Mohammad Reza Toliat

3PUBLICATIONS
16CO-AUTHORS
Gene mappingEpigenetics (incl. genome methylation and epigenomics)
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Publications (3)

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|Jun 29, 2026
Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families.

|Feb 05, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.

Mahmoud Koko, Maha A Elseed, Inaam N Mohammed

|Jan 01, 2021
Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B.

Tim Becker, Andreas Pich, Stephanie Tamm

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Frequent Collaborators

1 joint publications

Mahmoud Koko

1 joint publications

Inaam N Mohammed

1 joint publications

Ashraf Yahia

1 joint publications

Elhami A Ahmed

1 joint publications

Wasma A Abdelgadir

1 joint publications

Mohamed O M Ibrahim

1 joint publications

Mustafa A Salih

1 joint publications

Liena E O Elsayed

1 joint publications

Holger Lerche

1 joint publications

Dominika Oziębło

Frequent Collaborators

1 joint publications

Mahmoud Koko

1 joint publications

Inaam N Mohammed

1 joint publications

Ashraf Yahia

1 joint publications

Elhami A Ahmed

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