Christopher A Walsh

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William B. DobynsProfessor of PediatricsEmail verificata su umn.edu
Annapurna PoduriNeurology, Boston Children's Hospital, Harvard Medical SchoolEmail verificata su childrens.harvard.edu
Peter J ParkHarvard Medical SchoolEmail verificata su harvard.edu
Joseph G. GleesonUniversity of California, San DiegoEmail verificata su ucsd.edu
Ryan DoanBoston Children's HospitalEmail verificata su childrens.harvard.edu
Volney Sheenbeth israelEmail verificata su bidmc.harvard.edu
Timothy W. YuHarvard Medical School and Boston Children's HospitalEmail verificata su childrens.harvard.edu
Constance L CepkoProfessor of Genetics and Opthalmology, Harvard Medical School, Investigator of HHMIEmail verificata su genetics.med.harvard.edu
Michael A. LodatoUniversity of Massachusetts Medical SchoolEmail verificata su umassmed.edu
Russell FerlandProfessor & ChairEmail verificata su une.edu
Gilad D. EvronyAssistant Professor, New York UniversityEmail verificata su nyulangone.org
Margaret Elizabeth RossWeill Cornell Medical CollegeEmail verificata su med.cornell.edu
M. Chiara ManziniRutgers-Robert Wood Johnson Medical SchoolEmail verificata su rutgers.edu
christopher geoffrey woodsprofessor of human geneticsEmail verificata su cam.ac.uk
Alissa D'GamaBoston Children's Hospital and Harvard Medical SchoolEmail verificata su childrens.harvard.edu
Vijay S. Ganesh, M.D., Ph.D.Brigham and Women's Hospital, Boston, MAEmail verificata su post.harvard.edu
Anthony LaMantiaThe Fralin Biomedical Research Institute at Virginia Tech-Carilion School of MedicineEmail verificata su vt.edu
Renzo GuerriniProfessore di Neuropsichiatria Infantile, Università di FirenzeEmail verificata su meyer.it
Xuyu CaiScientist, Illumina, Inc.Email verificata su illumina.com
Basel-Salmon or Basel-Vanagaite or L...Director, The Raphael Recanati Genetics InstituteEmail verificata su tauex.tau.ac.il

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Christopher A Walsh

Boston Children's Hospital

Email verificata su childrens.harvard.edu - Home page

development neuroscience genetics


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
Synaptic, transcriptional and chromatin genes disrupted in autism S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ... Nature 515 (7526), 209-215, 2014	2876	2014
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature genetics 45 (9), 984-994, 2013	2403	2013
Association between microdeletion and microduplication at 16p11. 2 and autism LA Weiss, Y Shen, JM Korn, DE Arking, DT Miller, R Fossdal, ... New England Journal of Medicine 358 (7), 667-675, 2008	1977	2008
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ... Cell 180 (3), 568-584. e23, 2020	1944	2020
Regulation of cerebral cortical size by control of cell cycle exit in neural precursors A Chenn, CA Walsh Science 297 (5580), 365-369, 2002	1737	2002
Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons JG Gleeson, PT Lin, LA Flanagan, CA Walsh Neuron 23 (2), 257-271, 1999	1564	1999
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ... Neuron 87 (6), 1215-1233, 2015	1544	2015
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ... Neuron 70 (5), 863-885, 2011	1511	2011
Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1α/CXC chemokine receptor 4 pathway J Imitola, K Raddassi, KI Park, FJ Mueller, M Nieto, YD Teng, D Frenkel, ... Proceedings of the National Academy of Sciences 101 (52), 18117-18122, 2004	1321	2004
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein JG Gleeson, KM Allen, JW Fox, ED Lamperti, S Berkovic, I Scheffer, ... Cell 92 (1), 63-72, 1998	1162	1998
Multipotent neural cell lines can engraft and participate in development of mouse cerebellum EY Snyder, DL Deitcher, C Walsh, S Arnold-Aldea, EA Hartwieg, ... Cell 68 (1), 33-51, 1992	1044	1992
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations SE Hong, YY Shugart, DT Huang, SA Shahwan, PE Grant, ... Nature genetics 26 (1), 93-96, 2000	1023	2000
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia JW Fox, ED Lamperti, YZ Ekşioğlu, SE Hong, Y Feng, DA Graham, ... Neuron 21 (6), 1315-1325, 1998	970	1998
Identifying autism loci and genes by tracing recent shared ancestry EM Morrow, SY Yoo, SW Flavell, TK Kim, Y Lin, RS Hill, NM Mukaddes, ... science 321 (5886), 218-223, 2008	946	2008
A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009	808	2009
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome DBV de Bernabé, S Currier, A Steinbrecher, J Celli, E Van Beusekom, ... The American Journal of Human Genetics 71 (5), 1033-1043, 2002	802	2002
ASPM is a major determinant of cerebral cortical size J Bond, E Roberts, GH Mochida, DJ Hampshire, S Scott, JM Askham, ... Nature genetics 32 (2), 316-320, 2002	752	2002
Reelin binds α3β1 integrin and inhibits neuronal migration L Dulabon, EC Olson, MG Taglienti, S Eisenhuth, B McGrath, CA Walsh, ... Neuron 27 (1), 33-44, 2000	709	2000
The cerebrospinal fluid provides a proliferative niche for neural progenitor cells MK Lehtinen, MW Zappaterra, X Chen, YJ Yang, AD Hill, M Lun, ... Neuron 69 (5), 893-905, 2011	698	2011
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size J Bond, E Roberts, K Springell, S Lizarraga, S Scott, J Higgins, ... Nature genetics 37 (4), 353-355, 2005	668	2005

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