Meyer S - Search Results

1

Taylor AMR, Rothblum-Oviatt C, Ellis NA, Hickson ID, Meyer S, Crawford TO, Smogorzewska A, Pietrucha B, Weemaes C, Stewart GS. Taylor AMR, et al. Among authors: meyer s. Nat Rev Dis Primers. 2019 Sep 19;5(1):64. doi: 10.1038/s41572-019-0113-0. Nat Rev Dis Primers. 2019. PMID: 31537806 Free PMC article. Review.

2

Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site.

Meyer S, Kingston H, Taylor AM, Byrd PJ, Last JI, Brennan BM, Trueman S, Kelsey A, Taylor GM, Eden OB. Meyer S, et al. Cancer Genet Cytogenet. 2004 Oct 15;154(2):169-74. doi: 10.1016/j.cancergencyto.2004.02.022. Cancer Genet Cytogenet. 2004. PMID: 15474156

3

Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.

Popp I, Punekar M, Telford N, Stivaros S, Chandler K, Minnis M, Castleton A, Higham C, Hopewell L, Gareth Evans D, Raams A, Theil AF, Meyer S, Schindler D. Popp I, et al. Among authors: meyer s. BMC Med Genet. 2018 Jan 11;19(1):7. doi: 10.1186/s12881-018-0520-1. BMC Med Genet. 2018. PMID: 29325523 Free PMC article.

4

Genomic profiling of acute myeloid leukaemia associated with ataxia telangiectasia identifies a complex karyotype with wild-type TP53 and mutant KRAS, G3BP1 and IL7R.

Goldgraben MA, Fewings E, Larionov A, Scarth J, Redman J, Telford N, Arkwright PD, Bonney D, Wilks D, Kulkarni S, Taylor AMR, Tischkowitz MD, Meyer S. Goldgraben MA, et al. Among authors: meyer s. Pediatr Blood Cancer. 2020 Sep;67(9):e28354. doi: 10.1002/pbc.28354. Epub 2020 May 8. Pediatr Blood Cancer. 2020. PMID: 32383811 No abstract available.

5

No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia.

Meyer S, White DJ, Will AM, Eden T, Sim A, Brown R, Strathdee G. Meyer S, et al. Br J Haematol. 2006 Jul;134(1):61-3. doi: 10.1111/j.1365-2141.2006.06107.x. Br J Haematol. 2006. PMID: 16803569 Free article.

6

Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling.

Meyer S, Tischkowitz M, Chandler K, Gillespie A, Birch JM, Evans DG. Meyer S, et al. J Med Genet. 2014 Feb;51(2):71-5. doi: 10.1136/jmedgenet-2013-101642. Epub 2013 Nov 20. J Med Genet. 2014. PMID: 24259538 Review.

7

Fanconi anaemia: genetics, molecular biology, and cancer – implications for clinical management in children and adults.

Schneider M, Chandler K, Tischkowitz M, Meyer S. Schneider M, et al. Among authors: meyer s. Clin Genet. 2015 Jul;88(1):13-24. doi: 10.1111/cge.12517. Epub 2014 Nov 10. Clin Genet. 2015. PMID: 25307146 Review.

8

Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption.

Meyer S, Stevens A, Paredes R, Schneider M, Walker MJ, Williamson AJK, Gonzalez-Sanchez MB, Smetsers S, Dalal V, Teng HY, White DJ, Taylor S, Muter J, Pierce A, de Leonibus C, Rockx DAP, Rooimans MA, Spooncer E, Stauffer S, Biswas K, Godthelp B, Dorsman J, Clayton PE, Sharan SK, Whetton AD. Meyer S, et al. Cell Death Dis. 2017 Jun 15;8(6):e2875. doi: 10.1038/cddis.2017.264. Cell Death Dis. 2017. PMID: 28617445 Free PMC article.

9

Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome.

Huson SM, Staab T, Pereira M, Ward H, Paredes R, Evans DG, Baumhoer D, O'Sullivan J, Cheesman E, Schindler D, Meyer S. Huson SM, et al. Among authors: meyer s. Fam Cancer. 2022 Jan;21(1):85-90. doi: 10.1007/s10689-020-00221-1. Epub 2020 Nov 21. Fam Cancer. 2022. PMID: 33219493 Free PMC article.

10

Fanconi Anaemia, Childhood Cancer and the BRCA Genes.

Woodward ER, Meyer S. Woodward ER, et al. Among authors: meyer s. Genes (Basel). 2021 Sep 27;12(10):1520. doi: 10.3390/genes12101520. Genes (Basel). 2021. PMID: 34680915 Free PMC article. Review.

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