Ceren Alavanda

A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

Mehmet Eltan, Ceren Alavanda, Zehra Yavaş Abalı et al. · Calcified Tissue International · 2020 · 19 citations · Full text

Medicine, Endocrinology, Nephrology +12

Secondary findings in 622 Turkish clinical exome sequencing data

Esra Arslan Ateş, Ayberk Türkyılmaz, Özlem Yıldırım et al. · Journal of Human Genetics · 2021 · 19 citations

Life Sciences, Genetics, Molecular Genetics +12

Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency

Ayberk Türkyılmaz, Ceren Alavanda, Esra Arslan Ateş et al. · Journal of Assisted Reproduction and Genetics · 2022 · 15 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population

Nilgün Duman, Gülten Tuncel, Sevcan Tuğ Bozdoğan et al. · Journal of Medical Virology · 2022 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Clinical and genetic characterization of children with cubilin variants

Neslihan Çiçek, Harika Alpay, Serçin Güven et al. · Pediatric Nephrology · 2022 · 13 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11