المؤلفون: Domenighetti C., Sugier P.-E., Sreelatha A.A.K., Schulte C., Grover S., Mohamed O., Portugal B., May P., Bobbili D.R., Radivojkov-Blagojevic M., Lichtner P., Singleton A.B., Hernandez D.G., Edsall C., Mellick G.D., Zimprich A., Pirker W., Rogaeva E., Lang A.E., Koks S., Taba P., Lesage S., Brice A., Corvol J.-C., Chartier-Harlin M.-C., Mutez E., Brockmann K., Deutschländer A.B., Hadjigeorgiou G.M., Dardiotis E., Stefanis L., Simitsi A.M., Valente E.M., Petrucci S., Duga S., Straniero L., Zecchinelli A., Pezzoli G., Brighina L., Ferrarese C., Annesi G., Quattrone A., Gagliardi M., Matsuo H., Kawamura Y., Hattori N., Nishioka K., Chung S.J., Kim Y.J., Kolber P., Van De Warrenburg B.P.C., Bloem B.R., Aasly J., Toft M., Pihlstrøm L., Guedes L.C., Ferreira J.J., Bardien S., Carr J., Tolosa E., Ezquerra M., Pastor P., Diez-Fairen M., Wirdefeldt K., Pedersen N.L., Ran C., Belin A.C., Puschmann A., Hellberg C., Clarke C.E., Morrison K.E., Tan M., Krainc D., Burbulla L.F., Farrer M.J., Krüger R., Gasser T., Sharma M., Elbaz A.

المصدر: Journal of Parkinson's Disease ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85123813753&doi=10.3233%2fJPD-212851&partnerID=40&md5=bb722d2b2f2b7e79ffdcb4417ba894c4Test

مصطلحات موضوعية: aged, ancestry group, Article, case control study, coffee consumption, cohort analysis, controlled study, disease duration, drinking behavior, genetic polymorphism, genetic variability, genome-wide association study, human, incidence, lifestyle modification, major clinical study, Mendelian randomization analysis, observational study, Parkinson disease, patient participation, pleiotropy, prevalence, sample size, smoking, survival rate, coffee, epidemiology, genetics, risk factor, Alcohol Drinking

العلاقة: http://hdl.handle.net/11615/73411Test

الإتاحة: https://doi.org/10.3233/JPD-212851Test
http://hdl.handle.net/11615/73411Test

المؤلفون: Domenighetti C., Sugier P.-E., Ashok Kumar Sreelatha A., Schulte C., Grover S., Mohamed O., Portugal B., May P., Bobbili D.R., Radivojkov-Blagojevic M., Lichtner P., Singleton A.B., Hernandez D.G., Edsall C., Mellick G.D., Zimprich A., Pirker W., Rogaeva E., Lang A.E., Koks S., Taba P., Lesage S., Brice A., Corvol J.-C., Chartier-Harlin M.-C., Mutez E., Brockmann K., Deutschländer A.B., Hadjigeorgiou G.M., Dardiotis E., Stefanis L., Simitsi A.M., Valente E.M., Petrucci S., Duga S., Straniero L., Zecchinelli A., Pezzoli G., Brighina L., Ferrarese C., Annesi G., Quattrone A., Gagliardi M., Matsuo H., Kawamura Y., Hattori N., Nishioka K., Chung S.J., Kim Y.J., Kolber P., van de Warrenburg B.P.C., Bloem B.R., Aasly J., Toft M., Pihlstrøm L., Correia Guedes L., Ferreira J.J., Bardien S., Carr J., Tolosa E., Ezquerra M., Pastor P., Diez-Fairen M., Wirdefeldt K., Pedersen N.L., Ran C., Belin A.C., Puschmann A., Hellberg C., Clarke C.E., Morrison K.E., Tan M., Krainc D., Burbulla L.F., Farrer M.J., Krüger R., Gasser T., Sharma M., Elbaz A., and the Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease (Courage-PD) Consortium

المصدر: Movement Disorders ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128406510&doi=10.1002%2fmds.28902&partnerID=40&md5=1c6beb821e203be47bb0216393c0532fTest

مصطلحات موضوعية: lactase, low density lipoprotein, aged, allele, Article, cholesterol blood level, controlled study, dairy product, disease association, disease duration, female, food intake, genetic association, genetic predisposition, genetic susceptibility, genotype, human, major clinical study, male, Mendelian randomization analysis, obesity, Parkinson disease, randomized controlled trial, risk assessment, sex difference, single nucleotide polymorphism, John Wiley and Sons Inc

العلاقة: http://hdl.handle.net/11615/73410Test

الإتاحة: https://doi.org/10.1002/mds.28902Test
http://hdl.handle.net/11615/73410Test

المؤلفون: Grover S., Sreelatha A.A.K., Pihlstrom L., Domenighetti C., Schulte C., Sugier P.-E., Radivojkov-Blagojevic M., Lichtner P., Mohamed O., Portugal B., Landoulsi Z., May P., Bobbili D., Edsall C., Bartusch F., Hanussek M., Krüger J., Hernandez D.G., Blauwendraat C., Mellick G.D., Zimprich A., Pirker W., Tan M., Rogaeva E., Lang A., Koks S., Taba P., Lesage S., Brice A., Corvol J.-C., Chartier-Harlin M.-C., Mutez E., Brockmann K., Deutschländer A.B., Hadjigeorgiou G.M., Dardiotis E., Stefanis L., Simitsi A.M., Valente E.M., Petrucci S., Straniero L., Zecchinelli A., Pezzoli G., Brighina L., Ferrarese C., Annesi G., Quattrone A., Gagliardi M., Burbulla L.F., Matsuo H., Kawamura Y., Hattori N., Nishioka K., Chung S.J., Kim Y.J., Pavelka L., Van De Warrenburg B.P.C., Bloem B.R., Singleton A.B., Aasly J., Toft M., Guedes L.C., Ferreira J.J., Bardien S., Carr J., Tolosa E., Ezquerra M., Pastor P., Diez-Fairen M., Wirdefeldt K., Pedersen N.L., Ran C., Belin A.C., Puschmann A., Hellberg C., Clarke C.E., Morrison K.E., Krainc D., Farrer M.J., Kruger R., Elbaz A., Gasser T., Sharma M.

المصدر: Neurology ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85136019610&doi=10.1212%2fWNL.0000000000200699&partnerID=40&md5=7766b3a0615ef70c6f2a5cd8fcdabd2aTest

مصطلحات موضوعية: ADP ribosyl cyclase/cyclic ADP ribose hydrolase 1, adult, Article, BST1 gene, caudate nucleus, CD38 gene, chromosome 12, chromosome 4, chromosome 7, chromosome 8, controlled study, correlation analysis, expression quantitative trait locus, female, gene, gene expression, gene frequency, gene identification, gene linkage disequilibrium, genetic association, genome-wide association study, genotype, genotype phenotype correlation, heritability, human, human tissue, KNH3 gene, major clinical study, male, neuropathology

العلاقة: http://hdl.handle.net/11615/73726Test

الإتاحة: https://doi.org/10.1212/WNL.0000000000200699Test
http://hdl.handle.net/11615/73726Test

المؤلفون: Markopoulou K., Aasly J., Chung S.J., Dardiotis E., Wirdefeldt K., Premkumar A.P., Schoneburg B., Kartha N., Wilk G., Wei J., Simon K.C., Tideman S., Epshteyn A., Hadsell B., Garduno L., Pham A., Frigerio R., Maraganore D.

المصدر: Frontiers in Neurology ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85088429379&doi=10.3389%2ffneur.2020.00548&partnerID=40&md5=caed852c85080638276dc7880a217480Test

مصطلحات موضوعية: Article, blood sampling, bradykinesia, cohort analysis, disease exacerbation, educational status, Epworth sleepiness scale, ethnicity, family history, female, follow up, GBA gene, gene, genomics, Geriatric Depression Scale, Hoehn and Yahr scale, human, longitudinal study, LRRK2gene, major clinical study, male, Mini Mental State Examination, Montreal cognitive assessment, mortality rate, nursing home, onset age, Parkinson disease, phenotype, social status, tremor

العلاقة: http://hdl.handle.net/11615/76379Test

الإتاحة: https://doi.org/10.3389/fneur.2020.00548Test
http://hdl.handle.net/11615/76379Test

المؤلفون: Blauwendraat, C., Faghri, F., Pihlstrom, L., Geiger, J. T., Elbaz, A., Lesage, S., Corvol, J. -C., May, P., Nicolas, A., Abramzon, Y., Murphy, N. A., Gibbs, J. R., Ryten, M., Ferrari, R., Bras, J., Guerreiro, R., Williams, J., Sims, R., Lubbe, S., Hernandez, D. G., Mok, K. Y., Robak, L., Campbell, R. H., Rogaeva, E., Traynor, B. J., Chia, R., Chung, S. J., Hardy, J. A., Brice, A., Wood, N. W., Houlden, H., Shulman, J. M., Morris, H. R., Gasser, T., Kruger, R., Heutink, P., Sharma, M., Simon-Sanchez, J., Nalls, M. A., Singleton, A. B., Scholz, S. W., Noyce, A. J., Giri, A., Oehmig, A., Tucci, A., Schulte, C., Cookson, M. R., Kia, D., Danjou, F., Charlesworth, G., Plun-Favreau, H., Holmans, P., Jansen, I., Hardy, J., Bras, J. M., Quinn, J., Botia, J. A., Billingsley, K., R'Bibo, L., Lungu, C., Martinez, M., Escott-Price, V., Mencacci, N. E., Topley, Lewis, Denny, P., Rizzu, P., Taba, P., Lovering, R., Ogalla, R. D., Foulger, R., Finkbeiner, S., Sveinbjornsdottir, S., Scholz, S., Koks, S., Foltynie, T., Price, T. R., Sheerin, U. -M., Williams, N., Reed, X., Wang, L., Brockmann, K., Oertel, W., Klein, C., Mohamed, F., Malard, L., Corti, O., Drouet, V., Goldwurm, S., Tesei, S., Canesi, M., Valente, E. M., Petrucci, S., Ginevrino, M., Toft, M., Aasly, J., Henriksen, S. P., Saetehaug, C., Orr-Urtreger, A., Giladi, N., Ferreira, J., Guedes, L. C., Bouca-Machado, R., Coelho, M., Rosa, M. M., Tolosa, E., Fernandez-Santiago, R., Ezquerra, M., Marti, M. J., Glaab, E., Balling, R., Chung, S. -J.

المصدر: Neurobiology of Aging
Neurobiology of aging 57, 247.e9-247.e13 (2017). doi:10.1016/j.neurobiolaging.2017.05.009

مصطلحات موضوعية: 0301 basic medicine, Aging, methods [Genome-Wide Association Study], 0302 clinical medicine, Corticobasal degeneration, neurodegenerative diseases, humans, risk, high-throughput screening assays, education.field_of_study, General Neuroscience, neurodegeneration, genetics [Genetic Variation], 3. Good health, Neurochip, alleles, methods [Genotyping Techniques], Frontotemporal dementia, Risk, Population, methods [High-Throughput Screening Assays], Computational biology, Genetic screening, genotyping, NeuroChip, NeuroX, apolipoproteins E, genetic variation, genome-wide association study, genotyping techniques, Article, Progressive supranuclear palsy, 03 medical and health sciences, Apolipoproteins E, medicine, Humans, Dementia, ddc:610, education, Genotyping, Alleles, business.industry, medicine.disease, 030104 developmental biology, genetics [Neurodegenerative Diseases], genetics [Apolipoproteins E], Neurology (clinical), Geriatrics and Gerontology, business, Neuroscience, 030217 neurology & neurosurgery, Imputation (genetics), Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c65471285ddf63c5acb2ebcd54d52517Test
https://doi.org/10.1016Test/j.neurobiolaging.2017.05.009

المؤلفون: Heckman, M. G., Soto Ortolaza, A. I., Aasly, J. O., Abahuni, N., Annesi, G., Bacon, J. A., Bardien, S., Bozi, M., Brice, A., Brighina, L., Carr, J., Chartier Harlin, M., Dardiotis, E., Dickson, D. W., Diehl, N. N., Elbaz, A., Ferrarese, C., Fiske, B., Gibson, J. M., Gibson, R., Hadjigeorgiou, G. M., Hattori, N., J. P. A., Boczarska Jedynak, M., Jasinska Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lesage, S., Lin, C., Lynch, T., Maraganore, D. M., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Park, S. S., Petrucci, S., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Theuns, J., Tomiyama, H., Uitti, R. J., Valente, Enza Maria, Broeckhoven, C. V., S. v., De, Vassilatis, D. K., Vilariño Güell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R., Hentati, F., Farrer, M. J., Ross, O. A., G. E., Of

المساهمون: Heckman, M, Soto Ortolaza, A, Aasly, J, Abahuni, N, Annesi, G, Bacon, J, Bardien, S, Bozi, M, Brice, A, Brighina, L, Carr, J, Chartier Harlin, M, Dardiotis, E, Dickson, D, Diehl, N, Elbaz, A, Ferrarese, C, Fiske, B, Gibson, J, Gibson, R, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Boczarska Jedynak, M, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, C, Lynch, T, Maraganore, D, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Park, S, Petrucci, S, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, R, Valente, E, Van Broeckhoven, C, van de Loo, S, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Hentati, F, Farrer, M, Ross, O

المصدر: Movement disorders 28(12), 1740-1744 (2013). doi:10.1002/mds.25600

مصطلحات موضوعية: Molecular Epidemiology, Genotype, Parkinson's disease, LRRK2, Parkinson Disease, Protein Serine-Threonine Kinases, association study, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Protein-Serine-Threonine Kinases, Polymorphism, Single Nucleotide, genetics [Protein-Serine-Threonine Kinases], Article, Genetics, Population, Gene Frequency, Haplotypes, genetics [Parkinson Disease], Humans, genetics, lrrk2, parkinson's disease, genetic association studies, population, genotype, haplotypes, hHumans, leucine-rich repeat serine-threonine protein kinase-2, molecular epidemiology, parkinson disease, polymorphism, single nucleotide, protein-serine-threonine kinases, gene frequency, genetic predisposition to disease, Genetic Predisposition to Disease, ddc:610, epidemiology [Parkinson Disease], LRRK2 protein, human, genetic, Genetic Association Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::92643a5bf9a342d7d2a2a6f980f07057Test

المؤلفون: Heckman, M. G., Elbaz, A., Soto-Ortolaza, A. I., Serie, D. J., Aasly, J. O., Annesi, G., Auburger, G., Bacon, J. A., Boczarska-Jedynak, M., Bozi, M., Brighina, L., Chartier-Harlin, M. C., Dardiotis, E., Destée, A., Ferrarese, C., Ferraris, A., Fiske, B., Gispert, S., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lin, C. H., Lohmann, K., Loriot, M. A., Lynch, T., Mellick, G. D., Mutez, E., Opala, G., Park, S. S., Petrucci, S., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Tomiyama, H., Uitti, R. J., Valente, E. M., Vassilatis, D. K., Vilariño-Güell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R. M., Xiromerisiou, G., Maraganore, D. M., Farrer, M. J., Ross, O. A.

المصدر: Neurobiology of Aging ; http://www.scopus.com/inward/record.url?eid=2-s2.0-84885187895&partnerID=40&md5=c295b7406d4cd1619f495c332cc01beeTest

مصطلحات موضوعية: Genetics, Interaction, LRRK2, MAPT, Parkinson's disease, SNCA, alpha synuclein, leucine rich repeat kinase 2, tau protein, adult, article, Asian, Caucasian, controlled study, ethnic difference, female, gene, gene interaction, genetic analysis, genetic variability, genotype, haplotype, human, LRRK2 gene, major clinical study, male, MAPT gene, neuroprotection, Parkinson disease, priority journal

العلاقة: 1974580; http://hdl.handle.net/11615/28487Test

الإتاحة: https://doi.org/10.1016Test/j.neurobiolaging.2013.07.013
http://hdl.handle.net/11615/28487Test

المؤلفون: Sharma, M., Ioannidis, J. P. A., Aasly, J. O., Annesi, G., Brice, A., Van Broeckhoven, C., Bertram, L., Bozi, M., Crosiers, D., Clarke, C., Facheris, M., Farrer, M., Garraux, G., Gispert, S., Auburger, G., Vilariño-Güell, C., Hadjigeorgiou, G. M., Hicks, A. A., Hattori, N., Jeon, B., Lesage, S., Lill, C. M., Lin, J. J., Lynch, T., Lichtner, P., Lang, A. E., Mok, V., Jasinska-Myga, B., Mellick, G. D., Morrison, K. E., 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., Theuns, J., Tan, E. K., Toda, T., Tomiyama, H., Uitti, R. J., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Yueh, K. C., Zhao, Y., Gasser, T., Maraganore, D., Krüger, R.

المصدر: http://www.scopus.com/inward/record.url?eid=2-s2.0-84865196862&partnerID=40&md5=3c10498c7ff353916672f2f6dd321768Test.

مصطلحات موضوعية: ACMSD protein, alpha synuclein, BST1 protein, dendritic cell lysosome associated membrane protein, GAK1 protein, HIP1R protein, HLA DRB5 antigen, leucine rich repeat kinase 2, peptides and proteins, STK39 protein, SYT11 protein, tau protein, unclassified drug, article, Asian, Caucasian, controlled study, gene frequency, gene locus, gene replication, genetic association, genetic heterogeneity, genetic risk, genetic susceptibility, genetic variability, genotyping technique, human, major clinical study, Parkinson disease, population genetics

العلاقة: 283878; http://hdl.handle.net/11615/32977Test

الإتاحة: https://doi.org/10.1212/WNL.0b013e318264e353Test
http://hdl.handle.net/11615/32977Test

المؤلفون: Elbaz, A., Ross, O. A., Ioannidis, J. P. A., Soto-Ortolaza, A. I., Moisan, F., Aasly, J., Annesi, G., Bozi, M., Brighina, L., Chartier-Harlin, M. C., Destée, A., Ferrarese, C., Ferraris, A., Gibson, J. M., Gispert, S., Hadjigeorgiou, G. M., Jasinska-Myga, B., Klein, C., Krüger, R., Lambert, J. C., Lohmann, K., Van De Loo, S., Loriot, M. A., Lynch, T., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Stefanis, L., Uitti, R. J., Valente, E. M., Vilariño-Güell, C., Wirdefeldt, K., Wszolek, Z. K., Xiromerisiou, G., Maraganore, D. M., Farrer, M. J.

المصدر: http://www.scopus.com/inward/record.url?eid=2-s2.0-79955389000&partnerID=40&md5=4b9c83c2e73b12949fe939b7292f48bcTest.

مصطلحات موضوعية: alpha synuclein, tau protein, adult, article, Caucasian, controlled study, disease predisposition, gene interaction, genotype, haplotype, human, Parkinson disease, priority journal, single nucleotide polymorphism, Age of Onset, Aged, 80 and over, alpha-Synuclein, Case-Control Studies, Female, Genetic Predisposition to Disease, Humans, Logistic Models, Male, Middle Aged, Odds Ratio, Polymorphism, Single Nucleotide, Retrospective Studies, tau Proteins

العلاقة: 3645134; http://hdl.handle.net/11615/27297Test

الإتاحة: https://doi.org/10.1002/ana.22321Test
http://hdl.handle.net/11615/27297Test

المؤلفون: Krüger, R., Sharma, M., Riess, O., Gasser, T., Van Broeckhoven, C., Theuns, J., Aasly, J., Annesi, G., Bentivoglio, A. R., Brice, A., Djarmati, A., Elbaz, A., Farrer, M., Ferrarese, C., Gibson, J. M., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Klein, C., Lambert, J. C., Lesage, S., Lin, J. J., Lynch, T., Mellick, G. D., de Nigris, F., Opala, G., Prigione, A., Quattrone, A., Ross, O. A., Satake, W., Silburn, P. A., Tan, E. K., Toda, T., Tomiyama, H., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Maraganore, D. M.

المصدر: Neurobiology of Aging ; http://www.scopus.com/inward/record.url?eid=2-s2.0-79952900158&partnerID=40&md5=61623eef1476e5e0737058f20d4e29f0Test

مصطلحات موضوعية: Genetics, HtrA2, Omi, PARK13, Parkinson's disease, serine proteinase Omi, adult, age, article, Bayes theorem, controlled study, disease predisposition, ethnicity, family history, female, gender, gene, genetic association, genotype, human, major clinical study, male, Omi/Htra2 gene, onset age, Parkinson disease, pathogenesis, priority journal, protein variant, risk assessment, Scandinavia

العلاقة: 1974580; http://hdl.handle.net/11615/30055Test

الإتاحة: https://doi.org/10.1016Test/j.neurobiolaging.2009.11.021
http://hdl.handle.net/11615/30055Test