UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (302) 302
Patent (22) 22
Publication (9) 9
Conference Proceeding (6) 6
Book Chapter (3) 3
Book / eBook (2) 2
Compact Disc (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (208) 208
life sciences & biomedicine (198) 198
humans (174) 174
male (121) 121
female (118) 118
genetics & heredity (103) 103
mutation (78) 78
adult (60) 60
biological and medical sciences (58) 58
genetic aspects (57) 57
neurosciences & neurology (55) 55
pedigree (54) 54
neurology (51) 51
medical sciences (48) 48
clinical neurology (46) 46
middle aged (42) 42
neurosciences (40) 40
research (40) 40
genetic predisposition to disease (39) 39
child (38) 38
adolescent (37) 37
animals (35) 35
genetics (35) 35
risk factors (31) 31
fundamental and applied biological sciences. psychology (30) 30
molecular sequence data (30) 30
base sequence (29) 29
polymorphism, single nucleotide (29) 29
genotype (28) 28
amino acid sequence (27) 27
biochemistry & molecular biology (27) 27
genetics of eukaryotes. biological and molecular evolution (26) 26
aged (25) 25
genome-wide association study (25) 25
phenotype (25) 25
gene mutations (24) 24
case-control studies (23) 23
chemistry (23) 23
genes (23) 23
dna mutational analysis (22) 22
metallurgy (22) 22
migraine (22) 22
young adult (22) 22
child, preschool (20) 20
genomes (20) 20
medical genetics (20) 20
molecular and cellular biology (20) 20
medicin och hälsovetenskap (19) 19
proteins (19) 19
alleles (18) 18
human genetics (18) 18
mice (18) 18
genomics (17) 17
analysis (16) 16
gene expression (16) 16
haplotypes (16) 16
consanguinity (15) 15
genetic disorders (15) 15
chromosome mapping (14) 14
exons (14) 14
health aspects (14) 14
homozygote (14) 14
infant (14) 14
age of onset (13) 13
alloys (13) 13
ferrous or non-ferrous alloys (13) 13
genetic association studies (13) 13
medical and health sciences (13) 13
migraine disorders - genetics (13) 13
polymorphism, single nucleotide - genetics (13) 13
treatment of alloys or non-ferrous metals (13) 13
abridged index medicus (12) 12
biomedicine (12) 12
molecular medicine (12) 12
mutation, missense (12) 12
nervous system (12) 12
polymerase chain reaction (12) 12
gene frequency (11) 11
genetic research (11) 11
genetic testing (11) 11
genetic variation (11) 11
heterozygote (11) 11
intellectual disability - genetics (11) 11
magnetic resonance imaging (11) 11
medizin (11) 11
mutation - genetics (11) 11
physiological aspects (11) 11
syndrome (11) 11
vascular diseases and vascular malformations of the nervous system (11) 11
aged, 80 and over (10) 10
aging (10) 10
metabolic diseases (10) 10
migraine with aura - genetics (10) 10
stroke - genetics (10) 10
clinical medicine (9) 9
cloning, molecular (9) 9
family health (9) 9
gene function (9) 9
germany (9) 9
human (9) 9
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


European journal of epidemiology, ISSN 0393-2990, 02/2020, Volume 35, Issue 2, pp. 169 - 181
Journal Article
1992, Kunstgeschichte, ISBN 9783886605729, Volume Bd. 9, i, 117 p., [37] p. of plates
Book
Deutsches Ärzteblatt international, ISSN 1866-0452, 07/2019, Volume 116, Issue 29-30, pp. 489 - 496
Journal Article
Journal Article
by Gormley, A.M and Stefansson, Hreinn and Winsvold, Bendik and Palta, Priit and Esko, Tõnu and Pers, Tune and Farh, Kai-How and Cuenca-Leon, E and Muona, M and Furlotte, N.A and Kurth, Karl and Ingason, Anes and Mcmahon, George and Ligthart, Lannie and Terwindt, Gisela and Todt, Unda and Müller-Myhsok, Bertram and Ran, C and Gordon, S.G and Stam, Anine and Steinberg, Stacy and Göbel, Hartmut and Koiranen, Markku and Quaye, Lydia and Adams, H.H.H and Lehtimäki, Terho and Sarin, A.-P and Wedenoja, J and Hinds, David A and Buring, J.E and Schürks, Markus and Ridker, Paul and Hrafnsdottir, M.G and Ring, Susan and Hottenga, Jouke Jan and Penninx, Brenda and Färkkilä, Markus and Artto, Ville and Hämäläinen, Eija and Lucae, Susanne and Malik, Rainer and Heath, Anew C and Madden, Pamela and Martin, Nicholas and Montgomery, Grant and Kurki, M.I and Kals, Mart and Mägi, Reedik and Pärn, K and Huang, H and Byrnes, A.E and Franke, Lude and Huang, Jian and Stergiakouli, Evangelia and Lee, Phil and Sandor, C and Webber, C and Cader, Z and Müller-Myhsok, B and Schreiber, Stefan and Meitinger, Thomas and Hagen, Knut and Salomaa, Veikko and Heikkilä, Kauko and Loehrer, Elizabeth and Uitterlinden, Ané and Hofman, A and Duijn, Cornelia and Cherkas, Lynn and Pedersen, L.M and Stubhaug, A and Nielsen, C.S and Männikkö, M and Mihailov, Evelin and Milani, Lili and Esserlind, A.-L and Christensen, A.F and Hansen, T.F and Werge, Thomas and Kaprio, Jaakko and Aromaa, Arpo and Raitakari, Olli and Ikram, Arfan and Ikram, Kamran and Jarvelin, Marjo-Riitta and Metspalu, Anes and Kubisch, Christian and Strachan, David and Ferrari, Michel and Belin, A.C and Wessman, Maija and Maagdenberg, Arn and Zwart, John-Anker and Boomsma, Dorret and Smith, G.D and Stefansson, K and Eriksson, Nicholas and Daly, Mark and Neale, Benjamin and Olesen, Jes and ... and Int Headache Genetics Consortium and International Headache Genetics Consortium
Nature genetics, ISSN 1061-4036, 08/2016, Volume 48, Issue 8, pp. 856 - 866
Journal Article
Journal Article