Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: DLG1[original query] |
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Microdeletions of 3q29 confer high risk for schizophrenia. American journal of human genetics 2010 Aug 87 (2): 229-36. Mulle Jennifer Gladys, Dodd Anne F, McGrath John A, Wolyniec Paula S, Mitchell Adele A, Shetty Amol C, Sobreira Nara L, Valle David, Rudd M Katharine, Satten Glen, Cutler David J, Pulver Ann E, Warren Stephen |
Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Dec 156B (7): 844-9. Carroll L S, Williams H J, Walters J, Kirov G, O'Donovan M C, Owen M |
Peripheral blood gene expression as a novel genomic biomarker in complicated sarcoidosis. PloS one 2012 7 (9): e44818. Zhou Tong, Zhang Wei, Sweiss Nadera J, Chen Edward S, Moller David R, Knox Kenneth S, Ma Shwu-Fan, Wade Michael S, Noth Imre, Machado Roberto F, Garcia Joe G |
Population-specific haplotype association of the postsynaptic density gene DLG4 with schizophrenia, in family-based association studies. PloS one 2013 8 (7): e70302. Balan Shabeesh, Yamada Kazuo, Hattori Eiji, Iwayama Yoshimi, Toyota Tomoko, Ohnishi Tetsuo, Maekawa Motoko, Toyoshima Manabu, Iwata Yasuhide, Suzuki Katsuaki, Kikuchi Mitsuru, Yoshikawa Tak |
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 |
Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney. Kidney international 2015 Sep . Westland Rik, Verbitsky Miguel, Vukojevic Katarina, Perry Brittany J, Fasel David A, Zwijnenburg Petra J G, Bökenkamp Arend, Gille Johan J P, Saraga-Babic Mirna, Ghiggeri Gian Marco, D'Agati Vivette D, Schreuder Michiel F, Gharavi Ali G, van Wijk Joanna A E, Sanna-Cherchi Simo |
Reduced cortical expression of a newly identified splicing variant of the DLG1 gene in patients with early-onset schizophrenia. Translational psychiatry 2015 5 e654. Uezato A, Yamamoto N, Iwayama Y, Hiraoka S, Hiraaki E, Umino A, Haramo E, Umino M, Yoshikawa T, Nishikawa |
Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders. Scientific reports 2016 Jun 6 27491. Xing Jingrui, Kimura Hiroki, Wang Chenyao, Ishizuka Kanako, Kushima Itaru, Arioka Yuko, Yoshimi Akira, Nakamura Yukako, Shiino Tomoko, Oya-Ito Tomoko, Takasaki Yuto, Uno Yota, Okada Takashi, Iidaka Tetsuya, Aleksic Branko, Mori Daisuke, Ozaki Nor |
Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate. Clinical genetics 2017 Sep . Mostowska A, Gaczkowska A, ?ukowski K, Ludwig K U, Hozyasz K K, Wójcicki P, Mangold E, Böhmer A C, Heilmann-Heimbach S, Knapp M, Zadurska M, Biedziak B, Budner M, Lasota A, Daktera-Micker A, Jagodzi?ski P |
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS. Scientific reports 2017 8 7 (1): 8899. Taskesen E, Mishra A, van der Sluis S, Ferrari R, , Veldink J H, van Es M A, Smit A B, Posthuma D, Pijnenburg |
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathies. PloS one 2017 7 12 (7): e0181842. Forleo Cinzia, D'Erchia Anna Maria, Sorrentino Sandro, Manzari Caterina, Chiara Matteo, Iacoviello Massimo, Guaricci Andrea Igoren, De Santis Delia, Musci Rita Leonarda, La Spada Antonino, Marangelli Vito, Pesole Graziano, Favale Stefa |
Genetic and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Oct . Uezato Akihito, Yamamoto Naoki, Jitoku Daisuke, Haramo Emiko, Hiraaki Eri, Iwayama Yoshimi, Toyota Tomoko, Umino Masakazu, Umino Asami, Iwata Yasuhide, Suzuki Katsuaki, Kikuchi Mitsuru, Hashimoto Tasuku, Kanahara Nobuhisa, Kurumaji Akeo, Yoshikawa Takeo, Nishikawa To |
Detection of Molecular Alterations in Taiwanese Patients with Medullary Thyroid Cancer Using Whole-Exome Sequencing. Endocrine pathology 2018 Aug . Chang Ya-Sian, Chang Chun-Chi, Huang Hsi-Yuan, Lin Chien-Yu, Yeh Kun-Tu, Chang Jan-Gow |
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS genetics 2021 7 17 (7): e1009584. Ray Debashree, Venkataraghavan Sowmya, Zhang Wanying, Leslie Elizabeth J, Hetmanski Jacqueline B, Weinberg Seth M, Murray Jeffrey C, Marazita Mary L, Ruczinski Ingo, Taub Margaret A, Beaty Terri |
Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people.
Endokrynologia Polska 2022 8 . Lin Leweihua, Quan Huibiao, Fang Tuanyu, Lin Lu, Ou Qianying, Zhang Huachuan, Chen Kaining, Zhou Zhigua |
Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis. Genes 2022 5 13 (5): . Justice Cristina M, Musolf Anthony M, Cuellar Araceli, Lattanzi Wanda, Simeonov Emil, Kaneva Radka, Paschall Justin, Cunningham Michael, Wilkie Andrew O M, Wilson Alexander F, Romitti Paul A, Boyadjiev Simeon |
Genome-Wide Association Study for eGFR in a Taiwanese Population.
Clinical journal of the American Society of Nephrology : CJASN 2022 Oct . Chen Ying-Chun, Wong Henry Sung-Ching, Wu Mei-Yi, Chou Wan-Hsuan, Kao Chih-Chin, Chao Ching-Hsuan, Chang Wei-Chiao, Wu Mai-S |
Identification of Novel Risk Variants of Non-Syndromic Cleft Palate by Targeted Gene Panel Sequencing. Journal of clinical medicine 2023 3 12 (5): . D?browska Justyna, Biedziak Barbara, Bogdanowicz Agnieszka, Mostowska Adrian |
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- Page last updated:Apr 22, 2024
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