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Isis Atallah

8PUBLICATIONS

55CO-AUTHORS

NeurogeneticsCell and nuclear divisionNeurology and neuromuscular diseasesNeonatologyEpigenetics (incl. genome methylation and epigenomics)

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Publications (8)

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|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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Frequent Collaborators

2 joint publications

Amélie Piton

1 joint publications

Raffaele Renella

1 joint publications

Carlo Rivolta

1 joint publications

Sheila Unger

1 joint publications

Andrea Superti-Furga

1 joint publications

Mio Aerden

1 joint publications

Anne-Sophie Denommé-Pichon

1 joint publications

Ange-Line Bruel

1 joint publications

Benoît Mazel

1 joint publications

Christophe Philippe

Frequent Collaborators

2 joint publications

Amélie Piton

1 joint publications

Raffaele Renella

1 joint publications

Carlo Rivolta

1 joint publications

Sheila Unger

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