Author

Semra Kahraman

Istanbul Memorial HospitalORCID 0000-0002-2686-4240Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Murat ÇetinkayaiD· 2 shared Adrian M. E. PilatziD· 1 shared Ajuna AzadiD· 1 shared Albrecht RöpkeiD· 1 shared Alexandra Manuel LopesiD· 1 shared Antonio CapalboiD· 1 shared Beril Yüksel· 1 shared Burcu TürkgençiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Murat ÇetinkayaORCID

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2 papers

Recent·Most cited

A standardized approach for case selection and genomic data analysis of maternal exomes for the diagnosis of oocyte maturation and early embryonic developmental arrest in IVF

Antonio Capalbo, Silvia Buonaiuto, Matteo Figliuzzi, Gianluca Damaggio, Laura de Carvalho Girardi, Silvia Caroselli, Maurizio Poli, Cristina Patassini, Murat Çetinkaya, Beril Yüksel, Ajuna Azad, Marie Louise Grøndahl, Eva R. Hoffmann, Carlos Simón, Vincenza Colonna, Semra Kahraman

The paper develops a methodology for selecting IVF cases with oocyte maturation defects and preimplantation embryo lethality, using whole-exome sequencing and bioinformatics to identify causative genetic variants.

Reproductive BioMedicine Online · May 21, 2022Peer-reviewedGenetic & Genomic Medicine

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