Mehmet Alikasifoglu
Hacettepe Üniversitesi
H-index: 29
Asia-Turkey
Top articles of Mehmet Alikasifoglu
Rare variant analysis in CAD related loci in patients with premature CAD reveals possible targets for further functional studies
Atherosclerosis
2023/8/1
A novel variant in severe disease of DADA2: involving vasculitic and haematologic features
Scandinavian Journal of Rheumatology
2023/1/2
FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum
Journal of medical genetics
2022/11/1
Mehmet Alikasifoglu
H-Index: 14
Volker Straub
H-Index: 56
Reduced irisin levels in patients with acromegaly
Hormone Molecular Biology and Clinical Investigation
2022/9/28
Suleyman Nahit Sendur
H-Index: 5
Gokhan Baykal
H-Index: 11
Busra Aydin
H-Index: 4
Mehmet Alikasifoglu
H-Index: 14
Investigation of genetic causes in a developmental disorder: oculoauriculovertebral Spectrum
The Cleft Palate-Craniofacial Journal
2022/9
Specific FSTL1 polymorphism may determine the risk of cardiomyopathy in patients with acromegaly
Acta cardiologica
2022/4/21
Interaction between dietary fat intake and metabolic genetic risk score on 25-hydroxyvitamin D concentrations in a Turkish adult population
Nutrients
2022/1/17
Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: a rare disorder with neurologic regression and skeletal features
American Journal of Medical Genetics Part A
2021/6
Diagnostic yield of whole‐exome sequencing in non‐syndromic intellectual disability
Journal of Intellectual Disability Research
2021/6
FTO gene–lifestyle interactions on serum adiponectin concentrations and central obesity in a Turkish population
International Journal of Food Sciences and Nutrition
2021/4/3
Suleyman Nahit Sendur
H-Index: 5
Erdem Karabulut
H-Index: 32
Mehmet Alikasifoglu
H-Index: 14
Zehra Buyuktuncer
H-Index: 11
Klotho gene G395A and C1818T polymorphisms in acromegaly: Association with clinical presentation and comorbidities
Clinical endocrinology
2021/4
Erdem Karabulut
H-Index: 32
Mehmet Alikasifoglu
H-Index: 14
Genetic disorders with symptoms mimicking rheumatologic diseases: a single-center retrospective study
European Journal of Medical Genetics
2021/4/1
Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline?
Rheumatology
2021/2/1
Diagnostic yield of microarrays in individuals with non‐syndromic developmental delay and intellectual disability
Journal of Intellectual Disability Research
2021/12
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
2021/12/1
Mehmet Alikasifoglu
H-Index: 14
Is conventional treatment still the first choice in pediatric patients with PHEX mutations in an era of monoclonal FGF-23 antibody?
HORMONE RESEARCH IN PAEDIATRICS
2021/9/1
Mehmet Alikasifoglu
H-Index: 14
Molecular etiology of isolated congenital cataract using next-generation sequencing: single center exome sequencing data from Turkey
Molecular Syndromology
2020/12/18
A Revisited Diagnosis of Collagen VI Related Muscular Dystrophy in a Patient with a Novel COL6A2 Variant and 21q22. 3 Deletion
Neuropediatrics
2020/12
Pelin Ozlem Simsek-Kiper
H-Index: 17
Mehmet Alikasifoglu
H-Index: 14
Genetic IGF1R defects: new cases expand the spectrum of clinical features
Journal of Endocrinological Investigation
2020/12
Novel insights into diabetes mellitus due to DNAJC3‐defect: Evolution of neurological and endocrine phenotype in the pediatric age group
Pediatric Diabetes
2020/11
