Tinatin Tkemladze

8PUBLICATIONS
124CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapyCentral nervous systemCardiovascular medicine and haematology not elsewhere classified
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Publications (8)

|Oct 03, 2025
Evaluating DNA methylation episignatures as a first-tier diagnostic test in individuals with suspected genetic disorders.

Tinatin Tkemladze, Christopher Campbell, Kakha Bregvadze

|Jul 04, 2025
Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene.

Natasha L Rudy, Adriana Gomes, Tinatin Tkemaladze

|May 12, 2025
Clinical and Genetic Landscape of IGHMBP2 -Related Disorders: From Novel Variants to Phenotypic Insights.

Tinatin Tkemaladze, Kakha Bregvadze, Luka Abashishvili

|Nov 23, 2024
Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia.

Rauan Kaiyrzhanov, Nazira Zharkinbekova, Ulviyya Guliyeva

|Oct 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Angelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan

|Jul 04, 2024
Mining the diagnosis of rare disease with limited resources.

Tinatin Tkemaladze

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Frequent Collaborators

2 joint publications

Alain Verloes

2 joint publications

Aime Lumaka

2 joint publications

Tahsin Stefan Barakat

1 joint publications

Bekim Sadikovic