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Papers authored by Latourelle J

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Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).

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Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Wheeler V, Macdonald ME, Gusella JF, and Myers RH

American journal of medical genetics. Part A 149A(7):1375-81, 2009 Jul - Who cited this? | PubMed ID: 19507258 | Fulltext

Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

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Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH, and PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories

Human genetics 124(6):593-605, 2009 Jan - Who cited this? | PubMed ID: 18985386 | Fulltext

Genomewide association study for onset age in Parkinson disease.

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Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T, PROGENI Investigators, Coordinators and Molecular Genetic Laboratories, and GenePD Investigators, Coordinators and Molecular Genetic Laboratories

BMC medical genetics 10:98, 2009 - Who cited this? | PubMed ID: 19772629 | Fulltext

Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study.

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McNicoll CF, Latourelle JC, MacDonald ME, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA,

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Movement disorders : official journal of the Movement Disorder Society 23(11):1596-601, 2008 Aug 15 - Who cited this? | PubMed ID: 18649400 | Fulltext

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.

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Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, Goldwurm S,

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Neurology 71(1):28-34, 2008 Jul 1 - Who cited this? | PubMed ID: 18509094 | Fulltext

Replication of association between ELAVL4 and Parkinson disease: the GenePD study.

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Destefano AL, Latourelle J, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts R, Guttman M, Racette BA, Perlmutter JS, Marlor L, Shill HA, Singer C,

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Human genetics, 2008 Jun 29 - Who cited this? | PubMed ID: 18587682 | Fulltext

NYD-SP18 is associated with obesity in the NHLBI Family Heart Study.

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Wilk JB, Laramie JM, Latourelle JC, Williamson S, Nagle MW, Tobin JE, Foster CL, Eckfeldt JH, Province MA, Borecki IB, and Myers RH

International journal of obesity (2005) 32(6):930, 2008 Jun - Who cited this? | PubMed ID: 18317470 | Fulltext

Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study.

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Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, and Myers RH

BMC medical genetics 9:46, 2008 - Who cited this? | PubMed ID: 18498660 | Fulltext

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.

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Latourelle JC, Sun M, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA, Singer C,

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BMC medicine 6:32, 2008 - Who cited this? | PubMed ID: 18986508 | Fulltext

Sepiapterin reductase expression is increased in Parkinson's disease brain tissue.

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Tobin JE, Cui J, Wilk JB, Latourelle JC, Laramie JM, McKee AC, Guttman M, Karamohamed S, DeStefano AL, and Myers RH

Brain research 1139:42-7, 2007 Mar 30 - Who cited this? | PubMed ID: 17270157 | Fulltext

Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study.

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Wilk JB, Tobin JE, Suchowersky O, Shill HA, Klein C, Wooten GF, Lew MF, Mark MH, Guttman M, Watts RL, Singer C, Growdon JH, Latourelle JC, Saint-Hilaire MH, DeStefano AL, Prakash R,

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Neurology 67(12):2206-10, 2006 Dec 26 - Who cited this? | PubMed ID: 17190945 | Fulltext

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.

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Sun M, Latourelle JC, Wooten GF, Lew MF, Klein C, Shill HA, Golbe LI, Mark MH, Racette BA, Perlmutter JS, Parsian A, Guttman M, Nicholson G, Xu G, Wilk JB, Saint-Hilaire MH,

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Archives of neurology 63(6):826-32, 2006 Jun - Who cited this? | PubMed ID: 16769863 | Fulltext

BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study.

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Karamohamed S, Latourelle JC, Racette BA, Perlmutter JS, Wooten GF, Lew M, Klein C, Shill H, Golbe LI, Mark MH, Guttman M, Nicholson G, Wilk JB, Saint-Hilaire M, DeStefano AL, Prakash R,

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Neurology 65(11):1823-5, 2005 Dec 13 - Who cited this? | PubMed ID: 16344533 | Fulltext

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study.

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Karamohamed S, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Liu J, Shoemaker CM, Wilk JB, DeStefano AL,

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Movement disorders : official journal of the Movement Disorder Society 20(9):1188-91, 2005 Sep - Who cited this? | PubMed ID: 15966003 | Fulltext

Dynamic equilibration of airway smooth muscle contraction during physiological loading.

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Latourelle J, Fabry B, and Fredberg JJ

Journal of applied physiology (Bethesda, Md. : 1985) 92(2):771-9, 2002 Feb - Who cited this? | PubMed ID: 11796691 | Fulltext

Exact morphometric modeling of rat lungs for predicting mechanical impedance.

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Latourelle JC, Gillis HL, and Lutchen KR

Respiration physiology 127(1):75-85, 2001 Aug - Who cited this? | PubMed ID: 11445202 | Fulltext

[Malignant giant cell tumor of the soft tissues].

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Latourelle J and Boivin Y

L'union medicale du Canada 100(9):1792-3, 1971 Sep - Who cited this? | PubMed ID: 5112017 | Fulltext

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