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Fahrettin Duymuş
Observed names:
Duymuş, Fahrettin,
F., Duymus,
Fahrettin DUYMUŞ,
Fahrettin Duymus
Institutions:
Selçuk University,
Usak University,
Sağlık Bilimleri Üniversitesi,
Selçuk Üniversitesi Tıp Fakültesi Hastanesi,
Konya City Hospital
Observed institutions:
Selçuk University,
Usak University,
Sağlık Bilimleri Üniversitesi,
Selçuk Üniversitesi Tıp Fakültesi Hastanesi,
Konya City Hospital,
Muğla University
show all 6
ORCID:
0000-0002-8130-9792
Observed ORCID:
0000-0002-8130-9792
OpenAlex ID:
A5003099062
Relationship of endoplasmic reticulum stress with the etiopathogenesis of chronic tonsillitis and tonsillar hypertrophy in pediatric patients: a prospective, parallel-group study
2021
·
Merih Onal
, Nadir Kocak
, et al.
·
Molecular Biology Reports
·
8
PDF
Utility of Optical Genome Mapping in Repeat Disorders
2024
·
Mehmet Burak Mutlu
, Taner Karakaya
, et al.
·
Clinical Genetics
·
6
Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies
2023
·
Andrea Accogli
, Maha S Zaki
, et al.
·
Brain Communications
·
6
PDF
Assessment of Pathogenic Variants in the PAH Gene and Genotype–Phenotype Correlation in Phenylketonuria Patients from Turkey
2024
·
Özgür Balasar
, Banu Kadıoğlu Yılmaz
, et al.
·
Biochemical Genetics
·
3
Are decreased cocaine- and amphetamine regulated transcript and Agouti- related peptide levels associated Eating behavior in medication-free children with attention deficit and hyperactivity disorder?
2023
·
Mustafa Esad Tezcan
, Cüneyt Uğur
, et al.
·
Progress in Neuro-Psychopharmacology and Biological Psychiatry
·
3
Fetal Aberrant Subclavian Artery: A Retrospective Evaluation of Prenatal Findings and Postnatal Prognosis
2026
·
Nizamettin Bozbay
, Ayşe Ceren Duymuş
, et al.
·
Genel Tıp Dergisi
·
1
Influence of the IDOL Gene Variants on Low-Density Lipoprotein Cholesterol Levels in Turkish Patients with Familial Hypercholesterolemia
2024
·
Fahrettin Duymus
, Nadir Kocak
, et al.
·
Molecular Syndromology
·
1
PDF
A novel double hemizygous BTK mutation in a boy presenting withPseudomonasskin abscesses
2022
·
Tugba Guler
, Melike Emiroglu
, et al.
·
Clinical and Experimental Dermatology
·
1
Thrombolysis in pulmonary embolism: full-dose, low-dose, or catheter-directed thrombolysis?
2016
·
Murat Biteker
, Özcan Başaran
, et al.
·
The American Journal of Emergency Medicine
·
1
Supplemental Material for: ASPM-RELATED PRIMARY MICROCEPHALY PRESENTING WITH SEVERE GYRAL SIMPLIFICATION AND CEREBELLAR HYPOPLASIA: A CASE REPORT
2026
·
figshare admin karger
, Ali GÜLEN
, et al.
·
Figshare
ASPM-Related Primary Microcephaly Presenting with Severe Gyral Simplification and Cerebellar Hypoplasia: A Case Report
2026
·
Ali Gülen
, Fahrettin Duymuş
, et al.
·
Molecular Syndromology
Same mutation, different disease: intrafamilial clinical and radiological diversity in HPRT1-related gout—the first family series from Türkiye
2026
·
Reyhan Bilici
, Fahrettin Duymus
, et al.
·
Clinical Rheumatology
Characterization of FMR1 CGG Repeat Structure and AGG Interruption Patterns in Turkish and Syrian Individuals
2026
·
Hatice Koçak Eker
, Sümeyye Kara
, et al.
·
Gazi Medical Journal
PDF
Characterization of FMR1 CGG Repeat Structure and AGG Interruption Patterns in Turkish and Syrian Individuals: CGG Repeats and AGG Interruptions in FMR1
2026
·
Koçak Eker, Hatice
, Kara, Sümeyye
, et al.
·
Gazi Medical Journal
PDF
The Association of FMR1 Gene Low-Normal and High-Normal Alleles with Ovarian Dysfunctions: A Retrospective Analysis from the Turkish Population
2026
·
Hatice Kocak Eker
, Levent Simsek
, et al.
·
Molecular Syndromology
Supplementary Material for: The Association of FMR1 Gene Low-Normal and High-Normal Alleles with Ovarian Dysfunctions: A Retrospective Analysis from the Turkish Population
2026
·
karger, figshare admin
, H., KocakEker
, et al.
·
Figshare
Multimodal imaging of the autosomal recessive spastic ataxia of Charlevoix-Saguenay phenotype
2026
·
Mahmut Sami Biçimveren
, Ata Baytaroğlu
, et al.
·
Turkish Journal Of Neurology
PDF
Structural Variant and Repeat Expansion Findings Identified by Optical Genome Mapping in Complex Autism Spectrum Disorder With Concomitant Neurodevelopmental Disorders
2026
·
Mehmet Burak Mutlu
, Özge Beyza Gündoğdu Öğütlü
, et al.
·
Human Mutation
Familial Hyperekplexia Caused by a Novel Homozygous SLC6A5 Variant: A Case Report
2025
·
Fatma Hilal Yılmaz
, Ayça Burcu Kahraman
, et al.
·
Molecular Syndromology
High Diagnostic Yield of Next-Generation Sequencing in Charcot-Marie-Tooth Patients and a Novel Variant in the NDRG1 Gene
2025
·
Müşerref Başdemirci
, Özgür Balasar
, et al.
·
Molecular Syndromology
Featured Cover
2025
·
Mehmet Burak Mutlu
, Taner Karakaya
, et al.
·
Clinical Genetics
PDF
Author response for "Utility of Optical Genome Mapping in Repeat Disorders"
2024
·
Mehmet Burak Mutlu
, Taner Karakaya
, et al.
Author response for "Utility of Optical Genome Mapping in Repeat Disorders"
2024
·
Mehmet Burak Mutlu
, Taner Karakaya
, et al.
In silico analysis of similar protein sequences between Sars-Cov-2 and BCG vaccine
2021
·
Busra Goksel Tulgar
, Fahrettin Duymus
, et al.
·
Molecular Genetics and Metabolism
A case with a 552 kb deletion syndrome at 16p11.2
2021
·
Fahrettin Duymus
, Deniz Esin
, et al.
·
Molecular Genetics and Metabolism
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Works count:
26
Citation count:
30
H-index:
3
I10-index:
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