Two multiple sclerosis risk variants from a large genome-wide association study are associated with disease progression in a population-based case cohort

Michaela George; H. Quach; P. P. Ramsay; B. Acuna; L.  Shen; E. Mowry; C. Shaefer; L. F. Barcellos

Two multiple sclerosis risk variants from a large genome-wide association study are associated with disease progression in a population-based case cohort

Michaela George, H. Quach, P. P. Ramsay, B. Acuna, L. Shen, E. Mowry, C. Shaefer, L. F. Barcellos

University of California, Berkeley

Research output: Contribution to conference › Presentation › peer-review

Original language	American English
State	Published - 2012
Externally published	Yes
Event	Annual Meeting of the American Society of Human Genetics - San Francisco, United States Duration: Nov 6 2012 → Nov 10 2012 Conference number: 62

Conference

Conference	Annual Meeting of the American Society of Human Genetics
Abbreviated title	ASHG
Country/Territory	United States
City	San Francisco
Period	11/6/12 → 11/10/12

Disciplines

Public Health

OpenUrl availability

Full text

Cite this

Two multiple sclerosis risk variants from a large genome-wide association study are associated with disease progression in a population-based case cohort. / George, Michaela; Quach, H.; Ramsay, P. P. et al.
2012. Annual Meeting of the American Society of Human Genetics, San Francisco, California, United States.

Research output: Contribution to conference › Presentation › peer-review

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year = "2012",

language = "American English",

note = "Annual Meeting of the American Society of Human Genetics, ASHG ; Conference date: 06-11-2012 Through 10-11-2012",

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T1 - Two multiple sclerosis risk variants from a large genome-wide association study are associated with disease progression in a population-based case cohort

AU - George, Michaela

AU - Quach, H.

AU - Ramsay, P. P.

AU - Acuna, B.

AU - Shen, L.

AU - Mowry, E.

AU - Shaefer, C.

AU - Barcellos, L. F.

N1 - Conference code: 62

PY - 2012

Y1 - 2012

M3 - Presentation

T2 - Annual Meeting of the American Society of Human Genetics

Y2 - 6 November 2012 through 10 November 2012

ER -