Haplorhini < Haplotypes < Hardness

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 47.
[0-20] [0 - 20][0 - 47][20-40]

Ident.	Authors (with country if any)	Title
000853 (2013)	Michael G. Heckman [États-Unis] ; Alexandra I. Soto-Ortolaza ; Jan O. Aasly ; Nadine Abahuni ; Grazia Annesi ; Justin A. Bacon ; Soraya Bardien ; Maria Bozi ; Alexis Brice ; Laura Brighina ; Jonathan Carr ; Marie-Christine Chartier-Harlin ; Efthimios Dardiotis ; Dennis W. Dickson ; Nancy N. Diehl ; Alexis Elbaz ; Carlo Ferrarese ; Brian Fiske ; J Mark Gibson ; Rachel Gibson ; Georgios M. Hadjigeorgiou ; Nobutaka Hattori ; John P A. Ioannidis ; Magdalena Boczarska-Jedynak ; Barbara Jasinska-Myga ; Beom S. Jeon ; Yun Joong Kim ; Christine Klein ; Rejko Kruger ; Elli Kyratzi ; Suzanne Lesage ; Chin-Hsien Lin ; Timothy Lynch ; Demetrius M. Maraganore ; George D. Mellick ; Eugénie Mutez ; Christer Nilsson ; Grzegorz Opala ; Sung Sup Park ; Simona Petrucci ; Andreas Puschmann ; Aldo Quattrone ; Manu Sharma ; Peter A. Silburn ; Young Ho Sohn ; Leonidas Stefanis ; Vera Tadic ; Jessie Theuns ; Hiroyuki Tomiyama ; Ryan J. Uitti ; Enza Maria Valente ; Christine Van Broeckhoven ; Simone Van De Loo ; Demetrios K. Vassilatis ; Carles Vilari O-Güell ; Linda R. White ; Karin Wirdefeldt ; Zbigniew K. Wszolek ; Ruey-Meei Wu ; Faycal Hentati ; Matthew J. Farrer ; Owen A. Ross	Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.
000892 (2013)	Ignacio F. Mata ; Victoria Alvarez ; Renee Ribacoba ; Jon Infante ; María Sierra ; Pilar G Mez-Garre ; Pablo Mir ; Sarah Waldherr ; Dora Yearout ; Cyrus P. Zabetian	Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.
000964 (2013)	Justus L. Groen [Pays-Bas] ; Katja Ritz ; Michael W. Tanck ; Bart P. Van De Warrenburg ; Jacobus J. Van Hilten ; Majid Aramideh ; Frank Baas ; Marina A J. Tijssen	Is TOR1A a risk factor in adult-onset primary torsion dystonia?
000B66 (2012)	Maya Ando [Japon] ; Manabu Funayama ; Yuanzhe Li ; Kenichi Kashihara ; Yoshitake Murakami ; Nobutaka Ishizu ; Chizuko Toyoda ; Katsuhiko Noguchi ; Takashi Hashimoto ; Naoki Nakano ; Ryogen Sasaki ; Yasumasa Kokubo ; Shigeki Kuzuhara ; Kotaro Ogaki ; Chikara Yamashita ; Hiroyo Yoshino ; Taku Hatano ; Hiroyuki Tomiyama ; Nobutaka Hattori	VPS35 mutation in Japanese patients with typical Parkinson's disease.
000B91 (2012)	Tamara Pringsheim [Canada] ; Katie Wiltshire ; Lundy Day ; Jonathan Dykeman ; Thomas Steeves ; Nathalie Jette	The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis.
000D63 (2012)	Oswaldo Lorenzo-Betancor [Espagne] ; Lluís Samaranch ; Mario Ezquerra ; Eduardo Tolosa ; Elena Lorenzo ; Jaione Irigoyen ; Carles Gaig ; María A. Pastor ; Alexandra I. Soto-Ortolaza ; Owen A. Ross ; María C. Rodríguez-Oroz ; Francesc Valldeoriola ; María J. Martí ; María R. Luquin ; Jordi Perez-Tur ; Juan A. Burguera ; José A. Obeso ; Pau Pastor	LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation.
000E63 (2012)	Paolo Aridon ; Patrizia Tarantino ; Paolo Ragonese ; Marco D'Amelio ; Antono Cinturino ; Giuseppe Salemi ; Monica Gagliardi ; Vincenzina Lo Re ; Antonio Scarpitta ; Antonio Gambardella ; Aldo Quattrone ; Grazia Annesi ; Giovanni Savettieri	Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families.
000F36 (2012)	Ismaïl Ahmed [France] ; Ryad Tamouza ; Marc Delord ; Rajagopal Krishnamoorthy ; Christophe Tzourio ; Claire Mulot ; Magali Nacfer ; Jean-Charles Lambert ; Philippe Beaune ; Pierre Laurent-Puig ; Marie-Anne Loriot ; Dominique Charron ; Alexis Elbaz	Association between Parkinson's disease and the HLA-DRB1 locus.
001278 (2011)	Georgia Xiromerisiou ; Elli Kyratzi ; Efthimios Dardiotis ; Maria Bozi ; Vana Tsimourtou ; Eleftherios Stamboulis ; Styliani Ralli ; Demetrios Vassilatis ; Vanessa Gourbali ; Persa-Maria Kountra ; Kostas Fountas ; Alexandros Papadimitriou ; Leonidas Stefanis ; Georgios M. Hadjigeorgiou	Lack of association of the UCHL-1 gene with Parkinson's disease in a Greek cohort: a haplotype-tagging approach.
001411 (2011)	Sun Ju Chung [États-Unis] ; Sebastian M. Armasu ; Joanna M. Biernacka ; Timothy G. Lesnick ; David N. Rider ; Sarah J. Lincoln ; Alexandra I. Ortolaza ; Matthew J. Farrer ; Julie M. Cunningham ; Walter A. Rocca ; Demetrius M. Maraganore	Common variants in PARK loci and related genes and Parkinson's disease.
001B72 (2009)	Nadeeka N W. Dissanayaka [Australie] ; Peter A. Silburn ; John D. O'Sullivan ; George D. Mellick	Serotonin and dopamine transporter genes do not influence depression in Parkinson's disease.
001D19 (2009)	Prachi Mehta [Australie] ; George D. Mellick ; Dominic B. Rowe ; Glenda M. Halliday ; Michael M. Jones ; Neil Manwaring ; Himesha Vandebona ; Peter A. Silburn ; Jie Jin Wang ; Paul Mitchell ; Carolyn M. Sue	Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community.
001D86 (2009)	Greg T. Sutherland [Australie] ; Gerhard A. Siebert ; Jeremy R B. Newman ; Peter A. Silburn ; Richard S. Boyle ; John D. O'Sullivan ; George D. Mellick	Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease.
001D95 (2009)	Aleksandar Rakovic [Allemagne] ; Barbara Stiller ; Ana Djarmati ; Antonia Flaquer ; Jan Freudenberg ; Mohammad-Reza Toliat ; Michael Linnebank ; Vladimir Kostic ; Katja Lohmann ; Sebastian Paus ; Peter Nürnberg ; Christian Kubisch ; Christine Klein ; Ullrich Wüllner ; Alfredo Ramirez	Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
001F42 (2009)	Anastasia Levchenko [Canada] ; Jacques-Yves Montplaisir ; Géraldine Asselin ; Sylvie Provost ; Simon L. Girard ; Lan Xiong ; Emmanuelle Lemyre ; Judith St-Onge ; Pascale Thibodeau ; Alex Desautels ; Gustavo Turecki ; Claudia Gaspar ; Marie-Pierre Dubé ; Guy A. Rouleau	Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1.
001F78 (2009)	Donald L. Gilbert [États-Unis] ; Elizabeth J. Leslie ; Mehdi Keddache ; Nancy D. Leslie	A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.
002388 (2008)	Hiltrud Muhle [Allemagne] ; Anja Neumann ; Katja Lohmann-Hedrich ; Thora Lohnau ; Yang Lu ; Susen Winkler ; Stephan Waltz ; Anke Fischenbeck ; Patricia L. Kramer ; Christine Klein ; Ulrich Stephani	Childhood-onset restless legs syndrome: clinical and genetic features of 22 families.
002422 (2008)	Hiroyuki Soma [Japon] ; Ichiro Yabe ; Asako Takei ; Naoto Fujiki ; Tetsuro Yanagihara ; Hidenao Sasaki	Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 genes.
002510 (2007)	Cao Li [République populaire de Chine] ; Zhang Ting ; Xiao Qin ; Wang Ying ; Bai Li ; Lu Guo Qiang ; Ma Jian Fang ; Zhang Jing ; Ding Jian Qing ; Chen Sheng Di	The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease.
002754 (2007)	Eng-King Tan [Singapour] ; Lisa Skipper ; Louis Tan ; Jian-Jun Liu	LRRK2 G2019S founder haplotype in the Chinese population.
002818 (2007)	David Kemlink [Allemagne] ; Olli Polo ; Pasquale Montagna ; Federica Provini ; Karin Stiasny-Kolster ; Wolfgang Oertel ; Al De Weerd ; Sona Nevsimalova ; Karel Sonka ; Birgit Högl ; Birgit Frauscher ; Werner Poewe [Autriche] ; Claudia Trenkwalder ; Peter P. Pramstaller ; Luigi Ferini-Strambi ; Marco Zucconi ; Eric Konofal ; Isabelle Arnulf ; Georgios M. Hadjigeorgiou ; Svenja Happe ; Christine Klein ; Anja Hiller ; Peter Lichtner ; Thomas Meitinger ; Betram Müller-Myshok ; Juliane Winkelmann	Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.

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