Genomewide association, Parkinson disease, and PARK10 [3]

Matthew J. Farrer; Kristoffer Haugarvoll; Owen A. Ross; Jeremy T. Stone; Nicole M. Milkovic; Stephanie A. Cobb; Andrew J. Whittle; Sarah J. Lincoln; Mary M. Hulihan; Michael G. Heckman; Linda R. White; Jan O. Aasly; J. Mark Gibson; David Gosal; Timothy Lynch; Zbigniew K. Wszolek; Ryan J. Uitti; Mathias Toft

doi:10.1086/504728

Genomewide association, Parkinson disease, and PARK10 [3]

Matthew J. Farrer, Kristoffer Haugarvoll, Owen A. Ross, Jeremy T. Stone, Nicole M. Milkovic, Stephanie A. Cobb, Andrew J. Whittle, Sarah J. Lincoln, Mary M. Hulihan, Michael G. Heckman, Linda R. White, Jan O. Aasly, J. Mark Gibson, David Gosal, Timothy Lynch, Zbigniew K. Wszolek, Ryan J. Uitti, Mathias Toft

Research output: Contribution to journal › Letter › peer-review

48 Scopus citations

Original language	English (US)
Pages (from-to)	1084-1088
Number of pages	5
Journal	American journal of human genetics
Volume	78
Issue number	6
DOIs	https://doi.org/10.1086/504728
State	Published - Jun 2006

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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Farrer, M. J., Haugarvoll, K., Ross, O. A., Stone, J. T., Milkovic, N. M., Cobb, S. A., Whittle, A. J., Lincoln, S. J., Hulihan, M. M., Heckman, M. G., White, L. R., Aasly, J. O., Gibson, J. M., Gosal, D., Lynch, T., Wszolek, Z. K., Uitti, R. J., & Toft, M. (2006). Genomewide association, Parkinson disease, and PARK10 [3]. American journal of human genetics, 78(6), 1084-1088. https://doi.org/10.1086/504728

Farrer, MJ, Haugarvoll, K, Ross, OA, Stone, JT, Milkovic, NM, Cobb, SA, Whittle, AJ, Lincoln, SJ, Hulihan, MM, Heckman, MG, White, LR, Aasly, JO, Gibson, JM, Gosal, D, Lynch, T, Wszolek, ZK, Uitti, RJ & Toft, M 2006, 'Genomewide association, Parkinson disease, and PARK10 [3]', American journal of human genetics, vol. 78, no. 6, pp. 1084-1088. https://doi.org/10.1086/504728

@article{e183d358d3a94607b0f9eca502001919,

title = "Genomewide association, Parkinson disease, and PARK10 [3]",

author = "Farrer, {Matthew J.} and Kristoffer Haugarvoll and Ross, {Owen A.} and Stone, {Jeremy T.} and Milkovic, {Nicole M.} and Cobb, {Stephanie A.} and Whittle, {Andrew J.} and Lincoln, {Sarah J.} and Hulihan, {Mary M.} and Heckman, {Michael G.} and White, {Linda R.} and Aasly, {Jan O.} and Gibson, {J. Mark} and David Gosal and Timothy Lynch and Wszolek, {Zbigniew K.} and Uitti, {Ryan J.} and Mathias Toft",

note = "Funding Information: The authors thank the patients and families for their participation in this study. Mayo Clinic Jacksonville is an M. K. Udall Parkinson{\textquoteright}s Disease Research Center of Excellence (National Institute of Neurological Disorders and Stroke grant P01 NS40256), and the authors thank all collaborators at the Udall Center. This study was also supported by the National Institutes of Health grant R01 NS36960, the Research Council of Norway grant 153487/V50, and Reberg{\textquoteright}s Legacy. The Ireland research consortium was supported by a Programme for Research in Third-Level Institutions neurosciences award and by the Research and Development Office of the Health and Personal Social Services. O.A.R. and M.T. are partly funded by National Parkinson Foundation and Parkinson{\textquoteright}s Disease Foundation fellowships, respectively. We thank Minnie Schreiber for technical assistance. ",

year = "2006",

month = jun,

doi = "10.1086/504728",

language = "English (US)",

volume = "78",

pages = "1084--1088",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "6",

}

TY - JOUR

T1 - Genomewide association, Parkinson disease, and PARK10 [3]

AU - Farrer, Matthew J.

AU - Haugarvoll, Kristoffer

AU - Ross, Owen A.

AU - Stone, Jeremy T.

AU - Milkovic, Nicole M.

AU - Cobb, Stephanie A.

AU - Whittle, Andrew J.

AU - Lincoln, Sarah J.

AU - Hulihan, Mary M.

AU - Heckman, Michael G.

AU - White, Linda R.

AU - Aasly, Jan O.

AU - Gibson, J. Mark

AU - Gosal, David

AU - Lynch, Timothy

AU - Wszolek, Zbigniew K.

AU - Uitti, Ryan J.

AU - Toft, Mathias

N1 - Funding Information: The authors thank the patients and families for their participation in this study. Mayo Clinic Jacksonville is an M. K. Udall Parkinson’s Disease Research Center of Excellence (National Institute of Neurological Disorders and Stroke grant P01 NS40256), and the authors thank all collaborators at the Udall Center. This study was also supported by the National Institutes of Health grant R01 NS36960, the Research Council of Norway grant 153487/V50, and Reberg’s Legacy. The Ireland research consortium was supported by a Programme for Research in Third-Level Institutions neurosciences award and by the Research and Development Office of the Health and Personal Social Services. O.A.R. and M.T. are partly funded by National Parkinson Foundation and Parkinson’s Disease Foundation fellowships, respectively. We thank Minnie Schreiber for technical assistance.

PY - 2006/6

Y1 - 2006/6

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U2 - 10.1086/504728

DO - 10.1086/504728

M3 - Letter

C2 - 16685661

AN - SCOPUS:33646894113

SN - 0002-9297

VL - 78

SP - 1084

EP - 1088

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 6

ER -

Genomewide association, Parkinson disease, and PARK10 [3]

ASJC Scopus subject areas

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