Ethiraj Ravindran

Berlin, BE 10117, Germany

Last Updated: 09/26/2026

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Found 15 publications

Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiring.

Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiring.

Journal: Nature communications
Published: February 06, 2023

Case report: Compound heterozygous NUP85 variants cause autosomal recessive primary microcephaly.

Case report: Compound heterozygous NUP85 variants cause autosomal recessive primary microcephaly.

Journal: Frontiers in neurology
Published: December 15, 2022

PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients.

PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients.

Journal: Cerebellum (London, England)
Published: September 23, 2022

Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease.

Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease.

Journal: Frontiers in neurology
Published: August 12, 2022

Monoallelic CRMP1 gene variants cause neurodevelopmental disorder.

Monoallelic CRMP1 gene variants cause neurodevelopmental disorder.

Journal: eLife
Published: June 04, 2022

Proteome changes in autosomal recessive primary microcephaly.

Proteome changes in autosomal recessive primary microcephaly.

Journal: Annals of human genetics
Published: March 14, 2022

Arhgef2 regulates neural differentiation in the cerebral cortex through mRNA m6A-methylation of Npdc1 and Cend1.

Arhgef2 regulates neural differentiation in the cerebral cortex through mRNA m6A-methylation of Npdc1 and Cend1.

Journal: iScience
Published: February 09, 2021

Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders.

Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders.

Journal: Human molecular genetics
Published: February 08, 2021

Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability.

Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability.

Journal: Journal of medical genetics
Published: October 27, 2020

Congenital microcephaly-linked CDK5RAP2 affects eye development.

Congenital microcephaly-linked CDK5RAP2 affects eye development.

Journal: Annals of human genetics
Published: October 08, 2018

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

Journal: PLoS genetics
Published: June 23, 2016

Novel Alternative Splice Variants of Mouse Cdk5rap2.

Novel Alternative Splice Variants of Mouse Cdk5rap2.

Journal: PloS one
Published: June 10, 2015
Showing 1-12 of 15

Last Updated: 09/26/2026