo, Anne A; Mägi, Reedik R; Reschen, Michael E ME; Mahajan, Anubha A; Locke, Adam A; Rayner, N William NW; Robertson, Neil N; Scott, Robert A RA; Prokopenko, Inga I; Scott, Laura J LJ; Green, Todd T; Sparso, Thomas T; Thuillier, Dorothee D; Yengo, Loic L; Grallert, Harald H; Wahl, Simone S; Frånberg, Mattias M; Strawbridge, Rona J RJ; Kestler, Hans H; Chheda, Himanshu H; Eisele, Lewin L; Gustafsson, Stefan S; Steinthorsdottir, Valgerdur V; Thorleifsson, Gudmar G; Qi, Lu L; Karssen, Lennart C LC; van Leeuwen, Elisabeth M EM; Willems, Sara M SM; Li, Man M; Chen, Han H; Fuchsberger, Christian C; Kwan, Phoenix P; Ma, Clement C; Linderman, Michael M; Lu, Yingchang Y; Thomsen, Soren K SK; Rundle, Jana K JK; Beer, Nicola L NL; van de Bunt, Martijn M; Chalisey, Anil A; Kang, Hyun Min HM; Voight, Benjamin F BF; Abecasis, Gonçalo R GR; Almgren, Peter P; Baldassarre, Damiano D; Balkau, Beverley B; Benediktsson, Rafn R; Blüher, Matthias M; Boeing, Heiner H; Bonnycastle, Lori L LL; Bottinger, Erwin P EP; Burtt, Noël P NP; Carey, Jason J; Charpentier, Guillaume G; Chines, Peter S PS; Cornelis, Marilyn C MC; Couper, David J DJ; Crenshaw, Andrew T AT; van Dam, Rob M RM; Doney, Alex S F AS; Dorkhan, Mozhgan M; Edkins, Sarah S; Eriksson, Johan G JG; Esko, Tonu T; Eury, Elodie E; Fadista, João J; Flannick, Jason J; Fontanillas, Pierre P; Fox, Caroline C; Franks, Paul W PW; Gertow, Karl K; Gieger, Christian C; Gigante, Bruna B; Gottesman, Omri O; Grant, George B GB; Grarup, Niels N; Groves, Christopher J CJ; Hassinen, Maija M; Have, Christian T CT; Herder, Christian C; Holmen, Oddgeir L OL; Hreidarsson, Astradur B AB; Humphries, Steve E SE; Hunter, David J DJ; Jackson, Anne U AU; Jonsson, Anna A; Jørgensen, Marit E ME; Jørgensen, Torben T; Kao, Wen-Hong L WH; Kerrison, Nicola D ND; Kinnunen, Leena L; Klopp, Norman N; Kong, Augustine A; Kovacs, Peter P; Kraft, Peter P; Kravic, Jasmina J; Langford, Cordelia C; Leander, Karin K; Liang, Liming L; Lichtner, Peter P; Lindgren, Cecilia M CM; Lindholm, Eero E; Linneberg, Allan A; Liu, Ching-Ti CT; Lobbens, Stéphane S; Luan, Jian'an J; Lyssenko, Valeriya V; Männistö, Satu S; McLeod, Olga O; Meyer, Julia J; Mihailov, Evelin E; Mirza, Ghazala G; Mühleisen, Thomas W TW; Müller-Nurasyid, Martina M; Navarro, Carmen C; Nöthen, Markus M MM; Oskolkov, Nikolay N NN; Owen, Katharine R KR; Palli, Domenico D; Pechlivanis, Sonali S; Peltonen, Leena L; Perry, John R B JR; Platou, Carl G P CG; Roden, Michael M; Ruderfer, Douglas D; Rybin, Denis D; van der Schouw, Yvonne T YT; Sennblad, Bengt B; Sigurðsson, Gunnar G; Stančáková, Alena A; Steinbach, Gerald G; Storm, Petter P; Strauch, Konstantin K; Stringham, Heather M HM; Sun, Qi Q; Thorand, Barbara B; Tikkanen, Emmi E; Tonjes, Anke A; Trakalo, Joseph J; Tremoli, Elena E; Tuomi, Tiinamaija T; Wennauer, Roman R; Wiltshire, Steven S; Wood, Andrew R AR; Zeggini, Eleftheria E; Dunham, Ian I; Birney, Ewan E; Pasquali, Lorenzo L; Ferrer, Jorge J; Loos, Ruth J F RJ; Dupuis, Josée J; Florez, Jose C JC; Boerwinkle, Eric E; Pankow, James S JS; van Duijn, Cornelia C; Sijbrands, Eric E; Meigs, James B JB; Hu, Frank B FB; Thorsteinsdottir, Unnur U; Stefansson, Kari K; Lakka, Timo A TA; Rauramaa, Rainer R; Stumvoll, Michael M; Pedersen, Nancy L NL; Lind, Lars L; Keinanen-Kiukaanniemi, Sirkka M SM; Korpi-Hyövälti, Eeva E; Saaristo, Timo E TE; Saltevo, Juha J; Kuusisto, Johanna J; Laakso, Markku M; Metspalu, Andres A; Erbel, Raimund R; Jöcke, Karl-Heinz KH; Moebus, Susanne S; Ripatti, Samuli S; Salomaa, Veikko V; Ingelsson, Erik E; Boehm, Bernhard O BO; Bergman, Richard N RN; Collins, Francis S FS; Mohlke, Karen L KL; Koistinen, Heikki H; Tuomilehto, Jaakko J; Hveem, Kristian K; Njølstad, Inger I; Deloukas, Panagiotis P; Donnelly, Peter J PJ; Frayling, Timothy M TM; Hattersley, Andrew T AT; de Faire, Ulf U; Hamsten, Anders A; Illig, Thomas T; Peters, Annette A; Cauchi, Stephane S; Sladek, Rob R; Froguel, Philippe P; Hansen, Torben T; Pedersen, Oluf O; Morris, Andrew D AD; Palmer, Collin N A CN; Kathiresan, Sekar S; Melander, Olle O; Nilsson, Peter M PM; Groop, Leif C LC; Barroso, Inês I; Langenberg, Claudia C; Wareham, Nicholas J NJ; O'Callaghan, Christopher A CA; Gloyn, Anna L AL; Altshuler, David D; Boehnke, Michael M; Teslovich, Tanya M TM; McCarthy, Mark I MI; Morris, Andrew P AP; ,
Publication Date: 2015-12

Variant appearance in text: rs231361
PubMed Link: 26551672
Variant Present in the following documents:
  • Main text
  • emss-65542.pdf
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Association Between KCNQ1 Genetic Variants and Type 2 Diabetes in the Uyghur Population.

Genetic Testing And Molecular Biomarkers
Ma, Qi Q; Wang, Li L; Yao, Hua H; Wang, Ting-ting TT; Ma, Yan Y; Su, Yin-xia YX; Wang, Zhi-qiang ZQ; Zhu, Jun J; Wang, Shu-xia SX; Zhang, Zhao-Xia ZX; Hou, Qin-qin QQ; Cai, Ren R; Gong, Xue-li XL; Jiang, Xiao-yan XY
Publication Date: 2015-12

Variant appearance in text: rs231361
PubMed Link: 26540651
Variant Present in the following documents:
  • Main text
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Do variants associated with susceptibility to pancreatic cancer and type 2 diabetes reciprocally affect risk?

Plos One
Wu, Lang L; Rabe, Kari G KG; Petersen, Gloria M GM
Publication Date: 2015

Variant appearance in text: rs231361
PubMed Link: 25658847
Variant Present in the following documents:
  • Main text
  • pone.0117230.pdf
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Fine mapping of type 2 diabetes susceptibility loci.

Current Diabetes Reports
Morris, Andrew P AP
Publication Date: 2014

Variant appearance in text: rs231361
PubMed Link: 25239271
Variant Present in the following documents:
  • Main text
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Roles of lncRNAs in pancreatic beta cell identity and diabetes susceptibility.

Frontiers In Genetics
Pullen, Timothy J TJ; Rutter, Guy A GA
Publication Date: 2014

Variant appearance in text: rs231361
PubMed Link: 25071823
Variant Present in the following documents:
  • Main text
  • fgene-05-00193.pdf
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Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants.

Nature Genetics
Pasquali, Lorenzo L; Gaulton, Kyle J KJ; Rodríguez-Seguí, Santiago A SA; Mularoni, Loris L; Miguel-Escalada, Irene I; Akerman, İldem İ; Tena, Juan J JJ; Morán, Ignasi I; Gómez-Marín, Carlos C; van de Bunt, Martijn M; Ponsa-Cobas, Joan J; Castro, Natalia N; Nammo, Takao T; Cebola, Inês I; García-Hurtado, Javier J; Maestro, Miguel Angel MA; Pattou, François F; Piemonti, Lorenzo L; Berney, Thierry T; Gloyn, Anna L AL; Ravassard, Philippe P; Skarmeta, José Luis Gómez JLG; Müller, Ferenc F; McCarthy, Mark I MI; Ferrer, Jorge J
Publication Date: 2014-02

Variant appearance in text: rs231361
PubMed Link: 24413736
Variant Present in the following documents:
  • NIHMS56019-supplement-1.pdf
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Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study.

Diabetes
Ng, Maggie C Y MC; Saxena, Richa R; Li, Jiang J; Palmer, Nicholette D ND; Dimitrov, Latchezar L; Xu, Jianzhao J; Rasmussen-Torvik, Laura J LJ; Zmuda, Joseph M JM; Siscovick, David S DS; Patel, Sanjay R SR; Crook, Errol D ED; Sims, Mario M; Chen, Yii-Der I YD; Bertoni, Alain G AG; Li, Mingyao M; Grant, Struan F A SF; Dupuis, Josée J; Meigs, James B JB; Psaty, Bruce M BM; Pankow, James S JS; Langefeld, Carl D CD; Freedman, Barry I BI; Rotter, Jerome I JI; Wilson, James G JG; Bowden, Donald W DW
Publication Date: 2013-03

Variant appearance in text: rs231361
PubMed Link: 23193183
Variant Present in the following documents:
  • Main text
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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

Nature Genetics
Morris, Andrew P AP; Voight, Benjamin F BF; Teslovich, Tanya M TM; Ferreira, Teresa T; Segrè, Ayellet V AV; Steinthorsdottir, Valgerdur V; Strawbridge, Rona J RJ; Khan, Hassan H; Grallert, Harald H; Mahajan, Anubha A; Prokopenko, Inga I; Kang, Hyun Min HM; Dina, Christian C; Esko, Tonu T; Fraser, Ross M RM; Kanoni, Stavroula S; Kumar, Ashish A; Lagou, Vasiliki V; Langenberg, Claudia C; Luan, Jian'an J; Lindgren, Cecilia M CM; Müller-Nurasyid, Martina M; Pechlivanis, Sonali S; Rayner, N William NW; Scott, Laura J LJ; Wiltshire, Steven S; Yengo, Loic L; Kinnunen, Leena L; Rossin, Elizabeth J EJ; Raychaudhuri, Soumya S; Johnson, Andrew D AD; Dimas, Antigone S AS; Loos, Ruth J F RJ; Vedantam, Sailaja S; Chen, Han H; Florez, Jose C JC; Fox, Caroline C; Liu, Ching-Ti CT; Rybin, Denis D; Couper, David J DJ; Kao, Wen Hong L WH; Li, Man M; Cornelis, Marilyn C MC; Kraft, Peter P; Sun, Qi Q; van Dam, Rob M RM; Stringham, Heather M HM; Chines, Peter S PS; Fischer, Krista K; Fontanillas, Pierre P; Holmen, Oddgeir L OL; Hunt, Sarah E SE; Jackson, Anne U AU; Kong, Augustine A; Lawrence, Robert R; Meyer, Julia J; Perry, John R B JR; Platou, Carl G P CG; Potter, Simon S; Rehnberg, Emil E; Robertson, Neil N; Sivapalaratnam, Suthesh S; Stančáková, Alena A; Stirrups, Kathleen K; Thorleifsson, Gudmar G; Tikkanen, Emmi E; Wood, Andrew R AR; Almgren, Peter P; Atalay, Mustafa M; Benediktsson, Rafn R; Bonnycastle, Lori L LL; Burtt, Noël N; Carey, Jason J; Charpentier, Guillaume G; Crenshaw, Andrew T AT; Doney, Alex S F AS; Dorkhan, Mozhgan M; Edkins, Sarah S; Emilsson, Valur V; Eury, Elodie E; Forsen, Tom T; Gertow, Karl K; Gigante, Bruna B; Grant, George B GB; Groves, Christopher J CJ; Guiducci, Candace C; Herder, Christian C; Hreidarsson, Astradur B AB; Hui, Jennie J; James, Alan A; Jonsson, Anna A; Rathmann, Wolfgang W; Klopp, Norman N; Kravic, Jasmina J; Krjutškov, Kaarel K; Langford, Cordelia C; Leander, Karin K; Lindholm, Eero E; Lobbens, Stéphane S; Männistö, Satu S; Mirza, Ghazala G; Mühleisen, Thomas W TW; Musk, Bill B; Parkin, Melissa M; Rallidis, Loukianos L; Saramies, Jouko J; Sennblad, Bengt B; Shah, Sonia S; Sigurðsson, Gunnar G; Silveira, Angela A; Steinbach, Gerald G; Thorand, Barbara B; Trakalo, Joseph J; Veglia, Fabrizio F; Wennauer, Roman R; Winckler, Wendy W; Zabaneh, Delilah D; Campbell, Harry H; van Duijn, Cornelia C; Uitterlinden, Andre G AG; Hofman, Albert A; Sijbrands, Eric E; Abecasis, Goncalo R GR; Owen, Katharine R KR; Zeggini, Eleftheria E; Trip, Mieke D MD; Forouhi, Nita G NG; Syvänen, Ann-Christine AC; Eriksson, Johan G JG; Peltonen, Leena L; Nöthen, Markus M MM; Balkau, Beverley B; Palmer, Colin N A CN; Lyssenko, Valeriya V; Tuomi, Tiinamaija T; Isomaa, Bo B; Hunter, David J DJ; Qi, Lu L; , ; , ; , ; , ; , ; Shuldiner, Alan R AR; Roden, Michael M; Barroso, Ines I; Wilsgaard, Tom T; Beilby, John J; Hovingh, Kees K; Price, Jackie F JF; Wilson, James F JF; Rauramaa, Rainer R; Lakka, Timo A TA; Lind, Lars L; Dedoussis, George G; Njølstad, Inger I; Pedersen, Nancy L NL; Khaw, Kay-Tee KT; Wareham, Nicholas J NJ; Keinanen-Kiukaanniemi, Sirkka M SM; Saaristo, Timo E TE; Korpi-Hyövälti, Eeva E; Saltevo, Juha J; Laakso, Markku M; Kuusisto, Johanna J; Metspalu, Andres A; Collins, Francis S FS; Mohlke, Karen L KL; Bergman, Richard N RN; Tuomilehto, Jaakko J; Boehm, Bernhard O BO; Gieger, Christian C; Hveem, Kristian K; Cauchi, Stephane S; Froguel, Philippe P; Baldassarre, Damiano D; Tremoli, Elena E; Humphries, Steve E SE; Saleheen, Danish D; Danesh, John J; Ingelsson, Erik E; Ripatti, Samuli S; Salomaa, Veikko V; Erbel, Raimund R; Jöckel, Karl-Heinz KH; Moebus, Susanne S; Peters, Annette A; Illig, Thomas T; de Faire, Ulf U; Hamsten, Anders A; Morris, Andrew D AD; Donnelly, Peter J PJ; Frayling, Timothy M TM; Hattersley, Andrew T AT; Boerwinkle, Eric E; Melander, Olle O; Kathiresan, Sekar S; Nilsson, Peter M PM; Deloukas, Panos P; Thorsteinsdottir, Unnur U; Groop, Leif C LC; Stefansson, Kari K; Hu, Frank F; Pankow, James S JS; Dupuis, Josée J; Meigs, James B JB; Altshuler, David D; Boehnke, Michael M; McCarthy, Mark I MI; ,
Publication Date: 2012-09

Variant appearance in text: rs231361
PubMed Link: 22885922
Variant Present in the following documents:
  • Main text
  • ukmss-49214.pdf
  • NIHMS49214-supplement-2.pdf
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Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian population.

Journal Of Diabetes
Odgerel, Zagaa Z; Lee, Hee S HS; Erdenebileg, Narnygerel N; Gandbold, Suren S; Luvsanjamba, Munkhjargal M; Sambuughin, Nyamkhishig N; Sonomtseren, Sainbileg S; Sharavdorj, Purevdulam P; Jodov, Erdenezul E; Altaisaikhan, Khasag K; Goldfarb, Lev G LG
Publication Date: 2012-09

Variant appearance in text: rs231361
PubMed Link: 22151254
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.

Plos Genetics
Tsai, Fuu-Jen FJ; Yang, Chi-Fan CF; Chen, Ching-Chu CC; Chuang, Lee-Ming LM; Lu, Chieh-Hsiang CH; Chang, Chwen-Tzuei CT; Wang, Tzu-Yuan TY; Chen, Rong-Hsing RH; Shiu, Chiung-Fang CF; Liu, Yi-Min YM; Chang, Chih-Chun CC; Chen, Pei P; Chen, Chien-Hsiun CH; Fann, Cathy S J CS; Chen, Yuan-Tsong YT; Wu, Jer-Yuarn JY
Publication Date: 2010-02-19

Variant appearance in text: rs231361
PubMed Link: 20174558
Variant Present in the following documents:
  • Main text
  • pgen.1000847.pdf
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