Ad Geurts van Kessel

Author

Also Known As

A G van Kessel, A Geurts Van Kessel, A Geurts van Kessel, A. G. van Kessel, A. GEURTS VAN KESSEL, A. Geurts Van Kessel, A. Geurts van Kessel, A.G. van Kessel, A.Geurts van Kessel, AD GEURTS VAN KESSEL

377

Publications

22.2K

Citations

H-Index

168

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Erasmus University Rotterdam University of Groningen University Medical Center Groningen

About

Ad Geurts van Kessel is an author at Radboud University Nijmegen specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	53	120	15.3K
2	Natural Sciences	12	12	2.2K
3	Health Sciences	10	10	1.9K
4	Public Health	8	8	498
5	Engineering	2	2	96

Ad Geurts van Kessel

193

Publications

20.1K

Citations

H-Index

Page 1

	Year	Citations
A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia Annelies de Klein, Ad Geurts van Kessel, Gerard C. Grosveld, Nature Chronic Myelocytic LeukaemiaChromatinCellular OncogeneHematological MalignancyCytogenetics	1982	1.4K
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome Lisenka E.L.M. Vissers, Conny M.A. van Ravenswaaij, R.J.C. Admiraal, Nature Genetics ChromatinGenetic DisorderGeneticsCharge SyndromeMolecular Biology	2004	1.3K
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 Marjolijn J. L. Ligtenberg, Roland P. Kuiper, Tsun Leung Chan, Nature Genetics Heritable Somatic MethylationSomatic VariantMendelian DisorderGenetic DisorderMedicine	2008	803
Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia Claus R. Bartram, Annelies de Klein, Anne Hagemeijer, Nature Chronic Myelocytic LeukaemiaChromatinHematological MalignancyPhiladelphia ChromosomeHematology	1983	760
Acquired mutations in TET2 are common in myelodysplastic syndromes Saskia Langemeijer, Roland P. Kuiper, M Berends, Nature Genetics Hematological MalignancyGenetic DisorderMedicineGeneticsHematology	2009	740
Diagnostic Genome Profiling in Mental Retardation Bert B.A. de Vries, Rolph Pfundt, M.A.R. Leisink, The American Journal of Human Genetics PsychiatryGeneticsPsychiatric GeneticsSchizophreniaGenomics	2005	603
Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities Lisenka E.L.M. Vissers, Bert B.A. de Vries, Kazutoyo Osoegawa, The American Journal of Human Genetics Dna SequencingSequencingNext-generation SequencingGeneticsPathology	2003	471
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism David A. Koolen, Lisenka E.L.M. Vissers, Rolph Pfundt, Nature Genetics Genetic DisorderGeneticsCommon Inversion PolymorphismHuman PolymorphismPathology	2006	466
CHARGE syndrome: the phenotypic spectrum of mutations in the <i>CHD7</i> gene M.C.J. Jongmans, R.J.C. Admiraal, Kim P. van der Donk, Journal of Medical Genetics	2005	458
Cloning, structure and expression of a cDNA encoding the human androgen receptor Jan Trapman, Paul Klaassen, George G. J. M. Kuiper, Biochemical and Biophysical Research Communications Systems BiologyEndocrine MechanismHormonal ReceptorReceptor (Biochemistry)Human Androgen Receptor	1988	374

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