Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: CNTN6[original query] |
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A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.
Molecular psychiatry 2011 Sep 16 (9): 949-59. Wang K, Zhang H, Bloss C S, Duvvuri V, Kaye W, Schork N J, Berrettini W, Hakonarson H, |
Genome-wide association study in bipolar patients stratified by co-morbidity.
PloS one 2011 6 (12): e28477. Kerner Berit, Lambert Christophe G, Muthén Bengt |
Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis. International journal of cancer. Journal international du cancer 2015 Mar 136 (6): E578-89. Horpaopan Sukanya, Spier Isabel, Zink Alexander M, Altmüller Janine, Holzapfel Stefanie, Laner Andreas, Vogt Stefanie, Uhlhaas Siegfried, Heilmann Stefanie, Stienen Dietlinde, Pasternack Sandra M, Keppler Kathleen, Adam Ronja, Kayser Katrin, Moebus Susanne, Draaken Markus, Degenhardt Franziska, Engels Hartmut, Hofmann Andrea, Nöthen Markus M, Steinke Verena, Perez-Bouza Alberto, Herms Stefan, Holinski-Feder Elke, Fröhlich Holger, Thiele Holger, Hoffmann Per, Aretz Stef |
GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.
Genes and immunity 2014 Sep 15 (6): 347-54. Armstrong D L, Zidovetzki R, Alarcón-Riquelme M E, Tsao B P, Criswell L A, Kimberly R P, Harley J B, Sivils K L, Vyse T J, Gaffney P M, Langefeld C D, Jacob C |
A candidate gene association study further corroborates involvement of contactin genes in autism. Molecular syndromology 2014 Aug 5 (5): 229-35. Poot Mart |
CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders. Journal of neurodevelopmental disorders 2015 7 (1): 26. Hu Jie, Liao Jun, Sathanoori Malini, Kochmar Sally, Sebastian Jessica, Yatsenko Svetlana A, Surti Urvas |
[Estimation of association of CNTN6 copy number variation with idiopathic intellectual disability]. Genetika 2016 Sep 52 (9): 1109-12. Lopatkina M E, Kashevarova A A, Lebedev I |
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders. Molecular psychiatry 2016 May . Mercati O, Huguet G, Danckaert A, André-Leroux G, Maruani A, Bellinzoni M, Rolland T, Gouder L, Mathieu A, Buratti J, Amsellem F, Benabou M, Van-Gils J, Beggiato A, Konyukh M, Bourgeois J-P, Gazzellone M J, Yuen R K C, Walker S, Delépine M, Boland A, Régnault B, Francois M, Van Den Abbeele T, Mosca-Boidron A L, Faivre L, Shimoda Y, Watanabe K, Bonneau D, Rastam M, Leboyer M, Scherer S W, Gillberg C, Delorme R, Cloëz-Tayarani I, Bourgeron |
A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.
Clinical genetics 2016 Dec 90 (6): 518-525. Wakil S M, Ram R, Muiya N P, Andres E, Mazhar N, Hagos S, Alshahid M, Meyer B F, Morahan G, Dzimiri |
Association of host genome with intestinal microbial composition in a large healthy cohort. Nature genetics 2016 Oct . Turpin Williams, Espin-Garcia Osvaldo, Xu Wei, Silverberg Mark S, Kevans David, Smith Michelle I, Guttman David S, Griffiths Anne, Panaccione Remo, Otley Anthony, Xu Lizhen, Shestopaloff Konstantin, Moreno-Hagelsieb Gabriel, , Paterson Andrew D, Croitoru Kenne |
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron 2017 Jun 94 (6): 1101-1111.e7. Huang Alden Y, Yu Dongmei, Davis Lea K, Sul Jae Hoon, Tsetsos Fotis, Ramensky Vasily, Zelaya Ivette, Ramos Eliana Marisa, Osiecki Lisa, Chen Jason A, McGrath Lauren M, Illmann Cornelia, Sandor Paul, Barr Cathy L, Grados Marco, Singer Harvey S, Nöthen Markus M, Hebebrand Johannes, King Robert A, Dion Yves, Rouleau Guy, Budman Cathy L, Depienne Christel, Worbe Yulia, Hartmann Andreas, Müller-Vahl Kirsten R, Stuhrmann Manfred, Aschauer Harald, Stamenkovic Mara, Schloegelhofer Monika, Konstantinidis Anastasios, Lyon Gholson J, McMahon William M, Barta Csaba, Tarnok Zsanett, Nagy Peter, Batterson James R, Rizzo Renata, Cath Danielle C, Wolanczyk Tomasz, Berlin Cheston, Malaty Irene A, Okun Michael S, Woods Douglas W, Rees Elliott, Pato Carlos N, Pato Michele T, Knowles James A, Posthuma Danielle, Pauls David L, Cox Nancy J, Neale Benjamin M, Freimer Nelson B, Paschou Peristera, Mathews Carol A, Scharf Jeremiah M, Coppola Giovanni, , |
CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. European journal of medical genetics 2019 Mar . Repnikova Elena A, Lyalin Dmitry A, McDonald Kimberly, Astbury Caroline, Hansen-Kiss Emily, Cooley Linda D, Pfau Ruthann, Herman Gail E, Pyatt Robert E, Hickey Scott |
Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis.
Ophthalmology 2020 May . Meguro Akira, Yamane Takahiro, Takeuchi Masaki, Miyake Masahiro, Fan Qiao, Zhao Wanting, Wang I-Jong, Mizuki Yuki, Yamada Norihiro, Nomura Naoko, Tsujikawa Akitaka, Matsuda Fumihiko, Hosoda Yoshikatsu, Saw Seang-Mei, Cheng Ching-Yu, Tsai Tzu-Hsun, Yoshida Masao, Iijima Yasuhito, Teshigawara Takeshi, Okada Eiichi, Ota Masao, Inoko Hidetoshi, Mizuki Nobuhi |
Implications of venous thromboembolism GWAS reported genetic makeup in the clinical outcome of ovarian cancer patients. The pharmacogenomics journal 2020 Nov . Tavares Valéria, Pinto Ricardo, Assis Joana, Coelho Sara, Brandão Mariana, Alves Sara, Pereira Deolinda, Medeiros R |
Genome-wide copy number variation analysis of hepatitis B infection in a Japanese population. Human genome variation 2021 Jun 8 (1): 22. Kikuchi Masataka, Kobayashi Kaori, Nishida Nao, Sawai Hiromi, Sugiyama Masaya, Mizokami Masashi, Tokunaga Katsushi, Nakaya Akihi |
Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes. Frontiers in genetics 2021 4 12 622886. Pol-Fuster Josep, Cañellas Francesca, Ruiz-Guerra Laura, Medina-Dols Aina, Bisbal-Carrió Bàrbara, Asensio Víctor, Ortega-Vila Bernat, Marzese Diego, Vidal Carme, Santos Carmen, Lladó Jerònia, Olmos Gabriel, Heine-Suñer Damià, Strauch Konstantin, Flaquer Antònia, Vives-Bauzà Cristòf |
Interactions between genes involved in physiological dysregulation and axon guidance: role in Alzheimer's disease. Frontiers in genetics 2023 9 14 1236509. Konstantin G Arbeev, Svetlana Ukraintseva, Olivia Bagley, Hongzhe Duan, Deqing Wu, Igor Akushevich, Eric Stallard, Alexander Kulminski, Kaare Christensen, Mary F Feitosa, Jeffrey R O'Connell, Daniel Parker, Heather Whitson, Anatoliy I Yash |
Evaluation of myopia-associated genes in a Han Chinese population with high myopia. Ophthalmic genetics 2023 5 1-5. Zhenzhen Liu, Guangqi An, Yadan Huo, Youmei Xu, Pengyi Zhou, Kunpeng Xie, Haiyan Zhu, Bo Jin, Liping Du, Xuemin J |
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- Page last updated:Apr 22, 2024
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