نتائج البحث - Ravinesh A. Kumar
- يعرض 1 - 6 نتائج من 6
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TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins حسب Ravinesh A. Kumar, Daniela T. Pilz, Timothy D. Babatz, Thomas D. Cushion, Kirsten Harvey, Maya Topf, Laura Yates, S. Robb, Gökhan Uyanık, G.M.S. Mancini, Mark I. Rees, Victoria L. Harvey, William B. Dobyns
منشور في 2010Artigo -
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Association and Mutation Analyses of 16p11.2 Autism Candidate Genes حسب Ravinesh A. Kumar, Christian R. Marshall, Judith A. Badner, Timothy D. Babatz, Zohar Mukamel, Kimberly A. Aldinger, Jyotsna Sudi, Camille W. Brune, Gerald Goh, Samer Karamohamed, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, William B. Dobyns, Stephen W. Scherer, Susan L. Christian
منشور في 2009Artigo -
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Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder حسب Susan L. Christian, Camille W. Brune, Jyotsna Sudi, Ravinesh A. Kumar, Shaung Liu, Samer Karamohamed, Judith A. Badner, Seiichi Matsui, Jeffrey M. Conroy, Devin McQuaid, James Gergel, Eli Hatchwell, T. Conrad Gilliam, Elliot S. Gershon, Norma J. Nowak, William B. Dobyns, Edwin H. Cook
منشور في 2008Artigo -
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Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function حسب Alex R. Paciorkowski, Liu Lin Thio, Jill A. Rosenfeld, Marzena Gajęcka, Christina A. Gurnett, Shashikant Kulkarni, Wendy K. Chung, Eric D. Marsh, Mattia Gentile, James D. Reggin, James W. Wheless, Sandhya Balasubramanian, Ravinesh A. Kumar, Susan L. Christian, Carla Marini, Renzo Guerrini, Natalia Maltsev, Lisa G. Shaffer, William B. Dobyns
منشور في 2011Artigo -
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Microduplications of 16p11.2 are associated with schizophrenia حسب Shane McCarthy, Vladimir Makarov, George Kirov, Anjené Addington, Jon McClellan, Seungtai Yoon, Diana O. Perkins, Diane E. Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A. Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H. Zackai, Paige Kaplan, Jaya Ganesh, Ian D. Krantz, Nancy B. Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B. Lakshmi, Anthony Leotta, Jude Kendall, Yoon-ha Lee, Vladimir Vacic, Sydney Gary, Lilia M. Iakoucheva, Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimäki, Kaija Puura, Chad R. Haldeman‐Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nöthen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael O’Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith L. Rapoport, Deborah L. Levy, Mary‐Claire King, Jonathan Sebat
منشور في 2009Revisão
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Copy-number variation
Genome
Autism
Medicine
Phenotype
Psychiatry
Gene duplication
Neuroscience
Autism spectrum disorder
Candidate gene
Epilepsy
Neurodevelopmental disorder
Bacterial artificial chromosome
Central nervous system
Cerebellar hypoplasia (non-human)
Cerebellum
Chromosome
Cohort
Comparative genomic hybridization
Developmental disorder
Fluorescence in situ hybridization
Forebrain
Gene expression
Genetic association
Genotype
Heritability of autism
Hypotonia