Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Abnormalities and TCF4[original query] |
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TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders. Translational psychiatry 2012 Feb 2 . Wirgenes KV, Sønderby IE, Haukvik UK, Mattingsdal M, Tesli M, Athanasiu L, Sundet K, Røssberg JI, Dale AM, Brown AA, Agartz I, Melle I, Djurovic S, Andreassen OA |
Neurophysiologic effect of GWAS derived schizophrenia and bipolar risk variants. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Jan 165B (1): 9-18. Hall Mei-Hua, Levy Deborah L, Salisbury Dean F, Haddad Steve, Gallagher Patience, Lohan Mary, Cohen Bruce, Ongür Dost, Smoller Jordan |
Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis. European journal of human genetics : EJHG 2018 Apr . Mary Laura, Piton Amélie, Schaefer Elise, Mattioli Francesca, Nourisson Elsa, Feger Claire, Redin Claire, Barth Magali, El Chehadeh Salima, Colin Estelle, Coubes Christine, Faivre Laurence, Flori Elisabeth, Geneviève David, Capri Yline, Perrin Laurence, Fabre-Teste Jennifer, Timbolschi Dana, Verloes Alain, Olaso Robert, Boland Anne, Deleuze Jean-François, Mandel Jean-Louis, Gerard Bénédicte, Giurgea Iri |
[Association study of genetic markers of schizophrenia and its cognitive endophenotypes]. Genetika 2017 Jan 53 (1): 100-8. Bocharova A V, Stepanov V A, Marusin A V, Kharkov V N, Vagaitseva K V, Fedorenko O Yu, Bokhan N A, Semke A V, Ivanova S |
Genetic variants and cognitive functions in patients with brain tumors. Neuro-oncology 2019 May . Correa Denise D, Satagopan Jaya, Martin Axel, Braun Erica, Kryza-Lacombe Maria, Cheung Kenneth, Sharma Ajay, Dimitriadoy Sofia, O'Connell Kelli, Leong Siok, Karimi Sasan, Lyo John, DeAngelis Lisa M, Orlow Ire |
Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies. Journal of human genetics 2021 5 66 (11): 1061-1068. Miyamoto Sachiko, Kato Mitsuhiro, Hiraide Takuya, Shiohama Tadashi, Goto Tomohide, Hojo Akira, Ebata Akio, Suzuki Manabu, Kobayashi Kozue, Chong Pin Fee, Kira Ryutaro, Matsushita Hiroko Baber, Ikeda Hiroko, Hoshino Kyoko, Matsufuji Mayumi, Moriyama Nobuko, Furuyama Masayuki, Yamamoto Tatsuya, Nakashima Mitsuko, Saitsu Hiroto |
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- Page last updated:Apr 16, 2024
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