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List of works by Hanitra Randrianaivo

Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe

scientific article published on 31 May 2018

Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study

scientific article published on 11 December 2017

Case report: a prenatal case of Jarcho-Levin syndrome diagnosed during the first trimester of pregnancy

scientific article published in February 2003

Chikungunya virus-associated encephalitis: A cohort study on La Réunion Island, 2005-2009.

scientific article published on May 2016

Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

scientific article published on 2 July 2015

Congenital Zika syndrome: time to move from case series to case-control studies and data sharing

scientific article published on 14 September 2016

Congenital heart defects in La Réunion Island: a 6-year survey within a EUROCAT-affiliated congenital anomalies registry ⬇️

scientific article published on February 13, 2012

Cost and outcomes of the ultrasound screening program for birth defects over time: a population-based study in France

scientific article published on 20 July 2020

Discordant malformations in monochorionic twins: a retrospective cohort study in La Reunion Island

scientific article published on 25 March 2019

Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study

scientific article published on 12 July 2019

Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study

scientific article published on 26 June 2019

Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study.

scientific article published on 19 November 2014

Epidemiology of hypospadias in Europe: a registry-based study

scientific article

Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study

scholarly article by Ester Garne et al published September 2018 in European Journal of Medical Genetics

Epidemiology of small intestinal atresia in Europe: a register-based study

scholarly article by Kate E Best et al published 29 August 2012 in Archives of Disease in Childhood. Fetal and Neonatal Edition

Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data

scientific article

Expanding the clinical spectrum of B4GALT7 deficiency: homozygous p.R270C mutation with founder effect causes Larsen of Reunion Island syndrome

scientific article

Fetal fibrochondrogenesis at 26 weeks' gestation

scientific article

Gastroschisis in Europe - A Case-malformed-Control Study of Medication and Maternal Illness during Pregnancy as Risk Factors

scientific article published on 25 August 2017

High prevalence of Bardet-Biedl syndrome in La Réunion Island is due to a founder variant in ARL6/BBS3

scientific article published on 03 May 2020

Hirschsprung's disease prevalence in Europe: a register based study

scientific article

Low clinical burden of 2009 pandemic influenza A (H1N1) infection during pregnancy on the island of La Réunion

scientific article

Major congenital anomalies in babies born with Down syndrome: A EUROCAT population-based registry study

article by Joan K. Morris et al published 24 September 2014 in American Journal of Medical Genetics

Maternal risk factors for the VACTERL association: A EUROCAT case-control study

scientific article published on 22 April 2020

Multidisciplinary Prospective Study of Mother-to-Child Chikungunya Virus Infections on the Island of La Réunion

scientific article (publication date: 18 March 2008)

Pregnancy outcomes of Q fever: prospective follow-up study on Reunion island.

scientific article published on 27 November 2019

Prevalence of microcephaly in Europe: population based study

scientific article (publication date: 2016)

Recent decrease in the prevalence of congenital heart defects in Europe

scientific article published on 24 July 2012

Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome.

scientific article published on 12 January 2018

Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

scientific article published on 09 September 2019

Spectrum of the mutations in Bernard-Soulier syndrome

scientific article

Treacher Collins syndrome: a clinical and molecular study based on a large series of patients.

scientific article published on 19 March 2015

Trends in congenital anomalies in Europe from 1980 to 2012.

scientific article

Trends in resource use and effectiveness of ultrasound detection of fetal structural anomalies in France: a multiple registry-based study

article

Use of hierarchical models to analyze European trends in congenital anomaly prevalence

scientific article

[Early maternal-fetal transmission of the Chikungunya virus]

scientific article published on 01 November 2006

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