Kamel Jabbari
Koeln, NW, Germany
Last Updated: 09/26/2026
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Found 11 publications
mGlu3 Metabotropic Glutamate Receptors as a Target for the Treatment of Absence Epilepsy: Preclinical and Human Genetics Data.
Journal: Current neuropharmacology
Published: January 13, 2022
DNA sequence-dependent chromatin architecture and nuclear hubs formation.
Journal: Scientific reports
Published: June 20, 2019
A common genomic code for chromatin architecture and recombination landscape.
Journal: PloS one
Published: August 29, 2018
Rare gene deletions in genetic generalized and Rolandic epilepsies.
Journal: PloS one
Published: March 16, 2018
The Diverging Routes of BORIS and CTCF: An Interactomic and Phylogenomic Analysis.
Journal: Life (Basel, Switzerland)
Published: December 23, 2017
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.
Journal: The Lancet. Neurology
Published: August 02, 2017
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
Journal: European journal of human genetics : EJHG
Published: May 08, 2017
An Isochore Framework Underlies Chromatin Architecture.
Journal: PloS one
Published: September 28, 2016
Leveraging the power of high performance computing for next generation sequencing data analysis: tricks and twists from a high throughput exome workflow.
Journal: PloS one
Published: November 07, 2014
DEPDC5 mutations in genetic focal epilepsies of childhood.
Journal: Annals of neurology
Published: October 20, 2013
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Last Updated: 09/26/2026