Richard H. van Jaarsveld

Netherlands

Research Interests

Explore related searches

Professors in Netherlands Professors in Medical Science Medical Science professors in Netherlands

Contact this professor

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

Articles (10)

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Collaborators (8)

M. E. Suzanne Lewis

CANADA

View details

Mohamad Mikati

Duke University

UNITED STATES

View details

Rachel Schot

Erasmus University Medical Center

NETHERLANDS

View details

Damaris Lorenzo

Associate Professor

University of Pennsylvania

UNITED STATES

View details

Seth Berger

Assistant Professor

Children's National Health System

UNITED STATES

View details

Tomi Toler

Assistant Professor

Washington University in Saint Louis School of Medicine

UNITED STATES

View details

Marwan shinawi

Professor

Washington University in Saint Louis School of Medicine

UNITED STATES

View details

Kathryn Harper

Assistant Professor

University of North Carolina

UNITED STATES

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Richard H. van Jaarsveld

Research Interests

Explore related searches

Contact this professor

Articles (10)

Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature

Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder

De novo putative loss‐of‐function variants in <i>TAF4</i> are associated with a neuro‐developmental disorder

Nuclear chromosome locations dictate segregation error frequencies

Impaired activity of the fusogenic micropeptide Myomixer causes myopathy resembling Carey-Fineman-Ziter syndrome

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia

Collaborators (8)

M. E. Suzanne Lewis

Mohamad Mikati

Rachel Schot

Damaris Lorenzo

Seth Berger

Tomi Toler

Marwan shinawi

Kathryn Harper

Make your next move.