Cook MC - Search Results

1

Recurrent miscalling of missense variation from short-read genome sequence data.

Field MA, Burgio G, Chuah A, Al Shekaili J, Hassan B, Al Sukaiti N, Foote SJ, Cook MC, Andrews TD. Field MA, et al. Among authors: cook mc. BMC Genomics. 2019 Jul 16;20(Suppl 8):546. doi: 10.1186/s12864-019-5863-2. BMC Genomics. 2019. PMID: 31307400 Free PMC article.

2

Heterophile interference accounts for method-specific dsDNA antibodies in patients receiving anti-TNF treatment.

Alshekaili J, Li C, Cook MC. Alshekaili J, et al. Among authors: cook mc. Rheumatology (Oxford). 2010 May;49(5):891-7. doi: 10.1093/rheumatology/keq018. Epub 2010 Feb 23. Rheumatology (Oxford). 2010. PMID: 20179080

3

De novo infantile primary antiphospholipid antibody syndrome.

Alshekaili J, Reynolds G, Cook MC. Alshekaili J, et al. Among authors: cook mc. Lupus. 2010 Nov;19(13):1565-8. doi: 10.1177/0961203310375263. Epub 2010 Jul 27. Lupus. 2010. PMID: 20663842

4

Identification of a pathogenic variant in TREX1 in early-onset cerebral systemic lupus erythematosus by Whole-exome sequencing.

Ellyard JI, Jerjen R, Martin JL, Lee AY, Field MA, Jiang SH, Cappello J, Naumann SK, Andrews TD, Scott HS, Casarotto MG, Goodnow CC, Chaitow J, Pascual V, Hertzog P, Alexander SI, Cook MC, Vinuesa CG. Ellyard JI, et al. Among authors: cook mc. Arthritis Rheumatol. 2014 Dec;66(12):3382-6. doi: 10.1002/art.38824. Arthritis Rheumatol. 2014. PMID: 25138095

5

Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100.

Lee CE, Fulcher DA, Whittle B, Chand R, Fewings N, Field M, Andrews D, Goodnow CC, Cook MC. Lee CE, et al. Among authors: cook mc. Blood. 2014 Nov 6;124(19):2964-72. doi: 10.1182/blood-2014-06-578542. Epub 2014 Sep 18. Blood. 2014. PMID: 25237204 Free PMC article.

6

Reducing the search space for causal genetic variants with VASP.

Field MA, Cho V, Cook MC, Enders A, Vinuesa CG, Whittle B, Andrews TD, Goodnow CC. Field MA, et al. Among authors: cook mc. Bioinformatics. 2015 Jul 15;31(14):2377-9. doi: 10.1093/bioinformatics/btv135. Epub 2015 Mar 8. Bioinformatics. 2015. PMID: 25755272 Free PMC article.

7

A deleterious RNF43 germline mutation in a severely affected serrated polyposis kindred.

Taupin D, Lam W, Rangiah D, McCallum L, Whittle B, Zhang Y, Andrews D, Field M, Goodnow CC, Cook MC. Taupin D, et al. Among authors: cook mc. Hum Genome Var. 2015 Apr 16;2:15013. doi: 10.1038/hgv.2015.13. eCollection 2015. Hum Genome Var. 2015. PMID: 27081527 Free PMC article.

8

Heterogeneity of Human Neutrophil CD177 Expression Results from CD177P1 Pseudogene Conversion.

Wu Z, Liang R, Ohnesorg T, Cho V, Lam W, Abhayaratna WP, Gatenby PA, Perera C, Zhang Y, Whittle B, Sinclair A, Goodnow CC, Field M, Andrews TD, Cook MC. Wu Z, et al. Among authors: cook mc. PLoS Genet. 2016 May 26;12(5):e1006067. doi: 10.1371/journal.pgen.1006067. eCollection 2016 May. PLoS Genet. 2016. PMID: 27227454 Free PMC article.

9

Agammaglobulinaemia despite terminal B-cell differentiation in a patient with a novel LRBA mutation.

Al Sukaiti N, AbdelRahman K, AlShekaili J, Al Oraimi S, Al Sinani A, Al Rahbi N, Cho V, Field M, Cook MC. Al Sukaiti N, et al. Among authors: cook mc. Clin Transl Immunology. 2017 May 26;6(5):e144. doi: 10.1038/cti.2017.20. eCollection 2017 May. Clin Transl Immunology. 2017. PMID: 28690850 Free PMC article.

10

STAT3 regulates cytotoxicity of human CD57+ CD4+ T cells in blood and lymphoid follicles.

Alshekaili J, Chand R, Lee CE, Corley S, Kwong K, Papa I, Fulcher DA, Randall KL, Leiding JW, Ma CS, Wilkins MR, Uzel G, Goodnow CC, Vinuesa CG, Tangye SG, Cook MC. Alshekaili J, et al. Among authors: cook mc. Sci Rep. 2018 Feb 23;8(1):3529. doi: 10.1038/s41598-018-21389-8. Sci Rep. 2018. PMID: 29476109 Free PMC article.

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