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Author

Onur Yıldız

Observed names: O Yildiz, O. Yildiz, ONUR YILDIZ, Onur YILDIZ, Onur Yildiz, YILDIZ, ONUR
ORCID: 0000-0002-6507-7848
Observed ORCID: 0000-0002-6507-7848
OpenAlex ID: A5101698162
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
2019 · Davut Pehlivan, Yavuz Bayram, et al. · The American Journal of Human Genetics · 106
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Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population
2016 · S. Kilic, O. Ozdemir, et al. · Clinical and Experimental Dermatology · 11
Identification of a novel pathogenic variant in CKAP2L and literature review in a child with Filippi syndrome and congenital talipes equinovarus
2021 · Taner Karakaya, Ali Evren Bilgic, et al. · American Journal of Medical Genetics Part A · 8
Comparison of the thrombophilic gene polymorphisms and recurrent pregnancy loss: Results on combined gene effect of FVLeiden, FVR2, FXIII, MTHFR(A1298C and C677T), PAI-1 4G/5G and ACE I/D genes in RPL Women from Misk/Belarus and Canakkale - Sivas/Turkey
2016 · Fatma Silan, Irma Mosse, et al. · Biomedical Genetics and Genomics · 4
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Two siblings with GAPO syndrome: a novel missense variant in ANTXR1
2022 · Onur Yildiz, Elifcan Taşdelen, et al. · Clinical Dysmorphology · 2
Copy number variations in patients with idiopathic recurrent pregnancy loss: an arrayCGH approach
2022 · ONUR YILDIZ, FATMA SILAN, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 2
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The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report
2018 · Fatma Silan, Romyla Bourouba, et al. · Egyptian Journal of Medical Human Genetics · 1
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Tekrarlayan Gebelik Kaybı olan olguların kopya sayısı değişikliklerinin profillemesi
2020 · ÖZDEMİR, ÖZTÜRK, SILAN, FATMA, et al. · Çanakkale Onsekiz Mart University AVESIS
Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report
2020 · Fatma SILAN, Burcu ALBUZ, et al. · Cumhuriyet Tıp Dergisi/Cumhuriyet Üniversitesi Tıp Fakültesi dergisi
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BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q
2019 · ÖZTÜRK, MENEKŞE, ALBUZ, BURCU, et al. · Çanakkale Onsekiz Mart University AVESIS
Distal trisomy 3q and distal monosomy 11q in a mother and child with neurodevelopmental delay, short stature, facial dysmorphism and digital malformations
2018 · Ozturk Ozdemir, Taner Karakaya, et al. · Journal of Biotechnology
A case with 10q22.3q23.2 microdeletion syndrome and mosaic Klinefelter syndrome
2018 · Firdevs Dincsoy Bir, Özturk Özdemir, et al. · Journal of Biotechnology
Tekrarlayan gebelik kaybı olan olgularda array CGH analizinin yeri ve önemi
2018 · ONUR YILDIZ · Çanakkale Onsekiz Mart University AVESIS
Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?
2017 · Fatma Sılan, Baris Paksoy, et al. · Biodiscovery
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The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2 , and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), speech and motor delay
2017 · Ozturk Ozdemir, Onur Yildiz, et al. · Journal of Biotechnology
A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report
2017 · Fatma Silan, Taner Karakaya, et al. · Journal of Biotechnology
A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when comparing to the MicroArray-CGH technique
2017 · Ozturk Ozdemir, Mine Urfali, et al. · Journal of Biotechnology
A mental and motor retarded dysmorphic case withheterozygous 1p36 deletion Comparable results fromcytogenetic MicroArray CGH FISH and MLPAtechniques
2016 · SILAN, FATMA, ÖZDEMİR, ÖZTÜRK, et al. · Çanakkale Onsekiz Mart University AVESIS
An infertile case of 47,XYY syndrome without autistic spectrum: Cost effective well-define of extra Y chromosome by GTG, C bandings, QF-PCR and FISH analyses
2016 · Öztürk Özdemir, Barış Paksoy, et al. · Cumhuriyet Tıp Dergisi/Cumhuriyet Üniversitesi Tıp Fakültesi dergisi
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Mental ve motor geriliği olan dismorfik olguda heterozigot 1p36 delesyonu Sitogenetik moleküler sitogenetik ArrayCGH FISH ve MLPA tekniklerinin heterozigot delesyon saptama etkinliklerinin karşılaştırılması
2016 · YILDIZ, ONUR, SILAN, FATMA, et al. · Çanakkale Onsekiz Mart University AVESIS
An infertile case of 47 XYY syndromewithout autistic spectrum Cost effectivewell define of extra Y chromosome byGTG C bandings QF PCR and FISHanalyses
2016 · SILAN, FATMA, YILDIZ, ONUR, et al. · Çanakkale Onsekiz Mart University AVESIS
Pharmacogenetic analysis of CYP genes, VKORC1, UGT1A1 and MDR1 at West Anatolia Region
2016 · SILAN, COŞKUN, SILAN, FATMA, et al. · Çanakkale Onsekiz Mart University AVESIS
. Familial X chromosome translocation, Xq triplication and SHOX gene deletion with short stature;Conflicting results of QF-PCR analysis for Xq segmental triplication.
2016 · SILAN, FATMA, ÖZDEMİR, ÖZTÜRK, et al. · Çanakkale Onsekiz Mart University AVESIS
Pharmacogenetic analysis of CYP genes, VKORC1, UGT1A1 and MDR1 at West Anatolia Region
2016 · SILAN, FATMA, ÖZDEMİR, ÖZTÜRK, et al. · Çanakkale Onsekiz Mart University AVESIS
The possible role of chromosome 9q11.1-1.2 duplication resulting with infertility and recurrent pregnancy loss
2016 · SILAN, FATMA, ÖZDEMİR, ÖZTÜRK, et al. · Çanakkale Onsekiz Mart University AVESIS
Works count: 44
Citation count: 134
H-index: 4
I10-index: 2
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