Concepedia

Author

Szymon M. Kiełbasa

Leiden University Medical CenterORCID

Also Known As

Kielbasa, S., Kielbasa, Szymon, KiełBasa, Szymon, Kiełbasa, Szymon M., Louise Arseneault, Lude Franke, Maarten van Iterson, Riccardo E. Marioni, Rick Jansen, S Kielbasa

164

Publications

8.4K

Citations

37

H-Index

122

Concepts

All Affiliations

Leiden University Medical CenterErasmus MCUniversity Medical Center GroningenMax Planck Institute for Molecular GeneticsRadboud University Medical Center
SM

About

Szymon M. Kiełbasa is an author at Leiden University Medical Center specializing in medicine, genetics, and functional genomics.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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Public Health

4

4

736

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Natural Sciences

3

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Engineering

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Health Sciences

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Szymon M. Kiełbasa

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63

Publications

6.2K

Citations

34

H-Index

YearCitations

Adaptive seeds tame genomic sequence comparison

Szymon M. Kiełbasa, Raymond Wan, Kengo Sato,

Genome Research

2011

1.4K

Disease variants alter transcription factor levels and methylation of their binding sites

Marc Jan Bonder, René Luijk, Daria V. Zhernakova,

Nature Genetics

2016

544

Identification of context-dependent expression quantitative trait loci in whole blood

Daria V. Zhernakova, Patrick Deelen, Martijn Vermaat,

Nature Genetics

2016

502

Genetic and environmental influences interact with age and sex in shaping the human methylome

Jenny van Dongen, Michel G. Nivard, Gonneke Willemsen,

Nature Communications

2016

410

Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

Eleonora Porcu, Sina Rüeger, Kaido Lepik,

Nature Communications

2019

330

Regulation of Clock-Controlled Genes in Mammals

Katarzyna Bożek, Angela Relógio, Szymon M. Kiełbasa,

PLoS ONE

2009

288

RNA sequencing data integration reveals an miRNA interactome of osteoarthritis cartilage

Rodrigo Coutinho de Almeida, Y.F. Ramos, Ahmed Mahfouz,

Annals of the Rheumatic Diseases

2019

179

Skewed X-inactivation is common in the general female population

Ekaterina Shvetsova, Alina A. Sofronova, Ramin Monajemi,

European Journal of Human Genetics

2018

177

Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations

Sonia Shah, Marc Jan Bonder, Riccardo E. Marioni,

The American Journal of Human Genetics

2015

154

Mutations in PIGO, a Member of the GPI-Anchor-Synthesis Pathway, Cause Hyperphosphatasia with Mental Retardation

Peter Krawitz, Yoshiko Murakami, Jochen Hecht,

The American Journal of Human Genetics

2012

143

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