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The Turkish Journal of Pediatrics|March 4, 2010
A de novo complex chromosomal rearrangement involving chromosomes 2, 8 and 13 in a dysmorphic case with polysyndactylyBirsen Karaman, Rasim Ozgür Rosti, Kader Yilmaz, et al.Clinical Dysmorphology|February 2, 2002
Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocationAdnan Yuksel, Mehmet Seven, Birsen Karaman, et al.The Turkish Journal of Pediatrics|July 31, 2008
Angelman syndrome: clinical findings and follow-up data of 14 patientsBülent Kara, Birsen Karaman, Meral Ozmen, et al.Molecular Cytogenetics|August 25, 2018
Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 casesBirsen Karaman, Hülya Kayserili, Asadollah Ghanbari, et al.American Journal of Medical Genetics. Part A|September 1, 2021
Antenatal diagnostic dilemma in a pseudodominant pedigree with lamin-B receptor (LBR)-related regressive spondylometaphyseal dysplasiaGozde Tutku Turgut, Çağrı Güleç, Tugba Sarac Sivrikoz, et al.Molecular Syndromology|February 6, 2025
A Novel Truncating Variant in Sandestig-Stefanova Syndrome with HydrocephalusGülnihal Bulut, Gözde Tutku Turgut, Güven Toksoy, et al.Journal of Community Genetics|July 16, 2025
Awareness and attitudes of pregnant women about prenatal screening and diagnostic tests from TürkiyeDidem Kaymak, Tuğba Kalaycı, Gözde Yeşil Sayın, et al.Molecular Syndromology|June 16, 2023
Dicentric Recombinant Chromosome 18 due to Maternal Paracentric Inversion Analyzed by Array CGHÖzlem Anlaş, Akgün Ölmez, Birsen Karaman, et al.Archives of Gynecology and Obstetrics|June 19, 2021
Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary centerTugba Sarac Sivrikoz, Seher Basaran, Recep Has, et al.Journal of Gynecology Obstetrics and Human Reproduction|April 27, 2019
Clinical and Genetic Investigation of Premature Ovarian Insufficiency Cases from TurkeyEngin Oral, Guven Toksoy, Nigar Sofiyeva, et al.Pageof 6