X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (22) 22
humans (17) 17
schizophrenia (14) 14
genetics & heredity (13) 13
autism (12) 12
genetic aspects (12) 12
genomes (12) 12
genetics (11) 11
mental disorders (11) 11
research (11) 11
article (8) 8
consortia (8) 8
female (8) 8
genetic variation (8) 8
male (8) 8
mutation (8) 8
risk factors (8) 8
studies (8) 8
phenotype (7) 7
psychiatry (7) 7
risk (7) 7
analysis (6) 6
behavioral disciplines and activities (6) 6
genetic predisposition to disease (6) 6
genome-wide association study (6) 6
polymorphism, single nucleotide (6) 6
children (5) 5
genome-wide association (5) 5
genomics (5) 5
mutations (5) 5
neurosciences (5) 5
population (5) 5
schizophrenia - genetics (5) 5
variants (5) 5
child (4) 4
cohort studies (4) 4
disorders (4) 4
dk/atira/pure/researchoutput/pubmedpublicationtype/d016428 (4) 4
epidemiology (4) 4
genome, human (4) 4
journal article (4) 4
loci (4) 4
metaanalysis (4) 4
multidisciplinary sciences (4) 4
physiological aspects (4) 4
proteins (4) 4
science (4) 4
adolescent (3) 3
attention deficit disorder (3) 3
autism spectrum disorder - genetics (3) 3
autism spectrum disorders (3) 3
biology (3) 3
datasets (3) 3
datasets as topic (3) 3
de-novo (3) 3
development and progression (3) 3
disease (3) 3
dk/atira/pure/researchoutput/pubmedpublicationtype/d052061 (3) 3
dna mutational analysis (3) 3
epilepsy (3) 3
exome - genetics (3) 3
gene expression (3) 3
genes (3) 3
genetic research (3) 3
genetic risk (3) 3
genetic variation - genetics (3) 3
genome (3) 3
genome-wide association studies (3) 3
genotype (3) 3
health aspects (3) 3
homozygote (3) 3
intelligence (3) 3
medical and health sciences (3) 3
medical genetics (3) 3
medicin och hälsovetenskap (3) 3
medicine (3) 3
meta-analysis (3) 3
methods (3) 3
neurodevelopmental disorders (3) 3
pervasive developmental disorders (3) 3
phenotypes (3) 3
prevalence (3) 3
principal components analysis (3) 3
quality control (3) 3
research support, n.i.h., extramural (3) 3
sample size (3) 3
single nucleotide polymorphisms (3) 3
adult (2) 2
alleles (2) 2
attention deficit disorder with hyperactivity - genetics (2) 2
basic medicine (2) 2
bioinformatics (2) 2
bipolar disorder (2) 2
brain (2) 2
brain research (2) 2
candidate genes (2) 2
care and treatment (2) 2
case-control studies (2) 2
clinical medicine (2) 2
clinical psychology (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


NATURE COMMUNICATIONS, ISSN 2041-1723, 07/2019, Volume 10, Issue 1, pp. 3043 - 9
There are established associations between advanced paternal age and offspring risk for psychiatric and developmental disorders. These are commonly attributed... 
UNITED-STATES | SUPPORT | AUTISM | VARIANTS | MULTIDISCIPLINARY SCIENCES | SCHIZOPHRENIA | PREVALENCE | Mental disorders | Epilepsy | Disorders | Schizophrenia | Risk | Paternity | Nucleotides | Neurodevelopmental disorders | Epidemiology | Coronary artery disease | Autism | Offspring | Mutation | Cardiovascular diseases | Health risk assessment | Heart diseases | Age
Journal Article
Nature, ISSN 0028-0836, 2016, Volume 536, Issue 7616, pp. 285 - 291
Large-scale reference data sets of human genetic variation are critical for the medical and functional interpretation of DNA sequence changes. Here we describe... 
HUMAN-DISEASE | EVOLUTION | MULTIDISCIPLINARY SCIENCES | MUTATION | GUIDELINES | FRAMEWORK | SEQUENCE VARIANTS | NETWORKS | DISCOVERY | HUMAN-POPULATION HISTORY | Genetic aspects | Research | Man | Human beings | Genetic variation | Analysis | Datasets | Proteins | Disease | Genes | Principal components analysis | Genetics | Genomes | Data bases
Journal Article
by Grove, Jakob and Ripke, Stephan and Als, Thomas D and Mattheisen, Manuel and Walters, Raymond K and Won, Hyejung and Pallesen, Jonatan and Agerbo, Esben and Andreassen, Ole A and Anney, Richard and Awashti, Swapnil and Belliveau, Rich and Bettella, Francesco and Buxbaum, Joseph D and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Marie and Cerrato, Felecia and Chambert, Kimberly and Christensen, Jane H and Churchhouse, Claire and Dellenvall, Karin and Demontis, Ditte and De Rubeis, Silvia and Devlin, Bernie and Djurovic, Srdjan and Dumont, Ashley L and Goldstein, Jacqueline I and Hansen, Christine S and Hauberg, Mads Engel and Hollegaard, Mads V and Hope, Sigrun and Howrigan, Daniel P and Huang, Hailiang and Hultman, Christina M and Klei, Lambertus and Maller, Julian and Martin, Joanna and Martin, Alicia R and Moran, Jennifer L and Nyegaard, Mette and Nærland, Terje and Palmer, Duncan S and Palotie, Aarno and Pedersen, Carsten Bøcker and Pedersen, Marianne Giørtz and dPoterba, Timothy and Poulsen, Jesper Buchhave and Pourcain, Beate St and Qvist, Per and Rehnström, Karola and Reichenberg, Abraham and Reichert, Jennifer and Robinson, Elise B and Roeder, Kathryn and Roussos, Panos and Saemundsen, Evald and Sandin, Sven and Satterstrom, F. Kyle and Davey Smith, George and Stefansson, Hreinn and Steinberg, Stacy and Stevens, Christine R and Sullivan, Patrick F and Turley, Patrick and Walters, G. Bragi and Xu, Xinyi and Wray, Naomi R and Trzaskowski, Maciej and Byrne, Enda M and Abdellaoui, Abdel and Adams, Mark J and Air, Tracy M and Andlauer, Till F. M and Bacanu, Silviu-Alin and Beekman, Aartjan T. F and Bigdeli, Tim B and Binder, Elisabeth B and Blackwood, Douglas H. R and Bryois, Julien and Buttenschøn, Henriette N and Cai, Na and Castelao, Enrique and Clarke, Toni-Kim and Coleman, Jonathan R. I and Colodro-Conde, Lucía and Couvy-Duchesne, Baptiste and Craddock, Nick and Crawford, Gregory E and Davies, Gail and Deary, Ian J and Degenhardt, Franziska and Derks, Eske M and Direk, Nese and Dolan, Conor V and Dunn, Erin C and Eley, Thalia C and Escott-Price, Valentina and Kiadeh, Farnush Farhadi Hassan and Finucane, Hilary K and Forstner, Andreas J and ... and Psychiat Genomics Consortium and BUPGEN and 23andMe Res Team and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium and 23andMe Research Team and Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium
Nature Genetics, ISSN 1061-4036, 2019, Volume 51, Issue 3, pp. 431 - 431
Journal Article
by Demontis, Ditte and Walters, Raymond K and Martin, Joanna and Mattheisen, Manuel and Als, Thomas D and Agerbo, Esben and Baldursson, Gísli and Belliveau, Rich and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Marie and Cerrato, Felecia and Chambert, Kimberly and Churchhouse, Claire and Dumont, Ashley and Eriksson, Nicholas and Gandal, Michael and Goldstein, Jacqueline I and Grasby, Katrina L and Grove, Jakob and Gudmundsson, Olafur O and Hansen, Christine S and Hauberg, Mads Engel and Hollegaard, Mads V and Howrigan, Daniel P and Huang, Hailiang and Maller, Julian B and Martin, Alicia R and Martin, Nicholas G and Moran, Jennifer and Pallesen, Jonatan and Palmer, Duncan S and Pedersen, Carsten Bøcker and Pedersen, Marianne Giørtz and Poterba, Timothy and Poulsen, Jesper Buchhave and Ripke, Stephan and Robinson, Elise B and Satterstrom, F. Kyle and Stefansson, Hreinn and Stevens, Christine and Turley, Patrick and Walters, G. Bragi and Won, Hyejung and Wright, Margaret J and Albayrak, Özgür and Anney, Richard J. L and Arranz, Maria Jesús and Banaschewski, Tobias J and Bau, Claiton and Biederman, Joseph and Buitelaar, Jan K and Casas, Miguel and Charach, Alice and Crosbie, Jennifer and Dempfle, Astrid and Doyle, Alysa E and Ebstein, Richard P and Elia, Josephine and Freitag, Christine and Föcker, Manuel and Gill, Michael and Grevet, Eugenio and Hawi, Ziarih and Hebebrand, Johannes and Herpertz-Dahlmann, Beate and Hervas, Amaia and Hinney, Anke and Hohmann, Sarah and Holmans, Peter and Hutz, Mara and Ickowitz, Abel and Johansson, Stefan and Kent, Lindsey and Kittel-Schneider, Sarah and Lambregts-Rommelse, Nanda and Lehmkuhl, Gerd and Loo, Sandra K and McGough, James J and Meyer, Jobst and Mick, Eric and Middletion, Frank and Miranda, Ana and Mota, Nina Roth and Mulas, Fernando and Mulligan, Aisling and Nelson, Freimer and Nguyen, T. Trang and Oades, Robert D and O’Donovan, Michael C and Owen, Michael J and Palmason, Haukur and Ramos-Quiroga, Josep Antoni and Renner, Tobias J and Ribasés, Marta and Rietschel, Marcella and Rivero, Olga and Romanos, Jasmin and Romanos, Marcel and Rothenberger, Aribert and Royers, Herbert and ... and Early Lifecourse Genetic and ADHD Working Grp Psychiat Genomics and 23andMe Res Team and Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 23andMe Research Team and ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
Nature Genetics, ISSN 1061-4036, 01/2019, Volume 51, Issue 1, pp. 63 - 75
Journal Article
by Marshall, Christian R and Howrigan, Daniel P and Merico, Daniele and Thiruvahinapuram, Bhooma and Wu, Wenting and Greer, Douglas S and Antaki, Danny and Shetty, Aniket and Holmans, Peter A and Pinto, Dalila and Gujral, Madhusudan and Brandler, William M and Malhotra, Dheeraj and Wang, Zhouzhi and Fajarado, Karin V Fuentes and Maile, Michelle S and Ripke, Stephan and Agartz, Ingrid and Albus, Margot and Alexander, Madeline and Amin, Farooq and Atkins, Joshua and Bacanu, Silviu A and Belliveau, Richard A and Bergen, Sarah E and Bertalan, Marcelo and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Bulik-Sullivan, Brendan and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Cairns, Murray J and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberley D and Cheng, Wei and Cloninger, C Robert and Cohen, David and Cormican, Paul and Craddock, Nick and Crespo-Facorro, Benedicto and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and Del Favero, Jurgen and DeLisi, Lynn E and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farh, Kai-How and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedman, Joseph I and Forstner, Aneas J and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Gershon, Elliot S and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Gratten, Jacob and de Haan, Lieuwe and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Huang, Hailiang and Ikeda, Masashi and Joa, Inge and Kähler, Anna K and ... and Schizophrenia Working Grp and Psychosis Endophenotypes and CNV and Psychosis Endophenotypes International Consortium and CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature Genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 27 - 35
Journal Article