Yavuz Sahin

5PUBLICATIONS
12CO-AUTHORS
Medical infection agents (incl. prions)Haematological tumoursGene mappingDevelopmental genetics (incl. sex determination)Neurology and neuromuscular diseases
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Publications (5)

|Apr 28, 2025
Poikiloderma With Neutropenia due to Novel USB1 Mutation.

Kerem Balan, Basak Yalici-Armagan, Neslihan Akdogan

|Jan 11, 2024
Multiple Genomic Alterations, Including a Novel AFF4::IRF1 Fusion Gene, in a Treatment-Refractory Blastic Plasmacytoid Dendritic-Cell Neoplasm: A Case Report and Literature Review.

Yavuz Sahin, Y Lynn Wang, Jianming Pei

|May 08, 2020
Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide.

Claudia Gonzaga-Jauregui, Gozde Yesil, Harikiran Nistala

|Aug 18, 2017
Interstitial deletion 5p14.1-p15.2 and 5q14.3-q23.2 in a patient with clubfoot, blepharophimosis, arthrogryposis, and multiple congenital abnormalities.

Burhan Balta, Murat Erdogan, Ayse B Ergul

|Nov 16, 2016
Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy.

Yavuz Sahin, Olcay Güngör, Zeliha Gormez

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Frequent Collaborators

1 joint publications

Burhan Balta

1 joint publications

Claudia Gonzaga-Jauregui

1 joint publications

Harikiran Nistala

1 joint publications

Alper Gezdirici