Willy M. Nillesen - Concepedia

Author

Willy M. Nillesen

Also Known As

Lemmink, Henny H., Nillesen, W., Nillesen, Willy M., W M Nillesen, W Nillesen, W. M. Nillesen, W. Nillesen, W.M. Nillesen, Willy M Nillesen, Willy M. Nillesen

Publications

5.7K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center University Medical Center Groningen Inserm Maastricht University

About

Willy M. Nillesen is an author at Radboud University Nijmegen specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	27	3.2K
2	Natural Sciences	4	4	929
3	Public Health	2	2	33
4	Engineering	1	1	18
5	Health Sciences	1	1	46

Willy M. Nillesen

Publications

5.1K

Citations

H-Index

Page 1

	Year	Citations
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
Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome Tjitske Kleefstra, Han G. Brunner, Jeanne Amiel, The American Journal of Human Genetics Histone ModificationsChromatinGene Deletion DataChromatin StructureSubtelomeric Deletion Syndrome	2006	395
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
Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability Tjitske Kleefstra, Jamie M. Kramer, Kornelia Neveling, The American Journal of Human Genetics Histone ModificationsChromatinChromatin StructureChromatin RemodelingNatural Sciences	2012	267
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of <i>EHMT1</i> haploinsufficiency to the core phenotype Tjitske Kleefstra, W. A. van Zelst‐Stams, Willy M. Nillesen, Journal of Medical Genetics	2009	257
Heterozygous Germline Mutations in the CBL Tumor-Suppressor Gene Cause a Noonan Syndrome-like Phenotype Simone Martinelli, Alessandro De Luca, Emilia Stellacci, The American Journal of Human Genetics Tumor BiologySomatic VariantMendelian DisorderGenetic DisorderGenetics	2010	254
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome David A. Koolen, Jamie M. Kramer, Kornelia Neveling, Nature Genetics ChromatinGenome InstabilityGene Deletion DataChromatin StructureMicrodeletion Syndrome	2012	238
Chromosome 1p21.3 microdeletions comprising <i>DPYD</i> and <i>MIR137</i> are associated with intellectual disability Marjolein H. Willemsen, Astrid Vallès, Laurens A. M. H. Kirkels, Journal of Medical Genetics	2011	202
Update on Kleefstra Syndrome Marjolein H. Willemsen, Anneke T. Vulto‐van Silfhout, Willy M. Nillesen, Molecular Syndromology Down SyndromeChromatinDevelopmental BiologyMendelian DisorderEndocrine Disease	2011	178
Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation Marjolijn C.J. Jongmans, Ineke van der Burgt, Peter M. Hoogerbrugge, European Journal of Human Genetics	2011	171

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