Concepedia

Femke Hannes

FH

Statistics

Publications

11

Citations

892

H-Index

11

Active since

2005

Affiliations

KU Leuven(Current)

Sheffield Children's Hospital

University College London

Femke Hannes is an author at KU Leuven specializing in medicine, genetics, and molecular genetics.

Top concepts

Publications per year

2005–2012

11

Publications

11

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

Femke Hannes, Andrew J. Sharp, Heather C. Mefford et al. · Journal of Medical Genetics · 2008 · 346 citations · Full text

Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)

Nicole Maas, Griet Van Buggenhout, Femke Hannes et al. · Journal of Medical Genetics · 2007 · 178 citations · Full text

Nuclear speckles and nucleoli targeting by PIP2–PDZ domain interactions

Eva Mortier, Gunther Wuytens, Iris Leenaerts et al. · The EMBO Journal · 2005 · 103 citations · Full text

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Fine-grained facial phenotype–genotype analysis in Wolf–Hirschhorn syndrome

Peter Hammond, Femke Hannes, Michael Suttie et al. · European Journal of Human Genetics · 2011 · 73 citations · Full text

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Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf–Hirschhorn syndrome

Claudia Kerzendorfer, Femke Hannes, Rita Colnaghi et al. · Human Molecular Genetics · 2012 · 48 citations · Full text

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