TRIOBP c.3975G>A ;(p.Q1325=)

Variant ID: 22-38129332-G-A

NM_001039141.2(TRIOBP):c.3975G>A;(p.Q1325=)

This variant was identified in 23 publications

View GRCh38 version.




Publications:


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

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

Variant appearance in text: TRIOBP: Q1325Q; rs7284476
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



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: TRIOBP: 3975G>A; Q1325Q; rs7284476
PubMed Link: 36564540
Variant Present in the following documents:
  • 41598_2022_26850_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



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

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

Variant appearance in text: rs7284476
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.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: TRIOBP: 3975G>A; Q1325Q; rs7284476
PubMed Link: 36350814
Variant Present in the following documents:
  • pone.0276233.s004.xlsx, sheet 1
View BVdb publication page



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

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

Variant appearance in text: TRIOBP: Q1325Q
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM12_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM7_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
View BVdb publication page



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

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

Variant appearance in text: TRIOBP: Q1325Q; rs7284476
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



A 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: TRIOBP: 3975G>A; Q1325Q; rs7284476
PubMed Link: 35864542
Variant Present in the following documents:
  • 12920_2022_1315_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene.

Frontiers In Cell And Developmental Biology
Zhu, Yi-Ming YM; Li, Qi Q; Gao, Xue X; Li, Yan-Fei YF; Liu, You-Li YL; Dai, Pu P; Li, Xiang-Ping XP
Publication Date: 2021

Variant appearance in text: TRIOBP: 3975G>A; Q1325Q; rs7284476
PubMed Link: 34692690
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021

Variant appearance in text: TRIOBP: 3975G>A; Q1325Q; rs7284476
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: TRIOBP: Q1325Q; rs7284476
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family.

Biomed Research International
Huang, Shasha S; Gao, Xue X; Wang, Yufeng Y; Kang, Dongyang D; Zhang, Xin X; Yang, Suyan S; Dai, Pu P
Publication Date: 2020

Variant appearance in text: TRIOBP: 3975G>A; Q1325Q; rs7284476
PubMed Link: 32090102
Variant Present in the following documents:
  • 6370386.f1.xlsx, sheet 2
View BVdb publication page



An analysis of mutational signatures of synonymous mutations across 15 cancer types.

Bmc Medical Genetics
Bin, Yannan Y; Wang, Xiaojuan X; Zhao, Le L; Wen, Pengbo P; Xia, Junfeng J
Publication Date: 2019-12-09

Variant appearance in text: TRIOBP: 3975G>A
PubMed Link: 31815613
Variant Present in the following documents:
  • 12881_2019_926_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: TRIOBP: 3975G>A; Gln1325=; rs7284476
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: TRIOBP: Q1325Q; rs7284476
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports
Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS
Publication Date: 2018-12-04

Variant appearance in text: rs7284476
PubMed Link: 30514953
Variant Present in the following documents:
  • 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



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

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

Variant appearance in text: TRIOBP: 3975G>A; rs7284476
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_7.xlsx, sheet 1
View BVdb publication page



A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Molecular Genetics & Genomic Medicine
Yang, Junli J; Wang, Qiong Q; Zhuo, Qingcui Q; Tian, Huiling H; Li, Wen W; Luo, Fang F; Zhang, Jinghui J; Bi, Dan D; Peng, Jing J; Zhou, Dong D; Xin, Huawei H
Publication Date: 2018-09

Variant appearance in text: TRIOBP: 3975G>A; Q1325Q; rs7284476
PubMed Link: 29974678
Variant Present in the following documents:
  • MGG3-6-739-s002.xlsx, sheet 6
  • MGG3-6-739-s002.xlsx, sheet 5
  • MGG3-6-739-s002.xlsx, sheet 7
  • MGG3-6-739-s002.xlsx, sheet 4
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs7284476
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank.

Bmj (Clinical Research Ed.)
Tyrrell, Jessica J; Jones, Samuel E SE; Beaumont, Robin R; Astley, Christina M CM; Lovell, Rebecca R; Yaghootkar, Hanieh H; Tuke, Marcus M; Ruth, Katherine S KS; Freathy, Rachel M RM; Hirschhorn, Joel N JN; Wood, Andrew R AR; Murray, Anna A; Weedon, Michael N MN; Frayling, Timothy M TM
Publication Date: 2016-03-08

Variant appearance in text: rs7284476
PubMed Link: 26956984
Variant Present in the following documents:
  • tyrj029564.ww1_default.pdf
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: TRIOBP: Q1325Q; rs7284476
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 2
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 3
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: TRIOBP: Q1325Q; rs7284476
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: TRIOBP: Q1325Q; rs7284476
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



Defining the role of common variation in the genomic and biological architecture of adult human height.

Nature Genetics
Wood, Andrew R AR; Esko, Tonu T; Yang, Jian J; Vedantam, Sailaja S; Pers, Tune H TH; Gustafsson, Stefan S; Chu, Audrey Y AY; Estrada, Karol K; Luan, Jian'an J; Kutalik, Zoltán Z; Amin, Najaf N; Buchkovich, Martin L ML; Croteau-Chonka, Damien C DC; Day, Felix R FR; Duan, Yanan Y; Fall, Tove T; Fehrmann, Rudolf R; Ferreira, Teresa T; Jackson, Anne U AU; Karjalainen, Juha J; Lo, Ken Sin KS; Locke, Adam E AE; Mägi, Reedik R; Mihailov, Evelin E; Porcu, Eleonora E; Randall, Joshua C JC; Scherag, André A; Vinkhuyzen, Anna A E AA; Westra, Harm-Jan HJ; Winkler, Thomas W TW; Workalemahu, Tsegaselassie T; Zhao, Jing Hua JH; Absher, Devin D; Albrecht, Eva E; Anderson, Denise D; Baron, Jeffrey J; Beekman, Marian M; Demirkan, Ayse A; Ehret, Georg B GB; Feenstra, Bjarke B; Feitosa, Mary F MF; Fischer, Krista K; Fraser, Ross M RM; Goel, Anuj A; Gong, Jian J; Justice, Anne E AE; Kanoni, Stavroula S; Kleber, Marcus E ME; Kristiansson, Kati K; Lim, Unhee U; Lotay, Vaneet V; Lui, Julian C JC; Mangino, Massimo M; Mateo Leach, Irene I; Medina-Gomez, Carolina C; Nalls, Michael A MA; Nyholt, Dale R DR; Palmer, Cameron D CD; Pasko, Dorota D; Pechlivanis, Sonali S; Prokopenko, Inga I; Ried, Janina S JS; Ripke, Stephan S; Shungin, Dmitry D; Stancáková, Alena A; Strawbridge, Rona J RJ; Sung, Yun Ju YJ; Tanaka, Toshiko T; Teumer, Alexander A; Trompet, Stella S; van der Laan, Sander W SW; van Setten, Jessica J; Van Vliet-Ostaptchouk, Jana V JV; Wang, Zhaoming Z; Yengo, Loïc L; Zhang, Weihua W; Afzal, Uzma U; Arnlöv, Johan J; Arscott, Gillian M GM; Bandinelli, Stefania S; Barrett, Amy A; Bellis, Claire C; Bennett, Amanda J AJ; Berne, Christian C; Blüher, Matthias M; Bolton, Jennifer L JL; Böttcher, Yvonne Y; Boyd, Heather A HA; Bruinenberg, Marcel M; Buckley, Brendan M BM; Buyske, Steven S; Caspersen, Ida H IH; Chines, Peter S PS; Clarke, Robert R; Claudi-Boehm, Simone S; Cooper, Matthew M; Daw, E Warwick EW; De Jong, Pim A PA; Deelen, Joris J; Delgado, Graciela G; Denny, Josh C JC; Dhonukshe-Rutten, Rosalie R; Dimitriou, Maria M; Doney, Alex S F AS; Dörr, Marcus M; Eklund, Niina N; Eury, Elodie E; Folkersen, Lasse L; Garcia, Melissa E ME; Geller, Frank F; Giedraitis, Vilmantas V; Go, Alan S AS; Grallert, Harald H; Grammer, Tanja B TB; Gräßler, Jürgen J; Grönberg, Henrik H; de Groot, Lisette C P G M LC; Groves, Christopher J CJ; Haessler, Jeffrey J; Hall, Per P; Haller, Toomas T; Hallmans, Goran G; Hannemann, Anke A; Hartman, Catharina A CA; Hassinen, Maija M; Hayward, Caroline C; Heard-Costa, Nancy L NL; Helmer, Quinta Q; Hemani, Gibran G; Henders, Anjali K AK; Hillege, Hans L HL; Hlatky, Mark A MA; Hoffmann, Wolfgang W; Hoffmann, Per P; Holmen, Oddgeir O; Houwing-Duistermaat, Jeanine J JJ; Illig, Thomas T; Isaacs, Aaron A; James, Alan L AL; Jeff, Janina J; Johansen, Berit B; Johansson, Åsa Å; Jolley, Jennifer J; Juliusdottir, Thorhildur T; Junttila, Juhani J; Kho, Abel N AN; Kinnunen, Leena L; Klopp, Norman N; Kocher, Thomas T; Kratzer, Wolfgang W; Lichtner, Peter P; Lind, Lars L; Lindström, Jaana J; Lobbens, Stéphane S; Lorentzon, Mattias M; Lu, Yingchang Y; Lyssenko, Valeriya V; Magnusson, Patrik K E PK; Mahajan, Anubha A; Maillard, Marc M; McArdle, Wendy L WL; McKenzie, Colin A CA; McLachlan, Stela S; McLaren, Paul J PJ; Menni, Cristina C; Merger, Sigrun S; Milani, Lili L; Moayyeri, Alireza A; Monda, Keri L KL; Morken, Mario A MA; Müller, Gabriele G; Müller-Nurasyid, Martina M; Musk, Arthur W AW; Narisu, Narisu N; Nauck, Matthias M; Nolte, Ilja M IM; Nöthen, Markus M MM; Oozageer, Laticia L; Pilz, Stefan S; Rayner, Nigel W NW; Renstrom, Frida F; Robertson, Neil R NR; Rose, Lynda M LM; Roussel, Ronan R; Sanna, Serena S; Scharnagl, Hubert H; Scholtens, Salome S; Schumacher, Fredrick R FR; Schunkert, Heribert H; Scott, Robert A RA; Sehmi, Joban J; Seufferlein, Thomas T; Shi, Jianxin J; Silventoinen, Karri K; Smit, Johannes H JH; Smith, Albert Vernon AV; Smolonska, Joanna J; Stanton, Alice V AV; Stirrups, Kathleen K; Stott, David J DJ; Stringham, Heather M HM; Sundström, Johan J; Swertz, Morris A MA; Syvänen, Ann-Christine AC; Tayo, Bamidele O BO; Thorleifsson, Gudmar G; Tyrer, Jonathan P JP; van Dijk, Suzanne S; van Schoor, Natasja M NM; van der Velde, Nathalie N; van Heemst, Diana D; van Oort, Floor V A FV; Vermeulen, Sita H SH; Verweij, Niek N; Vonk, Judith M JM; Waite, Lindsay L LL; Waldenberger, Melanie M; Wennauer, Roman R; Wilkens, Lynne R LR; Willenborg, Christina C; Wilsgaard, Tom T; Wojczynski, Mary K MK; Wong, Andrew A; Wright, Alan F AF; Zhang, Qunyuan Q; Arveiler, Dominique D; Bakker, Stephan J L SJ; Beilby, John J; Bergman, Richard N RN; Bergmann, Sven S; Biffar, Reiner R; Blangero, John J; Boomsma, Dorret I DI; Bornstein, Stefan R SR; Bovet, Pascal P; Brambilla, Paolo P; Brown, Morris J MJ; Campbell, Harry H; Caulfield, Mark J MJ; Chakravarti, Aravinda A; Collins, Rory R; Collins, Francis S FS; Crawford, Dana C DC; Cupples, L Adrienne LA; Danesh, John J; de Faire, Ulf U; den Ruijter, Hester M HM; Erbel, Raimund R; Erdmann, Jeanette J; Eriksson, Johan G JG; Farrall, Martin M; Ferrannini, Ele E; Ferrières, Jean J; Ford, Ian I; Forouhi, Nita G NG; Forrester, Terrence T; Gansevoort, Ron T RT; Gejman, Pablo V PV; Gieger, Christian C; Golay, Alain A; Gottesman, Omri O; Gudnason, Vilmundur V; Gyllensten, Ulf U; Haas, David W DW; Hall, Alistair S AS; Harris, Tamara B TB; Hattersley, Andrew T AT; Heath, Andrew C AC; Hengstenberg, Christian C; Hicks, Andrew A AA; Hindorff, Lucia A LA; Hingorani, Aroon D AD; Hofman, Albert A; Hovingh, G Kees GK; Humphries, Steve E SE; Hunt, Steven C SC; Hypponen, Elina E; Jacobs, Kevin B KB; Jarvelin, Marjo-Riitta MR; Jousilahti, Pekka P; Jula, Antti M AM; Kaprio, Jaakko J; Kastelein, John J P JJ; Kayser, Manfred M; Kee, Frank F; Keinanen-Kiukaanniemi, Sirkka M SM; Kiemeney, Lambertus A LA; Kooner, Jaspal S JS; Kooperberg, Charles C; Koskinen, Seppo S; Kovacs, Peter P; Kraja, Aldi T AT; Kumari, Meena M; Kuusisto, Johanna J; Lakka, Timo A TA; Langenberg, Claudia C; Le Marchand, Loic L; Lehtimäki, Terho T; Lupoli, Sara S; Madden, Pamela A F PA; Männistö, Satu S; Manunta, Paolo P; Marette, André A; Matise, Tara C TC; McKnight, Barbara B; Meitinger, Thomas T; Moll, Frans L FL; Montgomery, Grant W GW; Morris, Andrew D AD; Morris, Andrew P AP; Murray, Jeffrey C JC; Nelis, Mari M; Ohlsson, Claes C; Oldehinkel, Albertine J AJ; Ong, Ken K KK; Ouwehand, Willem H WH; Pasterkamp, Gerard G; Peters, Annette A; Pramstaller, Peter P PP; Price, Jackie F JF; Qi, Lu L; Raitakari, Olli T OT; Rankinen, Tuomo T; Rao, D C DC; Rice, Treva K TK; Ritchie, Marylyn M; Rudan, Igor I; Salomaa, Veikko V; Samani, Nilesh J NJ; Saramies, Jouko J; Sarzynski, Mark A MA; Schwarz, Peter E H PE; Sebert, Sylvain S; Sever, Peter P; Shuldiner, Alan R AR; Sinisalo, Juha J; Steinthorsdottir, Valgerdur V; Stolk, Ronald P RP; Tardif, Jean-Claude JC; Tönjes, Anke A; Tremblay, Angelo A; Tremoli, Elena E; Virtamo, Jarmo J; Vohl, Marie-Claude MC; , ; , ; , ; , ; Amouyel, Philippe P; Asselbergs, Folkert W FW; Assimes, Themistocles L TL; Bochud, Murielle M; Boehm, Bernhard O BO; Boerwinkle, Eric E; Bottinger, Erwin P EP; Bouchard, Claude C; Cauchi, Stéphane S; Chambers, John C JC; Chanock, Stephen J SJ; Cooper, Richard S RS; de Bakker, Paul I W PI; Dedoussis, George G; Ferrucci, Luigi L; Franks, Paul W PW; Froguel, Philippe P; Groop, Leif C LC; Haiman, Christopher A CA; Hamsten, Anders A; Hayes, M Geoffrey MG; Hui, Jennie J; Hunter, David J DJ; Hveem, Kristian K; Jukema, J Wouter JW; Kaplan, Robert C RC; Kivimaki, Mika M; Kuh, Diana D; Laakso, Markku M; Liu, Yongmei Y; Martin, Nicholas G NG; März, Winfried W; Melbye, Mads M; Moebus, Susanne S; Munroe, Patricia B PB; Njølstad, Inger I; Oostra, Ben A BA; Palmer, Colin N A CN; Pedersen, Nancy L NL; Perola, Markus M; Pérusse, Louis L; Peters, Ulrike U; Powell, Joseph E JE; Power, Chris C; Quertermous, Thomas T; Rauramaa, Rainer R; Reinmaa, Eva E; Ridker, Paul M PM; Rivadeneira, Fernando F; Rotter, Jerome I JI; Saaristo, Timo E TE; Saleheen, Danish D; Schlessinger, David D; Slagboom, P Eline PE; Snieder, Harold H; Spector, Tim D TD; Strauch, Konstantin K; Stumvoll, Michael M; Tuomilehto, Jaakko J; Uusitupa, Matti M; van der Harst, Pim P; Völzke, Henry H; Walker, Mark M; Wareham, Nicholas J NJ; Watkins, Hugh H; Wichmann, H-Erich HE; Wilson, James F JF; Zanen, Pieter P; Deloukas, Panos P; Heid, Iris M IM; Lindgren, Cecilia M CM; Mohlke, Karen L KL; Speliotes, Elizabeth K EK; Thorsteinsdottir, Unnur U; Barroso, Inês I; Fox, Caroline S CS; North, Kari E KE; Strachan, David P DP; Beckmann, Jacques S JS; Berndt, Sonja I SI; Boehnke, Michael M; Borecki, Ingrid B IB; McCarthy, Mark I MI; Metspalu, Andres A; Stefansson, Kari K; Uitterlinden, André G AG; van Duijn, Cornelia M CM; Franke, Lude L; Willer, Cristen J CJ; Price, Alkes L AL; Lettre, Guillaume G; Loos, Ruth J F RJ; Weedon, Michael N MN; Ingelsson, Erik E; O'Connell, Jeffrey R JR; Abecasis, Goncalo R GR; Chasman, Daniel I DI; Goddard, Michael E ME; Visscher, Peter M PM; Hirschhorn, Joel N JN; Frayling, Timothy M TM
Publication Date: 2014-11

Variant appearance in text: rs7284476
PubMed Link: 25282103
Variant Present in the following documents:
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