| Zebrafish xenografts as a tool for in vivo studies on human cancer M Konantz, TB Balci, UF Hartwig, G Dellaire, MC André, JN Berman, ... Annals of the New York Academy of Sciences 1266 (1), 124-137, 2012 | 248 | 2012 |
| Evaluation of DNA methylation episignatures for diagnosis and phenotype correlations in 42 Mendelian neurodevelopmental disorders E Aref-Eshghi, J Kerkhof, VP Pedro, M Barat-Houari, N Ruiz-Pallares, ... The American Journal of Human Genetics 106 (3), 356-370, 2020 | 205 | 2020 |
| BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations A Basak, M Hancarova, JC Ulirsch, TB Balci, M Trkova, M Pelisek, ... The Journal of clinical investigation 125 (6), 2363-2368, 2015 | 153 | 2015 |
| Chromosome heteromorphisms: an impact on infertility FI Sahin, Z Yilmaz, OO Yuregir, T Bulakbasi, O Ozer, HB Zeyneloglu Journal of assisted reproduction and genetics 25, 191-195, 2008 | 134 | 2008 |
| Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders B Sadikovic, MA Levy, J Kerkhof, E Aref-Eshghi, L Schenkel, A Stuart, ... Genetics in Medicine 23 (6), 1065-1074, 2021 | 122 | 2021 |
| Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing TB Balci, T Hartley, Y Xi, DA Dyment, CL Beaulieu, FP Bernier, L Dupuis, ... Clinical genetics 92 (3), 281-289, 2017 | 108 | 2017 |
| Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders MA Levy, H McConkey, J Kerkhof, M Barat-Houari, S Bargiacchi, ... Human Genetics and Genomics Advances 3 (1), 2022 | 100 | 2022 |
| The zebrafish reveals dependence of the mast cell lineage on Notch signaling in vivo SI Da'as, AJ Coombs, TB Balci, CA Grondin, AA Ferrando, JN Berman Blood, The Journal of the American Society of Hematology 119 (15), 3585-3594, 2012 | 48 | 2012 |
| Genotype–phenotype correlations in individuals with pathogenic RERE variants VK Jordan, B Fregeau, X Ge, J Giordano, RJ Wapner, TB Balci, MT Carter, ... Human mutation 39 (5), 666-675, 2018 | 44 | 2018 |
| Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome TB Balci, J Davila, D Lewis, A Boafo, E Sell, J Richer, SM Nikkel, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018 | 38 | 2018 |
| Brain malformations in a patient with deletion 2p16. 1: A refinement of the phenotype to BCL11A TB Balci, SL Sawyer, J Davila, P Humphreys, DA Dyment European journal of medical genetics 58 (6-7), 351-354, 2015 | 37 | 2015 |
| Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders MA Levy, R Relator, H McConkey, E Pranckeviciene, J Kerkhof, ... Human mutation 43 (11), 1609-1628, 2022 | 30 | 2022 |
| The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®. BKM Hartley T, Balci TB, Rojas SK, Eaton A, Canada CR, Dyment DA Am J Med Genet C Semin Med Genet 178 (4), 458-463, 2018 | 28 | 2018 |
| Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants CA Chang, R Perrier, KC Kurek, J Estrada‐Veras, A Lehman, S Yip, ... American Journal of Medical Genetics Part A 185 (9), 2829-2845, 2021 | 27 | 2021 |
| Identification of Promoter Region Methylation Patterns of MGMT, CDKN2A, GSTP1, and THBS1 Genes in Intracranial Meningioma Patients F Aydemir, E Yurtcu, TB Balci, FI Sahin, S Gulsen, N Altinors Genetic Testing and Molecular Biomarkers 16 (5), 335-340, 2012 | 27 | 2012 |
| A transgenic zebrafish model expressing KIT‐D816V recapitulates features of aggressive systemic mastocytosis TB Balci, SV Prykhozhij, EM Teh, SI Da'as, E McBride, R Liwski, IC Chute, ... British journal of haematology 167 (1), 48-61, 2014 | 23* | 2014 |
| A unique role of GATA1s in Down syndrome acute megakaryocytic leukemia biology and therapy AC Xavier, H Edwards, AA Dombkowski, TB Balci, JN Berman, G Dellaire, ... PloS one 6 (11), e27486, 2011 | 23 | 2011 |
| BCL11B-related disorder in two canadian children: Expanding the clinical phenotype M Prasad, TB Balci, C Prasad, JD Andrews, R Lee, MT Jurkiewicz, ... European Journal of Medical Genetics 63 (9), 104007, 2020 | 21 | 2020 |
| Detection of a DNA methylation signature for the intellectual developmental disorder, X-linked, syndromic, armfield type S Haghshenas, MA Levy, J Kerkhof, E Aref-Eshghi, H McConkey, T Balci, ... International journal of molecular sciences 22 (3), 1111, 2021 | 16 | 2021 |
| Tatton‐Brown‐Rahman syndrome: Six individuals with novel features TB Balci, A Strong, JM Kalish, E Zackai, JM Maris, A Reilly, LF Surrey, ... American Journal of Medical Genetics Part A 182 (4), 673-680, 2020 | 14 | 2020 |
David DymentDepartment of Genetics; Children's Hospital of Eastern OntarioVerified email at cheo.on.ca
