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authorId(s): 3253547
Author(s): D. Geschwind
scorecitationCountPaperAuthorsyearMore like thisCompare & ContrastProNE-sSciNCLSpecterGNN
4435
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
M. Dejesus‐Hernandez, I. Mackenzie, ..., R. Rademakers
2011
2378
An anatomically comprehensive atlas of the adult human brain transcriptome
M. Hawrylycz, E. Lein, ..., Allan R. Jones
2012
2106
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. H. Lee, S. Ripke, ..., N. Wray
2013
1969
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Stephan J Sanders, M. Murtha, ..., M. State
2012
1905
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
B. Kunkle, B. Grenier‐Boley, ..., M. Pericak-Vance
2019
1569
Identification of common genetic risk variants for autism spectrum disorder
J. Grove, S. Ripke, ..., A. Børglum
2019
1560
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D. Demontis, R. Walters, ..., B. Neale
2018
1505
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, J. Kosmicki, ..., R. Walters
2019
1275
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
A. Pardiñas, P. Holmans, ..., J. Walters
2018
1254
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan J Sanders, A. Ercan-Sencicek, ..., M. State
2011

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