• 6043 Citations

Research output per year

If you made any changes in Pure these will be visible here soon.

Research Output


Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (Genetics in Medicine, (2019), 10.1038/s41436-019-0487-0)

on behalf of the ClinGen Hearing Loss Clinical Domain Working Group, Jan 1 2019, (Accepted/In press) In : Genetics in Medicine.

Research output: Contribution to journalComment/debate

Open Access
Open Access

Correction: Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. (PLoS ONE)

Diaz-Horta, O., Duman, D., Foster, J., Sirmaci, A., Gonzalez, M., Mahdieh, N., Fotouhi, N., Bonyadi, M., Cengiz, F. B., Menendez, I., Ulloa, R. H., Edwards, Y. J. K., Zuc̈hner, S., Blanton, S. & Tekin, M., May 17 2013, In : PloS one. 8, 5

Research output: Contribution to journalComment/debate


Erratum: GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome (American Journal of Human Genetics (2012) 90 (1088-1093))

Doherty, D., Chudley, A. E., Coghlan, G., Ishak, G. E., Innes, A. M., Lemire, E. G., Rogers, R. C., Mhanni, A. A., Phelps, I. G., Jones, S. J. M., Zhan, S. H., Fejes, A. P., Shahin, H., Kanaan, M., Akay, H., Tekin, M., Triggs-Raine, B. & Zelinski, T., Jul 13 2012, In : American journal of human genetics. 91, 1, 1 p.

Research output: Contribution to journalComment/debate


Erratum: Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia (Clinical Genetics (2005) vol. 67 (31-37))

Tekin, M., Boǧoclu, G., Arican, S. T., Orman, M. N., Tastan, H., Elsayed, S. & Akar, N., Mar 1 2005, In : Clinical Genetics. 67, 3, 1 p.

Research output: Contribution to journalComment/debate


Erratum: Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly (Hum Genet (2002) 110 (297-301))

Ming, J. E., Kaupas, M. E., Roessler, E., Brunner, H. G., Golabi, M., Tekin, M., Stratton, R. F., Sujansky, E., Bale, S. J. & Muenke, M., Oct 1 2002, In : Human Genetics. 111, 4-5, 1 p.

Research output: Contribution to journalComment/debate

1 Scopus citations

Erratum: Genotype-phenotype correlation in a large group of Turkish patients with familial Mediterranean fever: Evidence for mutation-independent amyloidosis (Rheumatology (2000) vol. 39 (67-72))

Yalcinkaya, F., Cakar, N., Misirlioglu, M., Tumer, N., Akar, N., Tekin, M., Tastan, H., Kocak, H., Ozkaya, N. & Elhan, A. H., Jan 1 2000, In : Rheumatology. 39, 10, 1 p.

Research output: Contribution to journalComment/debate