Byers HJ - Search Results

1

High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer.

Evans DG, van Veen EM, Byers HJ, Evans SJ, Burghel GJ, Woodward ER, Harkness EF, Eccles DM, Greville-Haygate SL, Ellingford JM, Bowers NL, Pereira M, Wallace AJ, Howell SJ, Howell A, Lalloo F, Newman WG, Smith MJ. Evans DG, et al. Among authors: byers hj. J Med Genet. 2022 Feb;59(2):115-121. doi: 10.1136/jmedgenet-2020-107347. Epub 2021 Mar 23. J Med Genet. 2022. PMID: 33758026 Free PMC article.

2

Is multiple SNP testing in BRCA2 and BRCA1 female carriers ready for use in clinical practice? Results from a large Genetic Centre in the UK.

Ingham SL, Warwick J, Byers H, Lalloo F, Newman WG, Evans DG. Ingham SL, et al. Clin Genet. 2013 Jul;84(1):37-42. doi: 10.1111/cge.12035. Epub 2012 Nov 20. Clin Genet. 2013. PMID: 23050611

3

G6PC3 mutations cause non-syndromic severe congenital neutropenia.

Banka S, Wynn R, Byers H, Arkwright PD, Newman WG. Banka S, et al. Mol Genet Metab. 2013 Feb;108(2):138-41. doi: 10.1016/j.ymgme.2012.12.001. Epub 2012 Dec 21. Mol Genet Metab. 2013. PMID: 23298686

4

Spontaneous ovarian hyperstimulation syndrome: case report, pathophysiological classification and diagnostic algorithm.

Panagiotopoulou N, Byers H, Newman WG, Bhatia K. Panagiotopoulou N, et al. Eur J Obstet Gynecol Reprod Biol. 2013 Jul;169(2):143-8. doi: 10.1016/j.ejogrb.2013.03.004. Epub 2013 Apr 3. Eur J Obstet Gynecol Reprod Biol. 2013. PMID: 23561021 Review.

5

FSH receptor genotype does not predict metaphase-II oocyte output or fertilization rates in ICSI patients.

Mohiyiddeen L, Newman WG, Cerra C, Horne G, Mulugeta B, Byers H, Roberts SA, Nardo LG. Mohiyiddeen L, et al. Reprod Biomed Online. 2013 Sep;27(3):305-9. doi: 10.1016/j.rbmo.2013.06.005. Epub 2013 Jun 20. Reprod Biomed Online. 2013. PMID: 23876973

6

Increased rate of phenocopies in all age groups in BRCA1/BRCA2 mutation kindred, but increased prospective breast cancer risk is confined to BRCA2 mutation carriers.

Evans DG, Ingham SL, Buchan I, Woodward ER, Byers H, Howell A, Maher ER, Newman WG, Lalloo F. Evans DG, et al. Cancer Epidemiol Biomarkers Prev. 2013 Dec;22(12):2269-76. doi: 10.1158/1055-9965.EPI-13-0316-T. Epub 2013 Nov 27. Cancer Epidemiol Biomarkers Prev. 2013. PMID: 24285840

7

Intronic splicing mutations in PTCH1 cause Gorlin syndrome.

Bholah Z, Smith MJ, Byers HJ, Miles EK, Evans DG, Newman WG. Bholah Z, et al. Among authors: byers hj. Fam Cancer. 2014 Sep;13(3):477-80. doi: 10.1007/s10689-014-9712-9. Fam Cancer. 2014. PMID: 24659465

8

Identification of a novel familial FGF16 mutation in metacarpal 4-5 fusion.

Jones B, Byers H, Watson JS, Newman WG. Jones B, et al. Clin Dysmorphol. 2014 Jul;23(3):95-97. doi: 10.1097/MCD.0000000000000043. Clin Dysmorphol. 2014. PMID: 24878828 No abstract available.

9

Common variants modify the age of onset for basal cell carcinomas in Gorlin syndrome.

Yasar B, Byers HJ, Smith MJ, Lear J, Oudit D, Bholah Z, Roberts SA, Newman WG, Evans DG. Yasar B, et al. Among authors: byers hj. Eur J Hum Genet. 2015 May;23(5):708-10. doi: 10.1038/ejhg.2014.167. Epub 2014 Aug 27. Eur J Hum Genet. 2015. PMID: 25159867 Free PMC article.

10

The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes.

Smith MJ, Urquhart JE, Harkness EF, Miles EK, Bowers NL, Byers HJ, Bulman M, Gokhale C, Wallace AJ, Newman WG, Evans DG. Smith MJ, et al. Among authors: byers hj. Hum Mutat. 2016 Mar;37(3):250-6. doi: 10.1002/humu.22938. Epub 2016 Jan 11. Hum Mutat. 2016. PMID: 26615784

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