X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (193) 193
Publication (44) 44
Newspaper Article (8) 8
Book / eBook (3) 3
Dissertation (2) 2
Patent (2) 2
Book Chapter (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (95) 95
index medicus (82) 82
male (63) 63
female (60) 60
genetics (52) 52
genetics & heredity (50) 50
article (46) 46
polymorphism, single nucleotide (37) 37
genetic aspects (36) 36
aged (35) 35
middle aged (35) 35
research (35) 35
risk factors (35) 35
adult (33) 33
genome-wide association (31) 31
genome-wide association study (30) 30
genotype (30) 30
genomes (27) 27
genetic predisposition to disease (26) 26
genomics (24) 24
parkinson disease - genetics (24) 24
aged, 80 and over (21) 21
epidemiology (21) 21
parkinson's disease (19) 19
genes (18) 18
mutation (18) 18
phenotype (18) 18
association (17) 17
genetic variation (17) 17
health aspects (17) 17
analysis (16) 16
case-control studies (15) 15
loci (15) 15
meta-analysis (15) 15
studies (15) 15
variants (15) 15
adolescent (14) 14
alleles (14) 14
clinical neurology (13) 13
diagnosis (13) 13
metaanalysis (13) 13
neurosciences (13) 13
population (13) 13
young adult (13) 13
cohort studies (12) 12
gene frequency (12) 12
genetic research (12) 12
genome-wide association studies (12) 12
medicine (12) 12
neurology (12) 12
physiological aspects (12) 12
research article (12) 12
disease (11) 11
gene (11) 11
genotype & phenotype (11) 11
risk (11) 11
risk-factors (11) 11
susceptibility (11) 11
alzheimers-disease (10) 10
cancer (10) 10
lod score (10) 10
medical and health sciences (10) 10
medical genetics (10) 10
medicin och hälsovetenskap (10) 10
single nucleotide polymorphisms (10) 10
abridged index medicus (9) 9
age (9) 9
age of onset (9) 9
alpha-synuclein (9) 9
basic medicine (9) 9
body mass index (9) 9
diabetes (9) 9
genetic loci (9) 9
internal medicine (9) 9
medicinsk genetik (9) 9
medicinska och farmaceutiska grundvetenskaper (9) 9
polymorphism, single nucleotide - genetics (9) 9
quantitative trait loci (9) 9
alzheimer disease - genetics (8) 8
alzheimer's disease (8) 8
coronary-heart-disease (8) 8
dna copy number variations (8) 8
exome (8) 8
exome - genetics (8) 8
expression (8) 8
genetic predisposition to disease - genetics (8) 8
hematology (8) 8
linkage disequilibrium (8) 8
mutations (8) 8
parkinson disease (8) 8
parkinsons disease (8) 8
wide association (8) 8
african-americans (7) 7
alzheimers disease (7) 7
atherosclerosis (7) 7
cardiovascular disease (7) 7
child (7) 7
endocrinology & metabolism (7) 7
european continental ancestry group - genetics (7) 7
family (7) 7
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Do, Ron and Stitziel, Nathan O and Won, Hong-Hee and Jørgensen, Anders Berg and Duga, Stefano and Angelica Merlini, Pier and Kiezun, Adam and Farrall, Martin and Goel, Anuj and Zuk, Or and Guella, Illaria and Asselta, Rosanna and Lange, Leslie A and Peloso, Gina M and Auer, Paul L and Girelli, Domenico and Martinelli, Nicola and Farlow, Deborah N and DePristo, Mark A and Roberts, Robert and Stewart, Alexander F. R and Saleheen, Danish and Danesh, John and Epstein, Stephen E and Sivapalaratnam, Suthesh and Hovingh, G. Kees and Kastelein, John J and Samani, Nilesh J and Schunkert, Heribert and Erdmann, Jeanette and Shah, Svati H and Kraus, William E and Davies, Robert and Nikpay, Majid and Johansen, Christopher T and Wang, Jian and Hegele, Robert A and Hechter, Eliana and Marz, Winfried and Kleber, Marcus E and Huang, Jie and Johnson, Anew D and Li, Mingyao and Burke, Greg L and Gross, Myron and Liu, Yongmei and Assimes, Themistocles L and Heiss, Gerardo and Lange, Ethan M and Folsom, Aaron R and Taylor, Herman A and Olivieri, Oliviero and Hamsten, Anders and Clarke, Robert and Reilly, Dermot F and Yin, Wu and Rivas, Manuel A and Donnelly, Peter and Rossouw, Jacques E and Psaty, Bruce M and Herrington, David M and Wilson, James G and Rich, Stephen S and Bamshad, Michael J and Tracy, Russell P and Cupples, L. Aienne and Rader, Daniel J and Reilly, Muredach P and Spertus, John A and Cresci, Sharon and Hartiala, Jaana and Tang, W. H. Wilson and Hazen, Stanley L and Allayee, Hooman and Reiner, Alex P and Carlson, Christopher S and Kooperberg, Charles and Jackson, Rebecca D and Boerwinkle, Eric and Lander, Eric S and Schwartz, Stephen M and Siscovick, David S and McPherson, Ruth and Tybjaerg-Hansen, Anne and Abecasis, Goncalo R and Watkins, Hugh and Nickerson, Deborah A and Ardissino, Diego and Sunyaev, Shamil R and O'Donnell, Christopher J and Altshuler, David and Gabriel, Stacey and Kathiresan, Sekar and Gabriel, Stacey B and Altshuler, David M and Abecasis, Gonçalo R and Daly, Mark J and de Bakker, Paul I. W and Fennell, Tim and Garimella, Kiran and ... and NHLBI Exome Sequencing Project
Nature, ISSN 0028-0836, 2015, Volume 518, Issue 7537, pp. 102 - +
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 02/2011, Volume 7, Issue 2, p. e1001308
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 03/2019, Volume 199, Issue 5, pp. 631 - 642
Journal Article
by Nalls, Mike A and Pankratz, Nathan and Lill, Christina M and Do, Chuong B and Hernandez, Dena G and Saad, Mohamad and DeStefano, Anita L and Kara, Eleanna and Bras, Jose and Sharma, Manu and Schulte, Claudia and Keller, Margaux F and Arepalli, Sampath and Letson, Christopher and Edsall, Connor and Stefansson, Hreinn and Liu, Xinmin and Pliner, Hannah and Lee, Joseph H and Cheng, Rong and Ikram, M. Arfan and Ioannidis, John P. A and Hadjigeorgiou, Georgios M and Bis, Joshua C and Martinez, Maria and Perlmutter, Joel S and Goate, Alison and Marder, Karen and Fiske, Brian and Sutherland, Margaret and Xiromerisiou, Georgia and Myers, Richard H and Clark, Lorraine N and Stefansson, Kari and Hardy, John A and Heutink, Peter and Chen, Honglei and Wood, Nicholas W and Houlden, Henry and Payami, Haydeh and Brice, Alexis and Scott, William K and Gasser, Thomas and Bertram, Lars and Eriksson, Nicholas and Foroud, Tatiana and Singleton, Anew B and Plagnol, Vincent and Sheerin, Una-Marie and Simón-Sánchez, Javier and Lesage, Suzanne and Sveinbjörnsdóttir, Sigurlaug and Barker, Roger and Ben-Shlomo, Yoav and Berendse, Henk W and Berg, Daniela and Bhatia, Kailash and de Bie, Rob M. A and Biffi, Alessano and Bloem, Bas and Bochdanovits, Zoltan and Bonin, Michael and Bras, Jose M and Brockmann, Kathrin and Brooks, Janet and Burn, David J and Charlesworth, Gavin and Chinnery, Patrick F and Chong, Sean and Clarke, Carl E and Cookson, Mark R and Cooper, J. Mark and Corvol, Jean Christophe and Counsell, Carl and Damier, Philippe and Dartigues, Jean-François and Deloukas, Panos and Deuschl, Günther and Dexter, David T and van Dijk, Karin D and Dillman, Allissa and Durif, Frank and Dürr, Alexana and Edkins, Sarah and Evans, Jonathan R and Foltynie, Thomas and Dong, Jing and Gardner, Michelle and Gibbs, J. Raphael and Gray, Emma and Guerreiro, Rita and Harris, Clare and van Hilten, Jacobus J and Hofman, Albert and Hollenbeck, Albert and Holton, Janice and Hu, Michele and Huang, Xuemei and Wurster, Isabel and Mätzler, Walter and ... and GenePD and IPDG and Ashkenazi Jewish Dataset Investiga and 23AndMe and NABEC and HIHG and Greek Parkinson's Dis Consortium and GParkinson's Study Grp PSG Parkins and NGRC and Alzheimer Genetic Analysis Gr and CHARGE and UKBEC and Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and Hussman Institute of Human Genomics (HIHG) and 23andMe and Greek Parkinson's Disease Consortium and International Parkinson's Disease Genomics Consortium (IPDGC) and Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE) and United Kingdom Brain Expression Consortium (UKBEC) and NeuroGenetics Research Consortium (NGRC) and Ashkenazi Jewish Dataset Investigator and North American Brain Expression Consortium (NABEC) and Alzheimer Genetic Analysis Group and The Ashkenazi Jewish Dataset Investigator
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 9, pp. 989 - +
Journal Article