# William B. Dobyns

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/william-b-dobyns/

## Facts

| Field | Value |
| --- | --- |
| Citations | 54,882 |
| Field | Fetal and Pediatric Neurological Disorders |
| h-index | 128 |
| i10-index | 419 |
| Last Known Institution | University of Minnesota |
| OpenAlex ID | https://openalex.org/A5057534469 |
| ORCID iD | https://orcid.org/0000-0002-7681-2844 |
| Works | 589 |

## Researcher papers

- [doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein](https://scholariq.org/papers/doublecortin-a-brain-specific-gene-mutated-in-human-x-linked-lissencephaly-and/)
- [A developmental and genetic classification for malformations of cortical development: update 2012](https://scholariq.org/papers/a-developmental-and-genetic-classification-for-malformations-of-cortical-2/)
- [A developmental and genetic classification for malformations of cortical development](https://scholariq.org/papers/a-developmental-and-genetic-classification-for-malformations-of-cortical/)
- [Classification system for malformations of cortical development](https://scholariq.org/papers/classification-system-for-malformations-of-cortical-development/)
- [Malformations of cortical development: clinical features and genetic causes](https://scholariq.org/papers/malformations-of-cortical-development-clinical-features-and-genetic-causes/)
- [A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases](https://scholariq.org/papers/a-drosophila-genetic-resource-of-mutants-to-study-mechanisms-underlying-human/)
- [<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects](https://scholariq.org/papers/i-grin2b-i-encephalopathy-novel-findings-on-phenotype-variant-clustering/)
- [Early-Life Epilepsies and the Emerging Role of Genetic Testing](https://scholariq.org/papers/early-life-epilepsies-and-the-emerging-role-of-genetic-testing/)

## Researcher topics

- [Fetal and Pediatric Neurological Disorders](https://scholariq.org/topics/fetal-and-pediatric-neurological-disorders/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)

## Researcher university

- [University of Minnesota](https://scholariq.org/institutions/university-of-minnesota/)

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