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Chris A. Walsh

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
Genes involved in the development and function of the cerebral cortex
Website:
http://www.walshlab.org/
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"Chris Walsh"
Mean distance: 12.78 (cluster 46)
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Parents

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Ray W. Guillery grad student Chicago
Constance L. Cepko post-doc Harvard

Children

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Timothy J. Cherry research assistant 2001-2002 Harvard Medical School
Kutay Deniz Atabay research assistant 2011-2013 Harvard Medical School - Boston Children's Hospital
Alissa D'Gama grad student
Teresa Hongmi Chae grad student 2004 Harvard
Sophie Christine Currier grad student 2004 Harvard
Thomas Andrew Deuel grad student 2004 Harvard
Jun Shen grad student 2005 Harvard
Mauro Dylan Zappaterra grad student 2008 Harvard
Jason Bennett Neal grad student 2010 Harvard
Vijay S. Ganesh grad student 2012 Harvard
Gilad David Evrony grad student 2013 Harvard
Michael E. Coulter grad student 2012-2018
Anjen Chenn post-doc Harvard Medical School
Noelle Dwyer post-doc Beth Israel Deaconess Medical Center / Harvard Medical School
Joseph G. Gleeson post-doc Harvard Medical School
Anthony D. Hill post-doc Harvard Medical School
Sofia B. Lizarraga post-doc Harvard Medical School
Christine Marshall-Walker post-doc Harvard
Edwin S. Monuki post-doc Harvard Medical School
Eric Morrow post-doc Harvard Medical School
Richard S. Smith post-doc Harvard Medical School
Matthew Bonser Johnson post-doc 2010- Harvard
August Yue Huang post-doc 2017- (GenetiTree)
Joseph C. Corbo post-doc 1999-2002 Beth Israel Deaconess Medical Center, Harvard Medical School
Marta Nieto post-doc 2000-2004
Russell J. Ferland post-doc 2000-2005 Beth Israel Deaconess Medical Center / Harvard Medical School
Tao Sun post-doc 2002-2005 Harvard
Seung-Yun Yoo post-doc 2004-2007 Harvard Medical School
Judy Shih-Hwa Liu post-doc 2004-2009 Harvard
Maria Kristiina Lehtinen post-doc 2007-2011 Boston Children's Hospital
Maria Chiara Manzini post-doc 2006-2013 Harvard Medical School, Beth Israel Deaconess Medical Center
Maria Chahrour post-doc 2009-2014 Harvard Medical School
Byoung-Il Bae post-doc 2006-2015 Children's Hospital Boston
Mollie Woodworth post-doc 2013-2016 Children's Hospital, Boston, Harvard University
Xiaochang Zhang post-doc 2011-2017 Harvard Medical School
Michael A Lodato post-doc 2013-2019 Children's Hospital Boston
Peter T. Lin research scientist 1998-1999 Harvard Institutes of Medicine

Collaborators

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David R. Beier collaborator Harvard Medical School
Anthony LaMantia collaborator Harvard
BETA: Related publications

Publications

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Shao DD, Achkar CM, Lai A, et al. (2020) Polymicrogyria is associated with pathogenic variants in PTEN. Annals of Neurology
Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, et al. (2020) Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045
Kim J, Zhao B, Huang AY, et al. (2020) APP gene copy number changes reflect exogenous contamination. Nature. 584: E20-E28
Lim ET, Uddin M, De Rubeis S, et al. (2020) Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience
Huang AY, Li P, Rodin RE, et al. (2020) Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain. Proceedings of the National Academy of Sciences of the United States of America
Khan A, Alaamery M, Massadeh S, et al. (2020) PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly. Clinical Genetics
Coulter ME, Musaev D, DeGennaro EM, et al. (2020) Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Smith RS, Walsh CA. (2020) Ion Channel Functions in Early Brain Development. Trends in Neurosciences
Dou Y, Kwon M, Rodin RE, et al. (2020) Accurate detection of mosaic variants in sequencing data without matched controls. Nature Biotechnology
Lodato MA, Walsh CA. (2019) Corrigendum: Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms. Human Molecular Genetics
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