Irmak Sakin

2PUBLICATIONS
15CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cell and nuclear division
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Publications (2)

|May 27, 2026
Evaluation of the NHS R67 Monogenic Hearing Loss Panel in a Single UK Centre.

|Aug 21, 2024
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow.

Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano

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Frequent Collaborators

1 joint publications

Angelina Haesoo Kim

1 joint publications

Stephen Viviano

1 joint publications

Canan Ceylan Kose

1 joint publications

Sukru Sadik Oner