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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 14, 2024. (Total: 231451Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Bipolar Disorder and NRXN1[original query]
Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility.
Molecular psychiatry 2011 Mar 16 (3): 286-92.
O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D, , Corvin
High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.
BMC medical genetics 2011 Nov 12 (1): 1.
Stewart LR, Hall AL, Kang SH, Shaw CA, Beaudet AL
Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain.
Schizophrenia research 2014 Oct 159 (1): 107-13.
Ivorra José Luis, Rivero Olga, Costas Javier, Iniesta Raquel, Arrojo Manuel, Ramos-Ríos Ramón, Carracedo Angel, Palomo Tomas, Rodriguez-Jimenez Roberto, Cervilla Jorge, Gutiérrez Blanca, Molina Esther, Arango Celso, Alvarez Mar, Pascual Juan C, Pérez Víctor, Saiz Pilar Alejandra, García-Portilla María Paz, Bobes Julio, González-Pinto Ana, Zorrilla Iñaki, Haro Josep María, Bernardo Miguel, Baca-García Enrique, González José Carlos, Hoenicka Janet, Moltó María Dolores, Sanjuán Jul
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Jun 165B (4): 303-13.
Noor Abdul, Lionel Anath C, Cohen-Woods Sarah, Moghimi Narges, Rucker James, Fennell Alanna, Thiruvahindrapuram Bhooma, Kaufman Liana, Degagne Bryan, Wei John, Parikh Sagar V, Muglia Pierandrea, Forte Julia, Scherer Stephen W, Kennedy James L, Xu Wei, McGuffin Peter, Farmer Anne, Strauss John, Vincent John
Genetics of long-term treatment outcome in bipolar disorder. GWAS Catalog
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24.
Fabbri Chiara, Serretti Alessand
Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.
Journal of psychiatric research 0 66-67 38-44.
Suárez-Rama José Javier, Arrojo Manuel, Sobrino Beatriz, Amigo Jorge, Brenlla Julio, Agra Santiago, Paz Eduardo, Brión María, Carracedo Ángel, Páramo Mario, Costas Javi
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