Yavuz Sahin

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 6

Top Topics

Duchenne Muscular Dystrophy

Intellectual Disability

Regulatory T Cells

Top Venues

International journal of molecular sciences

American journal of medical genetics. Part A

European journal of human genetics : EJHG

Acta neurologica Belgica

This page only lists publications with an associated author ORCID identifier.

Publications

Yavuz Sahin, Y Lynn Wang, Jianming Pei, Nashwa Mansoor, Michael Styler, Joseph R Testa, Reza Nejati
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. International journal of molecular sciences 25 (1) (2023)
Yavuz Sahin, Y Lynn Wang, Jianming Pei, Nashwa Mansoor, Michael Styler, Joseph R Testa, Reza Nejati
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. International journal of molecular sciences 25 (1) (2023)
Yavuz Sahin, Y Lynn Wang, Jianming Pei, Nashwa Mansoor, Michael Styler, Joseph R Testa, Reza Nejati
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. International journal of molecular sciences 25 (1) (2023)
Claudia Gonzaga-Jauregui, Gozde Yesil, Harikiran Nistala, Alper Gezdirici, Yavuz Bayram, Kalyan C Nannuru, Davut Pehlivan, Bo Yuan, Johanna Jimenez, Yavuz Sahin, Ingrid S Paine, Zeynep Coban Akdemir, Saathyaki Rajamani, Jeffrey Staples, John Dronzek, Kristen Howell, Jawid M Fatih, Silvia Smaldone, Alan E Schlesinger, Norman Ramírez, Alberto S Cornier, Melissa A Kelly, Robert Haber, Shek Man Chim, Kristy Nieman, Nan Wu, Johnathon Walls, null null, William Poueymirou, Chia-Jen Siao, V Reid Sutton, Marc S Williams, Jennifer E Posey, Richard A Gibbs, Simon Carlo, David H Tegay, Aris N Economides, James R Lupski
Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide. European journal of human genetics : EJHG 28 (9) (2020)
Burhan Balta, Murat Erdogan, Ayse B Ergul, Yavuz Sahin, Alper Ozcan
Interstitial deletion 5p14.1-p15.2 and 5q14.3-q23.2 in a patient with clubfoot, blepharophimosis, arthrogryposis, and multiple congenital abnormalities. American journal of medical genetics. Part A 173 (10) (2017)
Yavuz Sahin, Olcay Güngör, Zeliha Gormez, Huseyin Demirci, Bekir Ergüner, Gülay Güngör, Cengiz Dilber
Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy. Acta neurologica Belgica 117 (1) (2016)