Leman Damla Kotan (Damla Kotan, Leman D Kotan)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 7

Top Topics

Ejection Fraction

Mitochondrial Dna

Top Venues

Journal of clinical research in pediatric endocrinology

Journal of pediatric endocrinology & metabolism : JPEM

American journal of medical genetics. Part A

Journal of neuroendocrinology

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

Publications

Leman Damla Kotan, Melek Yildiz, Ihsan Turan, Can Celiloglu, Bilgin Yuksel, Ali Kemal Topaloglu
A novel homozygous nonsense NDNF variant in Kallmann syndrome. American journal of medical genetics. Part A (2022)
Bradley A Welch, Hyun-Ju Cho, Seyit Ahmet Ucakturk, Stephen Matthew Farmer, Semra Cetinkaya, Ayhan Abaci, Gamze Akkus, Enver Simsek, Leman Damla Kotan, Ihsan Turan, Fatih Gurbuz, Bilgin Yuksel, Susan Wray, A Kemal Topaloglu
PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism. Journal of neuroendocrinology 34 (4) (2022)
Leman Damla Kotan
Comparative Analyses of Turkish Variome and Widely Used Genomic Variation Databases for the Evaluation of Rare Sequence Variants in Turkish Individuals: Idiopathic Hypogonadotropic Hypogonadism as a Disease Model Journal of clinical research in pediatric endocrinology 14 (3) (2022)
Ihsan Turan, Sevcan Erdem, Leman Damla Kotan, Semine Özdemir Dilek, Mehmet Tastan, Fatih Gurbuz, Serdar Ceylaner, Aysun Karabay Bayazıt, Ali Kemal Topaloğlu, Bilgin Yuksel
Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets. Journal of pediatric endocrinology & metabolism : JPEM 34 (5) (2021)
Ibrahim Mert Erbas, Ahu Paketçi, Sezer Acar, Leman Damla Kotan, Korcan Demir, Ayhan Abaci, Ece Böber
A nonsense variant in FGFR1: a rare cause of combined pituitary hormone deficiency. Journal of pediatric endocrinology & metabolism : JPEM 33 (12) (2020)
Fatma Derya Bulut, Semine Özdemir Dilek, Leman Damla Kotan, Eda Mengen Ucakturk, Fatih Gurbuz, Bilgin Yuksel
Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency Journal of clinical research in pediatric endocrinology 12 (3) (2020)
Leman Damla Kotan, Emregul Isik, Ihsan Turan, Eda Mengen, Gamze Akkus, Mehmet Tastan, Fatih Gurbuz, Bilgin Yuksel, A Kemal Topaloglu
Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. Clinical genetics 95 (2) (2018)