Author

Şehime Gülsün Temel

Bursa Uludağ Üni̇versi̇tesi̇ORCID 0000-0002-9802-0880Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adrian M. E. PilatziD· 1 shared Albrecht RöpkeiD· 1 shared Alexandra Manuel LopesiD· 1 shared Burcu TürkgençiD· 1 shared Corinna FriedrichiD· 1 shared Daniela FietziD· 1 shared Donald F. ConradiD· 1 shared Filipa CarvalhoiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Adrian M. E. PilatzORCID

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1 paper

Recent·Most cited

Biallelic mutations in M1AP are a frequent cause of meiotic arrest leading to male infertility

Margot Julia Wyrwoll, Şehime Gülsün Temel, Liina Nagirnaja, Manon S. Oud, Alexandra Manuel Lopes, Godfried W. van der Heijden, James S. Heald, Nadja Rotte, Joachim Wistuba, Marius Wöste, Susanne Ledig, Henrike Krenz, Roos Marthe Smits, Filipa Carvalho, João Gonçalves, , Frank Tüttelmann

The paper identifies biallelic M1AP mutations as a cause of meiotic arrest and male infertility through whole exome sequencing and cohort screening.

The American Journal of Human Genetics · Jul 15, 2020Peer-reviewedGenetics