EFEMP1 c.1320+963T>C

Variant ID: 2-56096892-A-G

NM_001039348.2(EFEMP1):c.1320+963T>C

This variant was identified in 33 publications

View GRCh38 version.




Publications:


Genome-wide association analysis and replication in 810,625 individuals with varicose veins.

Nature Communications
Ahmed, Waheed-Ul-Rahman WU; Kleeman, Sam S; Ng, Michael M; Wang, Wei W; Auton, Adam A; , ; Lee, Regent R; Handa, Ashok A; Zondervan, Krina T KT; Wiberg, Akira A; Furniss, Dominic D
Publication Date: 2022-06-02

Variant appearance in text: rs3791679
PubMed Link: 35654884
Variant Present in the following documents:
  • Main text
  • 41467_2022_Article_30765.pdf
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A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.

Nature Communications
Skuladottir, Astros Th AT; Bjornsdottir, Gyda G; Ferkingstad, Egil E; Einarsson, Gudmundur G; Stefansdottir, Lilja L; Nawaz, Muhammad Sulaman MS; Oddsson, Asmundur A; Olafsdottir, Thorunn A TA; Saevarsdottir, Saedis S; Walters, G Bragi GB; Magnusson, Sigurdur H SH; Bjornsdottir, Anna A; Sveinsson, Olafur A OA; Vikingsson, Arnor A; Hansen, Thomas Folkmann TF; Jacobsen, Rikke Louise RL; Erikstrup, Christian C; Schwinn, Michael M; Brunak, Søren S; Banasik, Karina K; Ostrowski, Sisse Rye SR; Troelsen, Anders A; Henkel, Cecilie C; Pedersen, Ole Birger OB; , ; Jonsdottir, Ingileif I; Gudbjartsson, Daniel F DF; Sulem, Patrick P; Thorgeirsson, Thorgeir E TE; Stefansson, Hreinn H; Stefansson, Kari K
Publication Date: 2022-03-24

Variant appearance in text: EFEMP1: 1320+963T>C; rs3791679
PubMed Link: 35332129
Variant Present in the following documents:
  • 41467_2022_29133_MOESM4_ESM.xlsx, sheet 11
  • 41467_2022_29133_MOESM4_ESM.xlsx, sheet 3
  • 41467_2022_29133_MOESM4_ESM.xlsx, sheet 1
  • 41467_2022_29133_MOESM4_ESM.xlsx, sheet 9
  • 41467_2022_29133_MOESM4_ESM.xlsx, sheet 10
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Utility of EFEMP1 in the Prediction of Oncologic Outcomes of Urothelial Carcinoma.

Genes
Chen, Tzu-Ju TJ; Chan, Ti-Chun TC; Li, Wan-Shan WS; Li, Chien-Feng CF; Ke, Hung-Lung HL; Wei, Yu-Ching YC; Wu, Wen-Jeng WJ; Li, Wei-Ming WM
Publication Date: 2021-06-06

Variant appearance in text: rs3791679
PubMed Link: 34204134
Variant Present in the following documents:
  • Main text
View BVdb publication page



Instrumental Heterogeneity in Sex-Specific Two-Sample Mendelian Randomization: Empirical Results From the Relationship Between Anthropometric Traits and Breast/Prostate Cancer.

Frontiers In Genetics
Gao, Yixin Y; Zhang, Jinhui J; Zhao, Huashuo H; Guan, Fengjun F; Zeng, Ping P
Publication Date: 2021

Variant appearance in text: rs3791679
PubMed Link: 34178025
Variant Present in the following documents:
  • Main text
  • fgene-12-651332.pdf
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Genetics of Body Fat Distribution: Comparative Analyses in Populations with European, Asian and African Ancestries.

Genes
Sun, Chang C; Kovacs, Peter P; Guiu-Jurado, Esther E
Publication Date: 2021-05-29

Variant appearance in text: rs3791679
PubMed Link: 34072523
Variant Present in the following documents:
  • Main text
View BVdb publication page



Role of Fibulins in Embryonic Stage Development and Their Involvement in Various Diseases.

Biomolecules
Mahajan, Deviyani D; Kancharla, Sudhakar S; Kolli, Prachetha P; Sharma, Amarish Kumar AK; Singh, Sanjeev S; Kumar, Sudarshan S; Mohanty, Ashok Kumar AK; Jena, Manoj Kumar MK
Publication Date: 2021-05-02

Variant appearance in text: rs3791679
PubMed Link: 34063320
Variant Present in the following documents:
  • Main text
  • biomolecules-11-00685.pdf
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Systematic review and meta-analysis of genetic association studies of pelvic organ prolapse.

International Urogynecology Journal
Allen-Brady, Kristina K; Chua, John W F JWF; Cuffolo, Romana R; Koch, Marianne M; Sorrentino, Felice F; Cartwright, Rufus R
Publication Date: 2021-04-24

Variant appearance in text: rs3791679
PubMed Link: 33893823
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Pathophysiological Significance of Fibulin-3.

Biomolecules
Livingstone, Imogen I; Uversky, Vladimir N VN; Furniss, Dominic D; Wiberg, Akira A
Publication Date: 2020-09-08

Variant appearance in text: rs3791679
PubMed Link: 32911658
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.

Human Genetics
Hebbar, Prashantha P; Abubaker, Jehad Ahmed JA; Abu-Farha, Mohamed M; Alsmadi, Osama O; Elkum, Naser N; Alkayal, Fadi F; John, Sumi Elsa SE; Channanath, Arshad A; Iqbal, Rasheeba R; Pitkaniemi, Janne J; Tuomilehto, Jaakko J; Sladek, Robert R; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA
Publication Date: 2021-03

Variant appearance in text: rs3791679
PubMed Link: 32902719
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.

Communications Biology
Olafsdottir, Thorhildur T; Thorleifsson, Gudmar G; Sulem, Patrick P; Stefansson, Olafur A OA; Medek, Helga H; Olafsson, Karl K; Ingthorsson, Orri O; Gudmundsson, Valur V; Jonsdottir, Ingileif I; Halldorsson, Gisli H GH; Kristjansson, Ragnar P RP; Frigge, Michael L ML; Stefansdottir, Lilja L; Sigurdsson, Jon K JK; Oddsson, Asmundur A; Sigurdsson, Asgeir A; Eggertsson, Hannes P HP; Melsted, Pall P; Halldorsson, Bjarni V BV; Lund, Sigrun H SH; Styrkarsdottir, Unnur U; Steinthorsdottir, Valgerdur V; Gudmundsson, Julius J; Holm, Hilma H; Tragante, Vinicius V; Asselbergs, Folkert W FW; Thorsteinsdottir, Unnur U; Gudbjartsson, Daniel F DF; Jonsdottir, Kristin K; Rafnar, Thorunn T; Stefansson, Kari K
Publication Date: 2020-03-17

Variant appearance in text: rs3791679
PubMed Link: 32184442
Variant Present in the following documents:
  • Main text
  • 42003_2020_Article_857.pdf
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Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses.

Gastroenterology
Murphy, Neil N; Carreras-Torres, Robert R; Song, Mingyang M; Chan, Andrew T AT; Martin, Richard M RM; Papadimitriou, Nikos N; Dimou, Niki N; Tsilidis, Konstantinos K KK; Banbury, Barbara B; Bradbury, Kathryn E KE; Besevic, Jelena J; Rinaldi, Sabina S; Riboli, Elio E; Cross, Amanda J AJ; Travis, Ruth C RC; Agnoli, Claudia C; Albanes, Demetrius D; Berndt, Sonja I SI; Bézieau, Stéphane S; Bishop, D Timothy DT; Brenner, Hermann H; Buchanan, Daniel D DD; Onland-Moret, N Charlotte NC; Burnett-Hartman, Andrea A; Campbell, Peter T PT; Casey, Graham G; Castellví-Bel, Sergi S; Chang-Claude, Jenny J; Chirlaque, María-Dolores MD; de la Chapelle, Albert A; English, Dallas D; Figueiredo, Jane C JC; Gallinger, Steven J SJ; Giles, Graham G GG; Gruber, Stephen B SB; Gsur, Andrea A; Hampe, Jochen J; Hampel, Heather H; Harrison, Tabitha A TA; Hoffmeister, Michael M; Hsu, Li L; Huang, Wen-Yi WY; Huyghe, Jeroen R JR; Jenkins, Mark A MA; Keku, Temitope O TO; Kühn, Tilman T; Kweon, Sun-Seog SS; Le Marchand, Loic L; Li, Christopher I CI; Li, Li L; Lindblom, Annika A; Martín, Vicente V; Milne, Roger L RL; Moreno, Victor V; Newcomb, Polly A PA; Offit, Kenneth K; Ogino, Shuji S; Ose, Jennifer J; Perduca, Vittorio V; Phipps, Amanda I AI; Platz, Elizabeth A EA; Potter, John D JD; Qu, Conghui C; Rennert, Gad G; Sakoda, Lori C LC; Schafmayer, Clemens C; Schoen, Robert E RE; Slattery, Martha L ML; Tangen, Catherine M CM; Ulrich, Cornelia M CM; van Duijnhoven, Franzel J B FJB; Van Guelpen, Bethany B; Visvanathan, Kala K; Vodicka, Pavel P; Vodickova, Ludmila L; Vymetalkova, Veronika V; Wang, Hansong H; White, Emily E; Wolk, Alicja A; Woods, Michael O MO; Wu, Anna H AH; Zheng, Wei W; Peters, Ulrike U; Gunter, Marc J MJ
Publication Date: 2020-04

Variant appearance in text: rs3791679
PubMed Link: 31884074
Variant Present in the following documents:
  • Main text
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Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis.

American Journal Of Respiratory And Critical Care Medicine
Allen, Richard J RJ; Guillen-Guio, Beatriz B; Oldham, Justin M JM; Ma, Shwu-Fan SF; Dressen, Amy A; Paynton, Megan L ML; Kraven, Luke M LM; Obeidat, Ma'en M; Li, Xuan X; Ng, Michael M; Braybrooke, Rebecca R; Molina-Molina, Maria M; Hobbs, Brian D BD; Putman, Rachel K RK; Sakornsakolpat, Phuwanat P; Booth, Helen L HL; Fahy, William A WA; Hart, Simon P SP; Hill, Mike R MR; Hirani, Nik N; Hubbard, Richard B RB; McAnulty, Robin J RJ; Millar, Ann B AB; Navaratnam, Vidyia V; Oballa, Eunice E; Parfrey, Helen H; Saini, Gauri G; Whyte, Moira K B MKB; Zhang, Yingze Y; Kaminski, Naftali N; Adegunsoye, Ayodeji A; Strek, Mary E ME; Neighbors, Margaret M; Sheng, Xuting R XR; Gudmundsson, Gunnar G; Gudnason, Vilmundur V; Hatabu, Hiroto H; Lederer, David J DJ; Manichaikul, Ani A; Newell, John D JD; O'Connor, George T GT; Ortega, Victor E VE; Xu, Hanfei H; Fingerlin, Tasha E TE; Bossé, Yohan Y; Hao, Ke K; Joubert, Philippe P; Nickle, David C DC; Sin, Don D DD; Timens, Wim W; Furniss, Dominic D; Morris, Andrew P AP; Zondervan, Krina T KT; Hall, Ian P IP; Sayers, Ian I; Tobin, Martin D MD; Maher, Toby M TM; Cho, Michael H MH; Hunninghake, Gary M GM; Schwartz, David A DA; Yaspan, Brian L BL; Molyneaux, Philip L PL; Flores, Carlos C; Noth, Imre I; Jenkins, R Gisli RG; Wain, Louise V LV
Publication Date: 2020-03-01

Variant appearance in text: rs3791679
PubMed Link: 31710517
Variant Present in the following documents:
  • rccm.201905-1017OC_allen_data_supplement.pdf
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Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome.

Genomics, Proteomics & Bioinformatics
Du, Zhenglin Z; Ma, Liang L; Qu, Hongzhu H; Chen, Wei W; Zhang, Bing B; Lu, Xi X; Zhai, Weibo W; Sheng, Xin X; Sun, Yongqiao Y; Li, Wenjie W; Lei, Meng M; Qi, Qiuhui Q; Yuan, Na N; Shi, Shuo S; Zeng, Jingyao J; Wang, Jinyue J; Yang, Yadong Y; Liu, Qi Q; Hong, Yaqiang Y; Dong, Lili L; Zhang, Zhewen Z; Zou, Dong D; Wang, Yanqing Y; Song, Shuhui S; Liu, Fan F; Fang, Xiangdong X; Chen, Hua H; Liu, Xin X; Xiao, Jingfa J; Zeng, Changqing C
Publication Date: 2019-06

Variant appearance in text: rs3791679
PubMed Link: 31494266
Variant Present in the following documents:
  • Main text
  • main.pdf
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A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome.

Nature Communications
Wiberg, Akira A; Ng, Michael M; Schmid, Annina B AB; Smillie, Robert W RW; Baskozos, Georgios G; Holmes, Michael V MV; Künnapuu, K K; Mägi, R R; Bennett, David L DL; Furniss, Dominic D
Publication Date: 2019-03-04

Variant appearance in text: rs3791679
PubMed Link: 30833571
Variant Present in the following documents:
  • Main text
  • 41467_2019_8993_MOESM1_ESM.pdf
  • 41467_2019_Article_8993.pdf
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Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects.

Nature Communications
Rask-Andersen, Mathias M; Karlsson, Torgny T; Ek, Weronica E WE; Johansson, Åsa Å
Publication Date: 2019-01-21

Variant appearance in text: rs3791679
PubMed Link: 30664634
Variant Present in the following documents:
  • Main text
  • 41467_2018_Article_8000.pdf
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Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease.

Nature Communications
Yao, Chen C; Chen, George G; Song, Ci C; Keefe, Joshua J; Mendelson, Michael M; Huan, Tianxiao T; Sun, Benjamin B BB; Laser, Annika A; Maranville, Joseph C JC; Wu, Hongsheng H; Ho, Jennifer E JE; Courchesne, Paul P; Lyass, Asya A; Larson, Martin G MG; Gieger, Christian C; Graumann, Johannes J; Johnson, Andrew D AD; Danesh, John J; Runz, Heiko H; Hwang, Shih-Jen SJ; Liu, Chunyu C; Butterworth, Adam S AS; Suhre, Karsten K; Levy, Daniel D
Publication Date: 2018-08-15

Variant appearance in text: rs3791679
PubMed Link: 30111768
Variant Present in the following documents:
  • 41467_2018_Article_5512.pdf
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A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure.

Nature Communications
Choquet, Hélène H; Thai, Khanh K KK; Yin, Jie J; Hoffmann, Thomas J TJ; Kvale, Mark N MN; Banda, Yambazi Y; Schaefer, Catherine C; Risch, Neil N; Nair, K Saidas KS; Melles, Ronald R; Jorgenson, Eric E
Publication Date: 2017-12-13

Variant appearance in text: rs3791679
PubMed Link: 29235454
Variant Present in the following documents:
  • Main text
View BVdb publication page



The associations between common SNPs of EFEMP1 gene and glioma risk in Chinese population.

Oncotargets And Therapy
Hu, Jun J; Dong, Dong D; Lu, Dandan D
Publication Date: 2017

Variant appearance in text: rs3791679
PubMed Link: 29158681
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between EGFR gene polymorphisms and susceptibility to glioma: a systematic review and meta-analysis from GWAS and case-control studies.

Oncotarget
Yu, Xiao X; Sun, Nian Rong NR; Jang, Hai Tao HT; Guo, Shi Wen SW; Lian, Min Xue MX
Publication Date: 2017-10-17

Variant appearance in text: rs3791679
PubMed Link: 29156842
Variant Present in the following documents:
  • oncotarget-08-86877.pdf
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Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan.

Scientific Reports
Lin, Ying-Ju YJ; Liao, Wen-Ling WL; Wang, Chung-Hsing CH; Tsai, Li-Ping LP; Tang, Chih-Hsin CH; Chen, Chien-Hsiun CH; Wu, Jer-Yuarn JY; Liang, Wen-Miin WM; Hsieh, Ai-Ru AR; Cheng, Chi-Fung CF; Chen, Jin-Hua JH; Chien, Wen-Kuei WK; Lin, Ting-Hsu TH; Wu, Chia-Ming CM; Liao, Chiu-Chu CC; Huang, Shao-Mei SM; Tsai, Fuu-Jen FJ
Publication Date: 2017-07-25

Variant appearance in text: rs3791679
PubMed Link: 28744006
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_6766.pdf
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Impact of interaction between the G870A and EFEMP1 gene polymorphism on glioma risk in Chinese Han population.

Oncotarget
Yang, Libin L; Qu, Bo B; Xia, Xun X; Kuang, Yongqin Y; Li, Jian J; Fan, Kexia K; Guo, Heng H; Zheng, Hui H; Ma, Yuan Y
Publication Date: 2017-06-06

Variant appearance in text: rs3791679
PubMed Link: 28380465
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci.

Scientific Reports
Ellinghaus, Eva E; Ellinghaus, David D; Krusche, Petra P; Greiner, Aljoscha A; Schreiber, Claudia C; Nikolaus, Susanna S; Gieger, Christian C; Strauch, Konstantin K; Lieb, Wolfgang W; Rosenstiel, Philip P; Frings, Norbert N; Fiebig, Andreas A; Schreiber, Stefan S; Franke, Andre A
Publication Date: 2017-04-04

Variant appearance in text: rs3791679
PubMed Link: 28374850
Variant Present in the following documents:
  • Main text
  • srep45652.pdf
View BVdb publication page



New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.

Human Molecular Genetics
Springelkamp, Henriët H; Iglesias, Adriana I AI; Mishra, Aniket A; Höhn, René R; Wojciechowski, Robert R; Khawaja, Anthony P AP; Nag, Abhishek A; Wang, Ya Xing YX; Wang, Jie Jin JJ; Cuellar-Partida, Gabriel G; Gibson, Jane J; Bailey, Jessica N Cooke JN; Vithana, Eranga N EN; Gharahkhani, Puya P; Boutin, Thibaud T; Ramdas, Wishal D WD; Zeller, Tanja T; Luben, Robert N RN; Yonova-Doing, Ekaterina E; Viswanathan, Ananth C AC; Yazar, Seyhan S; Cree, Angela J AJ; Haines, Jonathan L JL; Koh, Jia Yu JY; Souzeau, Emmanuelle E; Wilson, James F JF; Amin, Najaf N; Müller, Christian C; Venturini, Cristina C; Kearns, Lisa S LS; Kang, Jae Hee JH; , ; Tham, Yih Chung YC; Zhou, Tiger T; van Leeuwen, Elisabeth M EM; Nickels, Stefan S; Sanfilippo, Paul P; Liao, Jiemin J; van der Linde, Herma H; Zhao, Wanting W; van Koolwijk, Leonieke M E LM; Zheng, Li L; Rivadeneira, Fernando F; Baskaran, Mani M; van der Lee, Sven J SJ; Perera, Shamira S; de Jong, Paulus T V M PT; Oostra, Ben A BA; Uitterlinden, André G AG; Fan, Qiao Q; Hofman, Albert A; Tai, E-Shyong ES; Vingerling, Johannes R JR; Sim, Xueling X; Wolfs, Roger C W RC; Teo, Yik Ying YY; Lemij, Hans G HG; Khor, Chiea Chuen CC; Willemsen, Rob R; Lackner, Karl J KJ; Aung, Tin T; Jansonius, Nomdo M NM; Montgomery, Grant G; Wild, Philipp S PS; Young, Terri L TL; Burdon, Kathryn P KP; Hysi, Pirro G PG; Pasquale, Louis R LR; Wong, Tien Yin TY; Klaver, Caroline C W CC; Hewitt, Alex W AW; Jonas, Jost B JB; Mitchell, Paul P; Lotery, Andrew J AJ; Foster, Paul J PJ; Vitart, Veronique V; Pfeiffer, Norbert N; Craig, Jamie E JE; Mackey, David A DA; Hammond, Christopher J CJ; Wiggs, Janey L JL; Cheng, Ching-Yu CY; van Duijn, Cornelia M CM; MacGregor, Stuart S
Publication Date: 2017-01-15

Variant appearance in text: rs3791679
PubMed Link: 28073927
Variant Present in the following documents:
  • Main text
View BVdb publication page



Detection and interpretation of shared genetic influences on 42 human traits.

Nature Genetics
Pickrell, Joseph K JK; Berisa, Tomaz T; Liu, Jimmy Z JZ; Ségurel, Laure L; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2016-07

Variant appearance in text: rs3791679
PubMed Link: 27182965
Variant Present in the following documents:
  • NIHMS780506-supplement-9.pdf
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EFEMP1 rs3791679 polymorphism was associated with susceptibility to glioma.

International Journal Of Clinical And Experimental Pathology
Qin, Guoqiang G; Qi, Songtao S; Lu, Dan D; Yu, Jiangjun J; Huang, Weimin W; Yu, Lei L
Publication Date: 2015

Variant appearance in text: rs3791679
PubMed Link: 26823870
Variant Present in the following documents:
  • Main text
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Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.

Scientific Reports
Wen, Wanqing W; Kato, Norihiro N; Hwang, Joo-Yeon JY; Guo, Xingyi X; Tabara, Yasuharu Y; Li, Huaixing H; Dorajoo, Rajkumar R; Yang, Xiaobo X; Tsai, Fuu-Jen FJ; Li, Shengxu S; Wu, Ying Y; Wu, Tangchun T; Kim, Soriul S; Guo, Xiuqing X; Liang, Jun J; Shungin, Dmitry D; Adair, Linda S LS; Akiyama, Koichi K; Allison, Matthew M; Cai, Qiuyin Q; Chang, Li-Ching LC; Chen, Chien-Hsiun CH; Chen, Yuan-Tsong YT; Cho, Yoon Shin YS; Choi, Bo Youl BY; Gao, Yutang Y; Go, Min Jin MJ; Gu, Dongfeng D; Han, Bok-Ghee BG; He, Meian M; Hixson, James E JE; Hu, Yanling Y; Huang, Tao T; Isono, Masato M; Jung, Keum Ji KJ; Kang, Daehee D; Kim, Young Jin YJ; Kita, Yoshikuni Y; Lee, Juyoung J; Lee, Nanette R NR; Lee, Jeannette J; Wang, Yiqin Y; Liu, Jian-Jun JJ; Long, Jirong J; Moon, Sanghoon S; Nakamura, Yasuyuki Y; Nakatochi, Masahiro M; Ohnaka, Keizo K; Rao, Dabeeru D; Shi, Jiajun J; Sull, Jae Woong JW; Tan, Aihua A; Ueshima, Hirotsugu H; Wu, Chen C; Xiang, Yong-Bing YB; Yamamoto, Ken K; Yao, Jie J; Ye, Xingwang X; Yokota, Mitsuhiro M; Zhang, Xiaomin X; Zheng, Yan Y; Qi, Lu L; Rotter, Jerome I JI; Jee, Sun Ha SH; Lin, Dongxin D; Mohlke, Karen L KL; He, Jiang J; Mo, Zengnan Z; Wu, Jer-Yuarn JY; Tai, E Shyong ES; Lin, Xu X; Miki, Tetsuro T; Kim, Bong-Jo BJ; Takeuchi, Fumihiko F; Zheng, Wei W; Shu, Xiao-Ou XO
Publication Date: 2016-01-20

Variant appearance in text: rs3791679
PubMed Link: 26785701
Variant Present in the following documents:
  • Main text
  • srep17958.pdf
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

Nature Genetics
Berndt, Sonja I SI; Gustafsson, Stefan S; Mägi, Reedik R; Ganna, Andrea A; Wheeler, Eleanor E; Feitosa, Mary F MF; Justice, Anne E AE; Monda, Keri L KL; Croteau-Chonka, Damien C DC; Day, Felix R FR; Esko, Tõnu T; Fall, Tove T; Ferreira, Teresa T; Gentilini, Davide D; Jackson, Anne U AU; Luan, Jian'an J; Randall, Joshua C JC; Vedantam, Sailaja S; Willer, Cristen J CJ; Winkler, Thomas W TW; Wood, Andrew R AR; Workalemahu, Tsegaselassie T; Hu, Yi-Juan YJ; Lee, Sang Hong SH; Liang, Liming L; Lin, Dan-Yu DY; Min, Josine L JL; Neale, Benjamin M BM; Thorleifsson, Gudmar G; Yang, Jian J; Albrecht, Eva E; Amin, Najaf N; Bragg-Gresham, Jennifer L JL; Cadby, Gemma G; den Heijer, Martin M; Eklund, Niina N; Fischer, Krista K; Goel, Anuj A; Hottenga, Jouke-Jan JJ; Huffman, Jennifer E JE; Jarick, Ivonne I; Johansson, Åsa Å; Johnson, Toby T; Kanoni, Stavroula S; Kleber, Marcus E ME; König, Inke R IR; Kristiansson, Kati K; Kutalik, Zoltán Z; Lamina, Claudia C; Lecoeur, Cecile C; Li, Guo G; Mangino, Massimo M; McArdle, Wendy L WL; Medina-Gomez, Carolina C; Müller-Nurasyid, Martina M; Ngwa, Julius S JS; Nolte, Ilja M IM; Paternoster, Lavinia L; Pechlivanis, Sonali S; Perola, Markus M; Peters, Marjolein J MJ; Preuss, Michael M; Rose, Lynda M LM; Shi, Jianxin J; Shungin, Dmitry D; Smith, Albert Vernon AV; Strawbridge, Rona J RJ; Surakka, Ida I; Teumer, Alexander A; Trip, Mieke D MD; Tyrer, Jonathan J; Van Vliet-Ostaptchouk, Jana V JV; Vandenput, Liesbeth L; Waite, Lindsay L LL; Zhao, Jing Hua JH; Absher, Devin D; Asselbergs, Folkert W FW; Atalay, Mustafa M; Attwood, Antony P AP; Balmforth, Anthony J AJ; Basart, Hanneke H; Beilby, John J; Bonnycastle, Lori L LL; Brambilla, Paolo P; Bruinenberg, Marcel M; Campbell, Harry H; Chasman, Daniel I DI; Chines, Peter S PS; Collins, Francis S FS; Connell, John M JM; Cookson, William O WO; de Faire, Ulf U; de Vegt, Femmie F; Dei, Mariano M; Dimitriou, Maria M; Edkins, Sarah S; Estrada, Karol K; Evans, David M DM; Farrall, Martin M; Ferrario, Marco M MM; Ferrières, Jean J; Franke, Lude L; Frau, Francesca F; Gejman, Pablo V PV; Grallert, Harald H; Grönberg, Henrik H; Gudnason, Vilmundur V; Hall, Alistair S AS; Hall, Per P; Hartikainen, Anna-Liisa AL; Hayward, Caroline C; Heard-Costa, Nancy L NL; Heath, Andrew C AC; Hebebrand, Johannes J; Homuth, Georg G; Hu, Frank B FB; Hunt, Sarah E SE; Hyppönen, Elina E; Iribarren, Carlos C; Jacobs, Kevin B KB; Jansson, John-Olov JO; Jula, Antti A; Kähönen, Mika M; Kathiresan, Sekar S; Kee, Frank F; Khaw, Kay-Tee KT; Kivimäki, Mika M; Koenig, Wolfgang W; Kraja, Aldi T AT; Kumari, Meena M; Kuulasmaa, Kari K; Kuusisto, Johanna J; Laitinen, Jaana H JH; Lakka, Timo A TA; Langenberg, Claudia C; Launer, Lenore J LJ; Lind, Lars L; Lindström, Jaana J; Liu, Jianjun J; Liuzzi, Antonio A; Lokki, Marja-Liisa ML; Lorentzon, Mattias M; Madden, Pamela A PA; Magnusson, Patrik K PK; Manunta, Paolo P; Marek, Diana D; März, Winfried W; Mateo Leach, Irene I; McKnight, Barbara B; Medland, Sarah E SE; Mihailov, Evelin E; Milani, Lili L; Montgomery, Grant W GW; Mooser, Vincent V; Mühleisen, Thomas W TW; Munroe, Patricia B PB; Musk, Arthur W AW; Narisu, Narisu N; Navis, Gerjan G; Nicholson, George G; Nohr, Ellen A EA; Ong, Ken K KK; Oostra, Ben A BA; Palmer, Colin N A CN; Palotie, Aarno A; Peden, John F JF; Pedersen, Nancy N; Peters, Annette A; Polasek, Ozren O; Pouta, Anneli A; Pramstaller, Peter P PP; Prokopenko, Inga I; Pütter, Carolin C; Radhakrishnan, Aparna A; Raitakari, Olli O; Rendon, Augusto A; Rivadeneira, Fernando F; Rudan, Igor I; Saaristo, Timo E TE; Sambrook, Jennifer G JG; Sanders, Alan R AR; Sanna, Serena S; Saramies, Jouko J; Schipf, Sabine S; Schreiber, Stefan S; Schunkert, Heribert H; Shin, So-Youn SY; Signorini, Stefano S; Sinisalo, Juha J; Skrobek, Boris B; Soranzo, Nicole N; Stančáková, Alena A; Stark, Klaus K; Stephens, Jonathan C JC; Stirrups, Kathleen K; Stolk, Ronald P RP; Stumvoll, Michael M; Swift, Amy J AJ; Theodoraki, Eirini V EV; Thorand, Barbara B; Tregouet, David-Alexandre DA; Tremoli, Elena E; Van der Klauw, Melanie M MM; van Meurs, Joyce B J JB; Vermeulen, Sita H SH; Viikari, Jorma J; Virtamo, Jarmo J; Vitart, Veronique V; Waeber, Gérard G; Wang, Zhaoming Z; Widén, Elisabeth E; Wild, Sarah H SH; Willemsen, Gonneke G; Winkelmann, Bernhard R BR; Witteman, Jacqueline C M JC; Wolffenbuttel, Bruce H R BH; Wong, Andrew A; Wright, Alan F AF; Zillikens, M Carola MC; Amouyel, Philippe P; Boehm, Bernhard O BO; Boerwinkle, Eric E; Boomsma, Dorret I DI; Caulfield, Mark J MJ; Chanock, Stephen J SJ; Cupples, L Adrienne LA; Cusi, Daniele D; Dedoussis, George V GV; Erdmann, Jeanette J; Eriksson, Johan G JG; Franks, Paul W PW; Froguel, Philippe P; Gieger, Christian C; Gyllensten, Ulf U; Hamsten, Anders A; Harris, Tamara B TB; Hengstenberg, Christian C; Hicks, Andrew A AA; Hingorani, Aroon A; Hinney, Anke A; Hofman, Albert A; Hovingh, Kees G KG; Hveem, Kristian K; Illig, Thomas T; Jarvelin, Marjo-Riitta MR; Jöckel, Karl-Heinz KH; Keinanen-Kiukaanniemi, Sirkka M SM; Kiemeney, Lambertus A LA; Kuh, Diana D; Laakso, Markku M; Lehtimäki, Terho T; Levinson, Douglas F DF; Martin, Nicholas G NG; Metspalu, Andres A; Morris, Andrew D AD; Nieminen, Markku S MS; Njølstad, Inger I; Ohlsson, Claes C; Oldehinkel, Albertine J AJ; Ouwehand, Willem H WH; Palmer, Lyle J LJ; Penninx, Brenda B; Power, Chris C; Province, Michael A MA; Psaty, Bruce M BM; Qi, Lu L; Rauramaa, Rainer R; Ridker, Paul M PM; Ripatti, Samuli S; Salomaa, Veikko V; Samani, Nilesh J NJ; Snieder, Harold H; Sørensen, Thorkild I A TI; Spector, Timothy D TD; Stefansson, Kari K; Tönjes, Anke A; Tuomilehto, Jaakko J; Uitterlinden, André G AG; Uusitupa, Matti M; van der Harst, Pim P; Vollenweider, Peter P; Wallaschofski, Henri H; Wareham, Nicholas J NJ; Watkins, Hugh H; Wichmann, H-Erich HE; Wilson, James F JF; Abecasis, Goncalo R GR; Assimes, Themistocles L TL; Barroso, Inês I; Boehnke, Michael M; Borecki, Ingrid B IB; Deloukas, Panos P; Fox, Caroline S CS; Frayling, Timothy T; Groop, Leif C LC; Haritunian, Talin T; Heid, Iris M IM; Hunter, David D; Kaplan, Robert C RC; Karpe, Fredrik F; Moffatt, Miriam F MF; Mohlke, Karen L KL; O'Connell, Jeffrey R JR; Pawitan, Yudi Y; Schadt, Eric E EE; Schlessinger, David D; Steinthorsdottir, Valgerdur V; Strachan, David P DP; Thorsteinsdottir, Unnur U; van Duijn, Cornelia M CM; Visscher, Peter M PM; Di Blasio, Anna Maria AM; Hirschhorn, Joel N JN; Lindgren, Cecilia M CM; Morris, Andrew P AP; Meyre, David D; Scherag, André A; McCarthy, Mark I MI; Speliotes, Elizabeth K EK; North, Kari E KE; Loos, Ruth J F RJ; Ingelsson, Erik E
Publication Date: 2013-05

Variant appearance in text: rs3791679
PubMed Link: 23563607
Variant Present in the following documents:
  • NIHMS536922-supplement-1.pdf
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Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia.

Plos One
Zhang, Ge G; Karns, Rebekah R; Sun, Guangyun G; Indugula, Subba Rao SR; Cheng, Hong H; Havas-Augustin, Dubravka D; Novokmet, Natalija N; Rudan, Dusko D; Durakovic, Zijad Z; Missoni, Sasa S; Chakraborty, Ranajit R; Rudan, Pavao P; Deka, Ranjan R
Publication Date: 2011

Variant appearance in text: rs3791679
PubMed Link: 22216288
Variant Present in the following documents:
  • Main text
  • pone.0029475.pdf
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Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women.

Obesity (Silver Spring, Md.)
Croteau-Chonka, Damien C DC; Marvelle, Amanda F AF; Lange, Ethan M EM; Lee, Nanette R NR; Adair, Linda S LS; Lange, Leslie A LA; Mohlke, Karen L KL
Publication Date: 2011-05

Variant appearance in text: rs3791679
PubMed Link: 20966902
Variant Present in the following documents:
  • Main text
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The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.

Bmc Medical Genetics
Zhao, Jianhua J; Li, Mingyao M; Bradfield, Jonathan P JP; Zhang, Haitao H; Mentch, Frank D FD; Wang, Kai K; Sleiman, Patrick M PM; Kim, Cecilia E CE; Glessner, Joseph T JT; Hou, Cuiping C; Keating, Brendan J BJ; Thomas, Kelly A KA; Garris, Maria L ML; Deliard, Sandra S; Frackelton, Edward C EC; Otieno, F George FG; Chiavacci, Rosetta M RM; Berkowitz, Robert I RI; Hakonarson, Hakon H; Grant, Struan F A SF
Publication Date: 2010-06-14

Variant appearance in text: rs3791679
PubMed Link: 20546612
Variant Present in the following documents:
  • Main text
  • 1471-2350-11-96.pdf
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Genome-wide association study of height and body mass index in Australian twin families.

Twin Research And Human Genetics : The Official Journal Of The International Society For Twin Studies
Liu, Jimmy Z JZ; Medland, Sarah E SE; Wright, Margaret J MJ; Henders, Anjali K AK; Heath, Andrew C AC; Madden, Pamela A F PA; Duncan, Alexis A; Montgomery, Grant W GW; Martin, Nicholas G NG; McRae, Allan F AF
Publication Date: 2010-04

Variant appearance in text: rs3791679
PubMed Link: 20397748
Variant Present in the following documents:
  • Main text
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Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.

Plos One
Shriner, Daniel D; Adeyemo, Adebowale A; Gerry, Norman P NP; Herbert, Alan A; Chen, Guanjie G; Doumatey, Ayo A; Huang, Hanxia H; Zhou, Jie J; Christman, Michael F MF; Rotimi, Charles N CN
Publication Date: 2009-12-22

Variant appearance in text: rs3791679
PubMed Link: 20027299
Variant Present in the following documents:
  • Main text
  • pone.0008398.pdf
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A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family.

Investigative Ophthalmology & Visual Science
Takeuchi, Tomokazu T; Hayashi, Takaaki T; Bedell, Matthew M; Zhang, Kang K; Yamada, Hisashi H; Tsuneoka, Hiroshi H
Publication Date: 2010-03

Variant appearance in text: rs3791679
PubMed Link: 19850834
Variant Present in the following documents:
  • Main text
View BVdb publication page