Author

Mircea Cretu-Stancu

Utrecht University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Sara L. PulitiD· 2 shared Wigard P. KloostermaniD· 2 shared Alejandro Fonollosa· 1 shared Alfredo AdániD· 1 shared Ana MárqueziD· 1 shared Anneke I. den HollanderiD· 1 shared Bobby P.C. KoelemaniD· 1 shared Carel B. HoyngiD· 1 shared

Activity by Year

2017-2018 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetics

Sara L. PulitORCID

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Author profile →

3 papers

Recent·Most cited

Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis.

Jonas J. W. Kuiper, Jessica van Setten, Matthew A.M. Devall, Mircea Cretu-Stancu, Sanne Hiddingh, Roel A. Ophoff, Tom Missotten, Mirjam E. J. van Velthoven, Anneke I. den Hollander, Carel B. Hoyng, Edward James, Emma Reeves, Miguel Cordero‐Coma, Alejandro Fonollosa, Alfredo Adán, , Timothy R. D. J. Radstake

This study identifies functionally distinct ERAP1 and ERAP2 haplotypes associated with Birdshot Uveitis and shows their combined effect enhances disease risk.

Human Molecular Genetics · Sep 10, 2018Peer-reviewedGenetics

No evidence that mate choice in humans is dependent on the MHC

Mircea Cretu-Stancu, Wigard P. Kloosterman, Sara L. Pulit

The paper analyzes 239 Dutch mate-pairs with whole-genome sequences to test if MHC genetic variation influences mate selection, finding no evidence of MHC-dependent mate choice.

bioRxiv · Jun 4, 2018 · PreprintGenetics

Mapping And Phasing Of Structural Variation In Patient Genomes Using Nanopore Sequencing

Mircea Cretu-Stancu, Markus J. van Roosmalen, Ivo Renkens, Marleen M. Nieboer, Sjors Middelkamp, Joep de Ligt, Giulia Pregno, Daniela Francesca Giachino, Giorgia Mandrile, Jose Espejo Valle-Inclán, Jerome Korzelius, Ewart de Bruijn, Edwin P. J. G. Cuppen, Michael E. Talkowski, Tobias Marschall, , Wigard P. Kloosterman

This study uses nanopore sequencing to detect and phase structural variants in patient genomes, identifying novel variants missed by short-read sequencing.

Nature Communications · Oct 31, 2017Peer-reviewedGenomics