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Henriette A. Delemarre-van de Waal
Researcher at Leiden University Medical Center
Publications - 114
Citations - 9369
Henriette A. Delemarre-van de Waal is an academic researcher from Leiden University Medical Center. The author has contributed to research in topics: Body mass index & Birth weight. The author has an hindex of 49, co-authored 114 publications receiving 8637 citations. Previous affiliations of Henriette A. Delemarre-van de Waal include Council on Education for Public Health & VU University Amsterdam.
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Journal ArticleDOI
Endocrine Treatment of Transsexual Persons: An Endocrine Society Clinical Practice Guideline
Wylie C. Hembree,Peggy T. Cohen-Kettenis,Henriette A. Delemarre-van de Waal,Henriette A. Delemarre-van de Waal,Louis J. G. Gooren,Walter J. Meyer,Norman P. Spack,Vin Tangpricha,Victor M. Montori +8 more
TL;DR: This evidence-based guideline was developed using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) system to describe the strength of recommendations and the quality of evidence, which was low or very low.
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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Catherine Dodé,Jacqueline Levilliers,Jean-Michel Dupont,Anne De Paepe,Nathalie Le Dû,Nadia Soussi-Yanicostas,Roney S. Coimbra,Sedigheh Delmaghani,Sylvie Compain-Nouaille,Françoise Baverel,Christophe Pêcheux,Dominique Le Tessier,Corinne Cruaud,Marc Delpech,Frank Speleman,Stefan Vermeulen,Andrea Amalfitano,Yvan Bachelot,Philippe Bouchard,Sylvie Cabrol,Jean-Claude Carel,Henriette A. Delemarre-van de Waal,Barbara Goulet-Salmon,Marie-Laure Kottler,Odile Richard,Franco Sánchez-Franco,Robert Saura,Jacques Young,Christine Petit,Jean-Pierre Hardelin +29 more
TL;DR: It is established here that loss- of-function mutations in FGFR1 underlie KAL2 whereas a gain-of-function mutation inFGFR1 has been shown to cause a form of craniosynostosis and suggested that the KAL1 gene product, the extracellular matrix protein anosmin-1, is involved in FGF signaling.
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The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
Renaud Legouis,Jean-Pierre Hardelin,Jacqueline Levilliers,Jean-Michel Claverie,Sylvia Compain,Véronique Wunderle,Véronique Wunderle,Philippe Millasseau,Philippe Millasseau,Denis Le Paslier,Daniel Cohen,Dominique Caterina,Lydie Bougueleret,Henriette A. Delemarre-van de Waal,Georges Lutfalla,Jean Weissenbach,Christine Petit +16 more
TL;DR: Two candidate exons, identified by multiparameter computer programs, were found in a cDNA encoding a protein of 679 amino acids that encodes a putative adhesion molecule, consistent with the defect of embryonic neuronal migration.
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Cardiometabolic differences in children born after in vitro fertilization: follow-up study.
Manon Ceelen,Mirjam M. van Weissenbruch,Jan P.W. Vermeiden,Flora E. van Leeuwen,Henriette A. Delemarre-van de Waal +4 more
TL;DR: The findings highlight the importance of continued cardiometabolic monitoring of IVF-conceived children and might contribute to current knowledge about periconceptional influences and their consequences in later life.
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Glucose tolerance, insulin sensitivity, and insulin secretion in children born small for gestational age.
TL;DR: During oral glucose tolerance tests, no differences were found in glucose tolerance and beta-cell function between the SGA and AGA groups, however, the hyperinsulinemic clamp showed a reduced insulin sensitivity in SGA children, which may contribute to the enhanced risk of developing NIDDM in adult life.