Barbara D′haene - Concepedia

Author

Barbara D′haene

Ghent University Hospital

Also Known As

B D'HAENE, B. D'haene, Barbara D'Haene, Barbara D'haene, Barbara D’haene, Barbara D′haene

Publications

Citations

H-Index

Concepts

All Affiliations

Ghent University Hospital University Medical Center Groningen University of Liège Institut Jacques Monod Délégation Paris 7

About

Barbara D′haene is an author at Ghent University Hospital specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	55
2	Molecular Genetics	2	2	39
3	Engineering	1	1	23
4	Neurology	1	1	16
5	Pathology	1	1	16

Barbara D′haene

Publications

685

Citations

H-Index

Page 1

	Year	Citations
miRNA Expression Profiling: From Reference Genes to Global Mean Normalization Barbara D′haene, Pieter Mestdagh, Jan Hellemans, Methods in molecular biology	2011	167
Renal micro<scp>RNA</scp>‐ and <scp>RNA</scp>‐profiles in progressive chronic kidney disease Michael A. Rudnicki, Paul Perco, Barbara D′haene, European Journal of Clinical Investigation	2015	109
Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening Barbara D′haene, Catia Attanasio, Diane Beysen, PLoS Genetics	2009	92
Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain Hannah Verdin, Barbara D′haene, Diane Beysen, PLoS Genetics	2013	90
Expanding the Spectrum of<i>FOXC1</i>and<i>PITX2</i>Mutations and Copy Number Changes in Patients with Anterior Segment Malformations Barbara D′haene, Françoise Meire, Ilse Claerhout, Investigative Ophthalmology & Visual Science	2010	87
Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G) Bérénice A. Benayoun, Sandrine Caburet, Aurélie Dipietromaria, PLoS ONE	2010	70
<i>FOXL2</i>copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions Barbara D′haene, Julián Nevado, M. Pugeat, Human Mutation EngineeringMolecular PathogenesisGeneticsMolecular GeneticsDisease Gene Identification	2010	23
Structural and numerical changes of chromosome X in patients with esophageal atresia Erwin Brosens, Elisabeth M. de Jong, Tahsin Stefan Barakat, European Journal of Human Genetics EsophagusEsophageal CancerEsophageal AtresiaCytogeneticsGenetics	2014	16
Identification of copy number variants associated with BPES-like phenotypes Antoinet C.J. Gijsbers, Barbara D′haene, Yvonne Hilhorst‐Hofstee, Human Genetics Developmental AnomalyDevelopmental BiologyGenotype-phenotype AssociationMendelian DisorderGenetic Disorder	2008	16
Improved Molecular Diagnostics of Idiopathic Short Stature and Allied Disorders: Quantitative Polymerase Chain Reaction-Based Copy Number Profiling of SHOX and Pseudoautosomal Region 1 Barbara D′haene, Jan Hellemans, Margarita Craen, The Journal of Clinical Endocrinology & Metabolism	2010	15

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