Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kai Wang"'
Autor:
Veronica J. Vieland, Stephen W. Scherer, Alison K. Merikangas, Naisha Shah, Edwin H. Cook, William M. McMahon, Kirsty Wing, Sabata C. Lund, Jacob A. S. Vorstman, Judith Conroy, Sabine M. Klauck, John B. Vincent, Astrid M. Vicente, Carine Mantoulan, Barbara Parrini, Jeremy R. Parr, Herman van Engeland, Jane McGrath, Guiomar Oliveira, Jonathan Green, James S. Sutcliffe, Peter Szatmari, Ann Le Couteur, Katerina Papanikolaou, Joseph Piven, Andrew Pickles, Gillian Baird, Inês Sousa, Gerard D. Schellenberg, Catarina Correia, Bennett L. Leventhal, Helen McConachie, Joseph T. Glessner, Fritz Poustka, Alistair T. Pagnamenta, Marion Leboyer, Nuala Sykes, Elena Maestrini, Penny Farrar, Maïté Tauber, Suzanne Foley, Richard Holt, Lonnie Zwaigenbaum, David J. Posey, John Tsiantis, Alexander Kolevzon, Agatino Battaglia, Maretha de Jonge, Hilary Coon, Gillian Hughes, John R. Gilbert, Patrick Bolton, Louise Gallagher, Jeff Munson, Kathy White, Michael L. Cuccaro, Annemarie Poustka, Daniel H. Geschwind, Richard Delorme, Annette Estes, Christine M. Freitag, Jillian P. Casey, Joana Almeida, Dalila Pinto, Simon Wallace, Sean Brennan, Stephen J. Guter, Stanley F. Nelson, Michael Rutter, Ghazala Mirza, Anthony J. Bailey, Christina Corsello, Kerstin Wittemeyer, Christian R. Marshall, Janine A. Lamb, Catherine Lord, Hakon Hakonarson, Jiannis Ragoussis, Catalina Betancur, Geraldine Dawson, Eftichia Duketis, Sean Ennis, Fiorella Minopoli, Christopher Gillberg, Vera Stoppioni, Bridget A. Fernandez, Frederico Duque, Eric Fombonne, Ellen M. Wijsman, Bernadette Rogé, Vanessa Hus, Susan E. Folstein, Jonathan L. Haines, Denis C. Shields, Tiago R. Magalhaes, Andrew Green, Thomas Bourgeron, Brian L. Yaspan, Ann P. Thompson, Gudrun Nygren, Judith Miller, Susanne Thomson, Roberta Igliozzi, Ana Filipa Sequeira, Kai Wang, Brett S. Abrahams, John I. Nurnberger, Michael Gill, Thomas H. Wassink, Christopher J. McDougle, Marc N. Coutanche, Anthony P. Monaco, Nadia Bolshakova, Cecilia Kim, Raffaella Tancredi, Rita M. Cantor, Phil Cali, Fred R. Volkmar, Tom Berney, Margaret A. Pericak-Vance, Joachim Hallmayer, Joseph D. Buxbaum, Elena Bacchelli, Latha Soorya, Richard Anney, Regina Regan
Publikováno v:
Human Genetics
Human Genetics, Springer Verlag, 2012, 131 (4), pp.565-79. ⟨10.1007/s00439-011-1094-6⟩
Human Genetics, 2012, 131 (4), pp.565-79. ⟨10.1007/s00439-011-1094-6⟩
Human Genetics, Springer Verlag, 2012, 131 (4), pp.565-79. ⟨10.1007/s00439-011-1094-6⟩
Human Genetics, 2012, 131 (4), pp.565-79. ⟨10.1007/s00439-011-1094-6⟩
Autism spectrum disorder (ASD) is a highly heritable disorder of complex and heterogeneous aetiology. It is primarily characterized by altered cognitive ability including impaired language and communication skills and fundamental deficits in social r
Autor:
Li-San Wang, Branimir Jernej, Dubravka Hranilović, Kai Wang, Nicole B. Gidaya, Ingrid E. Lindquist, Maja Bucan, Lindsay Yurcaba, Zorana-Bujas Petkovic, Hakon Hakonarson
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 11, Iss 1, p 134 (2010)
BMC Medical Genetics, Vol 11, Iss 1, p 134 (2010)
Background Genome-wide studies on autism spectrum disorders (ASDs) have mostly focused on large-scale population samples, but examination of rare variations in isolated populations may provide additional insights into the disease pathogenesis. Method
Autor:
Claus L. Andersen, Bodil Øster, Søren Laurberg, Mads Rasmussen, Troels Schepeler, Kasper Thorsen, Carsten Wiuf, Kristian Q Hansen, Philippe Lamy, Kirsti Laurila, Kai Wang, Lars Dyrskjøt, Francisco Mansilla, Torben F. Ørntoft, Jakob Skou Pedersen, Søren Vang, Asger Eller
Publikováno v:
Thorsen, K, Schepeler, T, Øster, B, Rasmussen, M H, Vang, S, Wang, K, Hansen, K Q, Lamy, P, Pedersen, J S, Eller, A Ø, Mansilla, F, Laurila, K, Wiuf, C H, Laurberg, S, Dyrskjot, L, Orntoft, T F & Andersen, C L 2011, ' Tumor-specific usage of alternative transcription start sites in colorectal cancer identified by genome-wide exon array analysis ', B M C Genomics, vol. 12, no. 1, pp. 505 . https://doi.org/10.1186/1471-2164-12-505
BMC Genomics, Vol 12, Iss 1, p 505 (2011)
BMC Genomics
BMC Genomics; Vol 12
BMC Genomics, Vol 12, Iss 1, p 505 (2011)
BMC Genomics
BMC Genomics; Vol 12
Background Approximately half of all human genes use alternative transcription start sites (TSSs) to control mRNA levels and broaden the transcriptional output in healthy tissues. Aberrant expression patterns promoting carcinogenesis, however, may ar
Autor:
Tao Jiang, Kai Wang, Lifeng Tian, Gholson J. Lyon, Jason O'Rawe, Jingchu Hu, Wei Min Wang, W. Evan Johnson, Hakon Hakonarson, Zhi Wei, Yiyang Wu, Guangqing Sun, Paul Bodily
Publikováno v:
Genome medicine, vol 5, iss 3
Genome Medicine
Genome Medicine
Background: To facilitate the clinical implementation of genomic medicine by next-generation sequencing, it will be critically important to obtain accurate and consistent variant calls on personal genomes. Multiple software tools for variant calling
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 4, Iss 1, p 158 (2011)
BMC Research Notes, Vol 4, Iss 1, p 158 (2011)
Background Gene-gene interaction in genetic association studies is computationally intensive when a large number of SNPs are involved. Most of the latest Central Processing Units (CPUs) have multiple cores, whereas Graphics Processing Units (GPUs) al
Autor:
Hakon Hakonarson, Elina Toskala, Kelly A. Thomas, Ryan Golhar, Jonathan P. Bradfield, Kai Wang, Gholson J. Lyon, Cecilia Kim, Yunfei Guo, Frederick G. Otieno, Christopher J. Cardinale, Cuiping Hou
Publikováno v:
Genome Medicine
Background: Whole-exome sequencing has identified the causes of several Mendelian diseases by analyzing multiple unrelated cases, but it is more challenging to resolve the cause of extremely rare and suspected Mendelian diseases from individual famil