Bhai P - Search Results

1

Secondary causes of elevated hemoglobin in patients undergoing molecular testing for suspected polycythemia vera in southwestern Ontario: a chart review.

Chin-Yee B, Matyashin M, Cheong I, Bhai P, Lazo-Langner A, Almanaseer A, Kawata E, Levy MA, Stuart A, Lin H, Chin-Yee I, Sadikovic B, Hsia C. Chin-Yee B, et al. Among authors: bhai p. CMAJ Open. 2022 Nov 8;10(4):E988-E992. doi: 10.9778/cmajo.20210322. Print 2022 Oct-Dec. CMAJ Open. 2022. PMID: 36347562 Free PMC article. Review.

2

Clinical and molecular characterization of Indian patients with fructose-1, 6-bisphosphatase deficiency: Identification of a frequent variant (E281K).

Bhai P, Bijarnia-Mahay S, Puri RD, Saxena R, Gupta D, Kotecha U, Sachdev A, Gupta D, Vyas V, Agarwal D, Jain V, Bansal RK, Kumar TG, Verma IC. Bhai P, et al. Ann Hum Genet. 2018 Sep;82(5):309-317. doi: 10.1111/ahg.12256. Epub 2018 May 18. Ann Hum Genet. 2018. PMID: 29774539

3

Mutation-Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype.

Khatter S, Puri RD, Mahay SB, Bhai P, Saxena R, Verma IC. Khatter S, et al. Among authors: bhai p. Indian J Dermatol. 2019 Mar-Apr;64(2):143-145. doi: 10.4103/ijd.IJD_510_17. Indian J Dermatol. 2019. PMID: 30983611 Free PMC article.

4

A novel CHEK2 variant identified by next generation sequencing in an Indian family with hereditary breast cancer syndrome.

Bhai P, Saxena R, Kulshrestha S, Verma IC. Bhai P, et al. Cancer Genet. 2019 Jun;235-236:13-17. doi: 10.1016/j.cancergen.2019.05.003. Epub 2019 May 31. Cancer Genet. 2019. PMID: 31296309

5

Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario.

Aref-Eshghi E, Kerkhof J, Carere DA, Volodarsky M, Bhai P, Colaiacovo S, Saleh M, Caudle M, Karp N, Prasad C, Balci T, Lin H, Campbell C, Siu VM, Sadikovic B. Aref-Eshghi E, et al. Among authors: bhai p. J Hum Genet. 2021 May;66(5):451-464. doi: 10.1038/s10038-020-00860-3. Epub 2020 Oct 23. J Hum Genet. 2021. PMID: 33093641

6

Diagnostic Utility of Genome-Wide DNA Methylation Analysis in Mendelian Neurodevelopmental Disorders.

Haghshenas S, Bhai P, Aref-Eshghi E, Sadikovic B. Haghshenas S, et al. Among authors: bhai p. Int J Mol Sci. 2020 Dec 6;21(23):9303. doi: 10.3390/ijms21239303. Int J Mol Sci. 2020. PMID: 33291301 Free PMC article. Review.

7

Validation and clinical performance of a combined nuclear-mitochondrial next-generation sequencing and copy number variant analysis panel in a Canadian population.

Levy MA, Kerkhof J, Belmonte FR, Kaufman BA, Bhai P, Brady L, Bursztyn LLCD, Tarnopolsky M, Rupar T, Sadikovic B. Levy MA, et al. Among authors: bhai p. Am J Med Genet A. 2021 Feb;185(2):486-499. doi: 10.1002/ajmg.a.61998. Epub 2020 Dec 10. Am J Med Genet A. 2021. PMID: 33300680

8

A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene.

Mansory EM, Bhai P, Stuart A, Laudenbach L, Sadikovic B, Lazo-Langner A. Mansory EM, et al. Among authors: bhai p. Res Pract Thromb Haemost. 2021 May 3;5(4):e12510. doi: 10.1002/rth2.12510. eCollection 2021 May. Res Pract Thromb Haemost. 2021. PMID: 33977210 Free PMC article.

9

Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach.

Bhai P, Levy MA, Rooney K, Carere DA, Reilly J, Kerkhof J, Volodarsky M, Stuart A, Kadour M, Panabaker K, Schenkel LC, Lin H, Ainsworth P, Sadikovic B. Bhai P, et al. Front Genet. 2021 Jul 13;12:698595. doi: 10.3389/fgene.2021.698595. eCollection 2021. Front Genet. 2021. PMID: 34326862 Free PMC article.

10

Reducing cytogenetic testing in the era of next generation sequencing: Are we choosing wisely?

Kawata E, Hedley BD, Chin-Yee B, Xenocostas A, Lazo-Langner A, Hsia CC, Howson-Jan K, Yang P, Levy MA, Santos S, Bhai P, Howlett C, Lin H, Kadour M, Sadikovic B, Chin-Yee I. Kawata E, et al. Among authors: bhai p. Int J Lab Hematol. 2022 Apr;44(2):333-341. doi: 10.1111/ijlh.13747. Epub 2021 Oct 29. Int J Lab Hematol. 2022. PMID: 34713980

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