X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (56) 56
gene expression (27) 27
brain (26) 26
female (25) 25
male (25) 25
mutation (21) 21
neurosciences (21) 21
genomics (20) 20
brain - metabolism (19) 19
genetic aspects (19) 19
genome-wide association (18) 18
genome-wide association study (18) 18
genomes (18) 18
middle aged (18) 18
adult (17) 17
aged (17) 17
clinical neurology (17) 17
genetics (17) 17
parkinson disease - genetics (16) 16
parkinson's disease (15) 15
quantitative trait loci (15) 15
genetic research (14) 14
genetics & heredity (14) 14
gene expression profiling (13) 13
risk factors (13) 13
aged, 80 and over (12) 12
expression (12) 12
genes (12) 12
metaanalysis (12) 12
polymorphism, single nucleotide (12) 12
polymorphism, single nucleotide - genetics (12) 12
research (12) 12
transcriptome (12) 12
adolescent (11) 11
genetic predisposition to disease (11) 11
genotype (11) 11
analysis (10) 10
biochemistry & molecular biology (10) 10
genetic predisposition to disease - genetics (10) 10
movement disorders (10) 10
neurology (10) 10
parkinsons disease (10) 10
case-control studies (9) 9
gene expression regulation (9) 9
gwas (9) 9
medical research (9) 9
multidisciplinary sciences (9) 9
neurodegenerative diseases (9) 9
neuroscience (9) 9
variants (9) 9
young adult (9) 9
aging (8) 8
brain research (8) 8
mutations (8) 8
studies (8) 8
alzheimers-disease (7) 7
association (7) 7
biology (7) 7
common variants (7) 7
disease (7) 7
dna methylation (7) 7
parkinsons-disease (7) 7
proteins (7) 7
quantitative genetics (7) 7
risk (7) 7
age (6) 6
animals (6) 6
brain - pathology (6) 6
exons - genetics (6) 6
frontal lobe - metabolism (6) 6
gene mutations (6) 6
gene-expression (6) 6
genetic association studies (6) 6
identification and classification (6) 6
internal medicine (6) 6
linkage disequilibrium (6) 6
lrrk2 protein (6) 6
medical and health sciences (6) 6
medicin och hälsovetenskap (6) 6
medicine, experimental (6) 6
neurons (6) 6
original (6) 6
pedigree (6) 6
population (6) 6
sequence (6) 6
splicing (6) 6
abridged index medicus (5) 5
basic medicine (5) 5
dystonia (5) 5
gene mapping (5) 5
genetic loci (5) 5
genetic variation (5) 5
genetic variation - genetics (5) 5
haplotypes (5) 5
human brain (5) 5
medical genetics (5) 5
medicinska och farmaceutiska grundvetenskaper (5) 5
parkinson’s disease (5) 5
pathogenesis (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Nature communications, ISSN 2041-1723, 2013, Volume 4, Issue 1, p. 2771
... and splicing in the adult human brain Daniah Trabzuni1,2,*, Adaikalavan Ramasamy3,*, Sabaena Imran1, Robert Walker4, Colin Smith4, Michael E. Weale3, John Hardy1, Mina... 
X-CHROMOSOME | AUTISM | METAANALYSIS | TRANSCRIPTOME | GENOTYPE | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | SEQUENCE | NEUROSCIENCE | GENDER-DIFFERENCES | PARKINSONS-DISEASE | Brain - metabolism | RNA Splicing | Spinal Cord - metabolism | Humans | Sex Factors | Gene Expression Regulation - physiology | Adult | Female | Male | Gene Expression Profiling | Genome | Quantitative Trait Loci
Journal Article
Journal of neurochemistry, ISSN 0022-3042, 2011, Volume 119, Issue 2, pp. 275 - 282
Journal Article
by Anttila, Verneri and Winsvold, Bendik S and Gormley, Padhraig and Kurth, Tobias and Bettella, Francesco and McMahon, George and Kallela, Mikko and Malik, Rainer and de Vries, Boukje and Terwindt, Gisela and Medland, Sarah E and Todt, Unda and McArdle, Wendy L and Quaye, Lydia and Koiranen, Markku and Ikram, M Arfan and Lehtimäki, Terho and Stam, Anine H and Ligthart, Lannie and Wedenoja, Juho and Dunham, Ian and Neale, Benjamin M and Palta, Priit and Hamalainen, Eija and Schürks, Markus and Rose, Lynda M and Buring, Julie E and Ridker, Paul M and Steinberg, Stacy and Stefansson, Hreinn and Jakobsson, Finnbogi and Lawlor, Debbie A and Evans, David M and Ring, Susan M and Färkkilä, Markus and Artto, Ville and Kaunisto, Mari A and Freilinger, Tobias and Schoenen, Jean and Frants, Rune R and Pelzer, Nadine and Weller, Claudia M and Zielman, Ronald and Heath, Andrew C and Madden, Pamela A F and Montgomery, Grant W and Martin, Nicholas G and Borck, Guntram and Göbel, Hartmut and Heinze, Axel and Heinze-Kuhn, Katja and Williams, Frances M K and Hartikainen, Anna-Liisa and Pouta, Anneli and van den Ende, Joyce and Uitterlinden, Andre G and Hofman, Albert and Amin, Najaf and Hottenga, Jouke-Jan and Vink, Jacqueline M and Heikkilä, Kauko and Alexander, Michael and Muller-Myhsok, Bertram and Schreiber, Stefan and Meitinger, Thomas and Wichmann, Heinz Erich and Aromaa, Arpo and Eriksson, Johan G and Traynor, Bryan J and Trabzuni, Daniah and Rossin, Elizabeth and Lage, Kasper and Jacobs, Suzanne B R and Gibbs, J Raphael and Birney, Ewan and Kaprio, Jaakko and Penninx, Brenda W and Boomsma, Dorret I and van Duijn, Cornelia and Raitakari, Olli and Jarvelin, Marjo-Riitta and Zwart, John-Anker and Cherkas, Lynn and Strachan, David P and Kubisch, Christian and Ferrari, Michel D and van den Maagdenberg, Arn M J M and Dichgans, Martin and Wessman, Maija and Smith, George Davey and Stefansson, Kari and Daly, Mark J and UK Brain Expression Consortium and the International Headache Genetics Consortium and North American Brain Expression Consortium and Int Headache Genetics Consortium and North Amer Brain Expression
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 8, pp. 912 - 917
Migraine is the most common brain disorder, affecting approximately 14% of the adult population, but its molecular mechanisms are poorly understood. We report... 
POPULATION | HUMAN-DISEASE | PROTEIN | NEURITE OUTGROWTH | DOWN-REGULATION | TRANSFORMING-GROWTH-FACTOR | PROTEOLYSIS | ASSOCIATION | EXPRESSION | FAMILY | LEWIS(X) | GENES | GENETICS & HEREDITY | MUTATIONS | Genetic susceptibility | Genetic variation | Migraine | Physiological aspects | Genetic aspects | Research | Risk factors | Studies | Proteins | Signal transduction | Headaches | Population | Genomes | Meta-analysis
Journal Article
Scientific reports, ISSN 2045-2322, 2019, Volume 9, Issue 1, pp. 19201 - 21
... analysis and insights using the UKBec dataset Letitia M. f. Sng1, peter c. thomson 1 and Daniah trabzuni 2,3* Understanding the complexity of the human brain... 
GENE-EXPRESSION | POLYMORPHISMS | TRANSCRIPTOME | MULTIDISCIPLINARY SCIENCES | REGIONS | Gene expression | Brain | Genomes
Journal Article
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 09/2018, Volume 19, Issue 9, p. 2784
... Dimitrios Vlachakis 1 , Nikolaos E. Labrou 2 , Costas Iliopoulos 3, John Hardy 4, Patrick A. Lewis 4,5, Hardy Rideout 6 and Daniah Trabzuni 4,7,* 1 Genetics Laboratory... 
Parkinson’s disease (PD) | Human brain substantia nigra | LRRK2 mRNA expression | ROC/COR domain splicing events | WD40 domain in protein structure | CROHNS-DISEASE | RNA ISOLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | Parkinson's disease (PD) | KINASE | SUSCEPTIBILITY LOCI | SINGLE-STEP METHOD | CHEMISTRY, MULTIDISCIPLINARY | PARKINSONS-DISEASE RISK | PHENOL-CHLOROFORM EXTRACTION | MUTATIONS | GENOME-WIDE ASSOCIATION | REVEALS | Gene Expression | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - chemistry | Humans | RNA, Messenger - genetics | Models, Molecular | Structure-Activity Relationship | Parkinson Disease - genetics | Substantia Nigra - metabolism | RNA Splicing | Protein Domains | Protein Conformation | Parkinson Disease - metabolism | Protein Interaction Domains and Motifs | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - metabolism | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics | Inflammatory bowel diseases | Parkinson's disease | Splicing | Neurodegenerative diseases | Pathogenesis | Copy number | Substantia nigra | Cortex (occipital) | Genomes | Biology | Leucine | Gene expression | Kinases | Proteins | Domains | Molecular modelling | Intestine | Isoforms | Dimers | Mutation | LRRK2 protein | Movement disorders | Biotechnology | Disease | Neurodegeneration | Localization | Studies | Brain research
Journal Article
Neurogenetics, ISSN 1364-6753, 2017, Volume 18, Issue 3, pp. 121 - 133
Journal Article
Journal Article
Behavior genetics, ISSN 1573-3297, 2018, Volume 48, Issue 5, pp. 374 - 385
Journal Article