Feride Iffet Sahin

7PUBLICATIONS
25CO-AUTHORS
Molecular targetsNeonatologyCancer geneticsMedical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|Dec 30, 2024
Rare STAT3 haplotypes cause a predisposition to developing congenital anomalies of the kidney and urinary tract disorder.

Mert Polat, Feride İffet Şahin, Esra Baskin

|Oct 02, 2024
Homologous recombination deficiency gene panel analysis results in synchronous endometrial and ovarian cancers.

Ferah Kazanci, Zerrin Yılmaz Çelik, Mert Polat

|Mar 15, 2023
The impact of developmental genes in non-syndromic cleft lip and/or palate

Nihal Şahin Uysal, Feride İffet Şahin, Yunus Kasım Terzi

|Jan 25, 2023
BRCA, infertility, and fertility preservation: a review for counseling.

Ege Baltacı, Ferah Kazancı, Feride İffet Şahin

|Jan 10, 2022
Comparison of diagnostic criteria for children with familial Mediterranean fever.

Esra Nagehan Akyol Onder, Kudret Ebru Ozcan, Feride Iffet Sahin

|Jul 08, 2020
The Role of Heredity and the Prevalence of Strabismus in Families with Accommodative, Partial Accommodative, and Infantile Esotropia

Fatma Çorak Eroğlu, Sibel Oto, Feride İffet Şahin

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Frequent Collaborators

4 joint publications

Yunus Terzi

2 joint publications

Mert Polat

2 joint publications

Ferah Kazancı

2 joint publications

Esra Baskin