Christopher A. Walsh

发表

Molecular contributions to cerebral cortical specification - Discussion

Jack Price, Tobias Bonhoeffer, Leah Krubitzer, 1995 .

The handshake hypothesis - General discussion III

Zoltán Molnár, Pasko Rakic, Jack Price, 1995 .

Cranking It Up a Notch

Christopher A. Walsh, Anjen Chenn, C. Walsh, 1999, Science.

Peter Huttenlocher (1931–2013)

Christopher A. Walsh, C. Walsh, 2013, Nature.

Rare variant association test in family-based sequencing studies

Seunggeun Lee, Xuefeng Wang, Tianxi Cai, 2016, Briefings Bioinform..

Aging and neurodegeneration are associated with increased mutations in single human neurons

Peter J. Park, Minseok Kwon, Thomas W. Chittenden, 2017 .

Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior

Soher Balkhy, Christopher A. Walsh, Byoung-Il Bae, 2016, Cell.

Comprehensive identification of somatic nucleotide variants in human brain tissue

Peter J. Park, Jonathan Pevsner, Eduardo Soriano, 2020, bioRxiv.

A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

Eric M. Morrow, Shrikant M. Mane, Edwin H. Cook, 2015, Biological Psychiatry.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Kathryn Roeder, Murim Choi, Eric M. Morrow, 2011, Neuron.

Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning

P. Ellen Grant, Hideyuki Okano, Kiho Im, 2014, Science.

Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

Eric M. Morrow, Annapurna Poduri, Fuki M. Hisama, 2013, Neuron.

Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1α/CXC chemokine receptor 4 pathway

Samia J. Khoury, Yang D. Teng, Richard L. Sidman, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism

Timothy W. Yu, Christopher A. Walsh, Michael E. Coulter, 2012, PLoS genetics.

Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex

Peter V. Kharchenko, Phillip A. Sharp, Nobuaki Yoshida, 2016, Cell.

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

William B. Dobyns, A. James Barkovich, Bernard S. Chang, 2004, Science.

Genes that regulate neuronal migration in the cerebral cortex

Christopher A. Walsh, C. Walsh, K. Allen, 1999, Epilepsy Research.

Targeted Disruption of Tgif, the Mouse Ortholog of a Human Holoprosencephaly Gene, Does Not Result in Holoprosencephaly in Mice

Christopher A. Walsh, C. Walsh, Jun Shen, 2005, Molecular and Cellular Biology.

Accurate detection of mosaic variants in sequencing data without matched controls

Peter J. Park, Minseok Kwon, Isidro Cortés-Ciriano, 2019, Nature Biotechnology.

Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

Annapurna Poduri, Christopher A. Walsh, C. Walsh, 2014, Cell reports.

Innovations in Primate Interneuron Repertoire

David Kulp, Bernardo Rudy, Qiangge Zhang, 2019, bioRxiv.

Aging and neurodegeneration are associated with increased mutations in single human neurons

Peter J. Park, Minseok Kwon, Thomas W. Chittenden, 2017, Science.

The Apical Complex Couples Cell Fate and Cell Survival to Cerebral Cortical Development

Jarema Malicki, Maria K. Lehtinen, Seonhee Kim, 2010, Neuron.

Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry

Eric M. Morrow, Soher Balkhy, Christopher A. Walsh, 2008, Science.

Mechanisms of cerebral cortical patterning in mice and humans

Christopher A. Walsh, Edwin S. Monuki, C. Walsh, 2001, Nature Neuroscience.

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes

Dian Donnai, Graeme C.M. Black, Nicolas Chassaing, 2007, Nature Genetics.

Molecular genetics of human microcephaly

Christopher A. Walsh, C. Walsh, G. Mochida, 2001, Current opinion in neurology.

The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles

David Haussler, Edward Yang, Eric T. Wong, 2018, Cell reports.

Somatic mutation in single human neurons tracks developmental and transcriptional history

Peter J. Park, Eunjung Lee, Thomas W. Chittenden, 2015, Science.

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact.

Christopher A. Walsh, C. Walsh, S. Shapiro, 2002, Human molecular genetics.

Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell

Kevin A. Pelphrey, Ellen M. Wijsman, Zachary Warren, 2012 .

A mapping label required for normal scale of body representation in the cortex

Ron D. Frostig, John G. Flanagan, Jonas Frisén, 2000, Nature Neuroscience.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Autism and Brain Development

Eric M. Morrow, John L.R. Rubenstein, Christopher A. Walsh, 2008, Cell.

Impact of PNKP mutations associated with microcephaly, seizures and developmental delay on enzyme activity and DNA strand break repair

Keith W. Caldecott, Christopher A. Walsh, C. Walsh, 2012, Nucleic acids research.

Identification of Neural Outgrowth Genes using Genome-Wide RNAi

Pengyu Hong, Norbert Perrimon, Christopher A. Walsh, 2008, PLoS genetics.

ASPM is a major determinant of cerebral cortical size

Alexander F. Markham, Emma Roberts, Christopher A. Walsh, 2002, Nature Genetics.

Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex

Renzo Guerrini, Hitoshi Takahashi, Christopher A. Walsh, 2002, Acta Neuropathologica.

Association between microdeletion and microduplication at 16p11.2 and autism

Joshua M. Korn, Yiping Shen, Manuel A. R. Ferreira, 2008 .

Detecting natural selection by empirical comparison to random regions of the genome

David Reich, Fuli Yu, Alon Keinan, 2009, Human molecular genetics.