Meyer S - Search Results

1

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.

2

Constitutional sequence variation in the Fanconi anaemia group C (FANCC) gene in childhood acute myeloid leukaemia.

Barber LM, McGrath HE, Meyer S, Will AM, Birch JM, Eden OB, Taylor GM. Barber LM, et al. Among authors: meyer s. Br J Haematol. 2003 Apr;121(1):57-62. doi: 10.1046/j.1365-2141.2003.04234.x. Br J Haematol. 2003. PMID: 12670332 Free article.

3

A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.

Meyer S, Fergusson WD, Oostra AB, Medhurst AL, Waisfisz Q, de Winter JP, Chen F, Carr TF, Clayton-Smith J, Clancy T, Green M, Barber L, Eden OB, Will AM, Joenje H, Taylor GM. Meyer S, et al. Genes Chromosomes Cancer. 2005 Apr;42(4):404-15. doi: 10.1002/gcc.20153. Genes Chromosomes Cancer. 2005. PMID: 15645491

4

Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia.

Meyer S, Barber LM, White DJ, Will AM, Birch JM, Kohler JA, Ersfeld K, Blom E, Joenje H, Eden TO, Malcolm Taylor G. Meyer S, et al. Br J Haematol. 2006 May;133(3):284-92. doi: 10.1111/j.1365-2141.2006.05985.x. Br J Haematol. 2006. PMID: 16643430 Free article.

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

Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption.

Meyer S, Fergusson WD, Whetton AD, Moreira-Leite F, Pepper SD, Miller C, Saunders EK, White DJ, Will AM, Eden T, Ikeda H, Ullmann R, Tuerkmen S, Gerlach A, Klopocki E, Tönnies H. Meyer S, et al. Genes Chromosomes Cancer. 2007 Apr;46(4):359-72. doi: 10.1002/gcc.20417. Genes Chromosomes Cancer. 2007. PMID: 17243162

7

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.

8

Pollicization of the index finger in Fanconi anaemia: appearances and functionality 40 years after the intervention.

Stivaros SM, Punekar M, Chandler K, Rost I, Schindler D, Meyer S. Stivaros SM, et al. Among authors: meyer s. Br J Haematol. 2014 Sep;166(6):807. doi: 10.1111/bjh.12996. Epub 2014 Jul 3. Br J Haematol. 2014. PMID: 24989649 Free article. No abstract available.

9

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.

10

Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imaging.

Stivaros SM, Alston R, Wright NB, Chandler K, Bonney D, Wynn RF, Will AM, Punekar M, Loughran S, Kilday JP, Schindler D, Patel L, Meyer S. Stivaros SM, et al. Among authors: meyer s. Br J Radiol. 2015;88(1056):20150088. doi: 10.1259/bjr.20150088. Epub 2015 Sep 15. Br J Radiol. 2015. PMID: 26369989 Free PMC article.

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