Ilse M. van der Werf

Author

University of Antwerp

Also Known As

I.M. van der Werf, Ilse M van der Werf, Ilse M. van der Werf

Publications

426

Citations

H-Index

Concepts

All Affiliations

University of Antwerp Antwerp University Hospital Ghent University Hospital Radboud University Nijmegen Radboud University Medical Center

About

Ilse M. van der Werf is an author at University of Antwerp specializing in medicine, genetics, and systems biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	383
2	Health Sciences	2	2	71
3	Engineering	1	1	16
4	Social Sciences	1	1	177
5	Biostatistics	1	1	16

Ilse M. van der Werf

Publications

421

Citations

H-Index

Page 1

	Year	Citations
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP Anke Van Dijck, Anneke T. Vulto‐van Silfhout, Elisa Cappuyns, Biological Psychiatry Neurodevelopmental DisordersDevelopmental BiologyMendelian DisorderBrain DevelopmentComplex Neurodevelopmental Disorder	2018	177
Novel microdeletions on chromosome 14q32.2 suggest a potential role for non-coding RNAs in Kagami-Ogata syndrome Ilse M. van der Werf, Karin Buiting, Johanna Christina Czeschik, European Journal of Human Genetics ChromatinGene Deletion DataDevelopmental BiologyChromosome 14Q32.2Cytogenetics	2016	62
Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities Anke Van Dijck, Ilse M. van der Werf, Edwin Reyniers, European Journal of Medical Genetics Triplication Show MacrocephalyChromatinChromosome 1Q21.1CytogeneticsMedicine	2015	48
New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome Jasmin Beygo, Alma Küchler, Gabriele Gillessen‐Kaesbach, European Journal of Human Genetics Imprinted Meg8-dmrMendelian DisorderGenetic DisorderPathologyDegenerative Disease	2017	43
Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability Ilse M. van der Werf, Anke Van Dijck, Edwin Reyniers, Gene Mendelian DisorderGenetic DisorderLarge PedigreesGeneticsFragile X Spectrum	2016	37
Behavioural characterization of AnkyrinG deficient mice, a model for ANK3 related disorders Ilse M. van der Werf, Debby Van Dam, Stephan Missault, Behavioural Brain Research Knockout MouseClinical DisordersSignal TransductionAnkyring Deficient MiceBehavioural Characterization	2017	23
A Robust Protocol to Increase NimbleGen SeqCap EZ Multiplexing Capacity to 96 Samples Ilse M. van der Werf, R. Frank Kooy, Geert Vandeweyer PLoS ONE EngineeringGeneticsGenomicsHigh Throughput SequencingTargeted Enrichment	2015	16
RNA‐Seq detects a <i>SAMD12‐EXT1</i> fusion transcript and leads to the discovery of an <i>EXT1</i> deletion in a child with multiple osteochondromas Gavin R. Oliver, Patrick R. Blackburn, Marissa S. Ellingson, Molecular Genetics & Genomic Medicine	2019	15

Page 1