Publications:

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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight

Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL

Publication Date: 2020-09-03

Variant appearance in text: rs13211507

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

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The schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studies.

Translational Psychiatry

Liu, Chenxing C; Kanazawa, Tetsufumi T; Tian, Ye Y; Mohamed Saini, Suriati S; Mancuso, Serafino S; Mostaid, Md Shaki MS; Takahashi, Atsushi A; Zhang, Dai D; Zhang, Fuquan F; Yu, Hao H; Doo Shin, Hyoung H; Sub Cheong, Hyun H; Ikeda, Masashi M; Kubo, Michiaki M; Iwata, Nakao N; Woo, Sung-Il SI; Yue, Weihua W; Kamatani, Yoichiro Y; Shi, Yongyong Y; Li, Zhiqiang Z; Everall, Ian I; Pantelis, Christos C; Bousman, Chad C

Publication Date: 2019-08-27

Variant appearance in text: rs13211507

PubMed Link: 31455759

Variant Present in the following documents:

• Main text
• 41398_2019_Article_532.pdf

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Transcription factor 4 gene rs9960767 polymorphism in bipolar disorder.

Biomedical Reports

Ozel, Mavi Deniz MD; Onder, Mehmet Emin ME; Sazci, Ali A

Publication Date: 2016-10

Variant appearance in text: rs13211507

PubMed Link: 27699022

Variant Present in the following documents:

• Main text

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Genome-wide association study of behavioural and psychiatric features in human prion disease.

Translational Psychiatry

Thompson, A G B AG; Uphill, J J; Lowe, J J; Porter, M-C MC; Lukic, A A; Carswell, C C; Rudge, P P; MacKay, A A; Collinge, J J; Mead, S S

Publication Date: 2015-04-21

Variant appearance in text: rs13211507

PubMed Link: 25897833

Variant Present in the following documents:

• Main text
• tp201542a.pdf

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GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.

Genes And Immunity

Armstrong, D L DL; Zidovetzki, R R; Alarcón-Riquelme, M E ME; Tsao, B P BP; Criswell, L A LA; Kimberly, R P RP; Harley, J B JB; Sivils, K L KL; Vyse, T J TJ; Gaffney, P M PM; Langefeld, C D CD; Jacob, C O CO

Publication Date: 2014-09

Variant appearance in text: rs13211507

PubMed Link: 24871463

Variant Present in the following documents:

• NIHMS583203-supplement-1.pdf

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Host genetics and immune control of HIV-1 infection: fine mapping for the extended human MHC region in an African cohort.

Genes And Immunity

Prentice, H A HA; Pajewski, N M NM; He, D D; Zhang, K K; Brown, E E EE; Kilembe, W W; Allen, S S; Hunter, E E; Kaslow, R A RA; Tang, J J

Publication Date: 2014

Variant appearance in text: rs13211507

PubMed Link: 24784026

Variant Present in the following documents:

• NIHMS580846-supplement-1.xlsx, sheet 3
• NIHMS580846-supplement-1.xlsx, sheet 2

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Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults.

Neuroimage

Braskie, Meredith N MN; Kohannim, Omid O; Jahanshad, Neda N; Chiang, Ming-Chang MC; Barysheva, Marina M; Toga, Arthur W AW; Ringman, John M JM; Montgomery, Grant W GW; McMahon, Katie L KL; de Zubicaray, Greig I GI; Martin, Nicholas G NG; Wright, Margaret J MJ; Thompson, Paul M PM

Publication Date: 2013-11-15

Variant appearance in text: rs13211507

PubMed Link: 23727532

Variant Present in the following documents:

• Main text

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Personalized medicine in psychiatry: problems and promises.

Bmc Medicine

Ozomaro, Uzoezi U; Wahlestedt, Claes C; Nemeroff, Charles B CB

Publication Date: 2013-05-16

Variant appearance in text: rs13211507

PubMed Link: 23680237

Variant Present in the following documents:

• Main text

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Using genetic, cognitive and multi-modal neuroimaging data to identify ultra-high-risk and first-episode psychosis at the individual level.

Psychological Medicine

Pettersson-Yeo, W W; Benetti, S S; Marquand, A F AF; Dell'acqua, F F; Williams, S C R SC; Allen, P P; Prata, D D; McGuire, P P; Mechelli, A A

Publication Date: 2013-12

Variant appearance in text: rs13211507

PubMed Link: 23507081

Variant Present in the following documents:

• Main text

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Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization.

Plos One

Ocklenburg, Sebastian S; Arning, Larissa L; Gerding, Wanda M WM; Epplen, Jörg T JT; Güntürkün, Onur O; Beste, Christian C

Publication Date: 2013

Variant appearance in text: rs13211507

PubMed Link: 23341962

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: rs13211507

PubMed Link: 23284144

Variant Present in the following documents:

• Main text

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Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.

Nature Genetics

Su, Zhan Z; Gay, Laura J LJ; Strange, Amy A; Palles, Claire C; Band, Gavin G; Whiteman, David C DC; Lescai, Francesco F; Langford, Cordelia C; Nanji, Manoj M; Edkins, Sarah S; van der Winkel, Anouk A; Levine, David D; Sasieni, Peter P; Bellenguez, Céline C; Howarth, Kimberley K; Freeman, Colin C; Trudgill, Nigel N; Tucker, Art T AT; Pirinen, Matti M; Peppelenbosch, Maikel P MP; van der Laan, Luc J W LJ; Kuipers, Ernst J EJ; Drenth, Joost P H JP; Peters, Wilbert H WH; Reynolds, John V JV; Kelleher, Dermot P DP; McManus, Ross R; Grabsch, Heike H; Prenen, Hans H; Bisschops, Raf R; Krishnadath, Kausila K; Siersema, Peter D PD; van Baal, Jantine W P M JW; Middleton, Mark M; Petty, Russell R; Gillies, Richard R; Burch, Nicola N; Bhandari, Pradeep P; Paterson, Stuart S; Edwards, Cathryn C; Penman, Ian I; Vaidya, Kishor K; Ang, Yeng Y; Murray, Iain I; Patel, Praful P; Ye, Weimin W; Mullins, Paul P; Wu, Anna H AH; Bird, Nigel C NC; Dallal, Helen H; Shaheen, Nicholas J NJ; Murray, Liam J LJ; Koss, Konrad K; Bernstein, Leslie L; Romero, Yvonne Y; Hardie, Laura J LJ; Zhang, Rui R; Winter, Helen H; Corley, Douglas A DA; Panter, Simon S; Risch, Harvey A HA; Reid, Brian J BJ; Sargeant, Ian I; Gammon, Marilie D MD; Smart, Howard H; Dhar, Anjan A; McMurtry, Hugh H; Ali, Haythem H; Liu, Geoffrey G; Casson, Alan G AG; Chow, Wong-Ho WH; Rutter, Matt M; Tawil, Ashref A; Morris, Danielle D; Nwokolo, Chuka C; Isaacs, Peter P; Rodgers, Colin C; Ragunath, Krish K; MacDonald, Chris C; Haigh, Chris C; Monk, David D; Davies, Gareth G; Wajed, Saj S; Johnston, David D; Gibbons, Michael M; Cullen, Sue S; Church, Nicholas N; Langley, Ruth R; Griffin, Michael M; Alderson, Derek D; Deloukas, Panos P; Hunt, Sarah E SE; Gray, Emma E; Dronov, Serge S; Potter, Simon C SC; Tashakkori-Ghanbaria, Avazeh A; Anderson, Mark M; Brooks, Claire C; Blackwell, Jenefer M JM; Bramon, Elvira E; Brown, Matthew A MA; Casas, Juan P JP; Corvin, Aiden A; Duncanson, Audrey A; 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; Viswanathan, Ananth C AC; Wood, Nicholas N; Trynka, Gosia G; Wijmenga, Cisca C; Cazier, Jean-Baptiste JB; Atherfold, Paul P; Nicholson, Anna M AM; Gellatly, Nichola L NL; Glancy, Deborah D; Cooper, Sheldon C SC; Cunningham, David D; Lind, Tore T; Hapeshi, Julie J; Ferry, David D; Rathbone, Barrie B; Brown, Julia J; Love, Sharon S; Attwood, Stephen S; MacGregor, Stuart S; Watson, Peter P; Sanders, Scott S; Ek, Weronica W; Harrison, Rebecca F RF; Moayyedi, Paul P; de Caestecker, John J; Barr, Hugh H; Stupka, Elia E; Vaughan, Thomas L TL; Peltonen, Leena L; Spencer, Chris C A CC; Tomlinson, Ian I; Donnelly, Peter P; Jankowski, Janusz A Z JA; , ; ,

Publication Date: 2012-10

Variant appearance in text: rs13211507

PubMed Link: 22961001

Variant Present in the following documents:

• Main text
• ukmss-49738.pdf

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Dissociation of accumulated genetic risk and disease severity in patients with schizophrenia.

Translational Psychiatry

Papiol, S S; Malzahn, D D; Kästner, A A; Sperling, S S; Begemann, M M; Stefansson, H H; Bickeböller, H H; Nave, K-A KA; Ehrenreich, H H

Publication Date: 2011-10-04

Variant appearance in text: rs13211507

PubMed Link: 22833191

Variant Present in the following documents:

• Main text

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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: rs13211507

PubMed Link: 22777127

Variant Present in the following documents:

• Main text

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Paradox of schizophrenia genetics: is a paradigm shift occurring?

Behavioral And Brain Functions : Bbf

Doi, Nagafumi N; Hoshi, Yoko Y; Itokawa, Masanari M; Yoshikawa, Takeo T; Ichikawa, Tomoe T; Arai, Makoto M; Usui, Chie C; Tachikawa, Hirokazu H

Publication Date: 2012-05-31

Variant appearance in text: rs13211507

PubMed Link: 22650965

Variant Present in the following documents:

• Main text

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The shock of the new: progress in schizophrenia genomics.

Current Genomics

Moore, Susan S; Kelleher, Eric E; Corvin, Aiden A

Publication Date: 2011-11

Variant appearance in text: rs13211507

PubMed Link: 22547958

Variant Present in the following documents:

• Main text

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Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults.

The Journal Of Neuroscience : The Official Journal Of The Society For Neuroscience

Braskie, Meredith N MN; Jahanshad, Neda N; Stein, Jason L JL; Barysheva, Marina M; Johnson, Kori K; McMahon, Katie L KL; de Zubicaray, Greig I GI; Martin, Nicholas G NG; Wright, Margaret J MJ; Ringman, John M JM; Toga, Arthur W AW; Thompson, Paul M PM

Publication Date: 2012-04-25

Variant appearance in text: rs13211507

PubMed Link: 22539856

Variant Present in the following documents:

• Main text

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Impact of the genome wide supported NRGN gene on anterior cingulate morphology in schizophrenia.

Plos One

Ohi, Kazutaka K; Hashimoto, Ryota R; Yasuda, Yuka Y; Nemoto, Kiyotaka K; Ohnishi, Takashi T; Fukumoto, Motoyuki M; Yamamori, Hidenaga H; Umeda-Yano, Satomi S; Okada, Takeya T; Iwase, Masao M; Kazui, Hiroaki H; Takeda, Masatoshi M

Publication Date: 2012

Variant appearance in text: rs13211507

PubMed Link: 22253779

Variant Present in the following documents:

• Main text

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Genome-wide association study of Alzheimer's disease with psychotic symptoms.

Molecular Psychiatry

Hollingworth, P P; Sweet, R R; Sims, R R; Harold, D D; Russo, G G; Abraham, R R; Stretton, A A; Jones, N N; Gerrish, A A; Chapman, J J; Ivanov, D D; Moskvina, V V; Lovestone, S S; Priotsi, P P; Lupton, M M; Brayne, C C; Gill, M M; Lawlor, B B; Lynch, A A; Craig, D D; McGuinness, B B; Johnston, J J; Holmes, C C; Livingston, G G; Bass, N J NJ; Gurling, H H; McQuillin, A A; , ; , ; Holmans, P P; Jones, L L; Devlin, B B; Klei, L L; Barmada, M M MM; Demirci, F Y FY; DeKosky, S T ST; Lopez, O L OL; Passmore, P P; Owen, M J MJ; O'Donovan, M C MC; Mayeux, R R; Kamboh, M I MI; Williams, J J

Publication Date: 2012-12

Variant appearance in text: rs13211507

PubMed Link: 22005930

Variant Present in the following documents:

• Main text

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Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

Human Molecular Genetics

Steinberg, Stacy S; de Jong, Simone S; , ; Andreassen, Ole A OA; Werge, Thomas T; Børglum, Anders D AD; Mors, Ole O; Mortensen, Preben B PB; Gustafsson, Omar O; Costas, Javier J; Pietiläinen, Olli P H OP; Demontis, Ditte D; Papiol, Sergi S; Huttenlocher, Johanna J; Mattheisen, Manuel M; Breuer, René R; Vassos, Evangelos E; Giegling, Ina I; Fraser, Gillian G; Walker, Nicholas N; Tuulio-Henriksson, Annamari A; Suvisaari, Jaana J; Lönnqvist, Jouko J; Paunio, Tiina T; Agartz, Ingrid I; Melle, Ingrid I; Djurovic, Srdjan S; Strengman, Eric E; , ; Jürgens, Gesche G; Glenthøj, Birte B; Terenius, Lars L; Hougaard, David M DM; Ørntoft, Torben T; Wiuf, Carsten C; Didriksen, Michael M; Hollegaard, Mads V MV; Nordentoft, Merete M; van Winkel, Ruud R; Kenis, Gunter G; Abramova, Lilia L; Kaleda, Vasily V; Arrojo, Manuel M; Sanjuán, Julio J; Arango, Celso C; Sperling, Swetlana S; Rossner, Moritz M; Ribolsi, Michele M; Magni, Valentina V; Siracusano, Alberto A; Christiansen, Claus C; Kiemeney, Lambertus A LA; Veldink, Jan J; van den Berg, Leonard L; Ingason, Andres A; Muglia, Pierandrea P; Murray, Robin R; Nöthen, Markus M MM; Sigurdsson, Engilbert E; Petursson, Hannes H; Thorsteinsdottir, Unnur U; Kong, Augustine A; Rubino, I Alex IA; De Hert, Marc M; Réthelyi, János M JM; Bitter, István I; Jönsson, Erik G EG; Golimbet, Vera V; Carracedo, Angel A; Ehrenreich, Hannelore H; Craddock, Nick N; Owen, Michael J MJ; O'Donovan, Michael C MC; , ; Ruggeri, Mirella M; Tosato, Sarah S; Peltonen, Leena L; Ophoff, Roel A RA; Collier, David A DA; St Clair, David D; Rietschel, Marcella M; Cichon, Sven S; Stefansson, Hreinn H; Rujescu, Dan D; Stefansson, Kari K

Publication Date: 2011-10-15

Variant appearance in text: rs13211507

PubMed Link: 21791550

Variant Present in the following documents:

• Main text

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Comparative linkage meta-analysis reveals regionally-distinct, disparate genetic architectures: application to bipolar disorder and schizophrenia.

Plos One

Tang, Brady B; Thornton-Wells, Tricia T; Askland, Kathleen D KD

Publication Date: 2011-04-29

Variant appearance in text: rs13211507

PubMed Link: 21559500

Variant Present in the following documents:

• Main text
• pone.0019073.pdf

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Genetics in schizophrenia: where are we and what next?

Dialogues In Clinical Neuroscience

Tiwari, Arun K AK; Zai, Clement C CC; Müller, Daniel J DJ; Kennedy, James L JL

Publication Date: 2010

Variant appearance in text: rs13211507

PubMed Link: 20954426

Variant Present in the following documents:

• Main text
• DialoguesClinNeurosci-12-289.pdf

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Genomics and pharmacogenomics of schizophrenia.

Cns Neuroscience & Therapeutics

Cacabelos, Ramón R; Martínez-Bouza, Rocío R

Publication Date: 2011-10

Variant appearance in text: rs13211507

PubMed Link: 20718829

Variant Present in the following documents:

• Main text

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Common variants in polygenic schizophrenia.

Genome Biology

Glessner, Joseph T JT; Hakonarson, Hakon H

Publication Date: 2009

Variant appearance in text: rs13211507

PubMed Link: 19785721

Variant Present in the following documents:

• Main text
• gb-2009-10-9-236.pdf

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Common variants conferring risk of schizophrenia.

Nature

Stefansson, Hreinn H; Ophoff, Roel A RA; Steinberg, Stacy S; Andreassen, Ole A OA; Cichon, Sven S; Rujescu, Dan D; Werge, Thomas T; Pietiläinen, Olli P H OP; Mors, Ole O; Mortensen, Preben B PB; Sigurdsson, Engilbert E; Gustafsson, Omar O; Nyegaard, Mette M; Tuulio-Henriksson, Annamari A; Ingason, Andres A; Hansen, Thomas T; Suvisaari, Jaana J; Lonnqvist, Jouko J; Paunio, Tiina T; Børglum, Anders D AD; Hartmann, Annette A; Fink-Jensen, Anders A; Nordentoft, Merete M; Hougaard, David D; Norgaard-Pedersen, Bent B; Böttcher, Yvonne Y; Olesen, Jes J; Breuer, René R; Möller, Hans-Jürgen HJ; Giegling, Ina I; Rasmussen, Henrik B HB; Timm, Sally S; Mattheisen, Manuel M; Bitter, István I; Réthelyi, János M JM; Magnusdottir, Brynja B BB; Sigmundsson, Thordur T; Olason, Pall P; Masson, Gisli G; Gulcher, Jeffrey R JR; Haraldsson, Magnus M; Fossdal, Ragnheidur R; Thorgeirsson, Thorgeir E TE; Thorsteinsdottir, Unnur U; Ruggeri, Mirella M; Tosato, Sarah S; Franke, Barbara B; Strengman, Eric E; Kiemeney, Lambertus A LA; , ; Melle, Ingrid I; Djurovic, Srdjan S; Abramova, Lilia L; Kaleda, Vasily V; Sanjuan, Julio J; de Frutos, Rosa R; Bramon, Elvira E; Vassos, Evangelos E; Fraser, Gillian G; Ettinger, Ulrich U; Picchioni, Marco M; Walker, Nicholas N; Toulopoulou, Timi T; Need, Anna C AC; Ge, Dongliang D; Yoon, Joeng Lim JL; Shianna, Kevin V KV; Freimer, Nelson B NB; Cantor, Rita M RM; Murray, Robin R; Kong, Augustine A; Golimbet, Vera V; Carracedo, Angel A; Arango, Celso C; Costas, Javier J; Jönsson, Erik G EG; Terenius, Lars L; Agartz, Ingrid I; Petursson, Hannes H; Nöthen, Markus M MM; Rietschel, Marcella M; Matthews, Paul M PM; Muglia, Pierandrea P; Peltonen, Leena L; St Clair, David D; Goldstein, David B DB; Stefansson, Kari K; Collier, David A DA

Publication Date: 2009-08-06

Variant appearance in text: rs13211507

PubMed Link: 19571808

Variant Present in the following documents:

• Main text

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