Fatma Tuba Eminoğlu

9PUBLICATIONS
36CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionNeurogeneticsMetabolic medicineGene expression (incl. microarray and other genome-wide approaches)
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Publications (9)

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

Duygu Duman, Memoona Ramzan, Asli Subasioglu

|Jun 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.

Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar

|May 11, 2022
Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss.

B Vona, D A Schwartzbaum, A A Rodriguez

|Dec 20, 2021
Whole Mitochondrial Genome Analysis in Turkish Patients with Mitochondrial Diseases

Emine Begüm Gencer Öncül, Duygu Duman, Fatma Tuba Eminoğlu

|Jan 06, 2019
Dysfunction of <i>GRAP</i>, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.

Chong Li, Guney Bademci, Asli Subasioglu

|Nov 08, 2017
Variants in CIB2 cause DFNB48 and not USH1J.

K T Booth, K Kahrizi, M Babanejad

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Frequent Collaborators

5 joint publications

Mustafa Tekin

4 joint publications

Guney Bademci

2 joint publications

Mustafa Türker Duman

2 joint publications

Süleyman Aktuna