Burhan Balta

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 10

Top Topics

Pseudomonas Aeruginosa

Molecular Dynamics Simulations

Hypertrophic Cardiomyopathy

Top Venues

American journal of medical genetics. Part A

Molecular biology reports

Turkish journal of haematology : official journal of Turkish Society of Haematology

Rheumatology international

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

Publications

Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A (2024)
Burhan Balta, Murat Erdogan, Aslıhan Kiraz, Tayfun Akalın, Funda Baştug, Arslan Bayram
A comprehensive molecular analysis and genotype-phenotype correlation in patients with familial mediterranean fever. Molecular biology reports 47 (3) (2020)
Burhan Balta, Murat Erdoğan, Aslıhan Kiraz, Serdal Korkmaz, Alperen Ağadayı
Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G Turkish journal of haematology : official journal of Turkish Society of Haematology 36 (1) (2018)
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)
Burhan Balta, Murat Erdogan, Murat Alisik, Aslihan Kiraz, Tayfun Akalin, Funda Bastug, Ozcan Erel
Does thiol-disulphide balance show oxidative stress in different MEFV mutations? Rheumatology international 38 (1) (2017)