Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Syndrome and NRG1[original query] |
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Association study of NRG1, DTNBP1, RGS4, G72/G30, and PIP5K2A with schizophrenia and symptom severity in a Hungarian sample. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Apr 153B (3): 792-801. Réthelyi János M, Bakker Steven C, Polgár Patrícia, Czobor Pál, Strengman Eric, Pásztor Péter I, Kahn René S, Bitter Istv |
Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects. Birth defects research. Part A, Clinical and molecular teratology 2011 Mar 91 (3): 162-8. McBride Kim L, Zender Gloria A, Fitzgerald-Butt Sara M, Seagraves Nikki J, Fernbach Susan D, Zapata Gladys, Lewin Mark, Towbin Jeffrey A, Belmont John |
Genetic variability testing of neurodevelopmental genes in schizophrenic patients. Journal of molecular neuroscience : MN 2015 May 56 (1): 205-11. Terzi? Tea, Kastelic Matej, Dolžan Vita, Plesni?ar Blanka Kor |
Genetic predictors of antipsychotic response to lurasidone identified in a genome wide association study and by schizophrenia risk genes. Schizophrenia research 2018 02 192 194-204. Li Jiang, Yoshikawa Akane, Brennan Mark D, Ramsey Timothy L, Meltzer Herbert |
Identifying the genetic risk factors for treatment response to lurasidone by genome-wide association study: A meta-analysis of samples from three independent clinical trials.
Schizophrenia research 2018 May . Li Jiang, Loebel Antony, Meltzer Herbert |
Prediction Analysis for Transition to Schizophrenia in Individuals at Clinical High Risk for Psychosis: The Relationship of DAO, DAOA, and NRG1 Variants with Negative Symptoms and Cognitive Deficits. Frontiers in psychiatry 2017 8 292. Jagannath Vinita, Theodoridou Anastasia, Gerstenberg Miriam, Franscini Maurizia, Heekeren Karsten, Correll Christoph U, Rössler Wulf, Grünblatt Edna, Walitza Susan |
Early-Onset Schizophrenia: A Special Phenotype of the Disease Characterized by Increased MTHFR Polymorphisms and Aggravating Symptoms. Neuropsychiatric disease and treatment 2021 8 17 2511-2525. Wan Lin, Wei Ji |
Pharmacogenetic associations of NRG1 polymorphisms with neurocognitive performance and clinical symptom response to risperidone in the untreated schizophrenia. Schizophrenia research 2021 Mar 231 67-69. Yang JianZhong, Kang ChuanYuan, Wu Changjiang, Lin Yuanyuan, Zeng Lei, Yuan Jing, Zhang Yan, Wei YuJun, Xu Li, Zhou Fa |
Correlation of rs35753505 polymorphism in Neuregulin 1 gene with psychopathology and intelligence of people with schizophrenia. Gene 2023 3 147285. Moradkhani Atefeh, Turki Jalil Abduladheem, Mahmood Saleh Marwan, Vanaki Elmira, Daghagh Hossein, Daghighazar Behrouz, Akbarpour Zahra, Ghahramani Almanghadim Hosse |
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