NCAN c.*1015G>A

Variant ID: 19-19361735-G-A

NM_004386.2(NCAN):c.*1015G>A

This variant was identified in 36 publications

View GRCh38 version.




Publications:


Genomic and neuroimaging approaches to bipolar disorder.

Bjpsych Open
Oraki Kohshour, Mojtaba M; Papiol, Sergi S; Ching, Christopher R K CRK; Schulze, Thomas G TG
Publication Date: 2022-02-01

Variant appearance in text: rs1064395
PubMed Link: 35101157
Variant Present in the following documents:
  • Main text
  • S2056472421010826a.pdf
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Long Non-Coding RNA- Associated Competing Endogenous RNA Axes in T-Cells in Multiple Sclerosis.

Frontiers In Immunology
Sabaie, Hani H; Salkhordeh, Zoha Z; Asadi, Mohammad Reza MR; Ghafouri-Fard, Soudeh S; Amirinejad, Nazanin N; Askarinejad Behzadi, Mahla M; Hussen, Bashdar Mahmud BM; Taheri, Mohammad M; Rezazadeh, Maryam M
Publication Date: 2021

Variant appearance in text: rs1064395
PubMed Link: 34956196
Variant Present in the following documents:
  • Main text
  • fimmu-12-770679.pdf
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The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder.

Brain Sciences
Georgitsi, Marianthi M; Dermitzakis, Iasonas I; Soumelidou, Evgenia E; Bonti, Eleni E
Publication Date: 2021-05-14

Variant appearance in text: rs1064395
PubMed Link: 34068951
Variant Present in the following documents:
  • Main text
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ADAMTS-12: Functions and Challenges for a Complex Metalloprotease.

Frontiers In Molecular Biosciences
Mohamedi, Yamina Y; Fontanil, Tania T; Cal, Santiago S; Cobo, Teresa T; Obaya, Álvaro J ÁJ
Publication Date: 2021

Variant appearance in text: rs1064395
PubMed Link: 33996918
Variant Present in the following documents:
  • Main text
  • fmolb-08-686763.pdf
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Molecular signature of extracellular matrix pathology in schizophrenia.

The European Journal Of Neuroscience
Pantazopoulos, Harry H; Katsel, Pavel P; Haroutunian, Vahram V; Chelini, Gabriele G; Klengel, Torsten T; Berretta, Sabina S
Publication Date: 2021-06

Variant appearance in text: rs1064395
PubMed Link: 33070392
Variant Present in the following documents:
  • Main text
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A shared genetic contribution to breast cancer and schizophrenia.

Nature Communications
Lu, Donghao D; Song, Jie J; Lu, Yi Y; Fall, Katja K; Chen, Xu X; Fang, Fang F; Landén, Mikael M; Hultman, Christina M CM; Czene, Kamila K; Sullivan, Patrick P; Tamimi, Rulla M RM; Valdimarsdóttir, Unnur A UA
Publication Date: 2020-09-15

Variant appearance in text: rs1064395
PubMed Link: 32934226
Variant Present in the following documents:
  • 41467_2020_18492_MOESM1_ESM.pdf
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Post-mortem multiple sclerosis lesion pathology is influenced by single nucleotide polymorphisms.

Brain Pathology (Zurich, Switzerland)
Fransen, Nina L NL; Crusius, Jakob B A JBA; Smolders, Joost J; Mizee, Mark R MR; van Eden, Corbert G CG; Luchetti, Sabina S; Remmerswaal, Ester B M EBM; Hamann, Jörg J; Mason, Matthew R J MRJ; Huitinga, Inge I
Publication Date: 2020-01

Variant appearance in text: rs1064395
PubMed Link: 31228212
Variant Present in the following documents:
  • Main text
  • BPA-30-106.pdf
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A review on shared clinical and molecular mechanisms between bipolar disorder and frontotemporal dementia.

Progress In Neuro-Psychopharmacology & Biological Psychiatry
Nascimento, Camila C; Nunes, Villela Paula VP; Diehl Rodriguez, Roberta R; Takada, Leonel L; Suemoto, Cláudia Kimie CK; Grinberg, Lea Tenenholz LT; Nitrini, Ricardo R; Lafer, Beny B
Publication Date: 2019-07-13

Variant appearance in text: rs1064395
PubMed Link: 31014945
Variant Present in the following documents:
  • Main text
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Association of Genetic Polymorphisms with Age at Onset in Han Chinese Patients with Bipolar Disorder.

Neuroscience Bulletin
Hu, Shao-Hua SH; Han, Yu-Qing YQ; Mou, Ting-Ting TT; Huang, Man-Li ML; Lai, Jian-Bo JB; Ng, Chee H CH; Lu, Jing J; Lu, Qiao-Qiao QQ; Lin, Qiu-Yan QY; Zhang, Yu-Zhi YZ; Hu, Jian-Bo JB; Wei, Ning N; Xu, Wei-Juan WJ; Zhou, Wei-Hua WH; Chen, Jing-Kai JK; Hu, Chan-Chan CC; Zhou, Xiao-Yi XY; Lu, Shao-Jia SJ; Xu, Yi Y
Publication Date: 2019-08

Variant appearance in text: rs1064395
PubMed Link: 30367335
Variant Present in the following documents:
  • Main text
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Further Evidence of an Association between NCAN rs1064395 and Bipolar Disorder.

Molecular Neuropsychiatry
Wang, Lu L; Liu, Weiqing W; Li, Xingxing X; Xiao, Xiao X; Li, Lingyi L; Liu, Fang F; He, Yuanfang Y; Bai, Yan Y; Chang, Hong H; Zhou, Dong-Sheng DS; Li, Ming M
Publication Date: 2018-06

Variant appearance in text: rs1064395
PubMed Link: 29998116
Variant Present in the following documents:
  • Main text
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Genetic Variants Involved in Bipolar Disorder, a Rough Road Ahead.

Clinical Practice And Epidemiology In Mental Health : Cp & Emh
Orrù, Germano G; Carta, Mauro Giovanni MG
Publication Date: 2018

Variant appearance in text: rs1064395
PubMed Link: 29541150
Variant Present in the following documents:
  • Main text
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Population-Wide Genetic Risk Prediction of Complex Diseases: A Pilot Feasibility Study in Macau Population for Precision Public Healthcare Planning.

Scientific Reports
Tsui, Nancy B Y NBY; Cheng, Gregory G; Chung, Teresa T; Lam, Christopher W K CWK; Yee, Anita A; Chung, Peter K C PKC; Kwan, Tsz-Ki TK; Ko, Elaine E; He, Daihai D; Wong, Wing-Tak WT; Lau, Johnson Y N JYN; Lau, Lok Ting LT; Fok, Manson M
Publication Date: 2018-01-30

Variant appearance in text: rs1064395
PubMed Link: 29382849
Variant Present in the following documents:
  • 41598_2017_19017_MOESM1_ESM.pdf
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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs1064395
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
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Identification of NCAN as a candidate gene for developmental dyslexia.

Scientific Reports
Einarsdottir, Elisabet E; Peyrard-Janvid, Myriam M; Darki, Fahimeh F; Tuulari, Jetro J JJ; Merisaari, Harri H; Karlsson, Linnea L; Scheinin, Noora M NM; Saunavaara, Jani J; Parkkola, Riitta R; Kantojärvi, Katri K; Ämmälä, Antti-Jussi AJ; Yiu-Lin Yu, Nancy N; Matsson, Hans H; Nopola-Hemmi, Jaana J; Karlsson, Hasse H; Paunio, Tiina T; Klingberg, Torkel T; Leinonen, Eira E; Kere, Juha J
Publication Date: 2017-08-24

Variant appearance in text: rs1064395
PubMed Link: 28839234
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_10175.pdf
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The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies.

Translational Psychiatry
Amare, A T AT; Schubert, K O KO; Klingler-Hoffmann, M M; Cohen-Woods, S S; Baune, B T BT
Publication Date: 2017-01-24

Variant appearance in text: rs1064395
PubMed Link: 28117839
Variant Present in the following documents:
  • Main text
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The NCAN gene: schizophrenia susceptibility and cognitive dysfunction.

Neuropsychiatric Disease And Treatment
Wang, Peirong P; Cai, Jun J; Ni, Jianliang J; Zhang, Jiangtao J; Tang, Wei W; Zhang, Chen C
Publication Date: 2016

Variant appearance in text: rs1064395
PubMed Link: 27853371
Variant Present in the following documents:
  • Main text
  • ndt-12-2875.pdf
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Genetics of Bipolar Disorder: Recent Update and Future Directions.

The Psychiatric Clinics Of North America
Goes, Fernando S FS
Publication Date: 2016-03

Variant appearance in text: rs1064395
PubMed Link: 26876324
Variant Present in the following documents:
  • Main text
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Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs.

Translational Psychiatry
den Braber, A A; Zilhão, N R NR; Fedko, I O IO; Hottenga, J-J JJ; Pool, R R; Smit, D J A DJ; Cath, D C DC; Boomsma, D I DI
Publication Date: 2016-02-09

Variant appearance in text: rs1064395
PubMed Link: 26859814
Variant Present in the following documents:
  • Main text
  • tp2015223a.pdf
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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: rs1064395
PubMed Link: 25897833
Variant Present in the following documents:
  • Main text
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Proteoglycans and neuronal migration in the cerebral cortex during development and disease.

Frontiers In Neuroscience
Maeda, Nobuaki N
Publication Date: 2015

Variant appearance in text: rs1064395
PubMed Link: 25852466
Variant Present in the following documents:
  • Main text
  • fnins-09-00098.pdf
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NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology
Dannlowski, Udo U; Kugel, Harald H; Grotegerd, Dominik D; Redlich, Ronny R; Suchy, Janina J; Opel, Nils N; Suslow, Thomas T; Konrad, Carsten C; Ohrmann, Patricia P; Bauer, Jochen J; Kircher, Tilo T; Krug, Axel A; Jansen, Andreas A; Baune, Bernhard T BT; Heindel, Walter W; Domschke, Katharina K; Forstner, Andreas J AJ; Nöthen, Markus M MM; Treutlein, Jens J; Arolt, Volker V; Hohoff, Christa C; Rietschel, Marcella M; Witt, Stephanie H SH
Publication Date: 2015-10

Variant appearance in text: rs1064395
PubMed Link: 25801500
Variant Present in the following documents:
  • Main text
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A genome-wide supported psychiatric risk variant in NCAN influences brain function and cognitive performance in healthy subjects.

Human Brain Mapping
Raum, Heidelore H; Dietsche, Bruno B; Nagels, Arne A; Witt, Stephanie H SH; Rietschel, Marcella M; Kircher, Tilo T; Krug, Axel A
Publication Date: 2015-01

Variant appearance in text: rs1064395
PubMed Link: 25220293
Variant Present in the following documents:
  • Main text
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Genome-wide association study combined with biological context can reveal more disease-related SNPs altering microRNA target seed sites.

Bmc Genomics
Wu, Di D; Yang, Gang G; Zhang, Lifang L; Xue, Jiwei J; Wen, Zhining Z; Li, Menglong M
Publication Date: 2014-08-08

Variant appearance in text: rs1064395
PubMed Link: 25106527
Variant Present in the following documents:
  • Main text
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Chondroitin sulfate proteoglycans: structure-function relationship with implication in neural development and brain disorders.

Biomed Research International
Avram, Speranta S; Shaposhnikov, Sergey S; Buiu, Catalin C; Mernea, Maria M
Publication Date: 2014

Variant appearance in text: rs1064395
PubMed Link: 24955366
Variant Present in the following documents:
  • Main text
  • BMRI2014-642798.pdf
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Genetics of bipolar disorder.

The Application Of Clinical Genetics
Kerner, Berit B
Publication Date: 2014

Variant appearance in text: rs1064395
PubMed Link: 24683306
Variant Present in the following documents:
  • Main text
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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.

Brain Imaging And Behavior
Thompson, Paul M PM; Stein, Jason L JL; Medland, Sarah E SE; Hibar, Derrek P DP; Vasquez, Alejandro Arias AA; Renteria, Miguel E ME; Toro, Roberto R; Jahanshad, Neda N; Schumann, Gunter G; Franke, Barbara B; Wright, Margaret J MJ; Martin, Nicholas G NG; Agartz, Ingrid I; Alda, Martin M; Alhusaini, Saud S; Almasy, Laura L; Almeida, Jorge J; Alpert, Kathryn K; Andreasen, Nancy C NC; Andreassen, Ole A OA; Apostolova, Liana G LG; Appel, Katja K; Armstrong, Nicola J NJ; Aribisala, Benjamin B; Bastin, Mark E ME; Bauer, Michael M; Bearden, Carrie E CE; Bergmann, Orjan O; Binder, Elisabeth B EB; Blangero, John J; Bockholt, Henry J HJ; Bøen, Erlend E; Bois, Catherine C; Boomsma, Dorret I DI; Booth, Tom T; Bowman, Ian J IJ; Bralten, Janita J; Brouwer, Rachel M RM; Brunner, Han G HG; Brohawn, David G DG; Buckner, Randy L RL; Buitelaar, Jan J; Bulayeva, Kazima K; Bustillo, Juan R JR; Calhoun, Vince D VD; Cannon, Dara M DM; Cantor, Rita M RM; Carless, Melanie A MA; Caseras, Xavier X; Cavalleri, Gianpiero L GL; Chakravarty, M Mallar MM; Chang, Kiki D KD; Ching, Christopher R K CR; Christoforou, Andrea A; Cichon, Sven S; Clark, Vincent P VP; Conrod, Patricia P; Coppola, Giovanni G; Crespo-Facorro, Benedicto B; Curran, Joanne E JE; Czisch, Michael M; Deary, Ian J IJ; de Geus, Eco J C EJ; den Braber, Anouk A; Delvecchio, Giuseppe G; Depondt, Chantal C; de Haan, Lieuwe L; de Zubicaray, Greig I GI; Dima, Danai D; Dimitrova, Rali R; Djurovic, Srdjan S; Dong, Hongwei H; Donohoe, Gary G; Duggirala, Ravindranath R; Dyer, Thomas D TD; Ehrlich, Stefan S; Ekman, Carl Johan CJ; Elvsåshagen, Torbjørn T; Emsell, Louise L; Erk, Susanne S; Espeseth, Thomas T; Fagerness, Jesen J; Fears, Scott S; Fedko, Iryna I; Fernández, Guillén G; Fisher, Simon E SE; Foroud, Tatiana T; Fox, Peter T PT; Francks, Clyde C; Frangou, Sophia S; Frey, Eva Maria EM; Frodl, Thomas T; Frouin, Vincent V; Garavan, Hugh H; Giddaluru, Sudheer S; Glahn, David C DC; Godlewska, Beata B; Goldstein, Rita Z RZ; Gollub, Randy L RL; Grabe, Hans J HJ; Grimm, Oliver O; Gruber, Oliver O; Guadalupe, Tulio T; Gur, Raquel E RE; Gur, Ruben C RC; Göring, Harald H H HH; Hagenaars, Saskia S; Hajek, Tomas T; Hall, Geoffrey B GB; Hall, Jeremy J; Hardy, John J; Hartman, Catharina A CA; Hass, Johanna J; Hatton, Sean N SN; Haukvik, Unn K UK; Hegenscheid, Katrin K; Heinz, Andreas A; Hickie, Ian B IB; Ho, Beng-Choon BC; Hoehn, David D; Hoekstra, Pieter J PJ; Hollinshead, Marisa M; Holmes, Avram J AJ; Homuth, Georg G; Hoogman, Martine M; Hong, L Elliot LE; Hosten, Norbert N; Hottenga, Jouke-Jan JJ; Hulshoff Pol, Hilleke E HE; Hwang, Kristy S KS; Jack, Clifford R CR; Jenkinson, Mark M; Johnston, Caroline C; Jönsson, Erik G EG; Kahn, René S RS; Kasperaviciute, Dalia D; Kelly, Sinead S; Kim, Sungeun S; Kochunov, Peter P; Koenders, Laura L; Krämer, Bernd B; Kwok, John B J JB; Lagopoulos, Jim J; Laje, Gonzalo G; Landen, Mikael M; Landman, Bennett A BA; Lauriello, John J; Lawrie, Stephen M SM; Lee, Phil H PH; Le Hellard, Stephanie S; Lemaître, Herve H; Leonardo, Cassandra D CD; Li, Chiang-Shan CS; Liberg, Benny B; Liewald, David C DC; Liu, Xinmin X; Lopez, Lorna M LM; Loth, Eva E; Lourdusamy, Anbarasu A; Luciano, Michelle M; Macciardi, Fabio F; Machielsen, Marise W J MW; Macqueen, Glenda M GM; Malt, Ulrik F UF; Mandl, René R; Manoach, Dara S DS; Martinot, Jean-Luc JL; Matarin, Mar M; Mather, Karen A KA; Mattheisen, Manuel M; Mattingsdal, Morten M; Meyer-Lindenberg, Andreas A; McDonald, Colm C; McIntosh, Andrew M AM; McMahon, Francis J FJ; McMahon, Katie L KL; Meisenzahl, Eva E; Melle, Ingrid I; Milaneschi, Yuri Y; Mohnke, Sebastian S; Montgomery, Grant W GW; Morris, Derek W DW; Moses, Eric K EK; Mueller, Bryon A BA; Muñoz Maniega, Susana S; Mühleisen, Thomas W TW; Müller-Myhsok, Bertram B; Mwangi, Benson B; Nauck, Matthias M; Nho, Kwangsik K; Nichols, Thomas E TE; Nilsson, Lars-Göran LG; Nugent, Allison C AC; Nyberg, Lars L; Olvera, Rene L RL; Oosterlaan, Jaap J; Ophoff, Roel A RA; Pandolfo, Massimo M; Papalampropoulou-Tsiridou, Melina M; Papmeyer, Martina M; Paus, Tomas T; Pausova, Zdenka Z; Pearlson, Godfrey D GD; Penninx, Brenda W BW; Peterson, Charles P CP; Pfennig, Andrea A; Phillips, Mary M; Pike, G Bruce GB; Poline, Jean-Baptiste JB; Potkin, Steven G SG; Pütz, Benno B; Ramasamy, Adaikalavan A; Rasmussen, Jerod J; Rietschel, Marcella M; Rijpkema, Mark M; Risacher, Shannon L SL; Roffman, Joshua L JL; Roiz-Santiañez, Roberto R; Romanczuk-Seiferth, Nina N; Rose, Emma J EJ; Royle, Natalie A NA; Rujescu, Dan D; Ryten, Mina M; Sachdev, Perminder S PS; Salami, Alireza A; Satterthwaite, Theodore D TD; Savitz, Jonathan J; Saykin, Andrew J AJ; Scanlon, Cathy C; Schmaal, Lianne L; Schnack, Hugo G HG; Schork, Andrew J AJ; Schulz, S Charles SC; Schür, Remmelt R; Seidman, Larry L; Shen, Li L; Shoemaker, Jody M JM; Simmons, Andrew A; Sisodiya, Sanjay M SM; Smith, Colin C; Smoller, Jordan W JW; Soares, Jair C JC; Sponheim, Scott R SR; Sprooten, Emma E; Starr, John M JM; Steen, Vidar M VM; Strakowski, Stephen S; Strike, Lachlan L; Sussmann, Jessika J; Sämann, Philipp G PG; Teumer, Alexander A; Toga, Arthur W AW; Tordesillas-Gutierrez, Diana D; Trabzuni, Daniah D; Trost, Sarah S; Turner, Jessica J; Van den Heuvel, Martijn M; van der Wee, Nic J NJ; van Eijk, Kristel K; van Erp, Theo G M TG; van Haren, Neeltje E M NE; van 't Ent, Dennis D; van Tol, Marie-Jose MJ; Valdés Hernández, Maria C MC; Veltman, Dick J DJ; Versace, Amelia A; Völzke, Henry H; Walker, Robert R; Walter, Henrik H; Wang, Lei L; Wardlaw, Joanna M JM; Weale, Michael E ME; Weiner, Michael W MW; Wen, Wei W; Westlye, Lars T LT; Whalley, Heather C HC; Whelan, Christopher D CD; White, Tonya T; Winkler, Anderson M AM; Wittfeld, Katharina K; Woldehawariat, Girma G; Wolf, Christiane C; Zilles, David D; Zwiers, Marcel P MP; Thalamuthu, Anbupalam A; Schofield, Peter R PR; Freimer, Nelson B NB; Lawrence, Natalia S NS; Drevets, Wayne W; ,
Publication Date: 2014-06

Variant appearance in text: rs1064395
PubMed Link: 24399358
Variant Present in the following documents:
  • Main text
  • 11682_2013_Article_9269.pdf
View BVdb publication page



Evidence for single nucleotide polymorphisms and their association with bipolar disorder.

Neuropsychiatric Disease And Treatment
Szczepankiewicz, Aleksandra A
Publication Date: 2013

Variant appearance in text: rs1064395
PubMed Link: 24143106
Variant Present in the following documents:
  • Main text
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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: rs1064395
PubMed Link: 23871474
Variant Present in the following documents:
  • Main text
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Biomarkers of bipolar disorder: specific or shared with schizophrenia?

Frontiers In Bioscience (Elite Edition)
Bellivier, Frank F; Geoffroy, Pierre Alexis PA; Scott, Jan J; Schurhoff, Franck F; Leboyer, Marion M; Etain, Bruno B
Publication Date: 2013-06-01

Variant appearance in text: rs1064395
PubMed Link: 23747901
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: rs1064395
PubMed Link: 23507081
Variant Present in the following documents:
  • Main text
  • S003329171300024Xa.pdf
View BVdb publication page



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: rs1064395
PubMed Link: 23284144
Variant Present in the following documents:
  • Main text
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Assessment of relatedness between neurocan gene as bipolar disorder susceptibility locus and schizophrenia.

Bosnian Journal Of Basic Medical Sciences
Oruč, Lilijana L; Kapur-Pojskić, Lejla L; Ramić, Jasmin J; Pojskić, Naris N; Bajrović, Kasim K
Publication Date: 2012-11

Variant appearance in text: rs1064395
PubMed Link: 23198940
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: rs1064395
PubMed Link: 22777127
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: rs1064395
PubMed Link: 22005930
Variant Present in the following documents:
  • Main text
  • ukmss-36376.pdf
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Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.

American Journal Of Human Genetics
Cichon, Sven S; Mühleisen, Thomas W TW; Degenhardt, Franziska A FA; Mattheisen, Manuel M; Miró, Xavier X; Strohmaier, Jana J; Steffens, Michael M; Meesters, Christian C; Herms, Stefan S; Weingarten, Moritz M; Priebe, Lutz L; Haenisch, Britta B; Alexander, Michael M; Vollmer, Jennifer J; Breuer, René R; Schmäl, Christine C; Tessmann, Peter P; Moebus, Susanne S; Wichmann, H-Erich HE; Schreiber, Stefan S; Müller-Myhsok, Bertram B; Lucae, Susanne S; Jamain, Stéphane S; Leboyer, Marion M; Bellivier, Frank F; Etain, Bruno B; Henry, Chantal C; Kahn, Jean-Pierre JP; Heath, Simon S; , ; Hamshere, Marian M; O'Donovan, Michael C MC; Owen, Michael J MJ; Craddock, Nick N; Schwarz, Markus M; Vedder, Helmut H; Kammerer-Ciernioch, Jutta J; Reif, Andreas A; Sasse, Johanna J; Bauer, Michael M; Hautzinger, Martin M; Wright, Adam A; Mitchell, Philip B PB; Schofield, Peter R PR; Montgomery, Grant W GW; Medland, Sarah E SE; Gordon, Scott D SD; Martin, Nicholas G NG; Gustafsson, Omar O; Andreassen, Ole O; Djurovic, Srdjan S; Sigurdsson, Engilbert E; Steinberg, Stacy S; Stefansson, Hreinn H; Stefansson, Kari K; Kapur-Pojskic, Lejla L; Oruc, Liliana L; Rivas, Fabio F; Mayoral, Fermín F; Chuchalin, Alexander A; Babadjanova, Gulja G; Tiganov, Alexander S AS; Pantelejeva, Galina G; Abramova, Lilia I LI; Grigoroiu-Serbanescu, Maria M; Diaconu, Carmen C CC; Czerski, Piotr M PM; Hauser, Joanna J; Zimmer, Andreas A; Lathrop, Mark M; Schulze, Thomas G TG; Wienker, Thomas F TF; Schumacher, Johannes J; Maier, Wolfgang W; Propping, Peter P; Rietschel, Marcella M; Nöthen, Markus M MM
Publication Date: 2011-03-11

Variant appearance in text: rs1064395
PubMed Link: 21353194
Variant Present in the following documents:
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