Research Explorer

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Researcher

Dorien Baetens

Awards & Distinctions

10 Results

2021

Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism

Celien GrijpSimon TavernierJana NeirinckMaha Abdullhadi-AtwanJulie Van De VeldeDorien BaetensHannah VerdinLieve MorbéeElfride De BaereDavid Zangen et al.

2019

Update on the genetics of differences of sex development (DSD)

Dorien BaetensHannah VerdinElfride De BaereMartine Cools

A1 Journal Article in BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

2018

Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development

Dorien BaetensTülay GüranBerenice B MendoncaNathalia L GomesLode De CauwerFrank PeelmanHannah VerdinMarnik VuylstekeMalaïka Van der LindenHans Stoop et al.

A1 Journal Article in GENETICS IN MEDICINE

2017

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development

Dorien BaetensHans StoopFrank PeelmanAnne-Laure TodeschiniToon RosseelFrauke CoppietersReiner VeitiaLeendert LooijengaElfride De BaereMartine Cools

A1 Journal Article in GENETICS IN MEDICINE

Non-coding variation in disorders of sex development

Dorien BaetensBerenice Bilharinho de MendonçaHannah VerdinMartine CoolsElfride De Baere

A1 Journal Article in CLINICAL GENETICS

SeX(X)Y genes : unraveling the molecular pathogenesis of disorders of sex development

Dorien BaetensMartine CoolsElfride De Baere

2016

De genetische revolutie in beeld gebracht : nieuwe diagnostische mogelijkheden voor aandoeningen van de geslachtsontwikkeling

Dorien BaetensMartine CoolsElfride De Baere

A4 Journal Article in GUNAÏKEIA (NEDERLANDSE EDITIE)

2015

Calcium and bone homeostasis in heterozygous carrier's of CYP24A1 mutations: a cross-sectional study

Martine CoolsStefan GoemaereDorien BaetensAnn RaesAn DesloovereJean KaufmanJean De SchepperIvo JansDirk VanderschuerenJaak Billen et al.

A1 Journal Article in BONE

2014

Extensive clinical, hormonal and genetic screening in a large consecutive series of 46, XY neonates and infants with atypical sexual development

Dorien BaetensWilhelm MladenovBarbara Delle ChiaeieBjörn MentenAn DesloovereVioleta IotovaBert CallewaertErik Van LaeckePiet HoebekeElfride De Baere et al.

A1 Journal Article in ORPHANET JOURNAL OF RARE DISEASES

2013

Forkhead transcription factors in genetic disease

Dorien BaetensHannah VerdinMartine CoolsElfride De Baere

Bookchapter in eLS