gender < gene < genepd

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List of bibliographic references indexed by gene

Number of relevant bibliographic references: 245.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000129 (2015)	Lasse Pihlstr M [Norvège] ; Victoria Berge ; Aina Rengmark ; Mathias Toft	Parkinson's disease correlates with promoter methylation in the α-synuclein gene.
000144 (2015)	Anat Mirelman [Israël] ; Roy N. Alcalay [États-Unis] ; Rachel Saunders-Pullman [États-Unis] ; Kira Yasinovsky [Israël] ; Avner Thaler [Israël] ; Tanya Gurevich [Israël] ; Helen Mejia-Santana [États-Unis] ; Deborah Raymond [États-Unis] ; Mali Gana-Weisz [Israël] ; Anat Bar-Shira [Israël] ; Laurie Ozelius [États-Unis] ; Lorraine Clark [États-Unis] ; Avi Orr-Urtreger [Israël] ; Susan Bressman [États-Unis] ; Karen Marder [États-Unis] ; Nir Giladi [Israël]	Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.
000162 (2015)	Ling-Yan Ma [République populaire de Chine] ; Lin Wang ; Ying-Mai Yang ; Tao Feng ; Xin-Hua Wan	Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families.
000216 (2015)	Bettina Balint [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	Hot topic: Recessive mutations in the a3(VI) collagen gene COL6A3 cause early-onset isolated dystonia.
000231 (2015)	Ismael Huertas-Fernández [Espagne] ; Pilar G Mez-Garre [Espagne] ; Marcos Madruga-Garrido [Espagne] ; Inmaculada Bernal-Bernal [Espagne] ; Marta Bonilla-Toribio [Espagne] ; Juan Francisco Martín-Rodríguez [Espagne] ; María Teresa Cáceres-Redondo [Espagne] ; Laura Vargas-González [Espagne] ; Fátima Carrillo [Espagne] ; Alberto Pascual [Espagne] ; Jay A. Tischfield [États-Unis] ; Robert A. King [États-Unis] ; Gary A. Heiman [États-Unis] ; Pablo Mir [Espagne]	GDNF gene is associated with tourette syndrome in a family study.
000261 (2015)	Brent L. Fogel [États-Unis] ; Sonya M. Hanson ; Esther B E. Becker	Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
000286 (2015)	Nathan C. Rowland [États-Unis] ; Philip A. Starr ; Paul S. Larson ; Jill L. Ostrem ; William J. Marks ; Daniel A. Lim	Combining cell transplants or gene therapy with deep brain stimulation for Parkinson's disease.
000305 (2015)	Chin-Hsien Lin [Taïwan] ; Eng-King Tan ; Chih-Chao Yang ; Zhao Yi ; Ruey-Meei Wu	COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese.
000349 (2015)	Ana Westenberger [Allemagne] ; Christine Klein [Allemagne]	A new gene for primary familial brain calcification: The importance of phosphate homeostasis.
000350 (2015)	Ebba Lohmann [Turquie] ; Anne-Sophie Coquel [France] ; Aurélie Honoré [France] ; Hakan Gurvit [Turquie] ; Hasmet Hanagasi [Turquie] ; Murat Emre [Turquie] ; Anne L. Leutenegger [France] ; Valérie Drouet [France] ; Mourad Sahbatou [France] ; Gamze Guven [Turquie] ; Nihan Erginel-Unaltuna [Turquie] ; Jean-Francois Deleuze [France] ; Suzanne Lesage [France] ; Alexis Brice [France]	A new F-box protein 7 gene mutation causing typical Parkinson's disease.
000494 (2014)	Geetanjali S. Rathore [États-Unis] ; Christian P. Schaaf ; Amber J. Stocco	Novel mutation of the WDR45 gene causing beta-propeller protein-associated neurodegeneration.
000533 (2014)	Karen M. Doherty [Royaume-Uni] ; Thomas T. Warner ; Andrew J. Lees	Late onset ataxia: MSA-C or SCA 17? A gene penetrance dilemma.
000556 (2014)	Neil Aronin [États-Unis] ; Marian Difiglia	Huntingtin-lowering strategies in Huntington's disease: antisense oligonucleotides, small RNAs, and gene editing.
000609 (2014)	Valerija Dobri I [Allemagne] ; Nikola Kresojevi ; Ana Westenberger ; Marina Svetel ; Aleksandra Tomi ; Vesna Rali ; Igor Petrovi ; Milica Je Menica Luki ; Katja Lohmann ; Ivana Novakovi ; Christine Klein ; Vladimir S. Kosti	De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
000667 (2014)	Sarah K. Abbott ; Hongyun Li ; Sonia Sanz Mu Oz ; Bianca Knoch ; Marijka Batterham ; Karen E. Murphy ; Glenda M. Halliday ; Brett Garner	Altered ceramide acyl chain length and ceramide synthase gene expression in Parkinson’s disease.
000685 (2014)	Amit Batla [Royaume-Uni] ; Kailash P. Bhatia	A new gene for Fahr's syndrome-PDGF-B.
000698 (2013)	Federica Agosta [Italie] ; Vladimir S. Kostic ; Kristina Davidovic ; Nikola Kresojevi ; Lidia Sarro ; Marina Svetel ; Iva Stankovi ; Giancarlo Comi ; Christine Klein ; Massimo Filippi	White matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutations.
000713 (2013)	Jeffrey H. Kordower [États-Unis] ; Anders Bjorklund	Trophic factor gene therapy for Parkinson's disease.
000747 (2013)	Hao Deng [République populaire de Chine] ; Kai Gao ; Joseph Jankovic [États-Unis]	The VPS35 gene and Parkinson's disease.
000785 (2013)	Jeremy R B. Newman [Australie] ; Alexander C. Lehn ; Richard S. Boyle ; Peter A. Silburn ; George D. Mellick	Screening for rare sequence variants in the THAP1 gene in a primary dystonia cohort.
000842 (2013)	Cathérine C S. Delnooz ; Ron A. Wevers ; Marialuisa Quadri ; Peter T. Clayton ; Philippa B. Mills ; Karin Tuschl ; Eric J. Steenbergen ; Vincenzo Bonifati ; Bart P C. Van De Warrenburg	Phenotypic variability in a dystonia family with mutations in the manganese transporter gene.

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