Meyer S - Search Results

1

Convergent somatic evolution commences in utero in a germline ribosomopathy.

Machado HE, Øbro NF, Williams N, Tan S, Boukerrou AZ, Davies M, Belmonte M, Mitchell E, Baxter EJ, Mende N, Clay A, Ancliff P, Köglmeier J, Killick SB, Kulasekararaj A, Meyer S, Laurenti E, Campbell PJ, Kent DG, Nangalia J, Warren AJ. Machado HE, et al. Among authors: meyer s. Nat Commun. 2023 Aug 22;14(1):5092. doi: 10.1038/s41467-023-40896-5. Nat Commun. 2023. PMID: 37608017 Free PMC article.

2

Chromosome instability syndromes.

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.

3

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.

4

Patterns and frequency of renal abnormalities in Fanconi anaemia: implications for long-term management.

Sathyanarayana V, Lee B, Wright NB, Santos R, Bonney D, Wynn R, Patel L, Chandler K, Cheesman E, Schindler D, Webb NJA, Meyer S. Sathyanarayana V, et al. Among authors: meyer s. Pediatr Nephrol. 2018 Sep;33(9):1547-1551. doi: 10.1007/s00467-018-3952-0. Epub 2018 Apr 12. Pediatr Nephrol. 2018. PMID: 29651604 Free PMC article.

5

Embryonal sarcoma of the liver in a girl with Cockayne syndrome.

Thorbinson C, Penn A, Nicola P, Hardcastle C, Waller S, Ramsden S, Coorens THH, Tang V, Cheesman E, Douzgou S, Meyer S. Thorbinson C, et al. Among authors: meyer s. Clin Genet. 2022 Mar;101(3):375-376. doi: 10.1111/cge.14094. Epub 2021 Dec 8. Clin Genet. 2022. PMID: 34878179

6

Proteomic Analysis of an Induced Pluripotent Stem Cell Model Reveals Strategies to Treat Juvenile Myelomonocytic Leukemia.

Pearson S, Guo B, Pierce A, Azadbakht N, Brazzatti JA, Patassini S, Mulero-Navarro S, Meyer S, Flotho C, Gelb BD, Whetton AD. Pearson S, et al. Among authors: meyer s. J Proteome Res. 2020 Jan 3;19(1):194-203. doi: 10.1021/acs.jproteome.9b00495. Epub 2019 Nov 12. J Proteome Res. 2020. PMID: 31657576 Free PMC article.

7

Chromosomal aberrations associated with clonal evolution and leukemic transformation in fanconi anemia: clinical and biological implications.

Meyer S, Neitzel H, Tönnies H. Meyer S, et al. Anemia. 2012;2012:349837. doi: 10.1155/2012/349837. Epub 2012 May 23. Anemia. 2012. PMID: 22675616 Free PMC article.

8

A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay.

Biswas K, Das R, Alter BP, Kuznetsov SG, Stauffer S, North SL, Burkett S, Brody LC, Meyer S, Byrd RA, Sharan SK. Biswas K, et al. Among authors: meyer s. Blood. 2011 Sep 1;118(9):2430-42. doi: 10.1182/blood-2010-12-324541. Epub 2011 Jun 30. Blood. 2011. PMID: 21719596 Free PMC article.

9

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.

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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