• 6170 Citations
19972022

Research output per year

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Research Output

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Review article

Whole-exome sequencing and its impact in hereditary hearing loss

Atik, T., Bademci, G., Diaz-Horta, O., Blanton, S. H. & Tekin, M., Mar 31 2015, In : Genetics research. 97, p. e4

Research output: Contribution to journalReview article

26 Scopus citations

The promise of whole-exome sequencing in medical genetics

Rabbani, B., Tekin, M. & Mahdieh, N., Jan 1 2014, In : Journal of Human Genetics. 59, 1, p. 5-15 11 p.

Research output: Contribution to journalReview article

228 Scopus citations

Research of genetic bases of hereditary non-syndromic hearing loss

Subaşıoğlu, A., Duman, D., Sırmacı, A., Bademci, G., Carkıt, F., Somdaş, M. A., Erkan, M., Tekin, M. & Dündar, M., Sep 1 2017, In : Turk Pediatri Arsivi. 52, 3, p. 122-132 11 p.

Research output: Contribution to journalReview article

1 Scopus citations

Next-generation sequencing in genetic hearing loss

Yan, D., Tekin, M., Blanton, S. H. & Liu, X. Z., Aug 1 2013, In : Genetic Testing and Molecular Biomarkers. 17, 8, p. 581-587 7 p.

Research output: Contribution to journalReview article

23 Scopus citations

Next generation sequencing: Implications in personalized medicine and pharmacogenomics

Rabbani, B., Nakaoka, H., Akhondzadeh, S., Tekin, M. & Mahdieh, N., 2016, In : Molecular BioSystems. 12, 6, p. 1818-1830 13 p.

Research output: Contribution to journalReview article

35 Scopus citations

KBG syndrome

Morel Swols, D., Foster, J. & Tekin, M., Dec 19 2017, In : Orphanet Journal of Rare Diseases. 12, 1, 183.

Research output: Contribution to journalReview article

9 Scopus citations

Genetic causes of inner ear anomalies: A review from the Turkish study group for inner ear anomalies

Ocak, E., Duman, D. & Tekin, M., Jul 2019, In : Balkan medical journal. 36, 4, p. 206-211 6 p.

Research output: Contribution to journalReview article

Open Access

Contrast-enhanced MR angiography of thoracic vascular malformations in children

Fitoz, S., Unsal, N., Tekin, M. & Tutar, E., Dec 15 2007, In : International Journal of Cardiology. 123, 1, p. 3-11 9 p.

Research output: Contribution to journalReview article

6 Scopus citations

Chudley-Mccullough syndrome: Expanded phenotype and review of the literature

Welch, K. O., Tekin, M., Nance, W. E., Blanton, S. H., Arnos, K. S. & Pandya, A., May 15 2003, In : American Journal of Medical Genetics. 119 A, 1, p. 71-76 6 p.

Research output: Contribution to journalReview article

12 Scopus citations

Café au lait spots: The pediatrician's perspective

Tekin, M., Bodurtha, J. N. & Riccardi, V. M., Jan 1 2001, In : Pediatrics in Review. 22, 3, p. 82-90 9 p.

Research output: Contribution to journalReview article

32 Scopus citations

Autosomal recessive nonsyndromic deafness genes: A review

Duman, D. & Tekin, M., Jun 1 2012, In : Frontiers in Bioscience. 17, 6, p. 2213-2236 24 p.

Research output: Contribution to journalReview article

70 Scopus citations