Wissenschaftliche Arbeiten

Uzm. Dr. Duygu Onur Cura

12 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  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 Quelle: 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 Frei zugänglicher VolltextQuelle: ORCID

  3. Dahili Hastalarda Özel Beslenme ve Diyet Yönetimi

    Akademisyen Kitabevi eBooks, 2022

    DOI 10.37609/akya.2182 Quelle: 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 Zitationen (Europe PMC) Quelle: ORCID

  5. Cinsiyet Disforisinde Genetik Faktörlerin Rolü

    DergiPark (Istanbul University), 2020

    Frei zugänglicher VolltextQuelle: 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 Frei zugänglicher VolltextQuelle: 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 Frei zugänglicher VolltextQuelle: 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 Quelle: 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 Frei zugänglicher VolltextQuelle: ORCID

  10. Genetik faktörlerin şiddet davranışı üzerine etkisi

    DergiPark (Istanbul University), 2017

    Frei zugänglicher VolltextQuelle: ORCID

  11. Three novel mutations of CHD7 gene in two turkish patients with charge syndrome; A double point mutation and an insertion.

    Balkan journal of medical genetics : BJMG, 2015

    DOI 10.1515/bjmg-2015-0007 PMID 26929907 Frei zugänglicher VolltextQuelle: ORCID

  12. Broncholithiasis with recurrent lithoptysis: a case report.

    Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 2013

    DOI 10.1159/000351816 PMID 23949189 Frei zugänglicher VolltextQuelle: ORCID