Uzm. Dr. Duygu Onur Cura
Is this your profile? Claim it and verify your details.
Claim profileTrust
Where does this information come from?
The source is stated next to each piece of information. If you see something wrong, you can suggest a correction.
- 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
-
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
-
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
-
Dahili Hastalarda Özel Beslenme ve Diyet Yönetimi
Akademisyen Kitabevi eBooks, 2022
DOI 10.37609/akya.2182 Source: OpenAlex
-
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
-
Cinsiyet Disforisinde Genetik Faktörlerin Rolü
DergiPark (Istanbul University), 2020
Open-access full textSource: ORCID
-
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
-
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
-
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
-
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
-
Genetik faktörlerin şiddet davranışı üzerine etkisi
DergiPark (Istanbul University), 2017
Open-access full textSource: ORCID