Isis Atallah

8PUBLICATIONS
55CO-AUTHORS
NeurogeneticsCell and nuclear divisionNeurology and neuromuscular diseasesNeonatologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (8)

|Jul 11, 2025
Structural and Functional Characterization of N-Glycanase-1 Pathogenic Variants.

Antje Banning, Lukas Hoeren, Isis Atallah

|Oct 30, 2024
Recurrent Increased Nuchal Translucency Led to the Identification of Novel NUP107 Variants.

Isis Atallah, Katarina Cisarova, Cécile Guenot

|Feb 24, 2024
Impact of neurofibromatosis type 1 on quality of life using the Skindex-29 questionnaire quality of life in NF1.

Ana M Cieza Rivera, Carlos Lobato Fuertes, Tania Fernández-Villa

|Nov 29, 2023
Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome.

Jérémie Courraud, Camille Engel, Angélique Quartier

|Aug 29, 2023
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.

Henry Oppermann, Elia Marcos-Grañeda, Linnea A Weiss

|Jun 23, 2023
Blunted circadian variation of blood pressure in individuals with neurofibromatosis type 1.

Ana M Cieza Rivera, Tania Fernández-Villa, Vicente Martín

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