Doç. Dr. Altuğ Koç
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Claim profilePerson ↔ Disease
Which diseases does this doctor work on?
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Abnormalities, Multiple 5 publicationsSource: OpenAlex / PubMed MeSHView publications
- Microcephaly 3 publications
- Intellectual Disability 2 publications
- Osteochondrodysplasias 2 publications
- Colorectal Neoplasms 2 publications
- Familial Mediterranean Fever 2 publications
- Abortion, Habitual 2 publications
- Heart Defects, Congenital 2 publications
- Developmental Disabilities 2 publications
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- SpecialtyMedical Geneticssaglik.gov.trFrom source
- Institutionİzmir Şehir Hastanesisaglik.gov.trFrom source
- Area of workAbnormalities, MultipleExtracted from 5 publications · Model version —From source
- Publications101 publicationsORCID, OpenAlexFrom source
- ORCID0000-0002-8366-6806ORCIDFrom source
- Last synchronised5 November 2026 09:07https://izmirsehir.saglik.gov.tr/TR-1046642/doktorlarimiz.html#altug-kocsaglik.gov.tr
Scientific work
Publications on Abnormalities, Multiple
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Clinical and Genetic Heterogeneity of Congenital Myasthenic Syndromes: Insights From a Large Cohort
Neurology and Clinical Neuroscience, 2026
DOI 10.1111/ncn3.70057 Open-access full textSource: ORCID
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Symptom-based classification of 16p11.2 copy number variations underlying the multidimensional autism spectrum disorder phenotype using machine learning methods
Research in Autism, 2026
DOI 10.1016/j.reia.2026.202865 Open-access full textSource: OpenAlex
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MCPH1 and DNA Damage Response Pathway Genes as Candidate Susceptibility Loci in Hereditary Breast Cancer
Diagnostics, 2026
DOI 10.3390/diagnostics16182967 PMID 42793752 Open-access full textSource: ORCID
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Genetic Landscape of Pediatric Dyslipidemia in a Turkish Cohort: Insights From a Single‐Center Experience
Annals of Human Genetics, 2026
DOI 10.1111/ahg.70028 PMID 41084934 Source: ORCID
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Characterization of the molecular and clinical features of Multilocus Inherited Neoplasia Allelic Syndrome (MINAS) cases in the Turkish population
Familial Cancer, 2026
DOI 10.1007/s10689-026-00577-w PMID 42258060 1 citation (Europe PMC) Source: ORCID
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Prenatal Diagnosis of HSPG2-Related Dyssegmental Dysplasia: The First Report From Turkey
American Journal of Medical Genetics Part A, 2025
DOI 10.1002/ajmg.a.64152 PMID 40503612 Source: ORCID
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Investigation of Epidermal Growth Factor Receptor Pathway Related, Exosomal miRNAs in Non-Small Cell Lung Cancer Cases
Journal of Basic and Clinical Health Sciences, 2025
DOI 10.30621/jbachs.1595106 Open-access full textSource: ORCID
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Effects of VDR and CYP24A1 gene polymorphisms on the outcome of supraglottic larynx cancer.
PubMed, 2024
DOI 10.26355/eurrev_202403_35720 PMID 38567579 1 citation (Europe PMC) Source: OpenAlex
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Prognostic and predictive role of liquid biopsy in lung cancer patients
Frontiers in Oncology, 2024
DOI 10.3389/fonc.2023.1275525 PMID 38304031 3 citations (Europe PMC) Open-access full textSource: ORCID
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Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome
Turkish Journal of Gastroenterology, 2024
DOI 10.5152/tjg.2024.23262 PMID 39115133 2 citations (Europe PMC) Open-access full textSource: ORCID