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Dan H. Geschwind

Observed names: Dan Geschwind, Dan H Geschwind, Geschwind, Dan H
OpenAlex ID: A5113595775
Accelerating axonal growth promotes motor recovery after peripheral nerve injury in mice
2011 · Chi Him Eddie Ma, Takao Omura, et al. · Journal of Clinical Investigation · 257
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative
2007 · Rosa Rademakers, Matt Baker, et al. · The Lancet Neurology · 216
Combined Intrinsic and Extrinsic Neuronal Mechanisms Facilitate Bridging Axonal Regeneration One Year after Spinal Cord Injury
2009 · Ken Kadoya, Shingo Tsukada, et al. · Neuron · 213
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Klinefelter syndrome: Expanding the phenotype and identifying new research directions
2003 · Joe Leigh Simpson, Felix de la Cruz, et al. · Genetics in Medicine · 184
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Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers
2016 · Suzee E. Lee, Ana C. Sias, et al. · NeuroImage Clinical · 164
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Divergent Whole-Genome Methylation Maps of Human and Chimpanzee Brains Reveal Epigenetic Basis of Human Regulatory Evolution
2012 · Jia Zeng, Genevieve Konopka, et al. · The American Journal of Human Genetics · 159
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Progranulin Mutations as Risk Factors for Alzheimer Disease
2013 · David C. Perry, Manja Lehmann, et al. · JAMA Neurology · 133
Patient-Tailored, Connectivity-Based Forecasts of Spreading Brain Atrophy
2019 · Jesse A. Brown, Jersey Deng, et al. · Neuron · 117
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Conditioning lesions before or after spinal cord injury recruit broad genetic mechanisms that sustain axonal regeneration: Superiority to camp-mediated effects
2011 · Armin Blesch, Paul Lu, et al. · Experimental Neurology · 105
The apolipoprotein E ε4 allele is not a significant risk factor for frontotemporal dementia
1998 · Dan Geschwind, Juliana Karrim, et al. · Annals of Neurology · 101
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
2013 · Marka van Blitterswijk, Matthew C. Baker, et al. · Neurology · 82
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Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers
2018 · Lieke H.H. Meeter, Tania F. Gendron, et al. · Annals of Clinical and Translational Neurology · 61
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Brain volumetric deficits in MAPT mutation carriers: a multisite study
2020 · Stephanie A. Chu, Taru M. Flagan, et al. · Annals of Clinical and Translational Neurology · 32
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GENSAT: a genomic resource for neuroscience research
2004 · Dan Geschwind · The Lancet Neurology · 28
Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy
2015 · Kellen D. Winden, Anatol Bragin, et al. · Neurobiology of Disease · 19
Pickʼs Disease and Frontotemporal Dementias
1999 · Bruce L Miller, Kyle Boone, et al. · The Neurologist · 14
Understanding the biological basis of psychiatric disease: What’s next?
2022 · Conor Liston, Angela Roberts, et al. · Cell · 13
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Genes and the long and winding road to cortical construction and cognition
2010 · M. Elizabeth Ross, Dan Geschwind · Neurobiology of Disease · 3
238. Transcriptome-Wide Isoform-Level Dysregulation in Schizophrenia, Autism, and Bipolar Disorder
2019 · Michael Gandal, Dalila Pinto, et al. · Biological Psychiatry · 1
Downregulation of the silent potassium channel Kv8.1 increases ALS motor neuron vulnerability
2023 · Xuan Huang, Seungkyu Lee, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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A microarray screen for genes involved in brain regionalization and morphogenesis
2003 · Zhouqing Luo, Dmitri Tentler, et al. · The American Journal of Human Genetics
Reply from the Authors
1996 · Dan Geschwind, Michael FitzPatrick, et al. · Neurology
Works count: 23
Citation count: 1,902
H-index: 15
I10-index: 17
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