Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: CDH9[original query] |
---|
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature 2009 May 459 (7246): 528-33. Wang Kai, Zhang Haitao, Ma Deqiong, Bucan Maja, Glessner Joseph T, Abrahams Brett S, Salyakina Daria, Imielinski Marcin, Bradfield Jonathan P, Sleiman Patrick M A, Kim Cecilia E, Hou Cuiping, Frackelton Edward, Chiavacci Rosetta, Takahashi Nagahide, Sakurai Takeshi, Rappaport Eric, Lajonchere Clara M, Munson Jeffrey, Estes Annette, Korvatska Olena, Piven Joseph, Sonnenblick Lisa I, Alvarez Retuerto Ana I, Herman Edward I, Dong Hongmei, Hutman Ted, Sigman Marian, Ozonoff Sally, Klin Ami, Owley Thomas, Sweeney John A, Brune Camille W, Cantor Rita M, Bernier Raphael, Gilbert John R, Cuccaro Michael L, McMahon William M, Miller Judith, State Matthew W, Wassink Thomas H, Coon Hilary, Levy Susan E, Schultz Robert T, Nurnberger John I, Haines Jonathan L, Sutcliffe James S, Cook Edwin H, Minshew Nancy J, Buxbaum Joseph D, Dawson Geraldine, Grant Struan F A, Geschwind Daniel H, Pericak-Vance Margaret A, Schellenberg Gerard D, Hakonarson Hak |
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, |
Analysis of four genes involved in the neurodevelopment shows association of rs4307059 polymorphism in the cadherin 9/10 region with completed suicide. Neuropsychobiology 2012 Jul 66 (2): 2. Chojnicka I, Strawa K, Fudalej S, Fudalej M, Pawlak A, Kostrzewa G, Wojnar M, Krajewski P, P?oski R |
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families. Psychiatric genetics 2012 Aug 22 (4): 177-81. Prandini Paola, Pasquali Alessandra, Malerba Giovanni, Marostica Andrea, Zusi Chiara, Xumerle Luciano, Muglia Pierandrea, Da Ros Lucio, Ratti Emiliangelo, Trabetti Elisabetta, Pignatti Pier Franco, |
Common genetic background in anorexia nervosa and obsessive compulsive disorder: preliminary results from an association study. Journal of psychiatric research 2013 Jun 47 (6): 747-54. Mas Sergi, Plana Maria Teresa, Castro-Fornieles Josefina, Gassó Patricia, Lafuente Amalia, Moreno Elena, Martinez Esteban, Milà Montserrat, Lazaro Lui |
Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10. Molecular autism 2014 5 (1): 55. Jonsson Lina, Zettergren Anna, Pettersson Erik, Hovey Daniel, Anckarsäter Henrik, Westberg Lars, Lichtenstein Paul, Lundström Sebastian, Melke Jon |
Association between genetic variants related to glutamatergic, dopaminergic and neurodevelopment pathways and white matter microstructure in child and adolescent patients with obsessive-compulsive disorder. Journal of affective disorders 2015 Nov 186 284-92. Gassó Patricia, Ortiz Ana E, Mas Sergi, Morer Astrid, Calvo Anna, Bargalló Nuria, Lafuente Amalia, Lázaro Lui |
Polygenic associations of neurodevelopmental genes in suicide attempt. Molecular psychiatry 2015 Dec . Sokolowski M, Wasserman J, Wasserman |
A novel relationship for schizophrenia, bipolar and major depressive disorder Part 5: a hint from chromosome 5 high density association screen. American journal of translational research 2017 9 (5): 2473-2491. Chen Xing, Long Feng, Cai Bin, Chen Xiaohong, Chen Ga |
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population. Genes 2020 Oct 11 (10): . Khalid Madiha, Raza Hashim, M Driessen Terri, J Lee Paul, Tejwani Leon, Sami Abdul, Nawaz Muhammad, Mehmood Baig Shahid, Lim Janghoo, Kaukab Raja Ghaza |
Mutations of METTL3 predict response to neoadjuvant chemotherapy in muscle-invasive bladder cancer. Journal of clinical and translational research 2021 7 7 (3): 386-413. Yang Zhao, Shen Zongyi, Jin Di, Zhang Nan, Wang Yue, Lei Wanjun, Zhang Zhiming, Chen Haige, Naz Faiza, Xu Lida, Wang Lei, Wang Shihui, Su Xin, Yu Changyuan, Li Cho |
Investigation of Association of Rare, Functional Genetic Variants With Heavy Drinking and Problem Drinking in Exome Sequenced UK Biobank Participants. Alcohol and alcoholism (Oxford, Oxfordshire) 2021 Apr . Curtis Dav |
Pleiotropy analysis between lobar intracerebral hemorrhage and CSF ?-amyloid highlights new and established associations. International journal of stroke : official journal of the International Stroke Society 2023 1 17474930231155816. Marini Sandro, Chung Jaeyoon, Han Xudong, Sun Xinyu, Parodi Livia, Farrer Lindsay A, Rosand Jonathan, Romero Jose Rafael, Anderson Christopher |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: