Christian Gilissen - Concepedia

Author

Christian Gilissen

Also Known As

Bart van de Warrenburg, C Gilissen, C. Gilissen, Christian Gilissen, Christian gilissen, Cornelius Boerkel, Dylan Henssen, Gilissen, C, Gilissen, C., Gilissen, Christian

352

Publications

27.6K

Citations

H-Index

217

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Radboud Institute for Molecular Life Sciences Maastricht University University Medical Center

About

Christian Gilissen is an author at Radboud University Nijmegen specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	63	106	14.4K
2	Public Health	13	14	1.3K
3	Natural Sciences	7	7	1.4K
4	Engineering	6	6	264
5	Health Sciences	4	4	198

Christian Gilissen

197

Publications

23.3K

Citations

H-Index

Page 1

	Year	Citations
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability Joep de Ligt, Marjolein H. Willemsen, Bregje W.M. van Bon, New England Journal of Medicine	2012	1.6K
Genome sequencing identifies major causes of severe intellectual disability Christian Gilissen, Jayne Y. Hehir‐Kwa, Djie Tjwan Thung, Nature Intellectual ImpairmentGeneticsSevere Intellectual DisabilityDisease Gene IdentificationGenomics	2014	1.1K
A de novo paradigm for mental retardation Lisenka E.L.M. Vissers, Joep de Ligt, Christian Gilissen, Nature Genetics Cognitive SciencePsychiatrySyndromic AutismSchizophreniaAutism	2010	849
Presence of Genetic Variants Among Young Men With Severe COVID-19 Caspar I. van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers, JAMA	2020	822
<i>STAT1</i> Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis Frank L. van de Veerdonk, Theo S. Plantinga, Alexander Hoischen, New England Journal of Medicine	2011	653
De novo mutations of SETBP1 cause Schinzel-Giedion syndrome Alexander Hoischen, Bregje W.M. van Bon, Christian Gilissen, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMedicine	2010	504
A recent bottleneck of Y chromosome diversity coincides with a global change in culture Monika Karmin, Lauri Saag, Mário Vicente, Genome Research	2015	484
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Catherine A. Brownstein, Alan H. Beggs, Nils Homer, Genome biology	2014	432
A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer Robbert D.A. Weren, Marjolijn J. L. Ligtenberg, C. Marleen Kets, Nature Genetics Genome InstabilityMedicineGeneticsColorectal CancerPathology	2015	372
Parent-of-origin-specific signatures of de novo mutations Jakob M. Goldmann, Wendy S.W. Wong, Michele Pinelli, Nature Genetics Somatic VariantGeneticsMolecular GeneticsParent-of-origin-specific SignaturesDisease Gene Identification	2016	359

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