Marc Pauper - Concepedia

Author

Marc Pauper

Radboud University Medical Center ORCID

Also Known As

Bradford, Yuki, Hilary C. Martin, M Pauper, M. Pauper, Marc Pauper, Martin, Hilary C., Pauper, Marc, Zmuda, Joseph M.

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

Radboud University Medical Center Radboud University Nijmegen Erasmus MC University of Oulu Leiden University Medical Center

About

Marc Pauper is an author at Radboud University Medical Center specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	959
2	Health Sciences	3	3	235
3	Public Health	2	2	53
4	Engineering	1	1	61
5	Natural Sciences	1	1	347

Marc Pauper

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
A saturated map of common genetic variants associated with human height Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Nature	2022	827
Transposons passively and actively contribute to evolution of the two-speed genome of a fungal pathogen Luigi Faino, Michael Seidl, Xiaoqian Shi‐Kunne, Genome Research Comparative GenomicsGeneticsMolecular GeneticsGenomicsMolecular Ecology	2016	347
Optical genome mapping enables constitutional chromosomal aberration detection Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard, The American Journal of Human Genetics ChromatinSpectral KaryotypingOptical Genome MappingGeneticsChromosomal Rearrangement	2021	239
Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping Kornelia Neveling, Tuomo Mantere, Susan Vermeulen, The American Journal of Human Genetics ChromatinNext-generation CytogeneticsSomatic VariantHealth SciencesTumor Heterogeneity	2021	185
Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation Laura Lorés‐Motta, Constantin C. Paun, Jordi Corominas, Ophthalmology	2018	66
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids Shweta Ramdas, Jonathan Judd, Sarah E. Graham, The American Journal of Human Genetics BioinformaticsGenetic AnalysisAllelic VariantEngineeringMolecular Ecology	2022	61
Long-read trio sequencing of individuals with unsolved intellectual disability Marc Pauper, Erdi Küçük, Aaron M. Wenger, European Journal of Human Genetics	2020	55
The Functional Effect of Rare Variants in Complement Genes on C3b Degradation in Patients With Age-Related Macular Degeneration Maartje J. Geerlings, Mariann Kremlitzka, Bjorn Bakker, JAMA Ophthalmology	2016	53
Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch’s Membrane Jordi Corominas, Johanna M. Colijn, Maartje J. Geerlings, Ophthalmology	2018	43
Association of Genetic Variants With Response to Anti–Vascular Endothelial Growth Factor Therapy in Age-Related Macular Degeneration Laura Lorés‐Motta, Moeen Riaz, Michelle Grunin, JAMA Ophthalmology	2018	42

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