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by Bandres‐Ciga, Sara and Ahmed, Sarah and Sabir, Marya S and Blauwendraat, Cornelis and Adarmes‐Gómez, Astrid D and Bernal‐Bernal, Inmaculada and Bonilla‐Toribio, Marta and Buiza‐Rueda, Dolores and Carrillo, Fátima and Carrión‐Claro, Mario and Gómez‐Garre, Pilar and Jesús, Silvia and Labrador‐Espinosa, Miguel A and Macias, Daniel and Méndez‐del‐Barrio, Carlota and Periñán‐Tocino, Teresa and Tejera‐Parrado, Cristina and Vargas‐González, Laura and Diez‐Fairen, Monica and Alvarez, Ignacio and Tartari, Juan Pablo and Buongiorno, Mariateresa and Aguilar, Miquel and Gorostidi, Ana and Bergareche, Jesús Alberto and Mondragon, Elisabet and Vinagre‐Aragon, Ana and Croitoru, Ioana and Ruiz‐Martínez, Javier and Dols‐Icardo, Oriol and Kulisevsky, Jaime and Marín‐Lahoz, Juan and Pagonabarraga, Javier and Pascual‐Sedano, Berta and Ezquerra, Mario and Cámara, Ana and Compta, Yaroslau and Fernández, Manel and Fernández‐Santiago, Rubén and Muñoz, Esteban and Tolosa, Eduard and Valldeoriola, Francesc and Gonzalez‐Aramburu, Isabel and Sanchez Rodriguez, Antonio and Sierra, María and Menéndez‐González, Manuel and Blazquez, Marta and Garcia, Ciara and Suarez‐San Martin, Esther and García‐Ruiz, Pedro and Martínez‐Castrillo, Juan Carlos and Vela‐Desojo, Lydia and Ruz, Clara and Barrero, Francisco Javier and Escamilla‐Sevilla, Francisco and Mínguez‐Castellanos, Adolfo and Cerdan, Debora and Tabernero, Cesar and Gomez Heredia, Maria Jose and Perez Errazquin, Francisco and Romero‐Acebal, Manolo and Feliz, Cici and Lopez‐Sendon, Jose Luis and Mata, Marina and Martínez Torres, Irene and Kim, Jonggeol Jeffrey and Dalgard, Clifton L and Brooks, Janet and Saez‐Atienzar, Sara and Gibbs, J. Raphael and Jorda, Rafael and Botia, Juan A and Bonet‐Ponce, Luis and Morrison, Karen E and Clarke, Carl and Tan, Manuela and Morris, Huw and Edsall, Connor and Hernandez, Dena and Simon‐Sanchez, Javier and Nalls, Mike A and Scholz, Sonja W and Jimenez‐Escrig, Adriano and Duarte, Jacinto and Vives, Francisco and Duran, Raquel and Hoenicka, Janet and Alvarez, Victoria and Infante, Jon and Marti, Maria José and Clarimón, Jordi and López de Munain, Adolfo and Pastor, Pau and Mir, Pablo and Singleton, Andrew and Noyce, Alastair J and Kaiyrzhanov, Rauan and Middlehurst, Ben and Kia, Demis A and Tan, Manuela and ... and The American Genome Center and on behalf of the International Parkinson Disease Genomics Consortium
Movement Disorders, ISSN 0885-3185, 10/2019
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
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
by Majounie, Elisa, PhD and Renton, Alan E, PhD and Mok, Kin, MSc and Dopper, Elise GP and Waite, Adrian, PhD and Rollinson, Sara, PhD and Chiò, Adriano, MD and Restagno, Gabriella, MD and Nicolaou, Nayia, MSc and Simon-Sanchez, Javier, PhD and van Swieten, John C, Prof and Abramzon, Yevgeniya and Johnson, Janel O, PhD and Sendtner, Michael, Prof and Pamphlett, Roger, MD and Orrell, Richard W, MD and Mead, Simon, MD and Sidle, Katie C, MD and Houlden, Henry, Prof and Rohrer, Jonathan D, MD and Morrison, Karen E, Prof and Pall, Hardev, MD and Talbot, Kevin, Prof and Ansorge, Olaf, MD and Hernandez, Dena G, MSc and Arepalli, Sampath, MS and Sabatelli, Mario, MD and Mora, Gabriele, MD and Corbo, Massimo, MD and Giannini, Fabio, MD and Calvo, Andrea, MD and Englund, Elisabet, MD and Borghero, Giuseppe, MD and Floris, Gian Luca, MD and Remes, Anne M, Prof and Laaksovirta, Hannu, MD and McCluskey, Leo, MD and Trojanowski, John Q, Prof and Van Deerlin, Vivianna M, MD and Schellenberg, Gerard D, Prof and Nalls, Michael A, PhD and Drory, Vivian E, MD and Lu, Chin-Song, Prof and Yeh, Tu-Hsueh, MD and Ishiura, Hiroyuki, MD and Takahashi, Yuji, MD and Tsuji, Shoji, Prof and Le Ber, Isabelle, MD and Brice, Alexis, Prof and Drepper, Carsten, PhD and Williams, Nigel, PhD and Kirby, Janine, PhD and Shaw, Pamela, Prof and Hardy, John, Prof and Tienari, Pentti J, MD and Heutink, Peter, Prof and Morris, Huw R, MD and Pickering-Brown, Stuart, Prof and Traynor, Bryan J, Dr and Chromosome 9-ALS FTD Consortium and French Res Network FTLD FTLD ALS and ITALSGEN Consortium and French research network on FTLD/FTLD/ALS and Chromosome 9-ALS/FTD Consortium and Oncology and Pathology, Kamprad Lab and Lund University and Lunds universitet and Onkologi och Patologi, Kampradlab
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 4, pp. 323 - 330
Summary Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9orf72 that has been associated with a large... 
Neurology | PREVALENCE | MUTATIONS | LOBAR DEGENERATION | GENETICS | TDP-43 | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Cross-Sectional Studies | DNA Repeat Expansion - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Child, Preschool | Genotype | Male | Genetic Loci | Open Reading Frames - genetics | Young Adult | Chromosomes, Human, Pair 9 - genetics | Adolescent | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Child | Cohort Studies | Medical research | Medical colleges | Care and treatment | Nervous system diseases | Neurosciences | Molecular genetics | Oncology, Experimental | Questions and answers | Amyotrophic lateral sclerosis | Research | Medicine, Experimental | Agriculture | Physicians (General practice) | Alzheimer's disease | Dementia | Cancer | Biomedical engineering | Haplotypes | Polymerase chain reaction | Neurodegenerative diseases | Ethnic groups | Data processing | Mutation | Frontotemporal dementia | Genetic counselling | Islands | Age | Toll-Like Receptor 4 | Open Reading Frames | Adaptor Proteins, Vesicular Transport | Lipopolysaccharides | Life Sciences | DNA Repeat Expansion | Interferon Regulatory Factor-3 | Transfection | Amyotrophic Lateral Sclerosis | RNA Interference | HEK293 Cells | Membrane Glycoproteins | Vesicular Transport Proteins | Protein Structure, Tertiary | Cell Line | Chemokine CCL5 | Frontotemporal Dementia | Signal Transduction | Myeloid Differentiation Factor 88 | Chromosomes, Human, Pair 9 | Protein Transport | Adaptor Proteins, Signal Transducing | Santé publique et épidémiologie | RNA, Small Interfering | Endosomes | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 6, pp. 585 - 596
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2014, Volume 111, Issue 7, pp. 2626 - 2631
Journal Article
Neurology, ISSN 0028-3878, 03/2015, Volume 84, Issue 10, pp. 966 - 967
Journal Article
by Jansen, Iris and Ye, H and Heetveld, S and Lechler, M.C and Michels, H and Seinstra, R.I and Lubbe, S.J and uet, V and Lesage, Suzanne and Majounie, Elisa and Gibbs, J.R and Nalls, Michael and Ryten, Mina and Botia, J.A and Vanovcova, Jana and Simón-Sánchez, Javier and Castillo-Lizardo, M and Rizzu, Patrizia and Blauwenaat, C and Chouhan, A.K and Li, Y and Yogi, P and Amin, Najaf and Duijn, Cornelia and Morris, H.R and Brice, A and Singleton, Anew and David, D.C and Nollen, E.A and Jain, Ashok and Shulman, J.M and Heutink, Peter and Hernandez, Dena and Arepalli, Sampath and Brooks, Janet and Price, R and Nicolas, A and Chong, Sean and Cookson, Mark and Dillman, Allissa and Moore, Matt and Traynor, Bryan and Plagnol, Vincent and Nicholas W Wood and Sheerin, Una-Marie and Jose M Bras and Charlesworth, Kate and Gardner, Mac and Guerreiro, Rita and Trabzuni, Danyah and Hardy, J and Sharma, M and Saad, Mohamad and Javier Simón-Sánchez and Schulte, Claudia and Corvol, Jean-Christophe and Dürr, A and Vidailhet, M and Sveinbjörnsdóttir, Sigurlaug and Barker, Roger and Caroline H Williams-Gray and Ben-Shlomo, Y and Berendse, Henk W and Dijk, Karin and Berg, Daniela and Brockmann, K and Wurster, Kathrin and Mätzler, W and Gasser, T and Martinez, Maria and Bie, Rob and Biffi, Alessano and Velseboer, Daan and Bloem, Bastiaan and Post, Bart and Wickremaratchi, Mirdhu and Warrenburg, Bart and Bochdanovits, Zoltan and Bonin, Malte and Pétursson, Hjörvar and Riess, Olaf and Burn, David and Lubbe, S and Cooper, J.M and McNeill, Nathan and Schapira, A and Lungu, C and Chen, H and Dong, J and Chinnery, P.F and Hudson, Gavin and Clarke, C.E and Moorby, Catriona and Counsell, Carl and Damier, Philippe and Dartigues, J.-F and Deloukas, Panagiotis and Gray, Emma and Edkins, Ted and Hunt, S.E and ... and IPGDC and International Parkinson’s Disease Genetics Consortium (IPGDC)
Genome Biology, ISSN 1474-7596, 01/2017, Volume 18, Issue 1, p. 22
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 10/2015, Volume 74, Issue 10, pp. 1875 - 1881
Journal Article