Yasemin Alanay

9PUBLICATIONS
57CO-AUTHORS
Adolescent healthGene expression (incl. microarray and other genome-wide approaches)Medical biotechnology not elsewhere classifiedAnthropological geneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (9)

|May 02, 2026
Fibrodysplasia ossificans progressiva in children: diagnostic pitfalls and ACVR1 genotype-phenotype spectrum.

|Mar 16, 2026
Periodic Genetic Reanalysis Identifies a Novel De Novo NOTCH1 Variant: A Case Report.

Eylul Aydin, Aybike S Bulut, Berkay Yildiz

|Jul 22, 2025
Undiagnosed Hackathon Ends Diagnostic Odyssey in a Patient With DNA2 -Related Rothmund-Thomson Syndrome.

Beril Ay, Ozlem Akgun-Dogan, Fulya Taylan

|Mar 17, 2025
Clinical and Molecular Analyses in 8 New Craniofrontonasal Syndrome Families: Revisiting the Mild End of the Phenotypic Spectrum in Females.

Umut Altunoglu, Birsen Karaman, Yasemin Alanay

|Jun 28, 2023
Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature.

Alejandro Parra, Rachel Rabin, John Pappas

|Jun 26, 2023
Real-world evidence in achondroplasia: considerations for a standardized data set.

Yasemin Alanay, Klaus Mohnike, Ola Nilsson

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Frequent Collaborators

3 joint publications

Ozlem Akgun-Dogan

1 joint publications

Ecenur Tuc

1 joint publications

Fuat Baris Bengur

1 joint publications

Sevinç Aksay