Haydar Bagis (Haydar Bağış)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Topics

Tyrosine Kinase

Mitochondrial Dna

Top Venues

Journal of pediatric genetics

Arquivos brasileiros de oftalmologia

Clinical case reports

Molecular biology reports

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

Publications

Esra Bozgeyik, Haydar Bagis, Ibrahim Bozgeyik, Sayad Kocahan
The roles of long non-coding RNAs in the necroptotic signaling of colon cancer cells. Molecular biology reports (2023)
Özden Öztürk, Haydar Bagis, Semih Bolu
Osteogenesis Imperfecta and Split Foot Malformation due to 7q21.2q21.3 Deletion Including COL1A2, DLX5/6 Genes: Review of the Literature. Journal of pediatric genetics 13 (1) (2021)
Özden Öztürk, Haydar Bagis, Semih Bolu
Osteogenesis Imperfecta and Split Foot Malformation due to 7q21.2q21.3 Deletion Including COL1A2, DLX5/6 Genes: Review of the Literature. Journal of pediatric genetics 13 (1) (2021)
Şemsettin Bilak, Muhammer Özgür Çevik, İbrahim Halil Erdoğdu, Haydar Bagis
Expression of Vitamin D Receptor and Vitamin D Receptor Gene Polymorphisms (BsmI, FokI, and TaqI) in Patients with Pterygium. Arquivos brasileiros de oftalmologia 84 (3) (2021)
Özden Öztürk, Haydar Bagis, Semih Bolu, Muhammer Özgür Çevik
Ellis-van Creveld syndrome novel pathogenic variant in the EVC2 gene a patient from Turkey. Clinical case reports 9 (4) (2021)
Haydar Bagis, Özden Öztürk, Semih Bolu, Bayram Taşkın
A Novel Mutation in NIPBL Gene with the Cornelia de Lange Syndrome and a 10q11.22-q11.23 Microdeletion in the Same Individual. Journal of pediatric genetics 11 (3) (2020)