Noémi Dahan-Oliel

29PUBLICATIONS
208CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Haematological tumoursInfant and child healthRehabilitationEpigenetics (incl. genome methylation and epigenomics)
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Publications (29)

|Jul 16, 2026
Two Novel ACTC1 Variants Cause Arthrogryposis Multiplex Congenita.

|Jun 26, 2026
The International Consortium for Arthrogryposis: A Collaborative Framework for Early Detection, Care, Research, and Education.

|Mar 16, 2026
Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors.

Ahlam Zidan, Sophia C Pasia, Emmanouil Rampakakis

|Oct 27, 2025
Implementation of a knowledge translation strategy to promote early evidence-based rehabilitation for children with cerebral palsy.

Jessica Hanson, Annette Majnemer, Keiko Shikako

|Oct 22, 2025
Psychometric properties of functional mobility outcome measures in children with arthrogryposis multiplex congenita.

Ahlam Zidan, Laurie Snider, Emmanouil Rampakakis

|Apr 03, 2025
Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita.

Shahrzad Nematollahi, Reggie C Hamdy, Harold van Bosse

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Frequent Collaborators

7 joint publications

Shahrzad Nematollahi

7 joint publications

Reggie Hamdy

6 joint publications

Bonita Sawatzky

5 joint publications

Klaus Dieterich