Petra de Vries - Concepedia

Author

Petra de Vries

Also Known As

P DEVRIES, P De Vries, P de Vries, P. D. Vries, P. DE VRIES, P. De Vries, P. de Vries, PETRA DE VRIES, PETRA de VRIES, Petra De Vries

Publications

6.6K

Citations

H-Index

105

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center National Institute for Public Health and the Environment Maastricht University Medical Centre Erasmus University Rotterdam

About

Petra de Vries is an author at Radboud University Nijmegen specializing in medicine, immunology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	27	3.7K
2	Engineering	3	3	66
3	Social Sciences	3	3	918
4	Health Sciences	2	2	131
5	Natural Sciences	1	1	238

Petra de Vries

Publications

5.7K

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
A de novo paradigm for mental retardation Lisenka E.L.M. Vissers, Joep de Ligt, Christian Gilissen, Nature Genetics Cognitive SciencePsychiatrySyndromic AutismSchizophreniaAutism	2010	849
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
Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta Jutta Becker, Oliver Semler, Christian Gilissen, The American Journal of Human Genetics SclerostinDevelopmental BiologyMendelian DisorderGenetic DisorderHuman Serpinf1	2011	354
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome Alexander Hoischen, Bregje W.M. van Bon, Benjamín Rodríguez‐Santiago, Nature Genetics Somatic VariantAutoimmune DiseaseMendelian DisorderGenetic DisorderGenetics	2011	277
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
Diagnostic Exome Sequencing in Persons With Severe Intellectual Disability Joep de Ligt, Marjolein H. Willemsen, Bregje W.M. van Bon, Obstetrical & Gynecological Survey Intellectual ImpairmentMendelian DisorderPsychiatryGenetic DisorderExome Sequencing	2013	201
Cantú Syndrome Is Caused by Mutations in ABCC9 Bregje W.M. van Bon, Christian Gilissen, Dorothy K. Grange, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathology	2012	166
Protective Immunity in Macaques Vaccinated with Live Attenuated, Recombinant, and Subunit Measles Vaccines in the Presence of Passively Acquired Antibodies Rob van Binnendijk, Martien C. M. Poelen, Geert van Amerongen, The Journal of Infectious Diseases VaccinationSubunit Measles VaccinesVaccine DevelopmentVaccine TargetImmunology	1997	133
Measles virus transmembrane fusion protein synthesized de novo or presented in immunostimulating complexes is endogenously processed for HLA class I- and class II-restricted cytotoxic T cell recognition. Rob van Binnendijk, Carel A. van Baalen, Martien C. M. Poelen, The Journal of Experimental Medicine Molecular VirologyNeurovirologyHla ImmunogeneticsImmunologyAntiviral Response	1992	126

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