P185
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brainAdvances in autismAdvances in autism genetics: on the threshold of a new neurobiologyAutism: many genes, common pathways?Neuroscience in the era of functional genomics and systems biologyWnt genes define distinct boundaries in the developing human brain: implications for human forebrain patterningLinkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneMolecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersGenome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathwaysA functional genetic link between distinct developmental language disordersMutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisReplication of autism linkage: fine-mapping peak at 17q21.A genomewide screen of 345 families for autism-susceptibility loci.Cancerous stem cells can arise from pediatric brain tumorsFunctional impact of global rare copy number variation in autism spectrum disordersCommon genetic variants on 5p14.1 associate with autism spectrum disordersAutism: Family connectionsDetecting network modules in fMRI time series: a weighted network analysis approachStrong association of de novo copy number mutations with autismExpanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSAtypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansionIdentification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brainHigh-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disordersHuman-specific transcriptional regulation of CNS development genes by FOXP2The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice.Early asymmetry of gene transcription in embryonic human left and right cerebral cortexSinging mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and languageA unified genetic theory for sporadic and inherited autismThe PsychENCODE projectGenetics and genomics of psychiatric diseaseEvidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonismHDAC inhibitors correct frataxin deficiency in a Friedreich ataxia mouse modelMapping autism risk loci using genetic linkage and chromosomal rearrangements.A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?A systems level, functional genomics analysis of chronic epilepsyRarity of the Alzheimer disease-protective APP A673T variant in the United StatesAdvancing the understanding of autism disease mechanisms through geneticsHuman ARX gene: genomic characterization and expressionSearch for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish familiesCloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue
P50
Q21144946-F008F3CF-B102-4DB6-AAB9-14132F9199D7Q22241976-B7FFF1DF-5D43-40E3-9032-A7FC51D92E47Q22251023-933E6F29-FD58-4D4E-A2E7-1D6C3BF68FAEQ22252315-45824576-C84B-424B-AFF3-3599F1926435Q22337243-AFBE218D-1450-4D0C-8DDE-11915CD53175Q24294389-E447998E-7A19-4BA0-93FB-9042ED26CCE6Q24305575-F7CAB2D0-D1B3-48FD-91F6-7DB5D2C8984CQ24305646-D8A420FF-B4FC-473B-AD6E-F2A278B7F531Q24306625-78ACB977-A473-42D6-8CEE-C58BB0500C59Q24312638-6263C75A-55B4-4AC1-BE45-03F414682350Q24337705-C9F0E5AF-AF2D-46DD-8700-1B9CB569D41BQ24530782-8A7737CF-D4BD-433C-97D9-3A637E266DF4Q24532783-9C196AD2-1328-44CA-A11C-DF9C8D9DF131Q24569653-9088DFA4-B519-4A8D-B302-486C02E8172FQ24596191-CB260324-4BF5-4C09-9A03-6F9A1ACB666EQ24603204-8E8F9B69-05CB-4FD1-B083-672A9C1B4070Q24629987-9AAAFC9F-956B-4AF7-A90C-502CC5544256Q24632511-2A3CF385-3319-4C74-A9DC-E3539B724EBBQ24633543-5A7FE0A5-8E14-4956-B8A9-3B690158129FQ24633692-B7AF6B70-D28B-4D63-9DE1-910760577664Q24633898-BDE87EBA-F3F8-4EEC-B8BA-721DDC7E1C71Q24648621-6AD8400E-20D8-4E03-92AB-3E58D96AF295Q24648773-A58DCA54-FBB5-459D-9121-AF89D170B2DBQ24655742-4F298ECB-8335-44FD-BA93-5754DFCBD098Q24656405-55896F9B-A3CA-4BA2-A5E5-C22225521C16Q24657807-C269522B-5D41-4A67-8A6C-139930282655Q24658435-73F6B61A-4942-4CA0-BCE2-BF10D23C1331Q24684315-DF6C1BD0-852A-41AF-9808-8A262E99CA9BQ26775498-5C465CA6-8CFE-46F0-86DB-E8BFC8219D44Q26781213-F274EB49-D417-4A69-9987-64665A0CFCF8Q26782028-52401FD7-D807-4AFD-8B11-E3665143FFCFQ27301415-0C485BF3-4E8A-4667-BEE1-D4BC41E89566Q27315912-D2925184-FDAA-494D-9349-B25C6636454AQ27326701-E04A90D6-A0FE-4BAA-9D13-F420D725CFC4Q27335505-7D22645C-C72F-40C1-833A-389B8AEEEDE9Q27346292-EFEF3321-9146-4A87-BD95-607AFD6BE8CBQ28069757-88AB0341-E419-4B9B-B3AB-60AB5DAF1503Q28160539-E31D16AF-4F06-4B4D-B3A0-C0928C93DEDDQ28281942-5D026498-B3A4-4755-BA7F-204387A2558BQ28289059-AB37160D-C1A9-4B75-928D-3449DED5F4C5
P50
description
American geneticist
@en
Amerikaans klinische genetica
@nl
genetista estadounidense
@es
jeneticiste american
@lfn
usona genetikisto
@eo
xenetista estauxunidense
@ast
عالم وراثة من الولايات المتحدة الأمريكية
@ar
name
Daniel Geschwind
@ast
Daniel Geschwind
@ca
Daniel Geschwind
@en
Daniel Geschwind
@es
Daniel Geschwind
@fr
Daniel Geschwind
@nl
Daniel Geschwind
@sl
دانیل قشویند
@azb
type
label
Daniel Geschwind
@ast
Daniel Geschwind
@ca
Daniel Geschwind
@en
Daniel Geschwind
@es
Daniel Geschwind
@fr
Daniel Geschwind
@nl
Daniel Geschwind
@sl
دانیل قشویند
@azb
altLabel
Daniel H Geschwind
@en
Daniel H. Geschwind
@en
prefLabel
Daniel Geschwind
@ast
Daniel Geschwind
@ca
Daniel Geschwind
@en
Daniel Geschwind
@es
Daniel Geschwind
@fr
Daniel Geschwind
@nl
Daniel Geschwind
@sl
دانیل قشویند
@azb
P1006
P214
P244
P269
P1006
P101
P184
P21
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P214
P244
n2001130764
P269
P31
P6023
P735
P7859
lccn-n2001130764