Hanitra Randrianaivo

Author

Inserm

Also Known As

H Randrianaivo, H. Randrianaivo, Hanitra Randrianaivo, Hanitra Randrianaivo (248063), Randrianaivo, Hanitra

Publications

Citations

H-Index

Concepts

All Affiliations

Inserm Health Service Executive Centre Hospitalier Universitaire de La Réunion Children's Hospital Zagreb University Medical Center Groningen

About

Hanitra Randrianaivo is an author at Inserm specializing in medicine, pediatrics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	464
2	Molecular Genetics	2	2	95
3	Family Medicine	1	1	82
4	Nephrology	1	1	83
5	Obstetrics	1	1	46

Hanitra Randrianaivo

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
Multidisciplinary Prospective Study of Mother-to-Child Chikungunya Virus Infections on the Island of La Réunion Patrick Gérardin, G. Barau, Alain Michault, PLoS Medicine	2008	498
Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study M McGivern, Kate Best, Judith Rankin, Archives of Disease in Childhood Fetal & Neonatal	2014	307
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data Breidge Boyle, Marie‐Claude Addor, Larraitz Arriola, Archives of Disease in Childhood Fetal & Neonatal	2017	210
Epidemiology of small intestinal atresia in Europe: a register-based study Kate Best, Peter W. G. Tennant, Marie‐Claude Addor, Archives of Disease in Childhood Fetal & Neonatal	2012	167
Trends in congenital anomalies in Europe from 1980 to 2012 Joan K. Morris, Anna Springett, Ruth Greenlees, PLoS ONE	2018	158
Epidemiology of hypospadias in Europe: a registry-based study Jorieke E. H. Bergman, Maria Loane, Martine Vrijheid, World Journal of Urology	2015	127
Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease Marie‐Pierre Audrézet, Christine Corbiere, Saïd Lebbah, Journal of the American Society of Nephrology Mendelian DisorderPkd2 Mutation AnalysisMedicineGeneticsRenal Pathology	2015	83
Major congenital anomalies in babies born with Down syndrome: A EUROCAT population‐based registry study Joan K. Morris, Ester Garne, Diana Wellesley, American Journal of Medical Genetics Part A Family MedicineCongenital Heart AnomalyDefectsNewborn ScreeningCongenital Disorders	2014	82
Prevalence of microcephaly in Europe: population based study Joan K. Morris, Judith Rankin, Ester Garne, BMJ	2016	82
Hirschsprung's disease prevalence in Europe: A register based study Kate Best, Marie‐Claude Addor, Larraitz Arriola, Birth Defects Research Part A Clinical and Molecular Teratology	2014	81

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