Medical Genetics

Uzm. Dr. Duygu Onur Cura

Doctor and researcher Denizli Devlet Hastanesi Denizli

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  • SpecialtyMedical Geneticssaglik.gov.trFrom source
  • InstitutionDenizli Devlet Hastanesisaglik.gov.trFrom source
  • Publications12 publicationsORCID, OpenAlexFrom source
  • ORCID0000-0001-7605-8047ORCIDFrom source
  • Last synchronised5 November 2026 07:59https://denizlidh.saglik.gov.tr/TR-641645/doktorlarimiz.html#duygu-onur-curasaglik.gov.tr

Scientific work

Publications

12 publications
  1. Rare Genetic Variants of Cell Adhesion Molecules in Transgender Men Suggest a Potential Role in Gender Dysphoria

    Sexual Development, 2025

    DOI 10.1159/000549011 PMID 41208545 Source: ORCID

  2. Genetic Analyses on Transgender Individuals: Impact on Physician Attitudes and Surgical Decision‐Making

    Brain and Behavior, 2025

    DOI 10.1002/brb3.70228 PMID 39789780 Open-access full textSource: ORCID

  3. Dahili Hastalarda Özel Beslenme ve Diyet Yönetimi

    Akademisyen Kitabevi eBooks, 2022

    DOI 10.37609/akya.2182 Source: OpenAlex

  4. Relationship between plasminogen activator inhibitor‐1 gene alterations and fibrosis in peritoneal dialysis patients

    Therapeutic Apheresis and Dialysis, 2021

    DOI 10.1111/1744-9987.13501 PMID 32301223 2 citations (Europe PMC) Source: ORCID

  5. Cinsiyet Disforisinde Genetik Faktörlerin Rolü

    DergiPark (Istanbul University), 2020

    Open-access full textSource: ORCID

  6. How Much do we Know About the Findings of 22q11.2 Deletion Syndrome?: A Single-Centre Study with 11-Year Follow-Up

    The Journal of Basic and Clinical Health Sciences, 2020

    DOI 10.30621/jbachs.2020.987 Open-access full textSource: ORCID

  7. Comment on: “Gene–Diet Interactions in Type 2 Diabetes: The Chicken and Egg Debate”

    International Journal of Molecular Sciences, 2019

    DOI 10.3390/ijms20194878 PMID 31581435 Open-access full textSource: ORCID

  8. Unexpected Coexistence of a Derivative t(21;21) and Complementary Mosaic r(21) in a Female with Multiple Miscarriages.

    Cytogenetic and genome research, 2019

    DOI 10.1159/000500986 PMID 31195399 Source: ORCID

  9. A newborn with monosomy X in association with corpus callosum agenesis

    Pediatrics & Neonatology, 2017

    DOI 10.1016/j.pedneo.2016.05.006 PMID 28117231 Open-access full textSource: ORCID

  10. Genetik faktörlerin şiddet davranışı üzerine etkisi

    DergiPark (Istanbul University), 2017

    Open-access full textSource: ORCID

View all 12 publications