Resultados da pesquisa

Genetic mechanisms of parenting Por Viara R. Mileva‐Seitz, Marian J. Bakermans‐Kranenburg, Marinus H. van IJzendoorn

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Genetics in schizophrenia: where are we and what next? Por Arun K. Tiwari, Clement C. Zai, Daniel J. Müller, James L. Kennedy

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Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals Por Suhua Chang, Kechi Fang, Kunlin Zhang, Jing Wang

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Genetics of Anorexia Nervosa Por Jessica H. Baker, Katherine Schaumberg, Melissa A. Munn‐Chernoff

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Pharmacogenomics in psychiatry: the relevance of receptor and transporter polymorphisms Por Gavin P. Reynolds, Olga O McGowan, Caroline Dalton

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A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease Por Vincent Plagnol, Michael A. Nalls, José Brás, D.G. Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Philippe Amouyel, Sampath Arepalli, Roger A. Barker, C. Bellinguez, Yoav Ben‐Shlomo, Henk W. Berendse, Daniela Berg, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, B.R. Bloem, Zoltán Bochdanovits, Marina de Nadai Bonin Gomes, Kathrin Brockmann, Janet Brooks, David J. Burn, Gavin Charlesworth, Honglei Chen, Patrick F. Chinnery, S. A. Chong, Carl E Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, J.F. Dartigues, Panos Deloukas, Günther Deuschl, David T. Dexter, Karin D. van Dijk, Allissa Dillman, F. Durif, Alexandra Dürr, Sarah Edkins, Jonathan Evans, Thomas Foltynie, Colin L. Freeman, Jingping Gao, Michelle Gardner, J. Raphael Gibbs, Alison Goate, Emma Gray, Rita Guerreiro, Ómar Gústafsson, Curtis C. Harris, Garrett Hellenthal, Jacobus J. van Hilten, Albert Hofman, A. R. Hollenbeck, Janice L. Holton, Joshua Shulman, Xia Huang, H Huber, Gavin Hudson, Sarah Hunt, Johanna Huttenlocher, Thomas Illig, Pálmi V. Jónsson, Cordelia Langford, Andrew J. Lees, Peter Lichtner, Patricia Limousin, Grisel Lopez, D. Lorenz, A. McNeill, Catriona Moorby, Matthew Moore, Huw R. Morris, Karen Morrison, Ese Mudanohwo, Sean S. O’Sullivan, John F. Pearson, Richard D. Pearson, Joel S. Perlmutter, Hannes Pétursson, M. Pirinen, Pierre Pollak, Bart Post, Sally Potter, Bernard Ravina, Tamás Révész, Olaf Rieß, Fernando Rivadeneira, Patrizia Rizzu, Mina Ryten, Stephen Sawcer, Peter Heutink, Nicholas Wood

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Candidate gene case‐control association studies: advantages and potential pitfalls Por Ann K. Daly, Christopher P. Day

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Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine Por Rod A. Lea, A. Dohy, Katherine W. Jordan, Sharon Quinlan, P. J. Brimage, Lyn R. Griffiths

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<i>MTHFR</i> and <i>MSX1</i> contribute to the risk of nonsyndromic cleft lip/palate Por Triin Jagomägi, Tiit Nikopensius, Kaarel Krjutškov, Veronika Tammekivi, Triin Viltrop, Mare Saag, Andres Metspalu

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The <i>Rc</i> and <i>Rd</i> genes are involved in proanthocyanidin synthesis in rice pericarp Por Tsutomu FURUKAWA, Masahiko Maekawa, Tomoyuki Oki, Ikuo Suda, Shigeru Iida, Hiroaki Shimada, Itsuro Takamure, Koh‐ichi Kadowaki

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Genome-Wide Transcriptome Directed Pathway Analysis of Maternal Pre-Eclampsia Susceptibility Genes Por Hannah E. J. Yong, Phillip E. Melton, Matthew P. Johnson, Katy A. Freed, Bill Kalionis, Padma Murthi, Shaun P. Brennecke, Rosemary J. Keogh, Eric K. Moses

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<i>NCAM1‐TTC12‐ANKK1‐DRD2</i> gene cluster and the clinical and genetic heterogeneity of adults with ADHD Por Nina Roth Mota, Diego Luiz Rovaris, Djenifer B. Kappel, Felipe Almeida Picon, Eduardo S. Vitola, Carlos Alberto Iglesias Salgado, Rafael G. Karam, Luís Augusto Rohde, Eugênio H. Grevet, Claiton Henrique Dotto Bau

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Febrile infection‐related epilepsy syndrome (FIRES) is not caused by <i>SCN1A, POLG, PCDH19</i> mutations or rare copy number variations Por Silke Appenzeller, Ingo Helbig, Ulrich Stephani, Martin Häusler, Gerhard Kluger, May Bungeroth, Stefanie H. Müller, Gregor Kuhlenbäumer, Andreas van Baalen

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Mutations in human IFT140 cause non-syndromic retinal degeneration Por Mingchu Xu, Lizhu Yang, Feng Wang, Huajin Li, Xia Wang, Weichen Wang, Zhongqi Ge, Keqing Wang, Li Zhao, Hui Li, Yumei Li, Ruifang Sui, Rui Chen

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Non-synonymous mutations mapped to chromosome X associated with andrological and growth traits in beef cattle Por Gregório Miguel Ferreira de Camargo, Laércio R. Porto-Neto, Matt Kelly, Rowan J. Bunch, Sean McWilliam, Humberto Tonhati, Sigrid A. Lehnert, Marina R. S. Fortes, S. S. Moore

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A genome‐wide association study for racing performances in Thoroughbreds clarifies a candidate region near the <i>MSTN</i> gene Por Teruaki Tozaki, Teruki Miyake, Hironaga KAKOI, Hitoshi Gawahara, Shigeo Sugita, T. Hasegawa, Nobushige Ishida, K. Hirota, Yasuko Nakano

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Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families Por Hanan E. Shamseldin, Maha Tulbah, Wesam Kurdi, Maha Nemer, Nada Alsahan, Elham Al Mardawi, Ola Khalifa, Amal Hashem, Ahmed M Kurdi, Zainab Babay, Dalal Bubshait, Niema Ibrahim, Firdous Abdulwahab, Zuhair Rahbeeni, Mais Hashem, Fowzan S. Alkuraya

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Genetic Epidemiology of Chagas Disease Por Sarah Williams‐Blangero, John L. VandeBerg, John Blangero, Rodrigo Corrêa‐Oliveira

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The Prevalence and Management of Diabetic Nephropathy in Asia Por Yasuhiko Tomino, Tomohito Gohda

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G2D: a tool for mining genes associated with disease Por Carolina Perez‐Iratxeta, Matthias Wjst, Peer Bork, Miguel A. Andrade‐Navarro

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