ITIH4 c.1540-83A>G

Variant ID: 3-52855229-T-C

NM_002218.4(ITIH4):c.1540-83A>G

This variant was identified in 24 publications

View GRCh38 version.




Publications:


Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: ITIH4: 1540-83A>G; rs2239547
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 1
  • CNR2-4-e1335-s003.xlsx, sheet 2
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An integrative analysis of genome-wide association study and regulatory SNP annotation datasets identified candidate genes for bipolar disorder.

International Journal Of Bipolar Disorders
Qi, Xin X; Wen, Yan Y; Li, Ping P; Liang, Chujun C; Cheng, Bolun B; Ma, Mei M; Cheng, Shiqiang S; Zhang, Lu L; Liu, Li L; Kafle, Om Prakash OP; Zhang, Feng F
Publication Date: 2020-02-03

Variant appearance in text: rs2239547
PubMed Link: 32009227
Variant Present in the following documents:
  • Main text
  • 40345_2019_Article_170.pdf
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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: ITIH4: 1540-83A>G; rs2239547
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1
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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.

Nature Genetics
Justice, Anne E AE; Karaderi, Tugce T; Highland, Heather M HM; Young, Kristin L KL; Graff, Mariaelisa M; Lu, Yingchang Y; Turcot, Valérie V; Auer, Paul L PL; Fine, Rebecca S RS; Guo, Xiuqing X; Schurmann, Claudia C; Lempradl, Adelheid A; Marouli, Eirini E; Mahajan, Anubha A; Winkler, Thomas W TW; Locke, Adam E AE; Medina-Gomez, Carolina C; Esko, Tõnu T; Vedantam, Sailaja S; Giri, Ayush A; Lo, Ken Sin KS; Alfred, Tamuno T; Mudgal, Poorva P; Ng, Maggie C Y MCY; Heard-Costa, Nancy L NL; Feitosa, Mary F MF; Manning, Alisa K AK; Willems, Sara M SM; Sivapalaratnam, Suthesh S; Abecasis, Goncalo G; Alam, Dewan S DS; Allison, Matthew M; Amouyel, Philippe P; Arzumanyan, Zorayr Z; Balkau, Beverley B; Bastarache, Lisa L; Bergmann, Sven S; Bielak, Lawrence F LF; Blüher, Matthias M; Boehnke, Michael M; Boeing, Heiner H; Boerwinkle, Eric E; Böger, Carsten A CA; Bork-Jensen, Jette J; Bottinger, Erwin P EP; Bowden, Donald W DW; Brandslund, Ivan I; Broer, Linda L; Burt, Amber A AA; Butterworth, Adam S AS; Caulfield, Mark J MJ; Cesana, Giancarlo G; Chambers, John C JC; Chasman, Daniel I DI; Chen, Yii-Der Ida YI; Chowdhury, Rajiv R; Christensen, Cramer C; Chu, Audrey Y AY; Collins, Francis S FS; Cook, James P JP; Cox, Amanda J AJ; Crosslin, David S DS; Danesh, John J; de Bakker, Paul I W PIW; Denus, Simon de S; Mutsert, Renée de R; Dedoussis, George G; Demerath, Ellen W EW; Dennis, Joe G JG; Denny, Josh C JC; Di Angelantonio, Emanuele E; Dörr, Marcus M; Drenos, Fotios F; Dubé, Marie-Pierre MP; Dunning, Alison M AM; Easton, Douglas F DF; Elliott, Paul P; Evangelou, Evangelos E; Farmaki, Aliki-Eleni AE; Feng, Shuang S; Ferrannini, Ele E; Ferrieres, Jean J; Florez, Jose C JC; Fornage, Myriam M; Fox, Caroline S CS; Franks, Paul W PW; Friedrich, Nele N; Gan, Wei W; Gandin, Ilaria I; Gasparini, Paolo P; Giedraitis, Vilmantas V; Girotto, Giorgia G; Gorski, Mathias M; Grallert, Harald H; Grarup, Niels N; Grove, Megan L ML; Gustafsson, Stefan S; Haessler, Jeff J; Hansen, Torben T; Hattersley, Andrew T AT; Hayward, Caroline C; Heid, Iris M IM; Holmen, Oddgeir L OL; Hovingh, G Kees GK; Howson, Joanna M M JMM; Hu, Yao Y; Hung, Yi-Jen YJ; Hveem, Kristian K; Ikram, M Arfan MA; Ingelsson, Erik E; Jackson, Anne U AU; Jarvik, Gail P GP; Jia, Yucheng Y; Jørgensen, Torben T; Jousilahti, Pekka P; Justesen, Johanne M JM; Kahali, Bratati B; Karaleftheri, Maria M; Kardia, Sharon L R SLR; Karpe, Fredrik F; Kee, Frank F; Kitajima, Hidetoshi H; Komulainen, Pirjo P; Kooner, Jaspal S JS; Kovacs, Peter P; Krämer, Bernhard K BK; Kuulasmaa, Kari K; Kuusisto, Johanna J; Laakso, Markku M; Lakka, Timo A TA; Lamparter, David D; Lange, Leslie A LA; Langenberg, Claudia C; Larson, Eric B EB; Lee, Nanette R NR; Lee, Wen-Jane WJ; Lehtimäki, Terho T; Lewis, Cora E CE; Li, Huaixing H; Li, Jin J; Li-Gao, Ruifang R; Lin, Li-An LA; Lin, Xu X; Lind, Lars L; Lindström, Jaana J; Linneberg, Allan A; Liu, Ching-Ti CT; Liu, Dajiang J DJ; Luan, Jian'an J; Lyytikäinen, Leo-Pekka LP; MacGregor, Stuart S; Mägi, Reedik R; Männistö, Satu S; Marenne, Gaëlle G; Marten, Jonathan J; Masca, Nicholas G D NGD; McCarthy, Mark I MI; Meidtner, Karina K; Mihailov, Evelin E; Moilanen, Leena L; Moitry, Marie M; Mook-Kanamori, Dennis O DO; Morgan, Anna A; Morris, Andrew P AP; Müller-Nurasyid, Martina M; Munroe, Patricia B PB; Narisu, Narisu N; Nelson, Christopher P CP; Neville, Matt M; Ntalla, Ioanna I; O'Connell, Jeffrey R JR; Owen, Katharine R KR; Pedersen, Oluf O; Peloso, Gina M GM; Pennell, Craig E CE; Perola, Markus M; Perry, James A JA; Perry, John R B JRB; Pers, Tune H TH; Ewing, Ailith A; Polasek, Ozren O; Raitakari, Olli T OT; Rasheed, Asif A; Raulerson, Chelsea K CK; Rauramaa, Rainer R; Reilly, Dermot F DF; Reiner, Alex P AP; Ridker, Paul M PM; Rivas, Manuel A MA; Robertson, Neil R NR; Robino, Antonietta A; Rudan, Igor I; Ruth, Katherine S KS; Saleheen, Danish D; Salomaa, Veikko V; Samani, Nilesh J NJ; Schreiner, Pamela J PJ; Schulze, Matthias B MB; Scott, Robert A RA; Segura-Lepe, Marcelo M; Sim, Xueling X; Slater, Andrew J AJ; Small, Kerrin S KS; Smith, Blair H BH; Smith, Jennifer A JA; Southam, Lorraine L; Spector, Timothy D TD; Speliotes, Elizabeth K EK; Stefansson, Kari K; Steinthorsdottir, Valgerdur V; Stirrups, Kathleen E KE; Strauch, Konstantin K; Stringham, Heather M HM; Stumvoll, Michael M; Sun, Liang L; Surendran, Praveen P; Swart, Karin M A KMA; Tardif, Jean-Claude JC; Taylor, Kent D KD; Teumer, Alexander A; Thompson, Deborah J DJ; Thorleifsson, Gudmar G; Thorsteinsdottir, Unnur U; Thuesen, Betina H BH; Tönjes, Anke A; Torres, Mina M; Tsafantakis, Emmanouil E; Tuomilehto, Jaakko J; Uitterlinden, André G AG; Uusitupa, Matti M; van Duijn, Cornelia M CM; Vanhala, Mauno M; Varma, Rohit R; Vermeulen, Sita H SH; Vestergaard, Henrik H; Vitart, Veronique V; Vogt, Thomas F TF; Vuckovic, Dragana D; Wagenknecht, Lynne E LE; Walker, Mark M; Wallentin, Lars L; Wang, Feijie F; Wang, Carol A CA; Wang, Shuai S; Wareham, Nicholas J NJ; Warren, Helen R HR; Waterworth, Dawn M DM; Wessel, Jennifer J; White, Harvey D HD; Willer, Cristen J CJ; Wilson, James G JG; Wood, Andrew R AR; Wu, Ying Y; Yaghootkar, Hanieh H; Yao, Jie J; Yerges-Armstrong, Laura M LM; Young, Robin R; Zeggini, Eleftheria E; Zhan, Xiaowei X; Zhang, Weihua W; Zhao, Jing Hua JH; Zhao, Wei W; Zheng, He H; Zhou, Wei W; Zillikens, M Carola MC; Rivadeneira, Fernando F; Borecki, Ingrid B IB; Pospisilik, J Andrew JA; Deloukas, Panos P; Frayling, Timothy M TM; Lettre, Guillaume G; Mohlke, Karen L KL; Rotter, Jerome I JI; Kutalik, Zoltán Z; Hirschhorn, Joel N JN; Cupples, L Adrienne LA; Loos, Ruth J F RJF; North, Kari E KE; Lindgren, Cecilia M CM; , ; , ; , ; , ; , ; , ; , ; , ; , ; ,
Publication Date: 2019-03

Variant appearance in text: rs2239547
PubMed Link: 30778226
Variant Present in the following documents:
  • NIHMS1016010-supplement-SupplementaryData14.xlsx, sheet 1
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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: ITIH4: 1540-83A>G; rs2239547
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
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Implications of Newly Identified Brain eQTL Genes and Their Interactors in Schizophrenia.

Molecular Therapy. Nucleic Acids
Cai, Lei L; Huang, Tao T; Su, Jingjing J; Zhang, Xinxin X; Chen, Wenzhong W; Zhang, Fuquan F; He, Lin L; Chou, Kuo-Chen KC
Publication Date: 2018-09-07

Variant appearance in text: rs2239547
PubMed Link: 30195780
Variant Present in the following documents:
  • Main text
  • mmc3.pdf
  • main.pdf
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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: rs2239547
PubMed Link: 29974678
Variant Present in the following documents:
  • MGG3-6-739-s002.xlsx, sheet 7
View BVdb publication page



Genetic Overlap Between Schizophrenia and Volumes of Hippocampus, Putamen, and Intracranial Volume Indicates Shared Molecular Genetic Mechanisms.

Schizophrenia Bulletin
Smeland, Olav B OB; Wang, Yunpeng Y; Frei, Oleksandr O; Li, Wen W; Hibar, Derrek P DP; Franke, Barbara B; Bettella, Francesco F; Witoelar, Aree A; Djurovic, Srdjan S; Chen, Chi-Hua CH; Thompson, Paul M PM; Dale, Anders M AM; Andreassen, Ole A OA
Publication Date: 2018-06-06

Variant appearance in text: rs2239547
PubMed Link: 29136250
Variant Present in the following documents:
  • Main text
View BVdb publication page



Progress in genome-wide association studies of schizophrenia in Han Chinese populations.

Npj Schizophrenia
Yue, Weihua W; Yu, Xin X; Zhang, Dai D
Publication Date: 2017-08-10

Variant appearance in text: rs2239547
PubMed Link: 28798405
Variant Present in the following documents:
  • Main text
  • 41537_2017_Article_29.pdf
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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: rs2239547
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
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Calcium-dependent intracellular signal pathways in primary cultured adipocytes and ANK3 gene variation in patients with bipolar disorder and healthy controls.

Molecular Psychiatry
Hayashi, A A; Le Gal, K K; Södersten, K K; Vizlin-Hodzic, D D; Ågren, H H; Funa, K K
Publication Date: 2015-08

Variant appearance in text: rs2239547
PubMed Link: 25311363
Variant Present in the following documents:
  • mp2014104a.pdf
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Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence?

Plos One
Sieradzka, Dominika D; Power, Robert A RA; Freeman, Daniel D; Cardno, Alastair G AG; McGuire, Philip P; Plomin, Robert R; Meaburn, Emma L EL; Dudbridge, Frank F; Ronald, Angelica A
Publication Date: 2014

Variant appearance in text: rs2239547
PubMed Link: 24718684
Variant Present in the following documents:
  • Main text
  • pone.0094398.pdf
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Analysis of schizophrenia-related genes and electrophysiological measures reveals ZNF804A association with amplitude of P300b elicited by novel sounds.

Translational Psychiatry
Del Re, E C EC; Bergen, S E SE; Mesholam-Gately, R I RI; Niznikiewicz, M A MA; Goldstein, J M JM; Woo, T U TU; Shenton, M E ME; Seidman, L J LJ; McCarley, R W RW; Petryshen, T L TL
Publication Date: 2014-01-14

Variant appearance in text: rs2239547
PubMed Link: 24424392
Variant Present in the following documents:
View BVdb publication page



A population-based study of genetic variation and psychotic experiences in adolescents.

Schizophrenia Bulletin
Zammit, Stanley S; Hamshere, Marian M; Dwyer, Sarah S; Georgiva, Lyudmila L; Timpson, Nic N; Moskvina, Valentina V; Richards, Alexander A; Evans, David M DM; Lewis, Glyn G; Jones, Peter P; Owen, Michael J MJ; O'Donovan, Michael C MC
Publication Date: 2014-11

Variant appearance in text: rs2239547
PubMed Link: 24174267
Variant Present in the following documents:
  • Main text
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Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.

Plos One
Kondo, Kenji K; Ikeda, Masashi M; Kajio, Yusuke Y; Saito, Takeo T; Iwayama, Yoshimi Y; Aleksic, Branko B; Yamada, Kazuo K; Toyota, Tomoko T; Hattori, Eiji E; Ujike, Hiroshi H; Inada, Toshiya T; Kunugi, Hiroshi H; Kato, Tadafumi T; Yoshikawa, Takeo T; Ozaki, Norio N; Iwata, Nakao N
Publication Date: 2013

Variant appearance in text: rs2239547
PubMed Link: 23967141
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.

Biological Psychiatry
, ; , ; Bramon, Elvira E; Pirinen, Matti M; Strange, Amy A; Lin, Kuang K; Freeman, Colin C; Bellenguez, Céline C; Su, Zhan Z; Band, Gavin G; Pearson, Richard R; Vukcevic, Damjan D; Langford, Cordelia C; Deloukas, Panos P; Hunt, Sarah S; Gray, Emma E; Dronov, Serge S; Potter, Simon C SC; Tashakkori-Ghanbaria, Avazeh A; Edkins, Sarah S; Bumpstead, Suzannah J SJ; Arranz, Maria J MJ; Bakker, Steven S; Bender, Stephan S; Bruggeman, Richard R; Cahn, Wiepke W; Chandler, David D; Collier, David A DA; Crespo-Facorro, Benedicto B; Dazzan, Paola P; de Haan, Lieuwe L; Di Forti, Marta M; Dragović, Milan M; Giegling, Ina I; Hall, Jeremy J; Iyegbe, Conrad C; Jablensky, Assen A; Kahn, René S RS; Kalaydjieva, Luba L; Kravariti, Eugenia E; Lawrie, Stephen S; Linszen, Don H DH; Mata, Ignacio I; McDonald, Colm C; McIntosh, Andrew A; Myin-Germeys, Inez I; Ophoff, Roel A RA; Pariante, Carmine M CM; Paunio, Tiina T; Picchioni, Marco M; , ; Ripke, Stephan S; Rujescu, Dan D; Sauer, Heinrich H; Shaikh, Madiha M; Sussmann, Jessika J; Suvisaari, Jaana J; Tosato, Sarah S; Toulopoulou, Timothea T; Van Os, Jim J; Walshe, Muriel M; Weisbrod, Matthias M; Whalley, Heather H; Wiersma, Durk D; Blackwell, Jenefer M JM; Brown, Matthew A MA; Casas, Juan P JP; Corvin, Aiden A; Duncanson, Audrey A; Jankowski, Janusz A Z JA; Markus, Hugh S HS; Mathew, Christopher G CG; Palmer, Colin N A CN; Plomin, Robert R; Rautanen, Anna A; Sawcer, Stephen J SJ; Trembath, Richard C RC; Wood, Nicholas W NW; Barroso, Ines I; Peltonen, Leena L; Lewis, Cathryn M CM; Murray, Robin M RM; Donnelly, Peter P; Powell, John J; Spencer, Chris C A CC
Publication Date: 2014-03-01

Variant appearance in text: rs2239547
PubMed Link: 23871474
Variant Present in the following documents:
  • Main text
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Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate.

Plos Genetics
Andreassen, Ole A OA; Thompson, Wesley K WK; Schork, Andrew J AJ; Ripke, Stephan S; Mattingsdal, Morten M; Kelsoe, John R JR; Kendler, Kenneth S KS; O'Donovan, Michael C MC; Rujescu, Dan D; Werge, Thomas T; Sklar, Pamela P; , ; , ; Roddey, J Cooper JC; Chen, Chi-Hua CH; McEvoy, Linda L; Desikan, Rahul S RS; Djurovic, Srdjan S; Dale, Anders M AM
Publication Date: 2013-04

Variant appearance in text: rs2239547
PubMed Link: 23637625
Variant Present in the following documents:
  • Main text
View BVdb publication page



Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors.

American Journal Of Human Genetics
Andreassen, Ole A OA; Djurovic, Srdjan S; Thompson, Wesley K WK; Schork, Andrew J AJ; Kendler, Kenneth S KS; O'Donovan, Michael C MC; Rujescu, Dan D; Werge, Thomas T; van de Bunt, Martijn M; Morris, Andrew P AP; McCarthy, Mark I MI; , ; , ; , ; Roddey, J Cooper JC; McEvoy, Linda K LK; Desikan, Rahul S RS; Dale, Anders M AM
Publication Date: 2013-02-07

Variant appearance in text: rs2239547
PubMed Link: 23375658
Variant Present in the following documents:
  • Main text
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Genome-wide association studies in psychiatry: what have we learned?

The British Journal Of Psychiatry : The Journal Of Mental Science
Collins, Ann L AL; Sullivan, Patrick F PF
Publication Date: 2013-01

Variant appearance in text: rs2239547
PubMed Link: 23284144
Variant Present in the following documents:
  • Main text
View BVdb publication page



Ankyrin 3: genetic association with bipolar disorder and relevance to disease pathophysiology.

Biology Of Mood & Anxiety Disorders
Leussis, Melanie P MP; Madison, Jon M JM; Petryshen, Tracey L TL
Publication Date: 2012-10-01

Variant appearance in text: rs2239547
PubMed Link: 23025490
Variant Present in the following documents:
  • Main text
  • 2045-5380-2-18.pdf
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Genetic architectures of psychiatric disorders: the emerging picture and its implications.

Nature Reviews. Genetics
Sullivan, Patrick F PF; Daly, Mark J MJ; O'Donovan, Michael M
Publication Date: 2012-07-10

Variant appearance in text: rs2239547
PubMed Link: 22777127
Variant Present in the following documents:
  • Main text
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Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

Molecular Psychiatry
Hamshere, M L ML; Walters, J T R JT; Smith, R R; Richards, A L AL; Green, E E; Grozeva, D D; Jones, I I; Forty, L L; Jones, L L; Gordon-Smith, K K; Riley, B B; O'Neill, F A FA; O'Neill, T T; Kendler, K S KS; Sklar, P P; Purcell, S S; Kranz, J J; , ; , ; , ; Morris, D D; Gill, M M; Holmans, P P; Craddock, N N; Corvin, A A; Owen, M J MJ; O'Donovan, M C MC
Publication Date: 2013-06

Variant appearance in text: rs2239547
PubMed Link: 22614287
Variant Present in the following documents:
  • Main text
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A mega-analysis of genome-wide association studies for major depressive disorder.

Molecular Psychiatry
, ; Ripke, Stephan S; Wray, Naomi R NR; Lewis, Cathryn M CM; Hamilton, Steven P SP; Weissman, Myrna M MM; Breen, Gerome G; Byrne, Enda M EM; Blackwood, Douglas H R DH; Boomsma, Dorret I DI; Cichon, Sven S; Heath, Andrew C AC; Holsboer, Florian F; Lucae, Susanne S; Madden, Pamela A F PA; Martin, Nicholas G NG; McGuffin, Peter P; Muglia, Pierandrea P; Noethen, Markus M MM; Penninx, Brenda P BP; Pergadia, Michele L ML; Potash, James B JB; Rietschel, Marcella M; Lin, Danyu D; Müller-Myhsok, Bertram B; Shi, Jianxin J; Steinberg, Stacy S; Grabe, Hans J HJ; Lichtenstein, Paul P; Magnusson, Patrik P; Perlis, Roy H RH; Preisig, Martin M; Smoller, Jordan W JW; Stefansson, Kari K; Uher, Rudolf R; Kutalik, Zoltan Z; Tansey, Katherine E KE; Teumer, Alexander A; Viktorin, Alexander A; Barnes, Michael R MR; Bettecken, Thomas T; Binder, Elisabeth B EB; Breuer, René R; Castro, Victor M VM; Churchill, Susanne E SE; Coryell, William H WH; Craddock, Nick N; Craig, Ian W IW; Czamara, Darina D; De Geus, Eco J EJ; Degenhardt, Franziska F; Farmer, Anne E AE; Fava, Maurizio M; Frank, Josef J; Gainer, Vivian S VS; Gallagher, Patience J PJ; Gordon, Scott D SD; Goryachev, Sergey S; Gross, Magdalena M; Guipponi, Michel M; Henders, Anjali K AK; Herms, Stefan S; Hickie, Ian B IB; Hoefels, Susanne S; Hoogendijk, Witte W; Hottenga, Jouke Jan JJ; Iosifescu, Dan V DV; Ising, Marcus M; Jones, Ian I; Jones, Lisa L; Jung-Ying, Tzeng T; Knowles, James A JA; Kohane, Isaac S IS; Kohli, Martin A MA; Korszun, Ania A; Landen, Mikael M; Lawson, William B WB; Lewis, Glyn G; Macintyre, Donald D; Maier, Wolfgang W; Mattheisen, Manuel M; McGrath, Patrick J PJ; McIntosh, Andrew A; McLean, Alan A; Middeldorp, Christel M CM; Middleton, Lefkos L; Montgomery, Grant M GM; Murphy, Shawn N SN; Nauck, Matthias M; Nolen, Willem A WA; Nyholt, Dale R DR; O'Donovan, Michael M; Oskarsson, Högni H; Pedersen, Nancy N; Scheftner, William A WA; Schulz, Andrea A; Schulze, Thomas G TG; Shyn, Stanley I SI; Sigurdsson, Engilbert E; Slager, Susan L SL; Smit, Johannes H JH; Stefansson, Hreinn H; Steffens, Michael M; Thorgeirsson, Thorgeir T; Tozzi, Federica F; Treutlein, Jens J; Uhr, Manfred M; van den Oord, Edwin J C G EJ; Van Grootheest, Gerard G; Völzke, Henry H; Weilburg, Jeffrey B JB; Willemsen, Gonneke G; Zitman, Frans G FG; Neale, Benjamin B; Daly, Mark M; Levinson, Douglas F DF; Sullivan, Patrick F PF
Publication Date: 2013-04

Variant appearance in text: rs2239547
PubMed Link: 22472876
Variant Present in the following documents:
  • Main text
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Genome-wide association study identifies five new schizophrenia loci.

Nature Genetics
,
Publication Date: 2011-09-18

Variant appearance in text: rs2239547
PubMed Link: 21926974
Variant Present in the following documents:
  • Main text
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