Medical Genetics

Prof. Dr. Taha Reşid Özdemir

Doctor and researcher İzmir Şehir Hastanesi İzmir
Prostatic NeoplasmsSpastic Paraplegia, Hereditary
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Person ↔ Disease

Which diseases does this doctor work on?

From source
  • Prostatic Neoplasms 2 publications
    Source: OpenAlex / PubMed MeSHView publications
  • Spastic Paraplegia, Hereditary 2 publications

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  • SpecialtyMedical Geneticssaglik.gov.trFrom source
  • Institutionİzmir Şehir Hastanesisaglik.gov.trFrom source
  • Area of workProstatic NeoplasmsExtracted from 2 publications · Model version —From source
  • Publications82 publicationsORCID, OpenAlexFrom source
  • ORCID0000-0003-4870-6945ORCIDFrom source
  • Last synchronised5 November 2026 09:07https://izmirsehir.saglik.gov.tr/TR-1046642/doktorlarimiz.html#taha-resid-ozdemirsaglik.gov.tr

Scientific work

Publications on Prostatic Neoplasms

82 publications

  1. 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

  2. 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

  3. Is Unidentified Cytopenia Truly Unidentified? Or Are We Overlooking Clonality?

    Medicina, 2026

    DOI 10.3390/medicina62050868 PMID 42195121 Open-access full textSource: OpenAlex

  4. 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

  5. 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

  6. 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

  7. Prevalence and impact of germline mutations in pancreatic ductal adenocarcinoma

    Tumori Journal, 2026

    DOI 10.1177/03008916251410475 PMID 41568754 Source: ORCID

  8. Dental Anomalies in a Pediatric Patient with 16p13.11 Recurrent Microdeletion Syndrome: A Case Report

    Journal of Dr Behcet Uz Children s Hospital, 2026

    DOI 10.4274/jbuch.galenos.2025.88234 Open-access full textSource: OpenAlex

  9. SCN1A DIŞINDAKİ SODYUM KANALOPATİLERİ: ÇOK MERKEZLİ ÇALIŞMA

    Kocaeli Üniversitesi - AVESİS, 2025

    Open-access full textSource: OpenAlex

  10. FKBP10 Variants: Differentiation Between Bruck Syndrome Type 1 And Osteogenesıs Imperfecta Type XI

    Journal of Clinical Research in Pediatric Endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2025.2025-8-4 PMID 41243835 Open-access full textSource: OpenAlex

View all 82 publications