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Author/Creator Gasser, Thomas

1. A genome-wide association study in multiple system atrophy. (11th October 2016)

Authors:
Sailer, Anna; Scholz, Sonja W.; Nalls, Michael A.; Schulte, Claudia; Federoff, Monica; Price, T. Ryan; Lees, Andrew; Ross, Owen A.; Dickson, Dennis W.; Mok, Kin; Mencacci, Niccolo E.; Schottlaender, Lucia; Chelban, Viorica; Ling, Helen; O'Sullivan, Sean S.; Wood, Nicholas W.; Traynor, Bryan J.; F...
Journal:
Neurology
Issue:
Volume 87:Number 15(2016)
Page Start:
Record Type:
Journal Article
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2. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Issue 11 (2nd November 2012)

Authors:
Sharma, Manu; Ioannidis, John P A; Aasly, Jan O; Annesi, Grazia; Brice, Alexis; Bertram, Lars; Bozi, Maria; Barcikowska, Maria; Crosiers, David; Clarke, Carl E; Facheris, Maurizio F; Farrer, Matthew; Garraux, Gaetan; Gispert, Suzana; Auburger, Georg; Vilariño-Güell, Carles; Hadjigeorgiou, Georgio...
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 11(2012)
Page Start:
721
Record Type:
Journal Article
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3. A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family. (August 2016)

Authors:
Hanagasi, Hasmet A.; Giri, Anamika; Kartal, Ece; Guven, Gamze; Bilgiç, Başar; Hauser, Ann-Kathrin; Emre, Murat; Heutink, Peter; Basak, Nazlı; Gasser, Thomas; Simón-Sánchez, Javier; Lohmann, Ebba
Journal:
Parkinsonism & related disorders
Issue:
Volume 29(2016)
Page Start:
117
Record Type:
Journal Article
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4. A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease. Issue 7 (22nd February 2021)

Authors:
Liu, Hui; Koros, Christos; Strohäker, Timo; Schulte, Claudia; Bozi, Maria; Varvaresos, Stefanos; Ibáñez de Opakua, Alain; Simitsi, Athina Maria; Bougea, Anastasia; Voumvourakis, Konstantinos; Maniati, Matina; Papageorgiou, Sokratis G.; Hauser, Ann‐Kathrin; Becker, Stefan; Zweckstetter, Markus; St...
Journal:
Movement disorders
Issue:
Volume 36:Issue 7(2021)
Page Start:
1624
Record Type:
Journal Article
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5. Abolishing the 1‐year rule: How much evidence will be enough?. Issue 11 (26th September 2016)

Authors:
Postuma, Ronald B.; Berg, Daniela; Stern, Matthew; Poewe, Werner; Olanow, C. Warren; Oertel, Wolfgang; Marek, Kenneth; Litvan, Irene; Lang, Anthony E.; Halliday, Glenda; Goetz, Christopher G.; Gasser, Thomas; Dubois, Bruno; Chan, Piu; Bloem, Bastiaan R.; Adler, Charles H.; Deuschl, Günther
Journal:
Movement disorders
Issue:
Volume 31:Issue 11(2016)
Page Start:
1623
Record Type:
Journal Article
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6. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. (18th October 2016)

Authors:
Lubbe, Steven J.; Escott-Price, Valentina; Gibbs, J. Raphael; Nalls, Mike A.; Bras, Jose; Price, T. Ryan; Nicolas, Aude; Jansen, Iris E.; Mok, Kin Y.; Pittman, Alan M.; Tomkins, James E.; Lewis, Patrick A.; Noyce, Alastair J.; Lesage, Suzanne; Sharma, Manu; Schiff, Elena R.; Levine, Adam P.; Bric...
Journal:
Human molecular genetics
Issue:
Volume 25:Number 24(2016:Dec. 15)
Page Start:
5483
Record Type:
Journal Article
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8. Analysis of slight precipitation in China during the past decades and its relationship with advanced very high radiometric resolution normalized difference vegetation index. (14th August 2018)

Authors:
Li, Xinyue; Balkanski, Yves; Wu, Zhengfang; Gasser, Thomas; Ciais, Philippe; Zhou, Feng; Li, Laurent; Tao, Shu; Peng, Shushi; Piao, Shilong; Wang, Rong; Wang, Tao; Li, Bengang
Journal:
International journal of climatology
Issue:
Volume 38:Number 15(2018)
Page Start:
5563
Record Type:
Journal Article
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