Kolexia
Randrianaivo Hanitra
Génétique médicale
Hôpital Saint Pierre
Saint-Pierre, France
64 Activités
88 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Malformations Cardiopathies congénitales Mort foetale Mortinatalité Anomalies morphologiques congénitales des membres Complications de la grossesse Complications infectieuses de la grossesse Prédisposition génétique à une maladie Syndrome de Down

Industries

Sanofi
2 collaboration(s)
Dernière en 2022
Novartis
1 collaboration(s)
Dernière en 2022
AstraZeneca
1 collaboration(s)
Dernière en 2021
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{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

Surveillance of multiple congenital anomalies; searching for new associations.
European journal of human genetics : EJHG   05 décembre 2023
Genetic testing in prolactinomas: a cohort study.
European journal of endocrinology   13 novembre 2023
Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies.
BMJ open   27 juillet 2023
Oncogenetics in the French overseas departments and regions: Situation in Reunion Island.
Bulletin du cancer   12 mai 2023
Amniotic band syndrome and limb body wall complex in Europe 1980-2019.
American journal of medical genetics. Part A   30 décembre 2022
Epidemiology of aplasia cutis congenita: A population-based study in Europe.
Journal of the European Academy of Dermatology and Venereology : JEADV   11 novembre 2022
The medikeye project: The first European study on in utero medicine exposure and congenital anomalies of eyes
Abstracts of the 38th International Conference on Pharmacoepidemiology: Advancing Pharmacoepidemiology and Real‐World Evidence for the Global Community, August 26–28, 2022, Copenhagen, Denmark   23 septembre 2022
QUALI-21: Qualitative Exploratory Study Among Reunionese Women and Their Partners Who Have a Child With Trisomy 21
Essai Clinique (CHU La Réunion)   31 mars 2022
Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT study.
Paediatric and perinatal epidemiology   16 juin 2021
Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders.
Genome medicine   21 mai 2021