Taha Reşid Özdemir

Author

Taha Reşid Özdemir

Also Known As

T Ozdemir, T. Ozdemir, T.R. Ozdemir, Taha Ozdemir, Taha R. Ozdemir, Taha R. Özdemir, Taha Resid Ozdemir, Taha Resid Ozdemır, Taha Resid Özdemir, Taha Reşid ÖZDEMİR

Publications

870

Citations

H-Index

Concepts

All Affiliations

Sağlık Bilimleri Üniversitesi Izmir University Ege University Izmir Kâtip Çelebi University Izmir Tepecik Eğitim ve Araştırma Hastanesi

About

Taha Reşid Özdemir is an author at Sağlık Bilimleri Üniversitesi specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	507
2	Language Studies	1	1	12
3	Public Health	1	1	30
4	Allergy	1	1	425
5	Comparative Literature	1	1	12

Taha Reşid Özdemir

Publications

693

Citations

H-Index

Page 1

	Year	Citations
The Arg753Gln polymorphism of the human Toll-like receptor 2 gene in tuberculosis disease A.C. Ogus, Burçak Yoldaş, Taha Reşid Özdemir, European Respiratory Journal Innate Immune SystemImmunologyGenetic EpidemiologyHuman PolymorphismInnate Immunity	2004	425
Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies Berk Özyılmaz, Taha Reşid Özdemir, Özge Özer Kaya, Annals of Human Genetics	2019	33
Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY) Taha Reşid Özdemir, Özgür Kırbıyık, Bumin Nuri Dündar, Journal of Pediatric Endocrinology and Metabolism GeneticsGenetic EpidemiologyPathologyDisease Gene IdentificationGenomics	2018	30
A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy Haruki Fujisawa, Mizuho S. Mimoto, Taha Reşid Özdemir, Thyroid Mendelian DisorderSelenium DeficiencyGenetic DisorderGeneticsPathogenesis	2018	23
Relationship Between IL1β-511C>T and ILRN VNTR Polymorphisms and Keratoconus Melis Palamar, Hüseyin Önay, Taha Reşid Özdemir, Cornea	2013	21
The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum Melis Köse, Ayça Aykut, Asude Durmaz, Journal of Pediatric Endocrinology and Metabolism	2021	20
SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey Melis Köse, Ebru Canda, Ayça Aykut, Molecular Genetics and Metabolism Reports	2020	17
Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey Melis Köse, Engi̇n Köse, Aycan Ünalp, Neurological Sciences Neuro-oncologyPathologyPhenotypic SpectrumNeurologyNeuropathology	2021	17
Mannose-binding lectin codon 54 gene polymorphism in relation to risk of nosocomial invasive fungal infection in preterm neonates in the neonatal intensive care unit Cumhur Aydemir, Hüseyin Önay, Şerife Suna Oğuz, The Journal of Maternal-Fetal & Neonatal Medicine	2010	16
Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study Taha Reşid Özdemir, Berk Özyılmaz, Özgür Çakmak, Turkish journal of urology	2019	16

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