Daniel H. Geschwind

Molecular Biology · 1997–2019

A researcher in the Science corpus: 47 papers; trusts 22 researchers and is trusted by 25 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 875 citations into it; #2,008 of 17,773 by trust here, #591 by citations
• Genetics — 700 citations into it; #789 of 6,854 by trust here, #100 by citations
• Cognitive Neuroscience — 318 citations into it; #1,845 of 10,852 by trust here, #181 by citations
• Cellular and Molecular Neuroscience — 111 citations into it
• Neurology — 110 citations into it
• Physiology — 93 citations into it
• Psychiatry and Mental health — 69 citations into it
• Clinical Psychology — 37 citations into it

Whom Daniel H. Geschwind trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Eric Fombonne
2. Eric Courchesne
3. H. Zoghbi
4. Steve Horvath
5. Bin Zhang
6. K. Pierce
7. Takao K. Hensch
8. Eric I. Knudsen
9. J. Constantino
10. Peter Langfelder

Who trusts Daniel H. Geschwind overall

1. Daniel P. Kennedy
2. Luis de la Torre-Ubieta
3. L. Weiss
4. Ralph Adolphs
5. Meng-Chuan Lai
6. Charity E. Onore
7. Xiao-Jing Wang
8. H. Won
9. Michael V. Lombardo
10. S. Wang

Papers from Daniel H. Geschwind's perspective

Ordered by how strongly the researchers Daniel H. Geschwind trusts endorse each paper. Same corpus, a different order for every researcher.

1. Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
2. Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
3. Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
4. Detection of large-scale variation in the human genome (Nature Genetics)
5. DAVID: Database for Annotation, Visualization, and Integrated Discovery (Genome Biology)
6. Advances in autism genetics: on the threshold of a new neurobiology (Nature reviews genetics)
7. FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism (Cell)
8. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. (American Journal of Human Genetics)
9. Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins. (Cell)
10. Neuroligins determine synapse maturation and function. (Neuron)

Their papers

• Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
• Functional organization of the transcriptome in human brain (2008) — 761 citations
• Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism (2015) — 682 citations
• Transcriptional Landscape of the Prenatal Human Brain (2014) — 1,286 citations
• Transcriptomic Analysis of Autistic Brain Reveals Convergent Molecular Pathology (2011) — 1,867 citations
• Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) — 1,286 citations
• A highly conserved program of neuronal microexons is misregulated in autistic brains (2014) — 652 citations
• An anatomically comprehensive atlas of the adult human brain transcriptome (2012) — 3,011 citations
• Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism (2013) — 1,012 citations
• Strategies for aggregating gene expression data: The collapseRows R function (2011) — 317 citations
• Cancerous stem cells can arise from pediatric brain tumors (2003) — 1,913 citations
• Advances in autism genetics: on the threshold of a new neurobiology (2008) — 1,905 citations
• Functional and Evolutionary Insights Into Human Brain Development Through Global Transcriptome Analysis (2009) — 606 citations
• Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder (2018) — 1,134 citations
• Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders (2015) — 392 citations
• Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease (2011) — 1,887 citations
• Advancing the understanding of autism disease mechanisms through genetics (2016) — 765 citations
• Comprehensive functional genomic resource and integrative model for the human brain (2018) — 946 citations
• Autism spectrum disorders: developmental disconnection syndromes (2007) — 1,460 citations
• A Functional Genetic Link between Distinct Developmental Language Disorders (2008) — 691 citations