1. J. M. Burgunder, J. Finsterer, Z. Szolnoki, B. Fontaine, J. Baets, C. Van Broeckhoven, S. Di Donato, P. De Jonghe, T. Lynch, C. Mariotti, L. Schols, A. Spinazzola, S. J. Tabrizi, C. Tallaksen, M. Zeviani, H. F. Harbo, and T. Gasser. EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias. Eur J Neurol, 2010. Note: Journal articlethe official journal of the European Federation of Neurological Societies. [WWW]



2. D. W. Dickson, H. Braak, J. E. Duda, C. Duyckaerts, T. Gasser, G. M. Halliday, J. Hardy, J. B. Leverenz, K. Del Tredici, Z. K. Wszolek, and I. Litvan. Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria. Lancet Neurol, 8(12):1150-7, 2009. Note: Journal ArticleReviewEngland. [WWW] Keyword(s): Humans, Lewy Bodies/pathology, Parkinson Disease/*diagnosis/genetics/*pathology, alpha-Synuclein/genetics.



3. J. Finsterer, H. F. Harbo, J. Baets, C. Van Broeckhoven, S. Di Donato, B. Fontaine, P. De Jonghe, A. Lossos, T. Lynch, C. Mariotti, L. Schols, A. Spinazzola, Z. Szolnoki, S. J. Tabrizi, C. M. Tallaksen, M. Zeviani, J. M. Burgunder, and T. Gasser. EFNS guidelines on the molecular diagnosis of mitochondrial disorders. Eur J Neurol, 16(12):1255-64, 2009. Note: Journal ArticleEnglandthe official journal of the European Federation of Neurological Societies. [WWW]



4. T. Gasser, J. Finsterer, J. Baets, C. Van Broeckhoven, S. Di Donato, B. Fontaine, P. De Jonghe, A. Lossos, T. Lynch, C. Mariotti, L. Schols, A. Spinazzola, Z. Szolnoki, S. J. Tabrizi, C. M. Tallaksen, M. Zeviani, J. M. Burgunder, and H. F. Harbo. EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. Eur J Neurol, 2009. Note: Journal articlethe official journal of the European Federation of Neurological Societies. [WWW]



5. H. F. Harbo, J. Finsterer, J. Baets, C. Van Broeckhoven, S. Di Donato, B. Fontaine, P. De Jonghe, A. Lossos, T. Lynch, C. Mariotti, L. Schols, A. Spinazzola, Z. Szolnoki, S. J. Tabrizi, C. Tallaksen, M. Zeviani, J. M. Burgunder, and T. Gasser. EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias. Eur J Neurol, 16(7):777-785, 2009. Note: Journal articlethe official journal of the European Federation of Neurological Societies. [WWW]



6. E. Sidransky, M. A. Nalls, J. O. Aasly, J. Aharon-Peretz, G. Annesi, E. R. Barbosa, A. Bar-Shira, D. Berg, J. Bras, A. Brice, C. M. Chen, L. N. Clark, C. Condroyer, E. V. De Marco, A. Durr, M. J. Eblan, S. Fahn, M. J. Farrer, H. C. Fung, Z. Gan-Or, T. Gasser, R. Gershoni-Baruch, N. Giladi, A. Griffith, T. Gurevich, C. Januario, P. Kropp, A. E. Lang, G. J. Lee-Chen, S. Lesage, K. Marder, I. F. Mata, A. Mirelman, J. Mitsui, I. Mizuta, G. Nicoletti, C. Oliveira, R. Ottman, A. Orr-Urtreger, L. V. Pereira, A. Quattrone, E. Rogaeva, A. Rolfs, H. Rosenbaum, R. Rozenberg, A. Samii, T. Samaddar, C. Schulte, M. Sharma, A. Singleton, M. Spitz, E. K. Tan, N. Tayebi, T. Toda, A. R. Troiano, S. Tsuji, M. Wittstock, T. G. Wolfsberg, Y. R. Wu, C. P. Zabetian, Y. Zhao, and S. G. Ziegler. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med, 361(17):1651-61, 2009. Note: NS050487/NS/NINDS NIH HHS/United StatesNS060113/NS/NINDS NIH HHS/United StatesNS40256/NS/NINDS NIH HHS/United StatesComparative StudyJournal ArticleMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, N.I.H., IntramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.United States. [WWW] Keyword(s): Aged, Case-Control Studies, Genotype, Glucosylceramidase/*genetics, Humans, Jews/genetics, Logistic Models, Middle Aged, Multivariate Analysis, *Mutation, Odds Ratio, Parkinson Disease/*genetics.



7. D. G. Healy, M. Falchi, S. S. O'Sullivan, V. Bonifati, A. Durr, S. Bressman, A. Brice, J. Aasly, C. P. Zabetian, S. Goldwurm, J. J. Ferreira, E. Tolosa, D. M. Kay, C. Klein, D. R. Williams, C. Marras, A. E. Lang, Z. K. Wszolek, J. Berciano, A. H. Schapira, T. Lynch, K. P. Bhatia, T. Gasser, A. J. Lees, and N. W. Wood. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol, 7(7):583-90, 2008. Note: International LRRK2 ConsortiumG0400000/United Kingdom Medical Research CouncilK08 NS044138/NS/United States NINDSNS R01-36960/NS/United States NINDSP01AG017216/AG/United States NIAP50NS40256/NS/United States NINDSR01AG015866/AG/United States NIAJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.England. [WWW]



8. I. Litvan, M. F. Chesselet, T. Gasser, D. A. Di Monte, D. Jr Parker, T. Hagg, J. Hardy, P. Jenner, R. H. Myers, D. Price, M. Hallett, W. J. Langston, A. E. Lang, G. Halliday, W. Rocca, C. Duyckaerts, D. W. Dickson, Y. Ben-Shlomo, C. G. Goetz, and E. Melamed. The etiopathogenesis of Parkinson disease and suggestions for future research. Part II. J Neuropathol Exp Neurol, 66(5):329-36, 2007. Note: Journal ArticleReviewUnited States. [WWW] Keyword(s): Animals, Disease Models, Animal, Forecasting, Humans, Oxidative Stress/physiology, Parkinson Disease/*etiology/*genetics/therapy, Research/*trends.



9. I. Litvan, G. Halliday, M. Hallett, C. G. Goetz, W. Rocca, C. Duyckaerts, Y. Ben-Shlomo, D. W. Dickson, A. E. Lang, M. F. Chesselet, W. J. Langston, D. A. Di Monte, T. Gasser, T. Hagg, J. Hardy, P. Jenner, E. Melamed, R. H. Myers, D. Jr Parker, and D. L. Price. The etiopathogenesis of Parkinson disease and suggestions for future research. Part I. J Neuropathol Exp Neurol, 66(4):251-7, 2007. Note: Journal ArticleReviewUnited States. [WWW] Keyword(s): Forecasting, Humans, Parkinson Disease/epidemiology/*etiology, Research/*trends.



10. M. Sharma, J. C. Mueller, A. Zimprich, P. Lichtner, A. Hofer, P. Leitner, S. Maass, D. Berg, A. Durr, V. Bonifati, G. De Michele, B. Oostra, A. Brice, N. W. Wood, B. Muller-Myhsok, and T. Gasser. The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations. J Med Genet, 43(7):557-62, 2006. Note: European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Age of Onset, Alcohol Oxidoreductases/*genetics, Chromosome Mapping, Genetic Markers, Germany/epidemiology, Humans, Lod Score, Parkinson Disease/*genetics, Parkinsonian Disorders/*genetics, Polymorphism, Genetic, Polymorphism, Single Nucleotide, Reference Values, Siblings.



11. P. G. Unschuld, J. Dachsel, F. Darios, A. Kohlmann, E. Casademunt, K. Lehmann-Horn, M. Dichgans, M. Ruberg, A. Brice, T. Gasser, and C. B. Lucking. Parkin modulates gene expression in control and ceramide-treated PC12 cells. Mol Biol Rep, 33(1):13-32, 2006. Note: Journal ArticleResearch Support, Non-U.S. Gov'tNetherlands. [WWW]



12. J. C. Dachsel, C. B. Lucking, S. Deeg, E. Schultz, M. Lalowski, E. Casademunt, O. Corti, C. Hampe, N. Patenge, K. Vaupel, A. Yamamoto, M. Dichgans, A. Brice, E. E. Wanker, P. J. Kahle, and T. Gasser. Parkin interacts with the proteasome subunit alpha4. FEBS Lett, 579(18):3913-9, 2005. Note: Journal ArticleResearch Support, Non-U.S. Gov'tNetherlands. [WWW] Keyword(s): Animals, Cell Line, Cysteine Endopeptidases/chemistry/*metabolism, DNA, Complementary/metabolism, Humans, Immunoprecipitation, Models, Genetic, Multienzyme Complexes/chemistry, Mutation, PC12 Cells, Plasmids/metabolism, Proteasome Endopeptidase Complex/chemistry/metabolism, Protein Binding, Protein Structure, Tertiary, Rats, Signal Transduction, Two-Hybrid System Techniques, Ubiquitin/chemistry, Ubiquitin-Protein Ligases/chemistry/*metabolism.



13. M. Martinez, A. Brice, J. R. Vaughan, A. Zimprich, M. M. Breteler, G. Meco, A. Filla, M. J. Farrer, C. Betard, A. Singleton, J. Hardy, G. De Michele, V. Bonifati, B. A. Oostra, T. Gasser, N. W. Wood, and A. Durr. Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet, 136(1):72-4, 2005. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesthe official publication of the International Society of Psychiatric Genetics. [WWW] Keyword(s): Alleles, Apolipoprotein E4, Apolipoproteins E/*genetics, Chromosomes, Human, Pair 19/*genetics, Family Health, Gene Frequency, Genotype, Humans, *Linkage (Genetics), Linkage Disequilibrium, Lod Score, Microsatellite Repeats, Parkinson Disease/*genetics, Siblings.



14. J. Prestel, M. Sharma, P. Leitner, A. Zimprich, J. R. Vaughan, A. Durr, V. Bonifati, G. De Michele, H. A. Hanagasi, M. Farrer, A. Hofer, F. Asmus, G. Volpe, G. Meco, A. Brice, N. W. Wood, B. Muller-Myhsok, and T. Gasser. PARK11 is not linked with Parkinson's disease in European families. Eur J Hum Genet, 13(2):193-7, 2005. Note: European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)P01 ns40256/ns/nindsJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.EnglandEjhg. [WWW] Keyword(s): Chromosomes, Human, Pair 2/*genetics, Europe, European Continental Ancestry Group, Humans, *Lod Score, Parkinson Disease/*genetics.



15. M. Martinez, A. Brice, J. R. Vaughan, A. Zimprich, M. M. Breteler, G. Meco, A. Filla, M. J. Farrer, C. Betard, J. Hardy, G. De Michele, V. Bonifati, B. Oostra, T. Gasser, N. W. Wood, and A. Durr. Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease. J Med Genet, 41(12):900-7, 2004. Note: French Parkinson's Disease Genetics Study GroupEuropean Consortium on Genetic Susceptibility in Parkinson's DiseaseNs41723-01a1/ns/nindsP01 ns40256/ns/nindsJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.England. [WWW] Keyword(s): Adult, Aged, Aged, 80 and over, Chromosome Mapping, Cohort Studies, Europe, Genetic Predisposition to Disease, Genetic Screening, Genome, Human, Genotype, Humans, *Linkage (Genetics), Lod Score, Microsatellite Repeats/genetics, Middle Aged, Parkinson Disease/*genetics, United States.



16. E. Lohmann, M. Periquet, V. Bonifati, N. W. Wood, G. De Michele, A. M. Bonnet, V. Fraix, E. Broussolle, M. W. Horstink, M. Vidailhet, P. Verpillat, T. Gasser, D. Nicholl, H. Teive, S. Raskin, O. Rascol, A. Destee, M. Ruberg, F. Gasparini, G. Meco, Y. Agid, A. Durr, and A. Brice. How much phenotypic variation can be attributed to parkin genotype?. Ann Neurol, 54(2):176-85, 2003. Note: French Parkinson's Disease Genetics Study GroupEuropean Consortium on Genetic Susceptibility in Parkinson's DiseaseNs41723-01a1/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.United States. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Aged, Aged, 80 and over, Antiparkinson Agents/therapeutic use, Disease Progression, Exons/genetics, Female, Genotype, Heterozygote, Humans, Levodopa/therapeutic use, Male, Middle Aged, Mutation/genetics, Mutation, Missense/genetics, Parkinson Disease/drug therapy/*genetics/physiopathology, Phenotype, Ubiquitin-Protein Ligases/*genetics, Variation (Genetics)/*genetics.



17. D. Sibbing, F. Asmus, I. R. Konig, S. Tezenas du Montcel, M. Vidailhet, S. Sangla, W. H. Oertel, A. Brice, A. Ziegler, T. Gasser, and O. Bandmann. Candidate gene studies in focal dystonia. Neurology, 61(8):1097-101, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/*genetics, Cystathionine beta-Synthase/genetics, Dystonic Disorders/*genetics, Female, France, Gene Frequency, Genetic Predisposition to Disease, Genotype, Germany, HLA-DR Antigens/*genetics, Haplotypes, Humans, Male, Methylenetetrahydrofolate Reductase (NADPH2)/genetics, Molecular Chaperones/*genetics, Polymerase Chain Reaction, *Polymorphism, Genetic, Receptors, Dopamine D1/*genetics, Receptors, Dopamine D5.

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