Author

Pieter B. T. Neerincx

University Medical Center GroningenORCID 0000-0002-9800-8638Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Research Focus:variant calling· 2 Approach:benchmark study· 1 Research Focus:GWAS / association mapping· 1 Assay:metagenomics· 1

Frequent Co-Authors

Cisca WijmengaiD· 2 shared Morris A. SwertziD· 2 shared Patrick DeeleniD· 2 shared Abdel AbdellaouiiD· 1 shared Adriaan van der GraafiD· 1 shared Albert Hofman DiD· 1 shared Alexander KurilshikoviD· 1 shared Alexandra ZhernakovaiD· 1 shared

Activity by Year

2018-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Cisca WijmengaORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

GeneticsNature GeneticsPeer-reviewedFeb 1, 2022

Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project

Esteban A. Lopera-Maya, Alexander Kurilshikov, Adriaan van der Graaf…·Alexandra Zhernakova

The paper identifies host genetic loci associated with gut microbiome composition and function in a large cohort, finding significant associations near LCT and ABO genes.

553 citationstop 1%

humanmetagenomics

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GeneticsBrainPeer-reviewedOct 29, 2018

Integrated Clinical and Omics Approach to Rare Diseases: Novel Genes and Oligogenic Inheritance in Holoprosencephaly

Artem Kim, Clara Savary, Christèle Dubourg…·Tania Attié‐Bitach

This study identifies novel HPE genes and oligogenic inheritance patterns in holoprosencephaly by integrating clinical data with exome sequencing and gene prioritization.

62 citationstop 2%

humanwhole-exome sequencing

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GenomicsNature GeneticsPeer-reviewedMar 1, 2018

Germline De Novo Mutation Clusters Arise During Oocyte Aging In Genomic Regions With Increased Double-Strand Break Incidence

Jakob M. Goldmann, Vladimir B. Seplyarskiy, Wendy S.W. Wong…·John E. Niederhuber

The paper identifies maternal age-related mutation clusters in germline de novo mutations linked to double-strand break processes.

89 citationstop 3%

humanwhole-genome sequencing

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