Christopher A Walsh

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William B. DobynsProfessor of PediatricsVerifisert e-postadresse på umn.edu
Annapurna PoduriNeurology, Boston Children's Hospital, Harvard Medical SchoolVerifisert e-postadresse på childrens.harvard.edu
Peter J ParkHarvard Medical SchoolVerifisert e-postadresse på harvard.edu
Joseph G. GleesonUniversity of California, San DiegoVerifisert e-postadresse på ucsd.edu
Timothy W. YuHarvard Medical School and Boston Children's HospitalVerifisert e-postadresse på childrens.harvard.edu
Ryan DoanBoston Children's HospitalVerifisert e-postadresse på childrens.harvard.edu
Volney Sheenbeth israelVerifisert e-postadresse på bidmc.harvard.edu
Michael A. LodatoUniversity of Massachusetts Medical SchoolVerifisert e-postadresse på umassmed.edu
Constance L CepkoProfessor of Genetics and Opthalmology, Harvard Medical School, Investigator of HHMIVerifisert e-postadresse på genetics.med.harvard.edu
Russell FerlandProfessor & ChairVerifisert e-postadresse på une.edu
Gilad D. EvronyAssistant Professor, New York UniversityVerifisert e-postadresse på nyulangone.org
Margaret Elizabeth RossWeill Cornell Medical CollegeVerifisert e-postadresse på med.cornell.edu
Alissa D'GamaBoston Children's Hospital and Harvard Medical SchoolVerifisert e-postadresse på childrens.harvard.edu
Anthony LaMantiaThe Fralin Biomedical Research Institute at Virginia Tech-Carilion School of MedicineVerifisert e-postadresse på vt.edu
Craig BohrsonHarvard Medical SchoolVerifisert e-postadresse på g.harvard.edu
christopher geoffrey woodsprofessor of human geneticsVerifisert e-postadresse på cam.ac.uk
M. Chiara ManziniRutgers-Robert Wood Johnson Medical SchoolVerifisert e-postadresse på rutgers.edu
Vijay S. Ganesh, M.D., Ph.D.Brigham and Women's Hospital, Boston, MAVerifisert e-postadresse på post.harvard.edu
Renzo GuerriniProfessore di Neuropsichiatria Infantile, Università di FirenzeVerifisert e-postadresse på meyer.it
Xuyu CaiScientist, Illumina, Inc.Verifisert e-postadresse på illumina.com

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Christopher A Walsh

Boston Children's Hospital

Verifisert e-postadresse på childrens.harvard.edu - Startside

development neuroscience genetics


Tittel Sorter etter sitater Sorter etter år Sorter etter tittel	Sitert av Sitert av	År
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	2973	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	2434	2013
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	2059	2020
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	2005	2008
Regulation of cerebral cortical size by control of cell cycle exit in neural precursors A Chenn, CA Walsh Science 297 (5580), 365-369, 2002	1743	2002
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	1592	2015
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	1576	1999
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	1539	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	1325	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	1180	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	1043	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	1038	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	980	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	951	2008
A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009	814	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	803	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	760	2002
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	720	2011
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	718	2000
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	674	2005

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