A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

10.1136/jmedgenet-2012-101155

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Main Authors: Sharma M., Ioannidis J.P.A., Aasly J.O., Annesi G., Brice A., Bertram L., Bozi M., Barcikowska M., Crosiers D., Clarke C.E., Facheris M.F., Farrer M., Garraux G., Gispert S., Auburger G., Vilariño-Güell C., Hadjigeorgiou G.M., Hicks A.A., Hattori N., Jeon B.S., Jamrozik Z., Krygowska-Wajs A., Lesage S., Lill C.M., Lin J.-J., Lynch T., Lichtner P., Lang A.E., Libioulle C., Murata M., Mok V., Jasinska-Myga B., Mellick G.D., Morrison K.E., Meitnger T., Zimprich A., Opala G., Pramstaller P.P., Pichler I., Park S.S., Quattrone A., Rogaeva E., Ross O.A., Stefanis L., Stockton J.D., Satake W., Silburn P.A., Strom T.M., Theuns J., Tan E.K., Toda T., Tomiyama H., Uitti R.J., Van Broeckhoven C., Wirdefeldt K., Wszolek Z., Xiromerisiou G., Yomono H.S., Yueh K.-C., Zhao Y., Gasser T., Maraganore D., Krüger R.
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: 2018
Online Access:http://scholarbank.nus.edu.sg/handle/10635/150112
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spelling sg-nus-scholar.10635-1501122023-11-01T07:58:02Z A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants Sharma M. Ioannidis J.P.A. Aasly J.O. Annesi G. Brice A. Bertram L. Bozi M. Barcikowska M. Crosiers D. Clarke C.E. Facheris M.F. Farrer M. Garraux G. Gispert S. Auburger G. Vilariño-Güell C. Hadjigeorgiou G.M. Hicks A.A. Hattori N. Jeon B.S. Jamrozik Z. Krygowska-Wajs A. Lesage S. Lill C.M. Lin J.-J. Lynch T. Lichtner P. Lang A.E. Libioulle C. Murata M. Mok V. Jasinska-Myga B. Mellick G.D. Morrison K.E. Meitnger T. Zimprich A. Opala G. Pramstaller P.P. Pichler I. Park S.S. Quattrone A. Rogaeva E. Ross O.A. Stefanis L. Stockton J.D. Satake W. Silburn P.A. Strom T.M. Theuns J. Tan E.K. Toda T. Tomiyama H. Uitti R.J. Van Broeckhoven C. Wirdefeldt K. Wszolek Z. Xiromerisiou G. Yomono H.S. Yueh K.-C. Zhao Y. Gasser T. Maraganore D. Krüger R. DUKE-NUS MEDICAL SCHOOL 10.1136/jmedgenet-2012-101155 Journal of Medical Genetics 49 11 721-726 2018-12-21T07:03:56Z 2018-12-21T07:03:56Z 2012 Article Sharma M., Ioannidis J.P.A., Aasly J.O., Annesi G., Brice A., Bertram L., Bozi M., Barcikowska M., Crosiers D., Clarke C.E., Facheris M.F., Farrer M., Garraux G., Gispert S., Auburger G., Vilariño-Güell C., Hadjigeorgiou G.M., Hicks A.A., Hattori N., Jeon B.S., Jamrozik Z., Krygowska-Wajs A., Lesage S., Lill C.M., Lin J.-J., Lynch T., Lichtner P., Lang A.E., Libioulle C., Murata M., Mok V., Jasinska-Myga B., Mellick G.D., Morrison K.E., Meitnger T., Zimprich A., Opala G., Pramstaller P.P., Pichler I., Park S.S., Quattrone A., Rogaeva E., Ross O.A., Stefanis L., Stockton J.D., Satake W., Silburn P.A., Strom T.M., Theuns J., Tan E.K., Toda T., Tomiyama H., Uitti R.J., Van Broeckhoven C., Wirdefeldt K., Wszolek Z., Xiromerisiou G., Yomono H.S., Yueh K.-C., Zhao Y., Gasser T., Maraganore D., Krüger R. (2012). A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics 49 (11) : 721-726. ScholarBank@NUS Repository. https://doi.org/10.1136/jmedgenet-2012-101155 222593 http://scholarbank.nus.edu.sg/handle/10635/150112 Scopus
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
description 10.1136/jmedgenet-2012-101155
author2 DUKE-NUS MEDICAL SCHOOL
author_facet DUKE-NUS MEDICAL SCHOOL
Sharma M.
Ioannidis J.P.A.
Aasly J.O.
Annesi G.
Brice A.
Bertram L.
Bozi M.
Barcikowska M.
Crosiers D.
Clarke C.E.
Facheris M.F.
Farrer M.
Garraux G.
Gispert S.
Auburger G.
Vilariño-Güell C.
Hadjigeorgiou G.M.
Hicks A.A.
Hattori N.
Jeon B.S.
Jamrozik Z.
Krygowska-Wajs A.
Lesage S.
Lill C.M.
Lin J.-J.
Lynch T.
Lichtner P.
Lang A.E.
Libioulle C.
Murata M.
Mok V.
Jasinska-Myga B.
Mellick G.D.
Morrison K.E.
Meitnger T.
Zimprich A.
Opala G.
Pramstaller P.P.
Pichler I.
Park S.S.
Quattrone A.
Rogaeva E.
Ross O.A.
Stefanis L.
Stockton J.D.
Satake W.
Silburn P.A.
Strom T.M.
Theuns J.
Tan E.K.
Toda T.
Tomiyama H.
Uitti R.J.
Van Broeckhoven C.
Wirdefeldt K.
Wszolek Z.
Xiromerisiou G.
Yomono H.S.
Yueh K.-C.
Zhao Y.
Gasser T.
Maraganore D.
Krüger R.
format Article
author Sharma M.
Ioannidis J.P.A.
Aasly J.O.
Annesi G.
Brice A.
Bertram L.
Bozi M.
Barcikowska M.
Crosiers D.
Clarke C.E.
Facheris M.F.
Farrer M.
Garraux G.
Gispert S.
Auburger G.
Vilariño-Güell C.
Hadjigeorgiou G.M.
Hicks A.A.
Hattori N.
Jeon B.S.
Jamrozik Z.
Krygowska-Wajs A.
Lesage S.
Lill C.M.
Lin J.-J.
Lynch T.
Lichtner P.
Lang A.E.
Libioulle C.
Murata M.
Mok V.
Jasinska-Myga B.
Mellick G.D.
Morrison K.E.
Meitnger T.
Zimprich A.
Opala G.
Pramstaller P.P.
Pichler I.
Park S.S.
Quattrone A.
Rogaeva E.
Ross O.A.
Stefanis L.
Stockton J.D.
Satake W.
Silburn P.A.
Strom T.M.
Theuns J.
Tan E.K.
Toda T.
Tomiyama H.
Uitti R.J.
Van Broeckhoven C.
Wirdefeldt K.
Wszolek Z.
Xiromerisiou G.
Yomono H.S.
Yueh K.-C.
Zhao Y.
Gasser T.
Maraganore D.
Krüger R.
spellingShingle Sharma M.
Ioannidis J.P.A.
Aasly J.O.
Annesi G.
Brice A.
Bertram L.
Bozi M.
Barcikowska M.
Crosiers D.
Clarke C.E.
Facheris M.F.
Farrer M.
Garraux G.
Gispert S.
Auburger G.
Vilariño-Güell C.
Hadjigeorgiou G.M.
Hicks A.A.
Hattori N.
Jeon B.S.
Jamrozik Z.
Krygowska-Wajs A.
Lesage S.
Lill C.M.
Lin J.-J.
Lynch T.
Lichtner P.
Lang A.E.
Libioulle C.
Murata M.
Mok V.
Jasinska-Myga B.
Mellick G.D.
Morrison K.E.
Meitnger T.
Zimprich A.
Opala G.
Pramstaller P.P.
Pichler I.
Park S.S.
Quattrone A.
Rogaeva E.
Ross O.A.
Stefanis L.
Stockton J.D.
Satake W.
Silburn P.A.
Strom T.M.
Theuns J.
Tan E.K.
Toda T.
Tomiyama H.
Uitti R.J.
Van Broeckhoven C.
Wirdefeldt K.
Wszolek Z.
Xiromerisiou G.
Yomono H.S.
Yueh K.-C.
Zhao Y.
Gasser T.
Maraganore D.
Krüger R.
A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
author_sort Sharma M.
title A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
title_short A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
title_full A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
title_fullStr A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
title_full_unstemmed A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
title_sort multi-centre clinico-genetic analysis of the vps35 gene in parkinson disease indicates reduced penetrance for disease-associated variants
publishDate 2018
url http://scholarbank.nus.edu.sg/handle/10635/150112
_version_ 1781791591276478464

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