Boris Keren
Université de Pau et des Pays de l'Adour(FR)Sorbonne Université(FR)Hôpital Armand-Trousseau(FR)Assistance Publique – Hôpitaux de Paris(FR)Tsehootsooi Medical Center(US)Pitié-Salpêtrière Hospital(FR)Institut Pierre Louis d‘Épidémiologie et de Santé Publique(FR)ERN ITHACA(FR)Université Paris 1 Panthéon-Sorbonne(FR)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, RNA modifications and cancer, Congenital heart defects research
Most-Cited Works
- → High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies(2017)451 cited
- → Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females(2009)368 cited
- → Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients(2008)362 cited
- → Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders(2020)319 cited
- → Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities(2015)292 cited
- → GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects(2017)252 cited