D. H. Geschwind

发表

Chunyu, Annie W Shieh, L. Iakoucheva, 2019 .

Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

D. Geschwind, R. Cantor, J. Lowe, 2014, Molecular Autism.

QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders

Daniel H. Geschwind, A. Lu, D. Geschwind, 2013, Molecular Psychiatry.

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs

D. Geschwind, R. Cantor, T. Gilliam, 2005, Molecular Psychiatry.

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.

D. Geschwind, R. Cantor, T. Gilliam, 2002, American journal of human genetics.

Global changes in patterning, splicing and primate specific lncRNAs in autism brain

Luis de la Torre Ubieta, S. Horvath, C. Hartl, 2016, bioRxiv.

Mapping the human genetic architecture of COVID-19

Mattia G. Bergomi, Christopher M. DeBoever, Matthew A. Wiles, 2021, Nature.

TOAD-64, a gene expressed early in neuronal differentiation in the rat, is related to unc-33, a C. elegans gene involved in axon outgrowth

S. Hockfield, D. Geschwind, H. Fryer, 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Disease-specific selective vulnerability and neuroimmune pathways in dementia revealed by single cell genomics

J. Trojanowski, D. Calini, R. Kawaguchi, 2023, bioRxiv.

Integrating de novo and inherited variants in over 42,607 autism cases 1 identifies mutations in new moderate risk genes 2

B. O’Roak, M. Dennis, L. Soorya, 2021 .

Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice

D. Geschwind, Y. Sano, W. Li, 2012, Molecular Psychiatry.

Neural responsivity to social rewards in autistic female youth

Katherine E. Lawrence, Zachary J. Jacokes, D. Geschwind, 2020, Translational Psychiatry.

Correspondence between Resting-State Activity and Brain Gene Expression

D. Geschwind, Hanzhang Lu, T. Preuss, 2015, Neuron.

Biophysical constraints of optogenetic inhibition at presynaptic terminals

J. D. Macklis, E. Ruzzo, B. Amilhon, 2016, Nature Neuroscience.

Prevalent iron metabolism gene variants associated with increased brain ferritin iron in healthy older men.

Jim Mintz, J Paul Finn, Anastasia Kosenko, 2010, Journal of Alzheimer's disease : JAD.

Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes

Pavel P. Kuksa, P. Kuksa, A. Naj, 2023, bioRxiv.

Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies LRRC4C, LHX5-AS1 and nominates ancestry-specific loci PTPRK, GRB14, and KIAA0825 as novel risk loci for Alzheimer disease: the Alzheimer Disease Genetics Consortium

Pavel P. Kuksa, Nicholas R. Wheeler, Timothy J. Hohman, 2023, medRxiv.

Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray.

D. Geschwind, S. Nelson, J. Ellison, 1998, Developmental genetics.

Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders

Daniel H. Geschwind, D. Geschwind, Neelroop N. Parikshak, 2016, Nature Communications.

Developmental disorders

Annette Karmiloff-Smith, A. Karmiloff-Smith, S. Jeste, 1998 .

phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing.

V. Swarup, M. Irimia, O. Peñagarikano, 2018 .

Tet3 regulates synaptic transmission and homeostatic plasticity via DNA oxidation and repair

Giovanni Coppola, Fuying Gao, Jaehoon Shin, 2015, Nature Neuroscience.

Whole genome‐wide sequence analysis of long‐lived families (Long‐Life Family Study) identifies MTUS2 gene associated with late‐onset Alzheimer's disease

A. Yashin, H. Hakonarson, M. Cuccaro, 2024, Alzheimer's & Dementia.

ATF4 Is an Oxidative Stress–Inducible, Prodeath Transcription ATF4 Is an Oxidative Stress–Inducible, Prodeath Transcription Factor in Neurons in Vitro and in Vivo Factor in Neurons in Vitro and in Vivo

T. Townes, R. Ratan, Chiao‐Wang Sun, 2022 .

Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer’s Disease

C. Lajonchere, E. Eskin, Timothy S. Chang, 2024, medRxiv.

Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy

L. Hazrati, B. Ghetti, M. Gearing, 2023, medRxiv.

Using iPS cell-derived neurons to uncover cellular phenotypes associated with Timothy Syndrome

D. Geschwind, R. Dolmetsch, T. Palmer, 2011, Nature Medicine.

Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants.

A. Ingason, T. Werge, M. Nordentoft, 2024, JAMA psychiatry.

Functional neurogenomics in autism spectrum disorders: A decade of progress

D. H. Geschwind, Lucy Bicks, 2024, Current Opinion in Neurobiology.

A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder.

M. Dapretto, Emily Neuhaus, Megha Santhosh, 2024, Autism research : official journal of the International Society for Autism Research.

Retooling spare parts: gene duplication and cognition

T. G. Belgard, D. H. Geschwind, 2012, Nature Neuroscience.