# Daniel H. Geschwind

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/daniel-h-geschwind/

## Facts

| Field | Value |
| --- | --- |
| Citations | 153,761 |
| Field | Autism Spectrum Disorder Research |
| h-index | 189 |
| i10-index | 597 |
| Last Known Institution | University of California, Los Angeles |
| OpenAlex ID | https://openalex.org/A5018481303 |
| ORCID iD | https://orcid.org/0000-0003-2896-3450 |
| Works | 970 |

## Researcher papers

Showing 12 of 28.

- [Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS](https://scholariq.org/papers/expanded-ggggcc-hexanucleotide-repeat-in-noncoding-region-of-c9orf72-causes/)
- [Strong Association of De Novo Copy Number Mutations with Autism](https://scholariq.org/papers/strong-association-of-de-novo-copy-number-mutations-with-autism/)
- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism](https://scholariq.org/papers/large-scale-exome-sequencing-study-implicates-both-developmental-and-functional/)
- [Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder](https://scholariq.org/papers/discovery-of-the-first-genome-wide-significant-risk-loci-for-attention-deficit/)
- [Analysis of shared heritability in common disorders of the brain](https://scholariq.org/papers/analysis-of-shared-heritability-in-common-disorders-of-the-brain/)
- [Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease](https://scholariq.org/papers/common-variants-at-ms4a4-ms4a6e-cd2ap-cd33-and-epha1-are-associated-with-late/)
- [Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection](https://scholariq.org/papers/common-schizophrenia-alleles-are-enriched-in-mutation-intolerant-genes-and-in/)
- [Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci](https://scholariq.org/papers/insights-into-autism-spectrum-disorder-genomic-architecture-and-biology-from-71/)
- [Mapping autism risk loci using genetic linkage and chromosomal rearrangements](https://scholariq.org/papers/mapping-autism-risk-loci-using-genetic-linkage-and-chromosomal-rearrangements/)
- [Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder](https://scholariq.org/papers/transcriptome-wide-isoform-level-dysregulation-in-asd-schizophrenia-and-bipolar/)
- [Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism](https://scholariq.org/papers/multiple-recurrent-de-novo-cnvs-including-duplications-of-the-7q11-23-williams/)

## Researcher topics

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Bioinformatics and Genomic Networks](https://scholariq.org/topics/bioinformatics-and-genomic-networks/)

## Researcher university

- [University of California, Los Angeles](https://scholariq.org/institutions/university-of-california-los-angeles/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.