Christopher A Walsh
Christopher A Walsh
Boston Children's Hospital
Dirección de correo verificada de childrens.harvard.edu - Página principal
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
16692013
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
16282008
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, AE Cicek, ...
Nature 515 (7526), 209-215, 2014
16222014
Regulation of cerebral cortical size by control of cell cycle exit in neural precursors
A Chenn, CA Walsh
Science 297 (5580), 365-369, 2002
14272002
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
12661999
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
11572004
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
11482011
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
10421998
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
10061992
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
SE Hong, YY Shugart, DT Huang, S Al Shahwan, PE Grant, ...
Nature genetics 26 (1), 93-96, 2000
8572000
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
8391998
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
7832015
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
7722008
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
7172002
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking
Nature 461 (7265), 802-808, 2009
6432009
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
6432002
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
6202000
Widespread dispersion of neuronal clones across functional regions of the cerebral cortex
C Walsh, CL Cepko
Science 255 (5043), 434-440, 1992
6051992
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
5412005
The many faces of filamin: a versatile molecular scaffold for cell motility and signalling
Y Feng, CA Walsh
Nature cell biology 6 (11), 1034-1038, 2004
5222004
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Artículos 1–20