Publications by authors named "Seher Basaran"

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Olfactory Receptor Gene Deletions: A Novel Genetic Findings in Idiopathic Prepubertal Gynecomastia and Juvenile Macromastia.
Firdevs Bas, Birsen Karaman, Asli Derya Kardelen, Somayyeh Heidargholizadeh, Adam Najafli, Seher Basaran

Horm Res Paediatr· November 2025

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Awareness and attitudes of pregnant women about prenatal screening and diagnostic tests from Türkiye.
Didem Kaymak, Tuğba Kalaycı, Gözde Yeşil Sayın, Birsen Karaman, Seher Başaran

J Community Genet· October 2025

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Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures.
Gozde Tutku Turgut, Umut Altunoglu, Cagri Gulec, Tugba Sarac Sivrikoz, Tuğba Kalaycı

Clin Genet· June 2024

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Association of Antenatal Evaluations with Postmortem and Genetic Findings in the Series of Fetal Osteogenesis Imperfecta.
Leyli Senturk, Cagri Gulec, Tugba Sarac Sivrikoz, Hulya Kayserili, Ibrahim Halil Kalelioglu, Seher Basaran

Fetal Diagn Ther· June 2024

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Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency.
Aslı Derya Kardelen, Adam Najafli, Firdevs Baş, Birsen Karaman, Güven Toksoy

J Clin Res Pediatr Endocrinol· November 2023

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Novel GALT variations and genetic spectrum in Turkish population with the correlation of genotype and phenotype.
Irem Kalay, Cagri Gulec, Mehmet Cihan Balcı, Guven Toksoy, Gulden Gokcay, Seher Basaran

Ann Hum Genet· November 2023

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A rare ring chromosome 21 abnormality is associated with azoospermia in two different phenotypically normal cases.
Ezgi Gizem Berkay, Birsen Karaman, Seher Başaran

Syst Biol Reprod Med· October 2023

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Predictive value of ultrasound in prenatal diagnosis of hypospadias: hints for accurate diagnosis.
Lutfiye Uygur, Tugba Sarac Sivrikoz, Ibrahim Halil Kalelioglu, Recep Has, Cigdem Kunt Isguder, Seher Basaran

J Perinat Med· September 2023

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Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases.
Asuman Gedikbasi, Guven Toksoy, Meryem Karaca, Cagri Gulec, Mehmet Cihan Balci, Seher Basaran

Front Genet· June 2023

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Fetal skeletal dysplasia cohort of a single tertiary referral center in Istanbul, Turkey.
Tugba Kalayci, Umut Altunoglu, Aytul Çorbacioglu Esmer, Şahin Avcı, Tugba Sarac Sivrikoz

Am J Med Genet A· February 2023

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A new enrichment approach for candidate gene detection in unexplained recurrent pregnancy loss and implantation failure.
Ezgi Gizem Berkay, Can Veysel Şoroğlu, Tuğba Kalaycı, Zehra Oya Uyguner, Günseli Bayram Akçapınar

Mol Genet Genomics· January 2023

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Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies.
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Tugba Sarac Sivrikoz, Birsen Karaman

Genes (Basel)· December 2022

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Mutations in or Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.
Neşe Akcan, Oya Uyguner, Firdevs Baş, Umut Altunoğlu, Güven Toksoy

J Clin Res Pediatr Endocrinol· June 2022

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Functional loss of ubiquitin-specific protease 14 may lead to a novel distal arthrogryposis phenotype.
Gozde Tutku Turgut, Umut Altunoglu, Tugba Sarac Sivrikoz, Guven Toksoy, Tuğba Kalaycı

Clin Genet· April 2022

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Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.
Tugba Sarac Sivrikoz, Seher Basaran, Recep Has, Birsen Karaman, Ibrahim Halil Kalelioglu

Arch Gynecol Obstet· February 2022

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Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey.
Inci Emekli, Fatih Tepgeç, Bedia Samancı, Güven Toksoy, Gizem Hasanoğulları Kına

Parkinsonism Relat Disord· December 2021

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Growth and relationship of phenotypic characteristics with gonadal pathology and tumour risk in patients with 45, X/46, XY mosaicism.
Sukran Poyrazoglu, Firdevs Bas, Birsen Karaman, Melek Yildiz, Seher Basaran

Clin Endocrinol (Oxf)· June 2021

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Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey.
Güven Toksoy, Dilek Uludağ Alkaya, Gülendam Bagirova, Şahin Avcı, Agharza Aghayev

Mol Syndromol· November 2020

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Follow-Up Studies of cf-DNA Testing from 101 Consecutive Fetuses and Related Ultrasound Findings.
Seher Basaran, Recep Has, Ibrahim Halil Kalelioglu, Birsen Karaman, Melike Kirgiz

Ultraschall Med· April 2020

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Clinical and Genetic Investigation of Premature Ovarian Insufficiency Cases from Turkey.
Engin Oral, Guven Toksoy, Nigar Sofiyeva, Hale Goksever Celik, Birsen Karaman, Seher Basaran

J Gynecol Obstet Hum Reprod· December 2019

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Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6.
Emmanuelle Szenker-Ravi, Umut Altunoglu, Marc Leushacke, Célia Bosso-Lefèvre, Muznah Khatoo

Nature· September 2018

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Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.
Birsen Karaman, Hülya Kayserili, Asadollah Ghanbari, Zehra Oya Uyguner, Güven Toksoy, Seher Basaran

Mol Cytogenet· August 2018

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A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations.
Aslı Derya Kardelen, Güven Toksoy, Firdevs Baş, Zehra Yavaş Abalı, Genco Gençay

J Clin Res Pediatr Endocrinol· July 2018

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Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene.
Firdevs Baş, Güven Toksoy, Berrin Ergun-Longmire, Zehra Oya Uyguner, Zehra Yavaş Abalı

J Steroid Biochem Mol Biol· July 2018

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RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6.
Emmanuelle Szenker-Ravi, Umut Altunoglu, Marc Leushacke, Célia Bosso-Lefèvre, Muznah Khatoo

Nature· May 2018

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