X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (14) 14
index medicus (14) 14
parkinson disease - genetics (11) 11
female (8) 8
male (8) 8
neurology (8) 8
neurosciences (8) 8
clinical neurology (7) 7
genetic predisposition to disease (7) 7
genetics (7) 7
genotype (7) 7
middle aged (7) 7
parkinson's disease (7) 7
aged (6) 6
gene (6) 6
gene frequency (5) 5
adult (4) 4
genetic aspects (4) 4
genome-wide association (4) 4
geriatrics & gerontology (4) 4
international cooperation (4) 4
medical and health sciences (4) 4
medical research (4) 4
medicin och hälsovetenskap (4) 4
mutation (4) 4
adolescent (3) 3
age of onset (3) 3
aged, 80 and over (3) 3
clinical medicine (3) 3
genetic association studies (3) 3
genetic predisposition to disease - genetics (3) 3
genome-wide association study - methods (3) 3
internal medicine (3) 3
klinisk medicin (3) 3
lrrk2 (3) 3
medical colleges (3) 3
medicine, experimental (3) 3
nervous system diseases (3) 3
polymorphism, single nucleotide - genetics (3) 3
risk (3) 3
risk factors (3) 3
snca (3) 3
165 (2) 2
abridged index medicus (2) 2
alpha-synuclein (2) 2
alpha-synuclein - genetics (2) 2
anopheles (2) 2
article (2) 2
association (2) 2
biological apparatus and supplies (2) 2
case-control studies (2) 2
cohort studies (2) 2
disease susceptibility (2) 2
europe (2) 2
family (2) 2
genetic research (2) 2
genome-wide association study (2) 2
leucine-rich repeat serine-threonine protein kinase-2 (2) 2
mapt (2) 2
medical genetics (2) 2
metaanalyses (2) 2
mutations (2) 2
neurologi (2) 2
parkinson disease (2) 2
parkinson disease - epidemiology (2) 2
parkinson disease - ethnology (2) 2
parkinson disease/genetics (2) 2
polymorphism, single nucleotide (2) 2
population (2) 2
protein-serine-threonine kinases - genetics (2) 2
psychiatry (2) 2
research (2) 2
stem cells (2) 2
uncertainty (2) 2
variability (2) 2
variants (2) 2
young adult (2) 2
1506 (1) 1
172 (1) 1
298 (1) 1
access to information (1) 1
agriculture (1) 1
alcohol oxidoreductases - genetics (1) 1
alleles (1) 1
allelic variation (1) 1
alzheimer disease (1) 1
alzheimers disease (1) 1
amyotrophic lateral sclerosis (1) 1
analysis (1) 1
animal models (1) 1
animals (1) 1
asia (1) 1
asian continental ancestry group - genetics (1) 1
ataxin-2 (1) 1
ataxins - genetics (1) 1
ataxins - metabolism (1) 1
autosomal dominant (1) 1
autosomal recessive parkinsonism (1) 1
autosomal-dominant parkinsonism (1) 1
biology (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Ross, Owen A, Dr and Soto-Ortolaza, Alexandra I, BSc and Heckman, Michael G, MS and Aasly, Jan O, Prof and Abahuni, Nadine, MD and Annesi, Grazia, Prof and Bacon, Justin A, BSc and Bardien, Soraya, PhD and Bozi, Maria, MD and Brice, Alexis, Prof and Brighina, Laura, MD and Van Broeckhoven, Christine, Prof and Carr, Jonathan, Prof and Chartier-Harlin, Marie-Christine, Prof and Dardiotis, Efthimios, MD and Dickson, Dennis W, Prof and Diehl, Nancy N, BS and Elbaz, Alexis, Prof and Ferrarese, Carlo, Prof and Ferraris, Alessandro, MD and Fiske, Brian, PhD and Gibson, J Mark, Prof and Gibson, Rachel, PhD and Hadjigeorgiou, Georgios M, MD and Hattori, Nobutaka, Prof and Ioannidis, John PA, Prof and Jasinska-Myga, Barbara, MD and Jeon, Beom S, Prof and Kim, Yun Joong, Prof and Klein, Christine, Prof and Kruger, Rejko, MD and Kyratzi, Elli, MD and Lesage, Suzanne, PhD and Lin, Chin-Hsien, MD and Lynch, Timothy, Prof and Maraganore, Demetrius M, Prof and Mellick, George D, PhD and Mutez, Eugénie, MD and Nilsson, Christer, Prof and Opala, Grzegorz, Prof and Park, Sung Sup, Prof and Puschmann, Andreas, MD and Quattrone, Aldo, Prof and Sharma, Manu, PhD and Silburn, Peter A, Prof and Sohn, Young Ho, Prof and Stefanis, Leonidas, MD and Tadic, Vera, MD and Theuns, Jessie, PhD and Tomiyama, Hiroyuki, MD and Uitti, Ryan J, Prof and Valente, Enza Maria, Prof and van de Loo, Simone, PhD and Vassilatis, Demetrios K, PhD and Vilariño-Güell, Carles, PhD and White, Linda R, Prof and Wirdefeldt, Karin, MD and Wszolek, Zbigniew K, Prof and Wu, Ruey-Meei, Prof and Farrer, Matthew J, Prof and Genetic Epidemiology Parkinson's D and Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium and Sektion IV and Lund University and Psychiatry (Lund) and Klinisk neurogenetik and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Psykiatri, Lund and Division IV and Clinical Neurogenetics and Lunds universitet
Lancet Neurology, The, ISSN 1474-4422, 2011, Volume 10, Issue 10, pp. 898 - 908
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/2012, Volume 49, Issue 11, pp. 721 - 726
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 2011, Volume 18, Issue 1, pp. S138 - S139
Summary Essential tremor (ET) is a prevalent condition manifesting with progressive action tremor. Although ET was traditionally viewed as a sporadic disease,... 
Neurology | LINGO1 | Genetics | Essential tremor | Polymorphism, Single Nucleotide - genetics | Animals | Essential Tremor - genetics | Genome-Wide Association Study - methods | Essential Tremor - diagnosis | Humans | Tremor | Genomics | Genes | Family | Genetic aspects | Dopamine receptors | Protein binding
Journal Article
Movement Disorders, ISSN 0885-3185, 07/2014, Volume 29, Issue 8, pp. 1053 - 1057
Journal Article
Neurology, ISSN 0028-3878, 08/2012, Volume 79, Issue 7, pp. 659 - 667
Objective: Eleven genetic loci have reached genome-wide significance in a recent meta-analysis of genome-wide association studies in Parkinson disease (PD)... 
VARIANTS | METAANALYSES | UNCERTAINTY | RISK | COMPLEX DISEASES | MAPT | SUSCEPTIBILITY GENES | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | SNCA | Genetic Predisposition to Disease | Genome-Wide Association Study | Gene Frequency | Humans | Middle Aged | Genotype | Male | Genetic Loci | Parkinson Disease - genetics | Case-Control Studies | Alleles | Female | Aged | Polymorphism, Single Nucleotide | 165 | 172
Journal Article
by Wray, Selina and Self, Matthew and Lewis, Patrick A and Taanman, Jan-Willem and Ryan, Natalie S and Mahoney, Colin J and Liang, Yuying and Devine, Michael J and Sheerin, Una-Marie and Houlden, Henry and Morris, Huw R and Healy, Daniel and Marti-Masso, Jose-Felix and Preza, Elisavet and Barker, Suzanne and Sutherland, Margaret and Corriveau, Roderick A and D'Andrea, Michael and Schapira, Anthony H. V and Uitti, Ryan J and Guttman, Mark and Opala, Grzegorz and Jasinska-Myga, Barbara and Puschmann, Andreas and Nilsson, Christer and Espay, Alberto J and Slawek, Jaroslaw and Gutmann, Ludwig and Boeve, Bradley F and Boylan, Kevin and Jon Stoessl, A and Ross, Owen A and Maragakis, Nicholas J and Van Gerpen, Jay and Gerstenhaber, Melissa and Gwinn, Katrina and Dawson, Ted M and Isacson, Ole and Marder, Karen S and Clark, Lorraine N and Przedborski, Serge E and Finkbeiner, Steven and Rothstein, Jeffrey D and Wszolek, Zbigniew K and Rossor, Martin N and Hardy, John and Gusella, James F and MacDonald, Marcy E and Wheeler, Vanessa C and Ross, Christopher A and Akimov, Sergey and Arjomand, Jamshid and Thompson, Leslie M and King, Alvin and Hermanowicz, Neal and Winokur, Sara and Svendsen, Clive N and Mattis, Virginia and Onorati, Marco and Cattaneo, Elena and Allen, Nicholas D and Kemp, Paul J and Kim, Kwang-Soo and Przedborski, Serge and Feng, Jian and Lee, Virginia M. Y and Trojanowski, John Q and James Surmeier, D and Henderson, Christopher E and Maniatis, Tom and Eggan, Kevin and Cudowicz, Merit E and NINDS ALS IPSC Consortium and NINDS Parkinson's Dis IPSC and NINDS Huntington's Dis IPSC and NINDS Huntington's Disease iPSC Consortium and NINDS Parkinson's Disease iPSC Consortium and NINDS ALS iPSC Consortium and Sektion IV and Lund University and Psychiatry (Lund) and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Division IV and Psykiatri, Lund and Lunds universitet
PLoS ONE, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, p. e43099
Our understanding of the molecular mechanisms of many neurological disorders has been greatly enhanced by the discovery of mutations in genes linked to... 
PLURIPOTENT STEM-CELLS | SOMATIC-CELLS | AUTOSOMAL-DOMINANT PARKINSONISM | GENE | MULTIDISCIPLINARY SCIENCES | FRONTOTEMPORAL DEMENTIA | EARLY-ONSET | FAMILIAL ALZHEIMERS-DISEASE | CLINICAL-FEATURES | TRIPLICATION | MISSENSE MUTATIONS | Cell Line | Tissue Banks | Cell Proliferation | Humans | Access to Information | Nervous System Diseases - genetics | Immunohistochemistry - methods | Biopsy | Cell Differentiation | Fibroblasts - cytology | Models, Genetic | Nervous System Diseases - physiopathology | Mutation | Induced Pluripotent Stem Cells - cytology | Databases, Factual | Fibroblasts - metabolism | Physiological aspects | Nervous system diseases | Genetic aspects | Research | Gene mutations | Huntingtons disease | Cell culture | Biotechnology | Neurosciences | Animal models | Parkinsons disease | Disorders | Stem cell transplantation | Neuronal-glial interactions | Consortia | Psychiatric-mental health nursing | Neurological disorders | Medical research | Stroke | Departments | Amyotrophic lateral sclerosis | Neurological diseases | Medicine | Neurology | Pathology | Molecular modelling | Cell lines | Stem cells | Surgeons | Collection | Alzheimers disease | Psychiatry | Pluripotency | Dementia | Geriatrics | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Psykiatri | Klinisk medicin | Geriatrik
Journal Article
Neurology, ISSN 0028-3878, 10/2015, Volume 85, Issue 15, pp. 1283 - 1292
Journal Article