Serdar Ceylaner

Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

Neil V. Morgan, Mark R. Morris, Hakan Cangül et al. · PLoS Genetics · 2010 · 222 citations · Full text

Genetics, Pathology, Molecular Genetics +16

<i>SALL4</i>mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders

Jürgen Kohlhase, David Chitayat, Dieter Kotzot et al. · Human Mutation · 2005 · 119 citations

Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

Sujal Ghosh, Sevgi Köstel Bal, Emily S.J. Edwards et al. · Blood · 2020 · 91 citations · Full text

Y chromosome azoospermia factor region microdeletions and recurrent pregnancy loss

Abdullah Karaer, Kadri Karaer, Gülnur Özakşit et al. · American Journal of Obstetrics and Gynecology · 2008 · 47 citations

Infertility, Fertility, Cytogenetics +10

Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing

Sebahat Yılmaz Ağladıoğlu, Zehra Aycan, Semra Çeti̇nkaya et al. · Journal of Pediatric Endocrinology and Metabolism · 2015 · 40 citations