Waye J - Search Results

1

Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty.

Tomkins DJ, Roux AF, Waye J, Freeman VC, Cox DW, Whelan DT. Tomkins DJ, et al. Among authors: waye j. Eur J Hum Genet. 1996;4(3):153-9. doi: 10.1159/000472189. Eur J Hum Genet. 1996. PMID: 8840115

2

B-cell lymphoma of recipient origin 9 years after allogeneic bone marrow transplantation for T-cell acute lymphoblastic leukaemia.

Trimble MS, Waye JS, Walker IR, Brain MC, Leber BF. Trimble MS, et al. Among authors: waye js. Br J Haematol. 1993 Sep;85(1):99-102. doi: 10.1111/j.1365-2141.1993.tb08651.x. Br J Haematol. 1993. PMID: 8251416

3

Forensic identity testing using highly polymorphic DNA markers: current status and emerging technologies.

Waye JS. Waye JS. Transfus Med Rev. 1993 Jul;7(3):193-205. doi: 10.1016/s0887-7963(93)70138-8. Transfus Med Rev. 1993. PMID: 8347985 Review. No abstract available.

4

Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes.

Diamandis M, Paterson AD, Rommens JM, Veljkovic DK, Blavignac J, Bulman DE, Waye JS, Derome F, Rivard GE, Hayward CP. Diamandis M, et al. Among authors: waye js. Blood. 2009 Feb 12;113(7):1543-6. doi: 10.1182/blood-2008-08-175216. Epub 2008 Nov 6. Blood. 2009. PMID: 18988861 Free PMC article.

5

The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytes.

Hayward CP, Liang M, Tasneem S, Soomro A, Waye JS, Paterson AD, Rivard GE, Wilson MD. Hayward CP, et al. PLoS One. 2017 Mar 16;12(3):e0173991. doi: 10.1371/journal.pone.0173991. eCollection 2017. PLoS One. 2017. PMID: 28301587 Free PMC article.

6

Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene.

Paterson AD, Rommens JM, Bharaj B, Blavignac J, Wong I, Diamandis M, Waye JS, Rivard GE, Hayward CP. Paterson AD, et al. Among authors: waye js. Blood. 2010 Feb 11;115(6):1264-6. doi: 10.1182/blood-2009-07-233965. Epub 2009 Dec 9. Blood. 2010. PMID: 20007542 Free article.

7

Dopamine D4 receptor variant, D4GLYCINE194, in Africans, but not in Caucasians: no association with schizophrenia.

Seeman P, Ulpian C, Chouinard G, Van Tol HH, Dwosh H, Lieberman JA, Siminovitch K, Liu IS, Waye J, Voruganti P, et al. Seeman P, et al. Among authors: waye j. Am J Med Genet. 1994 Dec 15;54(4):384-90. doi: 10.1002/ajmg.1320540419. Am J Med Genet. 1994. PMID: 7726213

8

Parentage testing implications of male fertility after allogeneic bone marrow transplantation.

Lipton JH, Marshall WH, Waye JS. Lipton JH, et al. Among authors: waye js. Bone Marrow Transplant. 1999 Jan;23(2):187-9. doi: 10.1038/sj.bmt.1701519. Bone Marrow Transplant. 1999. PMID: 10197807

9

Pregnancy outcomes in women with elevated levels of fetal hemoglobin.

Murji A, Sobel ML, Hasan L, McLeod A, Waye JS, Sermer M, Berger H. Murji A, et al. J Matern Fetal Neonatal Med. 2012 Feb;25(2):125-9. doi: 10.3109/14767058.2011.564241. Epub 2011 Apr 7. J Matern Fetal Neonatal Med. 2012. PMID: 21473677

10

Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR).

Lebo MS, Zakoor KR, Chun K, Speevak MD, Waye JS, McCready E, Parboosingh JS, Lamont RE, Feilotter H, Bosdet I, Tucker T, Young S, Karsan A, Charames GS, Agatep R, Spriggs EL, Chisholm C, Vasli N, Daoud H, Jarinova O, Tomaszewski R, Hume S, Taylor S, Akbari MR, Lerner-Ellis J; Canadian Open Genetics Repository Working Group. Lebo MS, et al. Among authors: waye js. Genet Med. 2018 Mar;20(3):294-302. doi: 10.1038/gim.2017.80. Epub 2017 Jul 20. Genet Med. 2018. PMID: 28726806 Free article.

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