Dan Geschwind
Dan Geschwind
Professor of Neurology, Psychiatry and Human Genetics, UCLA
Підтверджена електронна адреса в mednet.ucla.edu
НазваПосиланняРік
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
M DeJesus-Hernandez, IR Mackenzie, BF Boeve, AL Boxer, M Baker, ...
Neuron 72 (2), 245-256, 2011
30022011
Strong association of de novo copy number mutations with autism
J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ...
Science 316 (5823), 445-449, 2007
26312007
Cancerous stem cells can arise from pediatric brain tumors
HD Hemmati, I Nakano, JA Lazareff, M Masterman-Smith, DH Geschwind, ...
Proceedings of the National Academy of Sciences 100 (25), 15178-15183, 2003
19272003
Dentate granule cell neurogenesis is increased by seizures and contributes to aberrant network reorganization in the adult rat hippocampus
JM Parent, WY Timothy, RT Leibowitz, DH Geschwind, RS Sloviter, ...
Journal of Neuroscience 17 (10), 3727-3738, 1997
19081997
Advances in autism genetics: on the threshold of a new neurobiology
BS Abrahams, DH Geschwind
Nature reviews genetics 9 (5), 341, 2008
19052008
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368, 2010
16912010
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ...
Nature 485 (7397), 237, 2012
15452012
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ...
Nature genetics 43 (5), 436, 2011
13782011
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
13472007
Autism spectrum disorders: developmental disconnection syndromes
DH Geschwind, P Levitt
Current opinion in neurobiology 17 (1), 103-111, 2007
12532007
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
I Voineagu, X Wang, P Johnston, JK Lowe, Y Tian, S Horvath, J Mill, ...
Nature 474 (7351), 380, 2011
11872011
An anatomically comprehensive atlas of the adult human brain transcriptome
MJ Hawrylycz, ES Lein, AL Guillozet-Bongaarts, EH Shen, L Ng, JA Miller, ...
Nature 489 (7416), 391, 2012
11362012
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
10322011
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
9752013
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
M Hong, V Zhukareva, V Vogelsberg-Ragaglia, Z Wszolek, L Reed, ...
Science 282 (5395), 1914-1917, 1998
9241998
Common genetic variants on 5p14. 1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528, 2009
8912009
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
M Alarcón, BS Abrahams, JL Stone, JA Duvall, JV Perederiy, JM Bomar, ...
The American Journal of Human Genetics 82 (1), 150-159, 2008
7822008
Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease
AH Nagahara, DA Merrill, G Coppola, S Tsukada, BE Schroeder, ...
Nature medicine 15 (3), 331, 2009
7732009
A functional genetic link between distinct developmental language disorders
SC Vernes, DF Newbury, BS Abrahams, L Winchester, J Nicod, M Groszer, ...
New England Journal of Medicine 359 (22), 2337-2345, 2008
6722008
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
O Peñagarikano, BS Abrahams, EI Herman, KD Winden, A Gdalyahu, ...
Cell 147 (1), 235-246, 2011
6102011
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