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Charu Kaiwar

4PUBLICATIONS

18CO-AUTHORS

GenomicsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Vision science

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Publications (4)

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|Feb 10, 2019

Clinical spectrum of <i>STX1B</i>-related epileptic disorders.

Stefan Wolking, Patrick May, Davide Mei

|Jan 26, 2019

De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms.

Sandra Jansen, Ilse M van der Werf, A Micheil Innes

|Dec 15, 2018

A case of YY1-associated syndromic learning disability or Gabriele-de Vries syndrome with myasthenia gravis.

Joel A Morales-Rosado, Charu Kaiwar, Benn E Smith

|Oct 01, 2017

Novel <i>NR2F1</i> variants likely disrupt DNA binding: molecular modeling in two cases, review of published cases, genotype-phenotype correlation, and phenotypic expansion of the Bosch-Boonstra-Schaaf optic atrophy syndrome.

Charu Kaiwar, Michael T Zimmermann, Matthew J Ferber

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Frequent Collaborators

1 joint publications

Joel A Morales-Rosado

1 joint publications

Sandra Jansen

1 joint publications

Ilse M van der Werf

1 joint publications

A Micheil Innes

1 joint publications

Anke van Dijck

1 joint publications

Tuula Rinne

1 joint publications

Corrado Romano

1 joint publications

David A Sweetser

1 joint publications

Kristian Tveten

1 joint publications

R Frank Kooy

Frequent Collaborators

1 joint publications

Joel A Morales-Rosado

1 joint publications

Sandra Jansen

1 joint publications

Ilse M van der Werf

1 joint publications

A Micheil Innes

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