| Attention-deficit/hyperactivity disorder and very preterm/very low birth weight: a meta-analysis AP Franz, GU Bolat, H Bolat, A Matijasevich, IS Santos, RC Silveira, ... Pediatrics 141 (1), 2018 | 330 | 2018 |
| DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo H Bolat, ES Ercan, G Ünsel-Bolat, A Tahillioğlu, KU Yazici, A Bacanli, ... Brazilian Journal of Psychiatry 42, 630-637, 2020 | 16 | 2020 |
| Comparisons between sluggish cognitive tempo and ADHD-restrictive inattentive presentation phenotypes in a clinical ADHD sample G Ünsel-Bolat, ES Ercan, H Bolat, S Süren, A Bacanlı, KU Yazıcı, ... ADHD Attention Deficit and Hyperactivity Disorders 11, 363-372, 2019 | 15 | 2019 |
| Validity of proposed DSM-5 ADHD impulsivity symptoms in children G Ünsel Bolat, ES Ercan, GA Salum, Ö Bilaç, R Massuti, T Uysal Özaslan, ... European child & adolescent psychiatry 25, 1121-1132, 2016 | 12 | 2016 |
| Distinct Autism spectrum disorder phenotype and hand-flapping stereotypes: two siblings with novel homozygous mutation in TRAPPC9 gene and literature review H Bolat, G Ünsel-Bolat, H Derin, A Şen, S Ceylaner Molecular Syndromology 13 (4), 263-269, 2022 | 9 | 2022 |
| Clinical and genetic characteristics of patients with unexplained intellectual disability/developmental delay without epilepsy HB Gerik-Celebi, H Aydin, H Bolat, G Unsel-Bolat Molecular Syndromology 14 (3), 208-218, 2023 | 5 | 2023 |
| 20-year experience on prenatal diagnosis in a reference university medical geneticscenter in Turkey MB DURMAZ, H Bolat, Z Cengisiz, F Akercan, TS Türk, E Pariltay, ... Turkish Journal of Medical Sciences 51 (4), 1775-1780, 2021 | 5 | 2021 |
| 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 … H Bolat, G Ünsel-Bolat, S Özgül, E Parıltay, A Tahıllıoğlu, LA Rohde, ... Nordic Journal of Psychiatry 76 (8), 610-615, 2022 | 4 | 2022 |
| The Role of Copy Number Variations and FHIT Gene on Phenotypic Characteristics of Cases Diagnosed with Autism Spectrum Disorder G Ünsel Bolat, H Bolat Molecular Syndromology 12 (1), 12-19, 2021 | 4 | 2021 |
| Cytogenetic analysis of miscarriage materials of couples with recurrent pregnancy loss in a tertiary center H Akin, H Akin | 3 | 2019 |
| Autosomal recessive primary microcephaly (MCPH) and novel pathogenic variants in ASPM and WDR62 genes H Bolat, SG Sağer, A Türkyılmaz, AH Çebi, Y Akın, H Onay, F Özkınay, ... Molecular Syndromology 13 (5), 363-369, 2022 | 2 | 2022 |
| Sluggish Cognitive Tempo and Attention Deficit Hyperactivity Disorder: Similarities and Differences/Yavas Bilissel Tempo ve Dikkat Eksikligi Hiperaktivite Bozuklugu … GU Bolat, H Bolat, S Ozgul, S Suren, KU Yazici, A Bacanli, HA Tahillioglu, ... Turkish Journal of Child and Adolescent Mental Health 27 (3), 170-180, 2020 | 2 | 2020 |
| Analysis of the alpha galactosidase gene: mutation profile and description of two novel mutations with extensive literature review in Turkish population H Onay, H Bolat, GK Yıldırım, E Kose, SK Uçar, S Aşıkovalı, F Özkınay, ... Journal of Pediatric Endocrinology and Metabolism 33 (10), 1245-1250, 2020 | 2 | 2020 |
| Genetik tabanlı tanı ve tarama testlerine yaklaşım H AKIN, H BOLAT Turkiye Klinikleri Medical Genetics-Special Topics 5 (1), 1-5, 2020 | 2 | 2020 |
| BRCA and non-BRCA Variants Detected by Next Generation Sequencing in Patients with Hereditary Breast and/or Ovarian Cancer Syndrome HB Gerik-Çelebi, H Bolat Acta Oncologica Turcica 55 (2), 77-84, 0 | 2 | |
| Phenotypic and brain imaging findings associated with a 10p proximal deletion including the WAC gene: Case report and literature review H Bolat, H Derin, G Ünsel-Bolat Cognitive and Behavioral Neurology 35 (3), 221-226, 2022 | 1 | 2022 |
| Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders HB Gerik-Celebi, G Unsel-Bolat, H Bolat Molecular Syndromology 15 (1), 22-29, 2024 | | 2024 |
| Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders HB Gerik‐Celebi, H Bolat, G Unsel‐Bolat Developmental Neurobiology, 2024 | | 2024 |
| 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 … G Sahın Vural, H Bolat Graefe's Archive for Clinical and Experimental Ophthalmology 262 (3), 903-911, 2024 | | 2024 |
| Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders HB Gerik-Celebi, G Unsel-Bolat, H Bolat Molecular Syndromology, 1-8, 2024 | | 2024 |
Luis Augusto RohdeHospital de Clínicas de Porto Alegre - HCPA; Professor de Psiquiatria da Universidade Federal do RioVerified email at hcpa.edu.br
