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Hilmi Bolat

Observed names: BOLAT, HİLMİ, Bolat, Hilmi, H. Bolat, Hilmi BOLAT
ORCID: 0000-0001-6574-8149
Observed ORCID: 0000-0001-6574-8149
OpenAlex ID: A5050838706
Attention-Deficit/Hyperactivity Disorder and Very Preterm/Very Low Birth Weight: A Meta-analysis
2017 · Adelar Pedro Franz, Gul Unsel Bolat, et al. · PEDIATRICS · 358
DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
2020 · Hilmi Bolat, Eyüp S. Ercan, et al. · Brazilian Journal of Psychiatry · 36
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Comparisons between sluggish cognitive tempo and ADHD-restrictive inattentive presentation phenotypes in a clinical ADHD sample
2019 · Gül Ünsel-Bolat, Eyüp Sabri Ercan, et al. · ADHD Attention Deficit and Hyperactivity Disorders · 17
Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders
2024 · Hamide Betul Gerik‐Celebi, Hilmi Bolat, et al. · Developmental Neurobiology · 13
Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy
2023 · Hamide Betul Gerik-Celebi, Hilal Aydin, et al. · Molecular Syndromology · 13
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Investigation of possible associations of the BDNF, SNAP-25 and SYN III genes with the neurocognitive measures: BDNF and SNAP-25 genes might be involved in attention domain, SYN III gene in executive function
2022 · Hilmi Bolat, Gül Ünsel-Bolat, et al. · Nordic Journal of Psychiatry · 11
Distinct Autism Spectrum Disorder Phenotype and Hand-Flapping Stereotypes: Two Siblings with Novel Homozygous Mutation in TRAPPC9 Gene and Literature Review
2022 · Hilmi Bolat, Gül Ünsel-Bolat, et al. · Molecular Syndromology · 9
Autosomal Recessive Primary Microcephaly (MCPH) and Novel Pathogenic Variants in ASPM and WDR62 Genes
2022 · Hilmi Bolat, Safiye G. Sağer, et al. · Molecular Syndromology · 8
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey
2021 · Burak DURMAZ, Hilmi BOLAT, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 7
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Validity of proposed DSM-5 ADHD impulsivity symptoms in children
2016 · Gül Ünsel Bolat, Eyüp Sabri Ercan, et al. · European Child & Adolescent Psychiatry · 7
Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients
2025 · Gulcin Akinci, Berk Ozyilmaz, et al. · Neuromuscular Disorders · 6
Phenotypic and Brain Imaging Findings Associated With a 10p Proximal Deletion Including the WAC Gene: Case Report and Literature Review
2022 · Hilmi Bolat, Hatice Derin, et al. · Cognitive and Behavioral Neurology · 6
The Role of Copy Number Variations and FHIT Gene on Phenotypic Characteristics of Cases Diagnosed with Autism Spectrum Disorder
2020 · Gül Ünsel Bolat, Hilmi Bolat · Molecular Syndromology · 6
Sluggish Cognitive Tempo and Attention Deficit Hyperactivity Disorder: Similarities and Differences
2020 · Gül Ünsel Bolat, Hilmi Bolat, et al. · Çocuk ve Gençlik Ruh Sağlığı Dergisi / Turkish Journal of Child and Adolescent Mental Health · 6
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Analysis of the alpha galactosidase gene: mutation profile and description of two novel mutations with extensive literature review in Turkish population
2020 · Hüseyin Onay, Hilmi Bolat, et al. · Journal of Pediatric Endocrinology and Metabolism · 5
Cytogenetic analysis of miscarriage materials of couples with recurrent pregnancy loss in a tertiary center
2019 · H. Akin, E. Karaca, et al. · Clinical and Experimental Obstetrics & Gynecology · 4
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Novel RORA Variants Reveal Genotype–Phenotype Diversity and Variable Expressivity in Neurodevelopmental Disorders
2025 · Gul Unsel‐Bolat, Hilmi Bolat, et al. · Clinical Genetics · 3
Investigation of patients with childhood epilepsy in single center: Comprehensive genetic testing experience
2024 · Hamide Betul Gerik‐Celebi, İpek Dokurel Çetin, et al. · International Journal of Developmental Neuroscience · 3
Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders
2023 · Hamide Betul Gerik-Celebi, Gul Unsel-Bolat, et al. · Molecular Syndromology · 3
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Nanopore sequencing method for CTG18.1 expansion in TCF4 in late-onset Fuchs endothelial corneal dystrophy and a comparison of the structural features of cornea with first-degree relatives
2023 · Gozde Sahın Vural, Hilmi Bolat · Graefe s Archive for Clinical and Experimental Ophthalmology · 3
Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum
2025 · Zehra Manav Yiğit, Aydan Mengübaş Erbaş, et al. · Balkan Medical Journal · 2
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Cohen syndrome: Can early‐onset recurrent infections and hypotonia provide early diagnosis and intervention for intellectual disability?
2024 · Gül Ünsel‐Bolat, Ezgi Keskin‐Çelebi, et al. · International Journal of Developmental Neuroscience · 2
BRCA and non-BRCA Variants Detected by Next Generation Sequencing in Patients with Hereditary Breast and/or Ovarian Cancer Syndrome
2022 · Hamide Betül Gerik-Çelebi, Hilmi Bolat · Acta Oncologica Turcica · 2
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Identifying barriers and policy priorities for rare disease research in underrepresented European countries
2026 · Baiba Lace, Inna Inashkina, et al. · European Journal of Public Health · 1
Could Transforming Growth Factor Beta and Target MicroRNA Dysregulation Serve as Biomarkers of Symptom Severity in Patients With Obsessive‐Compulsive Disorder?
2025 · Sinan Altunoz, Nazan Dolapoglu, et al. · International Journal of Developmental Neuroscience · 1
Works count: 80
Citation count: 539
H-index: 8
I10-index: 6
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