William Dobyns

Has grant

Professor

University of Minnesota

United States

Research Interests

Explore related searches

Professors in United States

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

William Dobyns is a Professor at the University of Minnesota, USA. His research primarily focuses on neurodevelopmental disorders, brain malformations, and the genetic underpinnings of various neurological conditions. His recent articles include reviews and studies on topics such as congenital infections, X-linked inheritance patterns, and innovative phenotyping techniques for rare disorders.

Recent Grants

Grant: Close

Mosaic: post-zygotic mutations in vascular and lymphatic developmental disorders

Open Date: 2016-02-08

Close Date: 2020-01-31

Grant: Close

Megalencephaly and segmental brain overgrowth in humans

Open Date: 2015-09-30

Close Date: 2020-07-31

Grant: Close

A comparative study of sudden unexpected death in mouse models of focal cortical dysplasia and Dravet syndrome

Open Date: 2014-09-01

Close Date: 2015-08-31

Grant: Close

A genomic approach to identify novel genes associated with human brain malformations

Open Date: 2011-06-01

Close Date: 2012-08-24

Grant: Close

Genomic Imbalances In Autism

Open Date: 2008-04-01

Close Date: 2010-04-01

Articles (17)

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Collaborators (16)

Elizabeth Pierpont

University of Minnesota

UNITED STATES

William Dobyns

Research Interests

Explore related searches

Contact this professor

About

Recent Grants

Articles (17)

Pathogenic de novo variants in PPP2R5C cause a neurodevelopmental disorder within the Houge-Janssens syndrome spectrum

Beyond hearing loss: exploring neurological and neurodevelopmental sequelae in asymptomatic congenital cytomegalovirus infection

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

Pontocerebellar hypoplasia: a review from 1912 to 2022

Patterns of X-linked inheritance: A new approach for the genome era

Disruptive lesions can cause developmental anomalies in the fetal brain: Mini-review

P253 Next-generation phenotyping facilitates the identification of structural brain malformations in rare disorders through computational brain MRI analysis

Diffusion Tensor Imaging in Boys With Adrenoleukodystrophy

Undifferentiated psychosis or schizophrenia associated with vermis‐predominant cerebellar hypoplasia

Diffuse CNS cortical vein malformations with chromosome 17q microduplication

Delphi Consensus on Diagnostic Criteria for LUMBAR Syndrome

Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes

Mary Ella Mascia Pierpont: Geneticist, scientist, mentor, friend (1945–2020)

Recurrent constellations of embryonic malformations re‐conceptualized as an overlapping group of disorders with shared pathogenesis

Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome?

Genotype–phenotype correlation at codon 1740 of SETD2

Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations

Collaborators (16)

Elizabeth Pierpont

Pamela Trapane

Anna Ruiz

Christiane Zweier

David Nascene

Sally Ann Lynch

Veerle Janssens

Youssef A Kousa, MS, DO, PhD

Igor Nestrasil

Manuela Morleo

Ilona Frieden

Lauren Haisley

roberta battini

Cristina Dias

Alison Leslie

Jeffrey Wozniak

Make your next move.