Elifcan Taşdelen

14PUBLICATIONS
46CO-AUTHORS
Medical infection agents (incl. prions)Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)AutoimmunityInnate immunity
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Publications (14)

|Jul 06, 2026
Biallelic Variants in MIMS1 Produce a Form of Spondyloepimetaphyseal Dysplasia With Tracheal Stenosis and Ectodermal Dysplasia (SEMDTSED).

|Jun 19, 2026
Atypical Biallelic Inheritance in "Dominant" Genes: Evidence From a Large-Scale Consanguineus Exome Cohort.

|Jun 02, 2026
Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon.

|Mar 08, 2026
Expanding the Coffin-Siris syndrome spectrum: genetic, dysmorphic, and endocrine findings in eight cases.

Abdulkerim Kolkiran, Melike Ataseven Kulalı, Tuğba Daşar

|Feb 15, 2026
Lipoid proteinosis mimicking Sjögren's syndrome: a diagnostic challenge in rheumatology practice.

Mehmet Akif Baltaci, Elifcan Taşdelen, Gokhan Toptas

|Oct 08, 2025
Ectodermal dysplasias and isolated ectodermal anomalies: expanding the clinical and molecular spectrum in a cohort of 36 patients.

Ayşe Burcu Doğan Arı, Ayberk Türkyılmaz, Abdulkerim Kolkıran

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Frequent Collaborators

3 joint publications

Abdulkerim Kolkıran

3 joint publications

Abdullah Sezer

3 joint publications

Ahmet Kablan

2 joint publications

Melike Ataseven Kulalı