Frank Speleman - Concepedia

Author

Frank Speleman

Also Known As

F Speleman, F. Speleman, FRANK SPELEMAN, Frank Speleman, Frank Speleman (800), Franki Speleman, James Nicholson, Jo Vandesompele, Katleen De Preter, Liselot Mus

814

Publications

26.4K

Citations

H-Index

174

Concepts

All Affiliations

Ghent University Hospital Ghent University KU Leuven University of Amsterdam Heidelberg University

About

Frank Speleman is an author at Ghent University Hospital specializing in medicine, cell biology, and tumor biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	51	117	12.6K
2	Engineering	10	11	1.1K
3	Natural Sciences	10	10	524
4	Health Sciences	5	5	323
5	Public Health	3	3	206

Frank Speleman

239

Publications

23.5K

Citations

H-Index

Page 1

	Year	Citations
Identification of ALK as a major familial neuroblastoma predisposition gene Yaël P. Mossé, Marci Laudenslager, Luca Longo, Nature Genetic DisorderGeneticsPathologyNeuroblastsNeuropathology	2008	1.4K
miR-9, a MYC/MYCN-activated microRNA, regulates E-cadherin and cancer metastasis Li Ma, Jennifer J. Young, Harsha Prabhala, Nature Cell Biology Tumor BiologyMedicineMyc/mycn-activated MicrornaSmall RnaMicrorna Detection	2010	1.3K
A novel and universal method for microRNA RT-qPCR data normalization Pieter Mestdagh, Pieter Van Vlierberghe, An De Weer, Genome biology	2009	1K
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsLoss-of-function Mutations	2003	825
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Heather C. Mefford, Andrew J. Sharp, Carl Baker, New England Journal of Medicine	2008	803
RNA G-quadruplexes cause eIF4A-dependent oncogene translation in cancer Andrew L. Wolfe, Kamini Singh, Philipp Drewe, Nature MedicineCancer Cell BiologyCancer GeneticsGene ExpressionCancer Biology	2014	617
Exhaustive mutation analysis of theNF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects Ludwine Messiaen, Tom Callens, Geert Mortier, Human Mutation	2000	496
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis Jan Hellemans, Olena Preobrazhenska, Andy Willaert, Nature Genetics Lemd3 ResultDevelopmental BiologySclerostinBone Morphogenic ProteinPathogenesis	2004	454
International consensus for neuroblastoma molecular diagnostics: report from the International Neuroblastoma Risk Group (INRG) Biology Committee Peter F. Ambros, I.M. Ambros, G M Brodeur, British Journal of Cancer Prognostic BiomarkersNeuroblastoma Treatment PlanningMedicineInternational ConsensusPathology	2009	397
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome Bregje W.M. van Bon, Heather C. Mefford, Björn Menten, Journal of Medical Genetics	2009	366

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