Medical Genetics

Uzm. Dr. Hande Özkalaycı

Doctor and researcher İstanbul Eğitim Araştırma Hastanesi İstanbul
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  • SpecialtyMedical Geneticssaglik.gov.trFrom source
  • Institutionİstanbul Eğitim Araştırma Hastanesisaglik.gov.trFrom source
  • Publications9 publicationsORCID, Europe PMC, OpenAlexFrom source
  • ORCID0000-0002-8520-623XORCIDFrom source
  • Last synchronised5 November 2026 08:56https://istanbuleah.saglik.gov.tr/TR-1039956/doktorlar.html#hande-ozkalaycisaglik.gov.tr

Scientific work

Publications

9 publications

  1. Comparison of chromosome analysis, factor V Leiden, and prothrombin G20210A mutation results according to the number of pregnancy losses in recurrent pregnancy loss

    Meandros Medical And Dental Journal, 2025

    DOI 10.69601/meandrosmdj.1570237 Open-access full textSource: ORCID

  2. Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patients

    Neurogenetics, 2024

    DOI 10.1007/s10048-024-00765-9 PMID 38850354 2 citations (Europe PMC) Source: ORCID

  3. Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single center

    International Journal of Developmental Neuroscience, 2023

    DOI 10.1002/jdn.10278 PMID 37280783 Source: ORCID

  4. A Turkish Patient with Aceruloplasminemia Found to Have a Novel Pathogenic Variant Presenting with High Ferritin Level and Microcytic Anemia

    Turkish journal of haematology : official journal of Turkish Society of Haematology, 2023

    DOI 10.4274/tjh.galenos.2023.2023.0270 PMID 37698253 Open-access full textSource: Europe PMC

  5. Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation sequencing panel and MLPA analysis in Turkey

    Cancer Genetics, 2022

    DOI 10.1016/j.cancergen.2022.02.006 PMID 35220195 11 citations (OpenAlex) Source: OpenAlex

  6. Genetik Tabanlı Tarama Testlerinde Genetik Danışmanlık

    2020

    Source: OpenAlex

  7. 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

  8. Kistik Fibroza Genetik Yaklaşım

    Turkiye Klinikleri Medical Genetics - Special Topics, 2019

    Source: OpenAlex

  9. Thanatophoric Dysplasia Detected During Prenatal Period

    Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi, 2017

    DOI 10.5505/deutfd.2017.04909 Open-access full textSource: OpenAlex