Newman WG - Search Results

1

Geroderma osteodysplastica maps to a 4 Mb locus on chromosome 1q24.

Newman WG, Clayton-Smith J, Metcalfe K, Cole R, Tartaglia M, Brancati F, Morara S, Novelli A, Liu X, Siminovitch KA, Mundlos S, Tassabehji M, Black GC. Newman WG, et al. Am J Med Genet A. 2008 Dec 1;146A(23):3034-7. doi: 10.1002/ajmg.a.32564. Am J Med Genet A. 2008. PMID: 19006212

2

DLG5 variants contribute to Crohn disease risk in a Canadian population.

Newman WG, Gu X, Wintle RF, Liu X, van Oene M, Amos CI, Siminovitch KA. Newman WG, et al. Hum Mutat. 2006 Apr;27(4):353-8. doi: 10.1002/humu.20301. Hum Mutat. 2006. PMID: 16450402

3

Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population.

Newman WG, Zhang Q, Liu X, Walker E, Ternan H, Owen J, Johnson B, Greer W, Mosher DP, Maksymowych WP, Bykerk VP, Keystone EC, Amos CI, Siminovitch KA. Newman WG, et al. Arthritis Rheum. 2006 Dec;54(12):3820-7. doi: 10.1002/art.22270. Arthritis Rheum. 2006. PMID: 17133579 Free article.

4

Array comparative genomic hybridization for diagnosis of developmental delay: an exploratory cost-consequences analysis.

Newman WG, Hamilton S, Ayres J, Sanghera N, Smith A, Gaunt L, Davies LM, Clayton-Smith J. Newman WG, et al. Clin Genet. 2007 Mar;71(3):254-9. doi: 10.1111/j.1399-0004.2007.00756.x. Clin Genet. 2007. PMID: 17309648

5

A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25-q26.

Cilliers DD, Parveen R, Clayton P, Cairns SA, Clarke S, Shalet SM, Black GC, Newman WG, Clayton-Smith J. Cilliers DD, et al. Among authors: newman wg. Eur J Med Genet. 2007 May-Jun;50(3):216-23. doi: 10.1016/j.ejmg.2007.01.003. Epub 2007 Jan 27. Eur J Med Genet. 2007. PMID: 17369115

6

Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis.

Hadfield KD, Newman WG, Bowers NL, Wallace A, Bolger C, Colley A, McCann E, Trump D, Prescott T, Evans DG. Hadfield KD, et al. Among authors: newman wg. J Med Genet. 2008 Jun;45(6):332-9. doi: 10.1136/jmg.2007.056499. Epub 2008 Feb 19. J Med Genet. 2008. PMID: 18285426

7

Genetic variants in IL-23R and ATG16L1 independently predispose to increased susceptibility to Crohn's disease in a Canadian population.

Newman WG, Zhang Q, Liu X, Amos CI, Siminovitch KA. Newman WG, et al. J Clin Gastroenterol. 2009 May-Jun;43(5):444-7. doi: 10.1097/MCG.0b013e318168bdf0. J Clin Gastroenterol. 2009. PMID: 19276991

8

Breast cancer susceptibility variants alter risks in familial disease.

Latif A, Hadfield KD, Roberts SA, Shenton A, Lalloo F, Black GC, Howell A, Evans DG, Newman WG. Latif A, et al. Among authors: newman wg. J Med Genet. 2010 Feb;47(2):126-31. doi: 10.1136/jmg.2009.067256. Epub 2009 Jul 16. J Med Genet. 2010. PMID: 19617217

9

Genetic dissection of inflammatory bowel disease: unravelling etiology and improving diagnostics.

Limdi JK, Siminovitch KA, Newman W. Limdi JK, et al. Expert Rev Clin Immunol. 2005 Nov;1(4):609-17. doi: 10.1586/1744666X.1.4.609. Expert Rev Clin Immunol. 2005. PMID: 20477602

10

Mutations in HPSE2 cause urofacial syndrome.

Daly SB, Urquhart JE, Hilton E, McKenzie EA, Kammerer RA, Lewis M, Kerr B, Stuart H, Donnai D, Long DA, Burgu B, Aydogdu O, Derbent M, Garcia-Minaur S, Reardon W, Gener B, Shalev S, Smith R, Woolf AS, Black GC, Newman WG. Daly SB, et al. Among authors: newman wg. Am J Hum Genet. 2010 Jun 11;86(6):963-9. doi: 10.1016/j.ajhg.2010.05.006. Am J Hum Genet. 2010. PMID: 20560210 Free PMC article.

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