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Publications 2008

Structural variation of chromosomes in autism spectrum disorder.
Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW. Am J Hum Genet. 2008 Feb;82(2):477-88. Epub 2008 Jan 17.
PMID: 18252227

IL5RA and TNFRSF6B Gene Variants Are Associated With Sporadic IgA Nephropathy.
Liu XQ, Paterson AD, He N, St George-Hyslop P, Rauta V, Gronhagen-Riska C, Laakso M, Thibaudin L, Berthoux F, Cattran D, Pei Y. J Am Soc Nephrol. 2008 Feb 6; [Epub ahead of print]
PMID: 18256354

Very high and increasing incidence of type 1 diabetes mellitus in Newfoundland and Labrador, Canada.
Newhook LA, Grant M, Sloka S, Hoque M, Paterson AD, Hagerty D, Curtis J. Pediatr Diabetes. 2008 Jan 24; [Epub ahead of print]
PMID: 18221421

Association of LY9 in UK and Canadian SLE families.
Graham DS, Vyse TJ, Fortin PR, Montpetit A, Cai YC, Lim S, McKenzie T, Farwell L, Rhodes B, Chad L, Hudson TJ, Sharpe A, Terhorst C, Greenwood CM, Wither J, Rioux JD. Genes Immun. 2008 Jan 24; [Epub ahead of print]
PMID: 18216865

Parental effect of DNA (Cytosine-5) methyltransferase 1 on grandparental-origin-dependent transmission ratio distortion in mouse crosses and human families.
Yang L, Andrade MF, Labialle S, Moussette S, Geneau G, Sinnett D, Belisle A, Greenwood CM, Naumova AK. Genetics. 2008 Jan;178(1):35-45.
PMID: 18202356

Genomic rearrangements in the spotlight.
Osborne LR. Nat Genet. 2008 Jan;40(1):6-7.
PMID: 18163126

Molecular diagnostics in autosomal dominant polycystic kidney disease: utility and limitations.
Zhao X, Paterson AD, Zahirieh A, He N, Wang K, Pei Y. Clin J Am Soc Nephrol. 2008 Jan;3(1):146-52. Epub 2007 Dec 12.
PMID: 18077784

Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study.
Al-Kateb H, Boright AP, Mirea L, Xie X, Sutradhar R, Mowjoodi A, Bharaj B, Liu M, Bucksa JM, Arends VL, Steffes MW, Cleary PA, Sun W, Lachin JM, Thorner PS, Ho M, McKnight AJ, Maxwell AP, Savage DA, Kidd KK, Kidd JR, Speed WC, Orchard TJ, Miller RG, Sun L, Bull SB, Paterson AD; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group. Diabetes. 2008 Jan;57(1):218-28. Epub 2007 Oct 3.
PMID: 17914031

A Nurr1 point mutant, implicated in Parkinson's disease, uncouples ERK1/2-dependent regulation of tyrosine hydroxylase transcription.
Jacobsen KX, MacDonald H, Lemonde S, Daigle M, Grimes DA, Bulman DE, Albert PR. Neurobiol Dis. 2008 Jan;29(1):117-22. Epub 2007 Aug 21.
PMID: 17890097