Mehmet Alikaşifoğlu

Hacettepe University — Turkey

Biochemistry, Genetics and Molecular Biology · Life Sciences

26h-index3.0kcitations176works0.52yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(21), Genetics and Neurodevelopmental Disorders(21), Genomics and Rare Diseases(16), Congenital heart defects research(11), Connective tissue disorders research(9)

Publications175 total

miR-770-5p: A novel molecular target regulating KLF4/EGFR signaling through PRMT5 interaction
Medical Oncology·2025
POS1360 THE SECOND KICK FOR FMF PATIENTS WITH ONE MUTATION ONLY: THE TALENTED MR. INTERFERON
Annals of the Rheumatic Diseases·2025Open Access
Association of HIF-1α and TNFα single nucleotide polymorphisms with periodontal disease in diabetic patients
Acta Medica·2025Open Access
Investigation of the genetic background of familial hypercholesterolemia in a Turkish cohort and its clinical implications
Journal of clinical lipidology·2025· 2 cited
Long‐term follow‐up of anti‐<scp>TNF</scp> treatment in adult and pediatric <scp>DADA2</scp> patients: Insights from real‐world data
International Journal of Rheumatic Diseases·2024· 2 cited
Ex vivo disease modelling of Rett syndrome: the transcriptomic and metabolomic implications of direct neuronal conversion
Molecular Biology Reports·2024
POS0863 REAL-LIFE DATA COMPARING THE LONG-TERM OUTCOME AND TREATMENT IN ADULT AND PEDIATRIC DADA2 PATIENTS: SINGLE CENTER EXPERIENCE OVER 10 YEARS
Annals of the Rheumatic Diseases·2024
AB0846 MOLECULAR PROFILING OF AN EASTERN MEDITERRANEAN FAMILY REVEALS NOT ONLY KNOWN BUT ALSO NEW CANDIDATE GENETIC RISK FOR AUTOIMMUNE DISEASES
Annals of the Rheumatic Diseases·2024
Rare variant analysis in CAD related loci in patients with premature CAD reveals possible targets for further functional studies
Atherosclerosis·2023Open Access
A novel variant in severe disease of DADA2: involving vasculitic and haematologic features
Scandinavian Journal of Rheumatology·2022· 1 cited
Reduced irisin levels in patients with acromegaly
Hormone Molecular Biology and Clinical Investigation·2022· 3 cited
<i>FXR1</i>-related congenital myopathy: expansion of the clinical and genetic spectrum
Journal of Medical Genetics·2022· 4 citedOpen Access
Interaction between Dietary Fat Intake and Metabolic Genetic Risk Score on 25-Hydroxyvitamin D Concentrations in a Turkish Adult Population
Nutrients·2022· 9 citedOpen Access
Diagnostic yield of microarrays in individuals with non‐syndromic developmental delay and intellectual disability
Journal of Intellectual Disability Research·2021· 11 cited
Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation
Journal of Pediatric Endocrinology and Metabolism·2021· 6 cited
Investigation of Genetic Causes in a Developmental Disorder: Oculoauriculovertebral Spectrum
The Cleft Palate-Craniofacial Journal·2021· 6 cited
Specific FSTL1 polymorphism may determine the risk of cardiomyopathy in patients with acromegaly
Acta cardiologica. Supplementum·2021· 2 cited
Further expanding the mutational spectrum of <scp>brain abnormalities, neurodegeneration, and dysosteosclerosis</scp>: A rare disorder with neurologic regression and skeletal features
American Journal of Medical Genetics Part A·2021· 17 cited
Diagnostic yield of whole‐exome sequencing in non‐syndromic intellectual disability
Journal of Intellectual Disability Research·2021· 26 cited
Genetic disorders with symptoms mimicking rheumatologic diseases: A single-center retrospective study
European Journal of Medical Genetics·2021· 6 cited
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Frequent Co-authors

Dilek Aktaş(17), Koray Boduroğlu(14), Ergül Tunçbılek(11), Ekim Z. Taşkıran(11), Yasemin Alanay(10), Can Koşukçu(10), E Tunçbilek(9), Pelin Özlem Şimşek‐Kiper(9), Gülen Eda Ütine(7), Nurten Akarsu(5), Göknur Haliloğlu(5), Bilge Volkan Salancı(5), Ezgi Deniz Batu(4), Özlem Akgün Doğan(4), Seza Özen(3), Yelda Bilginer(3), K. Yüce(3), Beren Karaosmanoğlu(3), Eda G. Utine(3), Ender Karaca(2)