Birsen Karaman

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 9

Top Venues

Genes

American journal of medical genetics. Part A

Molecular cytogenetics

EMBO molecular medicine

Istanbul Universitesi

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Istanbul Universitesi Mar 21 1998

Turkey

Responsible for molecular cytogenetics :: Medical Genetics

Publications

Arjan F Theil, Alex Pines, Tuğba Kalaycı, José M Heredia-Genestar, Anja Raams, Marion H Rietveld, Sriram Sridharan, Sabine Ej Tanis, Klaas W Mulder, Nesimi Buyukbabani, Birsen Karaman, Zehra O Uyguner, Hülya Kayserili, Jan Hj Hoeijmakers, Hannes Lans, Jeroen Aa Demmers, Joris Pothof, Umut Altunoglu, Abdoelwaheb El Ghalbzouri, Wim Vermeulen
Trichothiodystrophy-associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation. EMBO molecular medicine (2023)
Ezgi Gizem Berkay, Birsen Karaman, Seher Başaran
A rare ring chromosome 21 abnormality is associated with azoospermia in two different phenotypically normal cases. Systems biology in reproductive medicine (2023)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (2022)
Tuğba Kalaycı, Umut Altunoglu, Aytul Çorbacioglu Esmer, Sahin Avci, Tugba Sarac Sivrikoz, Birsen Karaman, İbrahim Kalelioğlu, Recep Has, Zehra Oya Uyguner, Atıl Yüksel, Seher Başaran, Hülya Kayserili
Fetal skeletal dysplasia cohort of a single tertiary referral center in Istanbul, Turkey. American journal of medical genetics. Part A (2022)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (2022)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (2022)
Neşe Akcan, Zehra Oya Uyguner, Firdevs Baş, Umut Altunoglu, Güven Toksoy, Birsen Karaman, Sahin Avci, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendelıler
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD Journal of clinical research in pediatric endocrinology 14 (2) (2022)
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman, Melike Kirgiz, Tahir Dehgan, Tuğba Kalaycı, Bilge Ozsait Selcuk, Peter Miny, Atil Yuksel
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies. Genes 13 (12) (2022)
Birsen Karaman, Hülya Kayserili, Asadollah Ghanbari, Zehra Oya Uyguner, Güven Toksoy, Umut Altunoglu, Seher Basaran
Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases. Molecular cytogenetics 11 (2018)

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Publication Activity (10 Years)

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Birsen Karaman