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Cellular and molecular life sciences, ISSN 1420-9071, 01/2013, Volume 70, Issue 1, pp. 121 - 36
Journal Article
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 08/2010, Volume 69, Issue 8, pp. 789 - 800
Journal Article
by Premi, Enrico and Calhoun, Vince D and Diano, Matteo and Gazzina, Stefano and Cosseddu, Maura and Alberici, Antonella and Archetti, Silvana and Paternicò, Donata and Gasparotti, Roberto and van Swieten, John and Galimberti, Daniela and Sanchez-Valle, Raquel and Laforce, Robert and Moreno, Fermin and Synofzik, Matthis and Graff, Caroline and Masellis, Mario and Tartaglia, Maria Carmela and Rowe, James and Vandenberghe, Rik and Finger, Elizabeth and Tagliavini, Fabrizio and de Mendonça, Alexandre and Santana, Isabel and Butler, Chris and Ducharme, Simon and Gerhard, Alex and Danek, Adrian and Levin, Johannes and Otto, Markus and Frisoni, Giovanni and Cappa, Stefano and Sorbi, Sandro and Padovani, Alessandro and Rohrer, Jonathan D and Borroni, Barbara and Almeida, Maria Rosario and Anderl-Straub, Sarah and Andersson, Christin and Antonell, Anna and Arighi, Andrea and Balasa, Mircea and Barandiaran, Myriam and Bargalló, Nuria and Bartha, Robart and Bender, Benjamin and Benussi, Luisa and Binetti, Giuliano and Black, Sandra and Bocchetta, Martina and Borrego-Ecija, Sergi and Bras, Jose and Bruffaerts, Rose and Caroppo, Paola and Cash, David and Castelo-Branco, Miguel and Convery, Rhian and Cope, Thomas and de Arriba, María and Di Fede, Giuseppe and Díaz, Zigor and Dick, Katrina M and Duro, Diana and Fenoglio, Chiara and Ferreira, Catarina B and Ferreira, Carlos and Flanagan, Toby and Fox, Nick and Freedman, Morris and Fumagalli, Giorgio and Gabilondo, Alazne and Gauthier, Serge and Ghidoni, Roberta and Giaccone, Giorgio and Gorostidi, Ana and Greaves, Caroline and Guerreiro, Rita and Heller, Carolin and Hoegen, Tobias and Indakoetxea, Begoña and Jelic, Vesna and Jiskoot, Lize and Karnath, Hans-Otto and Keren, Ron and Leitão, Maria João and Lladó, Albert and Lombardi, Gemma and Loosli, Sandra and Maruta, Carolina and Mead, Simon and Meeter, Lieke and Miltenberger, Gabriel and van Minkelen, Rick and Mitchell, Sara and Nacmias, Benedetta and Neason, Mollie and Nicholas, Jennifer and Öijerstedt, Linn and Olives, Jaume and Panman, Jessica and ... and GENFI and Genetic FTD Initiative and Genetic FTD Initiative, GENFI
NeuroImage, ISSN 1053-8119, 04/2019, Volume 189, pp. 645 - 654
Journal Article
by Nalls, Mike A and Blauwendraat, Cornelis and Vallerga, Costanza L and Heilbron, Karl and Bandres-Ciga, Sara and Chang, Diana and Tan, Manuela X and Tan, Manuela and Kia, Demis A and Noyce, Alastair J and Xue, Angli and Bras, Jose and Young, Emily and von Coelln, Rainer and Simón-Sánchez, Javier and Schulte, Claudia and Sharma, Manu and Krohn, Lynne and Pihlstrøm, Lasse and Siitonen, Ari and Iwaki, Hirotaka and Leonard, Hampton and Leonard, Hampton L and Faghri, Faraz and Gibbs, J Raphael and Hernandez, Dena G and Scholz, Sonja W and Botia, Juan A and Martinez, Maria and Corvol, Jean-Christophe and Lesage, Suzanne and Jankovic, Joseph and Shulman, Lisa M and Shulman, Joshua M and Sutherland, Margaret and Tienari, Pentti and Majamaa, Kari and Toft, Mathias and Andreassen, Ole A and Bangale, Tushar and Brice, Alexis and Yang, Jian and Gan-Or, Ziv and Gasser, Thomas and Heutink, Peter and Wood, Nicholas W and Hinds, David A and Hardy, John and Hardy, John A and Morris, Huw R and Gratten, Jacob and Visscher, Peter M and Graham, Robert R and Singleton, Andrew B and Adarmes-Gómez, Astrid D and Aguilar, Miquel and Aitkulova, Akbota and Akhmetzhanov, Vadim and Alcalay, Roy N and Alvarez, Ignacio and Alvarez, Victoria and Barrero, Francisco Javier and Bergareche Yarza, Jesús Alberto and Bernal-Bernal, Inmaculada and Billingsley, Kimberley and Blazquez, Marta and Bonilla-Toribio, Marta and Botía, Juan A and Boungiorno, María Teresa and Brockmann, Kathrin and Bubb, Vivien and Buiza-Rueda, Dolores and Cámara, Ana and Carrillo, Fátima and Carrión-Claro, Mario and Cerdan, Debora and Chelban, Viorica and Clarimón, Jordi and Clarke, Carl and Compta, Yaroslau and Cookson, Mark R and Craig, David W and Danjou, Fabrice and Diez-Fairen, Monica and Dols-Icardo, Oriol and Duarte, Jacinto and Duran, Raquel and Escamilla-Sevilla, Francisco and Escott-Price, Valentina and Ezquerra, Mario and Feliz, Cici and Fernández, Manel and Fernández-Santiago, Rubén and Finkbeiner, Steven and Foltynie, Thomas and Garcia, Ciara and García-Ruiz, Pedro and Gomez Heredia, Maria Jose and Gómez-Garre, Pilar and González, Manuel Menéndez and ... and Int Parkinson's Dis Genomics and Syst Genomics Parkinson's Dis and 23 Me Res Team
The Lancet Neurology, ISSN 1474-4422, 12/2019, Volume 18, Issue 12, pp. 1091 - 1102
Genome-wide association studies (GWAS) in Parkinson's disease have increased the scope of biological knowledge about the disease over the past decade. We aimed... 
PHENOTYPES | GWAS | GENE | VARIANTS | EFFICIENT | CLINICAL NEUROLOGY | Phenotypes | Parkinson's disease | Neurodegenerative diseases | Genomics | Parkinsons disease | Cognitive ability | Clinical trials | Genomes | Single-nucleotide polymorphism | Gene expression | Putamen | Risk factors | Datasets | Studies | Prediction models | DNA methylation | Aging | Heritability | Movement disorders
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2014, Volume 35, Issue 2, pp. 444.e1 - 444.e4
Journal Article
by Kia, Demis A and Sabir, Marya S and Ahmed, Sarah and Trinh, Joanne and Bandres-Ciga, Sara and Noyce, Alastair J and Kaiyrzhanov, Rauan and Middlehurst, Ben and Tan, Manuela and Houlden, Henry and Morris, Huw R and Plun-Favreau, Helene and Holmans, Peter and Hardy, John and Trabzuni, Daniah and Bras, Jose and Quinn, John and Mok, Kin Y and Kinghorn, Kerri J and Billingsley, Kimberley and Wood, Nicholas W and Lewis, Patrick and Schreglmann, Sebastian and Guerreiro, Rita and Lovering, Ruth and R'Bibo, Lea and Rizig, Mie and Ryten, Mina and Guelfi, Sebastian and Escott-Price, Valentina and Chelban, Viorica and Foltynie, Thomas and Williams, Nigel and Brice, Alexis and Danjou, Fabrice and Lesage, Suzanne and Corvol, Jean-Christophe and Martinez, Maria and Schulte, Claudia and Brockmann, Kathrin and Simón-Sánchez, Javier and Heutink, Peter and Rizzu, Patrizia and Sharma, Manu and Gasser, Thomas and Nicolas, Aude and Cookson, Mark R and Blauwendraat, Cornelis and Craig, David W and Faghri, Faraz and Gibbs, Raphael J and Hernandez, Dena G and Van Keuren-Jensen, Kendall and Shulman, Joshua M and Iwaki, Hirotaka and Leonard, Hampton L and Nalls, Mike A and Robak, Laurie and Lubbe, Steven and Finkbeiner, Steven and Mencacci, Niccolo E and Lungu, Codrin and Singleton, Andrew B and Scholz, Sonja W and Reed, Xylena and Alcalay, Roy N and Gan-Or, Ziv and Rouleau, Guy A and van Hilten, Jacobus J and Marinus, Johan and Adarmes-Gómez, Astrid D and Aguilar, Miquel and Alvarez, Victoria and Alvarez, Ignacio and Barrero, Francisco J and Bergareche Yarza, Jesús A and Bernal-Bernal, Inmaculada and Blazquez, Marta and Bonilla-Toribio, Marta and Botía, Juan A and Boungiorno, María Teresa and Buiza-Rueda, Dolores and Cámara, Ana and Carrillo, Fátima and Carrión-Claro, Mario and Cerdan, Debora and Clarimón, Jordi and Diez-Farien, Monica and Dols-Icardo, Oriol and Duarte, Jacinto and Duran, Raquel and Escamilla-Sevilla, Francisco and Ezquerra, Mario and Feliz, Cici and Fernández, Manel and Fernández-Santiago, Rubén and Garcia, Ciara and García-Ruiz, Pedro and Gómez-Garre, Pilar and Gomez Heredia, Maria Jose and ... and Int DLB Genetics Consortium and International DLB Genetics Consortium
The Lancet Neurology, ISSN 1474-4422, 12/2018, Volume 17, Issue 12, pp. 1032 - 1032
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 10/2015, Volume 60, Issue 10, pp. 637 - 640
Although in the last two decades there has been considerable progress in understanding the genetic basis of Parkinson's disease (PD), the majority of PD is... 
INSULIN | DOMAIN | EXPRESSION | GENETICS & HEREDITY | FAMILY | Exome | Carrier Proteins - genetics | Humans | Cognition Disorders - metabolism | Female | Male | Cognition Disorders - genetics | Parkinson Disease - metabolism | Mutation, Missense | Parkinson Disease - genetics | Amino Acid Substitution
Journal Article
Journal Article
by Bandres‐Ciga, Sara and Saez‐Atienzar, Sara and Bonet‐Ponce, Luis and Billingsley, Kimberley and Vitale, Dan and Blauwendraat, Cornelis and Gibbs, Jesse Raphael and Pihlstrøm, Lasse and Gan‐Or, Ziv and Noyce, Alastair J and Kaiyrzhanov, Rauan and Middlehurst, Ben and Kia, Demis A and Tan, Manuela and Houlden, Henry and Morris, Huw R and Plun‐Favreau, Helene and Holmans, Peter and Hardy, John and Trabzuni, Daniah and Bras, Jose and Quinn, John and Mok, Kin Y and Kinghorn, Kerri J and Billingsley, Kimberley and Wood, Nicholas W and Lewis, Patrick and Schreglmann, Sebastian and Guerreiro, Rita and Lovering, Ruth and RņBibo, Lea and Manzoni, Claudia and Rizig, Mie and Ryten, Mina and Guelfi, Sebastian and Escott‐Price, Valentina and Chelban, Viorica and Foltynie, Thomas and Williams, Nigel and Morrison, Karen E and Brice, Alexis and Danjou, Fabrice and Lesage, Suzanne and Corvol, Jean‐Christophe and Martinez, Maria and Schulte, Claudia and Brockmann, Kathrin and SimɃn‐Sȥnchez, Javier and Heutink, Peter and Rizzu, Patrizia and Sharma, Manu and Gasser, Thomas and Nicolas, Aude and Cookson, Mark R and Bandres‐Ciga, Sara and Blauwendraat, Cornelis and Craig, David W and Faghri, Faraz and Gibbs, J Raphael and Hernandez, Dena G and Van Keuren‐Jensen, Kendall and Shulman, Joshua M and Iwaki, Hirotaka and Leonard, Hampton L and Nalls, Mike A and Robak, Laurie and Lubbe, Steven and Finkbeiner, Steven and Mencacci, Niccolo E and Lungu, Codrin and Singleton, Andrew B and Scholz, Sonja W and Reed, Xylena and Alcalay, Roy N and Gan‐Or, Ziv and Rouleau, Guy A and Hilten, Jacobus J and Marinus, Johan and Adarmes‐GɃmez, Astrid D and Aguilar, Miquel and Alvarez, Ignacio and Alvarez, Victoria and Barrero, Francisco Javier and Yarza, Jesɐs Alberto Bergareche and Bernal‐Bernal, Inmaculada and Blazquez, Marta and Bonilla‐Toribio, Marta and Botȷa, Juan A and Boungiorno, Marȷa Teresa and Buiza‐Rueda, Dolores and Cȥmara, Ana and Carrillo, Fȥtima and CarriɃn‐Claro, Mario and Cerdan, Debora and ClarimɃn, Jordi and Compta, Yaroslau and Casa, Beatrȷz and Diez‐Fairen, Monica and Dols‐Icardo, Oriol and Duarte, Jacinto and ... and Int Parkinsons Dis Genomics Consor and International Parkinson's Disease Genomics Consortium (IPDGC)
Movement Disorders, ISSN 0885-3185, 04/2019, Volume 34, Issue 4, pp. 460 - 468
ABSTRACT Background PD is a complex polygenic disorder. In recent years, several genes from the endocytic membrane‐trafficking pathway have been suggested to... 
endocytosis | Parkinson's disease | polygenic risk score | genetic risk | heritability | COMPLEX | METAANALYSIS | TRANSCRIPTOME | CLINICAL NEUROLOGY | DATABASE | DISORDER | LD SCORE REGRESSION | GENOME-WIDE ASSOCIATION | POLYGENIC RISK | Quantitative genetics | Genetic research | Medicine, Experimental | Medical research | Genetic polymorphisms
Journal Article