• 5973 Citations
19972022
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Research Output 1997 2020

  • 5973 Citations
  • 209 Article
  • 4 Review article
  • 2 Comment/debate
  • 1 Chapter
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Review article
Review article
6 Citations (Scopus)

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

Haploinsufficiency
Genetic Counseling
Incisor
Lip
Nose
33 Citations (Scopus)

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

Precision Medicine
Pharmacogenetics
Genome
Exome
Transcriptome
1 Citation (Scopus)

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

Genetic Research
Hearing Loss
Mutation
Genes
Single Nucleotide Polymorphism
26 Citations (Scopus)

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

Exome
Hearing Loss
Deafness
Technology
Genes