X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (207) 207
schizophrenia (141) 141
female (121) 121
male (118) 118
psychiatry (117) 117
genetics & heredity (98) 98
genetics (94) 94
neurosciences (82) 82
genome-wide association study (76) 76
bipolar disorder (75) 75
genomes (75) 75
genetic aspects (74) 74
genome-wide association (74) 74
adult (72) 72
genetic predisposition to disease (71) 71
genomics (68) 68
mental disorders (64) 64
schizophrenia - genetics (64) 64
polymorphism, single nucleotide (61) 61
case-control studies (59) 59
middle aged (57) 57
research (56) 56
risk factors (54) 54
gene expression (49) 49
genotype (46) 46
risk (46) 46
genes (45) 45
polymorphism, single nucleotide - genetics (42) 42
analysis (39) 39
disease (39) 39
genetic variation (36) 36
studies (36) 36
brain (33) 33
medicin och hälsovetenskap (33) 33
metaanalysis (33) 33
alleles (32) 32
association (32) 32
genetic research (32) 32
medical and health sciences (32) 32
aged (31) 31
biochemistry & molecular biology (31) 31
meta-analysis (31) 31
phenotype (31) 31
young adult (31) 31
common variants (30) 30
loci (29) 29
expression (28) 28
susceptibility (28) 28
variants (28) 28
psychiatry and mental health (27) 27
adolescent (26) 26
medical research (26) 26
research article (25) 25
heritability (24) 24
clinical neurology (23) 23
consortia (23) 23
multidisciplinary sciences (23) 23
mutations (23) 23
population (23) 23
autism (22) 22
linkage disequilibrium (22) 22
medical genetics (22) 22
animals (21) 21
psychosis (21) 21
quantitative trait loci (21) 21
single nucleotide polymorphisms (21) 21
single-nucleotide polymorphism (21) 21
biology (20) 20
medicine (20) 20
neurology (20) 20
umcg approved (20) 20
identification (19) 19
genetic predisposition to disease - genetics (18) 18
genome, human (18) 18
linkage (18) 18
no (18) 18
european continental ancestry group - genetics (17) 17
medicinska och farmaceutiska grundvetenskaper (17) 17
polymorphism (17) 17
susceptibility loci (17) 17
age (16) 16
basic medicine (16) 16
child (16) 16
gene (16) 16
genetic markers (16) 16
medicine, experimental (16) 16
mutation (16) 16
neuroscience (16) 16
amyotrophic lateral sclerosis (15) 15
amyotrophic lateral sclerosis - genetics (15) 15
biological psychiatry (15) 15
chromosomes (15) 15
clinical medicine (15) 15
disorders (15) 15
dna methylation (15) 15
gene expression profiling (15) 15
haplotypes (15) 15
klinisk medicin (15) 15
aged, 80 and over (14) 14
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS genetics, ISSN 1553-7390, 08/2011, Volume 7, Issue 8, p. e1002197
Journal Article
PLoS genetics, ISSN 1553-7404, 2012, Volume 8, Issue 1, p. e1002431
Journal Article
BMC genomics, ISSN 1471-2164, 2012, Volume 13, Issue 1, pp. 636 - 636
Journal Article
by Davis, Lea K and Yu, Dongmei and Keenan, Clare L and Gamazon, Eric R and Konkashbaev, Anuar I and Derks, Eske M and Neale, Benjamin M and Yang, Jian and Lee, S. Hong and Evans, Patrick and Barr, Cathy L and Bellodi, Laura and Benarroch, Fortu and Berrio, Gabriel Bedoya and Bienvenu, Oscar J and Bloch, Michael H and Blom, Rianne M and Bruun, Ruth D and Budman, Cathy L and Camarena, Beatriz and Campbell, Desmond and Cappi, Carolina and Cardona Silgado, Julio C and Cath, Danielle C and Cavallini, Maria C and Chavira, Denise A and Chouinard, Sylvain and Conti, David V and Cook, Edwin H and Coric, Vladimir and Cullen, Bernadette A and Deforce, Dieter and Delorme, Richard and Dion, Yves and Edlund, Christopher K and Egberts, Karin and Falkai, Peter and Fernandez, Thomas V and Gallagher, Patience J and Garrido, Helena and Geller, Daniel and Girard, Simon L and Grabe, Hans J and Grados, Marco A and Greenberg, Benjamin D and Gross-Tsur, Varda and Haddad, Stephen and Heiman, Gary A and Hemmings, Sian M. J and Hounie, Ana G and Illmann, Cornelia and Jankovic, Joseph and Jenike, Michael A and Kennedy, James L and King, Robert A and Kremeyer, Barbara and Kurlan, Roger and Lanzagorta, Nuria and Leboyer, Marion and Leckman, James F and Lennertz, Leonhard and Liu, Chunyu and Lochner, Christine and Lowe, Thomas L and Macciardi, Fabio and McCracken, James T and McGrath, Lauren M and Mesa Restrepo, Sandra C and Moessner, Rainald and Morgan, Jubel and Muller, Heike and Murphy, Dennis L and Naarden, Allan L and Ochoa, William Cornejo and Ophoff, Roel A and Osiecki, Lisa and Pakstis, Andrew J and Pato, Michele T and Pato, Carlos N and Piacentini, John and Pittenger, Christopher and Pollak, Yehuda and Rauch, Scott L and Renner, Tobias J and Reus, Victor I and Richter, Margaret A and Riddle, Mark A and Robertson, Mary M and Romero, Roxana and Rosàrio, Maria C and Rosenberg, David and Rouleau, Guy A and Ruhrmann, Stephan and Ruiz-Linares, Andres and Sampaio, Aline S and Samuels, Jack and Sandor, Paul and Sheppard, Brooke and Singer, Harvey S and Smit, Jan H and ...
PLoS genetics, ISSN 1553-7404, 2013, Volume 9, Issue 10, p. e1003864
Journal Article
Lancet neurology, ISSN 1474-4422, 2007, Volume 6, Issue 6, pp. 521 - 532
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 6, p. e39498
Journal Article