Dan Geschwind
Dan Geschwind
Distinguished Professor of Neurology, Psychiatry and Human Genetics, UCLA
Verified email at mednet.ucla.edu - Homepage
Title
Cited by
Cited by
Year
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
37592011
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
29262007
Advances in autism genetics: on the threshold of a new neurobiology
BS Abrahams, DH Geschwind
Nature reviews genetics 9 (5), 341-355, 2008
21122008
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
20652003
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
20581997
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), 368-372, 2010
19382010
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), 237-241, 2012
18372012
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
17612013
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), 436-441, 2011
16412011
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), 391-399, 2012
15902012
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
14492007
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), 380-384, 2011
14452011
Autism spectrum disorders: developmental disconnection syndromes
DH Geschwind, P Levitt
Current opinion in neurobiology 17 (1), 103-111, 2007
14412007
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
11932011
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
10041998
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), 528-533, 2009
9792009
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), 331-337, 2009
8932009
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
8712015
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
8672008
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
8192019
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