Burhan Balta

7PUBLICATIONS
14CO-AUTHORS
Gene mappingMedical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)Medical virologyCell and nuclear division
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Publications (7)

|Nov 15, 2025
A novel homozygous c.301T > C, p.Y101H variant in the GNA11 gene is implicated in familial hypocalciuric hypercalcemia type 2 in a proband with the heterozygous variant present in mother and father - A case report.

Serkan Bilge Koca, Burhan Balta

|Apr 17, 2025
A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.

Murat Erdogan, Aysel Unal, Muhammet Ensar Dogan

|Feb 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss.

Duygu Duman, Memoona Ramzan, Asli Subasioglu

|Jan 29, 2020
A comprehensive molecular analysis and genotype-phenotype correlation in patients with familial mediterranean fever.

Burhan Balta, Murat Erdogan, Aslıhan Kiraz

|Nov 08, 2018
Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G

Burhan Balta, Murat Erdoğan, Aslıhan Kiraz

|Dec 21, 2017
Does thiol-disulphide balance show oxidative stress in different MEFV mutations?

Burhan Balta, Murat Erdogan, Murat Alisik

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Frequent Collaborators

2 joint publications

Murat Erdoğan

2 joint publications

Aslıhan Kiraz

1 joint publications

Yavuz Sahin

1 joint publications

Serdal Korkmaz