| Analysis of microRNA transcriptome by deep sequencing of small RNA libraries of peripheral blood AB Candida Vaz 1, Hafiz M Ahmad, Pratibha Sharma, Rashi Gupta, Lalit Kumar ... BMC Genomics 11, 2010 | 194 | 2010 |
| Response to Imatinib mesylate in chronic myeloid leukemia patients with variant BCR-ABL fusion transcripts VK Pratibha Sharma, Lalit Kumar, Sujata Mohanty Annals of hematology 89 (3), 241, 2010 | 69 | 2010 |
| Diagnostic utility of genome-wide DNA methylation analysis in mendelian neurodevelopmental disorders S Haghshenas, P Bhai, E Aref-Eshghi, B Sadikovic International journal of molecular sciences 21 (23), 9303, 2020 | 35 | 2020 |
| Mutations in ABL kinase domain are associated with inferior progression-free survival LK Pratibha Sharma, Sujata Mohanty, Vinod Kochupillai Leukemia Lymphoma 6, 1072, 2010 | 22* | 2010 |
| Clinical and molecular characterization of Indian patients with fructose‐1, 6‐bisphosphatase deficiency: identification of a frequent variant (E281K) P Bhai, S Bijarnia‐Mahay, RD Puri, R Saxena, D Gupta, U Kotecha, ... Annals of Human Genetics 82 (5), 309-317, 2018 | 19 | 2018 |
| Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases K Singh, RD Puri, P Bhai, AD Arya, G Chawla, R Saxena, IC Verma Journal of Pediatric Endocrinology and Metabolism 31 (7), 799-807, 2018 | 19 | 2018 |
| Mutation–proved Clouston syndrome in a large Indian family with a variant phenotype S Khatter, RD Puri, SB Mahay, P Bhai, R Saxena, IC Verma Indian Journal of Dermatology 64 (2), 143-145, 2019 | 15 | 2019 |
| The first case of antenatal presentation in COG8‐congenital disorder of glycosylation with a novel splice site mutation and an extended phenotype V Arora, RD Puri, P Bhai, N Sharma, S Bijarnia–Mahay, N Dimri, A Baijal, ... American journal of medical genetics Part A 179 (3), 480-485, 2019 | 14 | 2019 |
| Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome A Foroutan, S Haghshenas, P Bhai, MA Levy, J Kerkhof, H McConkey, ... International journal of molecular sciences 23 (3), 1815, 2022 | 12 | 2022 |
| Secondary causes of elevated hemoglobin in patients undergoing molecular testing for suspected polycythemia vera in southwestern Ontario: a chart review B Chin-Yee, M Matyashin, I Cheong, P Bhai, A Lazo-Langner, ... Canadian Medical Association Open Access Journal 10 (4), E988-E992, 2022 | 10 | 2022 |
| Clinical utility of implementing a frontline NGS-based DNA and RNA fusion panel test for patients with suspected myeloid malignancies P Bhai, CC Hsia, LC Schenkel, BD Hedley, MA Levy, J Kerkhof, S Santos, ... Molecular diagnosis & therapy 26 (3), 333-343, 2022 | 8 | 2022 |
| Validation and clinical performance of a combined nuclear‐mitochondrial next‐generation sequencing and copy number variant analysis panel in a Canadian population MA Levy, J Kerkhof, FR Belmonte, BA Kaufman, P Bhai, L Brady, ... American Journal of Medical Genetics Part A 185 (2), 486-499, 2021 | 8 | 2021 |
| Serum erythropoietin levels in 696 patients investigated for erythrocytosis with JAK2 mutation analysis B Chin-Yee, I Cheong, M Matyashin, A Lazo-Langner, I Chin-Yee, ... | 7 | 2022 |
| Next-generation sequencing reveals a nonsense mutation (p. Arg364Ter) in MRE11A gene in an indian patient with familial breast cancer P Sharma Bhai, D Sharma, R Saxena, IC Verma Breast Care 12 (2), 112-114, 2017 | 7 | 2017 |
| Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome DM Connaughton, P Bhai, P Isenring, M Mahdi, B Sadikovic, LC Schenkel Journal of Molecular Medicine 101 (8), 1029-1040, 2023 | 5 | 2023 |
| Clinical features and long-term outcomes of a Pan-Canadian cohort of adolescents and young adults with myeloproliferative neoplasms: a Canadian MPN Group study JT England, N Szuber, S Sirhan, T Dunne, S Cerquozzi, M Hill, ... Leukemia 38 (3), 570-578, 2024 | 4 | 2024 |
| Identification of a DNA methylation signature for Renpenning syndrome (RENS1), a spliceopathy S Haghshenas, A Foroutan, P Bhai, MA Levy, R Relator, J Kerkhof, ... European Journal of Human Genetics 31 (8), 879-886, 2023 | 4 | 2023 |
| Molecular profiling of solid tumors by next-generation sequencing: an experience from a clinical laboratory P Bhai, J Turowec, S Santos, J Kerkhof, LA Pickard, A Foroutan, ... Frontiers in Oncology 13, 1208244, 2023 | 4 | 2023 |
| Analysis of sequence and copy number variants in Canadian patient cohort with familial cancer syndromes using a unique next generation sequencing based approach P Bhai, MA Levy, K Rooney, DA Carere, J Reilly, J Kerkhof, M Volodarsky, ... Frontiers in genetics 12, 698595, 2021 | 4 | 2021 |
| An Approach to the Investigation of Thrombocytosis: Differentiating between Essential Thrombocythemia and Secondary Thrombocytosis A Almanaseer, B Chin-Yee, J Ho, A Lazo-Langner, L Schenkel, P Bhai, ... Advances in Hematology 2024 (1), 3056216, 2024 | 3 | 2024 |
