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Daniel Geschwind
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American geneticist
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Works
13
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
scientific article
Selenium Drives a Transcriptional Adaptive Program to Block Ferroptosis and Treat Stroke
scientific article published on 02 May 2019
Functional impact of global rare copy number variation in autism spectrum disorders
scientific article published on 15 July 2010
Common genetic variants, acting additively, are a major source of risk for autism
scientific article
Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage
scientific article published on 26 August 2019
Chromosome conformation elucidates regulatory relationships in developing human brain.
scientific article published on 19 October 2016
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
scientific article
Human Disease Variation in the Light of Population Genomics
scientific article published on 01 March 2019
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
scientific article
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
scientific article (publication date: June 2011)
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Daniel H. Geschwind is an American physician-scientist whose laboratory has made pioneering discoveries in the biology of brain disorders and the genetic and genomic analyses of the nervous system.

Instance of
Human
Occupation
Geneticist
Neuroscientist
Researcher
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