X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
genome-wide association (3) 3
all-cause mortality (2) 2
bipolar disorder (2) 2
cardiovascular-disease (2) 2
common variants (2) 2
coronary-heart-disease (2) 2
genetic-variants (2) 2
genome-wide association study (2) 2
humans (2) 2
index medicus (2) 2
research (2) 2
risk factors (2) 2
risk loci (2) 2
analysis (1) 1
asperger-syndrome (1) 1
autism (1) 1
autism spectrum disorder (1) 1
autism spectrum disorder - diagnosis (1) 1
autism spectrum disorder - genetics (1) 1
autism spectrum disorder - physiopathology (1) 1
autism spectrum disorder, genome-wide association study, meta-analysis, genetic correlation, heritability, gene-set analysis, schizophrenia, neurodevelopment (1) 1
biology and life sciences (1) 1
blood-pressure (1) 1
body-mass index (1) 1
c-reactive protein (1) 1
c-reactive protein - genetics (1) 1
c-reactive protein - metabolism (1) 1
carrier proteins - genetics (1) 1
case-control studies (1) 1
chromosomes, human, pair 10 - chemistry (1) 1
common (1) 1
copy number variation (1) 1
de-novo mutations (1) 1
developmental biology (1) 1
developmental neuroscience (1) 1
female (1) 1
forkhead transcription factors - genetics (1) 1
foxp1 (1) 1
gene expression (1) 1
gene-set analysis (1) 1
genetic (1) 1
genetic aspects (1) 1
genetic correlation (1) 1
genetic loci (1) 1
genetic predisposition to disease (1) 1
genetic susceptibility (1) 1
genetics (1) 1
genetics & heredity (1) 1
genomes (1) 1
genotype (1) 1
health risk assessment (1) 1
heart diseases - genetics (1) 1
heritability (1) 1
homeodomain proteins - genetics (1) 1
immune system diseases - genetics (1) 1
immune-system (1) 1
inflammatory markers (1) 1
intellectual disability (1) 1
life sciences (1) 1
linkage (1) 1
male (1) 1
medical research (1) 1
medicine and health sciences (1) 1
medicine, general & internal (1) 1
membrane proteins - genetics (1) 1
mendelian randomization analysis (1) 1
mental disorders (1) 1
mental disorders - genetics (1) 1
mental illness (1) 1
mental-retardation (1) 1
meta-analysis (1) 1
metabolic diseases - genetics (1) 1
molecular biology (1) 1
neurodevelopment (1) 1
neurologi (1) 1
neurology (1) 1
neuronal migration (1) 1
neurosciences (1) 1
neurosciences & neurology (1) 1
outcome and process assessment (1) 1
pervasive developmental disorders (1) 1
plasma membrane calcium-transporting atpases - genetics (1) 1
polymorphism, single nucleotide (1) 1
psychiatry and mental health (1) 1
repressor proteins - genetics (1) 1
resource exchange (1) 1
reveals (1) 1
scan (1) 1
schizophrenia (1) 1
schizophrenia - diagnosis (1) 1
schizophrenia - genetics (1) 1
schizophrenia - physiopathology (1) 1
social sciences (1) 1
studies (1) 1
susceptibility locus (1) 1
transcription factors - genetics (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Prins, B.P and Abbasi, A and Wong, A and Vaez, Ahmad and Nolte, Ilja and Franceschini, Nora and Stuart, P.E and Guterriez Achury, J and Mistry, V and Bradfield, Jonathan and Valdes, Ana Maria and Bras, Jose and Shatunov, Aleksey and Lu, Chao and Han, B and Raychaudhuri, Soumya and Bevan, Steve and Mayes, M.D and Tsoi, L.C and Evangelou, Evangelos and Nair, Rajan P and Grant, Struan and Polychronakos, Constantin and Radstake, Timothy and Heel, David and Dunstan, M.L and Wood, Nicholas and Al-Chalabi, Ammar and Dehghan, Abbas and Hakonarson, Hakon and Markus, H.S and Elder, James and Knight, J and Arking, Dan and Spector, Timothy and Koeleman, Bobby and Duijn, Cornelia and Martín, Javier and Morris, Anew and Weersma, Rinse K and Wijmenga, Cisca and Munroe, Patricia and Perry, John and Pouget, J.G and Jamshidi, Yalda and Snieder, Harold and Alizadeh, Behrooz and Inflammation Working Grp CHARGE Co and Autism Spectrum Disorder Working G and PAGE Consortium and Int Consortium Blood Pressure and Int Parkinson Dis Genomics Consort and Schizophrenia Working Grp Psychiat and DIAGRAM Consortium and CARDIoGRAMplusC4d Consortium and Int Stroke Genetics Consortium and Treat OA Consortium and ALS Consortium and CKDGen Consortium and Systemic Sclerosis Consortium and GERAD1 Consortium and International Consortium for Blood Pressure and International Stroke Genetics Consortium and Treat OA consortium and ALS consortium and CKDGen consortium and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Systemic Sclerosis consortium and Inflammation Working Group of the CHARGE Consortium and International Parkinson’s Disease Genomics Consortium and CARDIoGRAMplusC4D Consortium and Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium
PLoS Medicine, ISSN 1549-1277, 06/2016, Volume 13, Issue 6, p. e1001976
Journal Article
by Anney, Richard J. L and Ripke, Stephan and Anttila, Verneri and Grove, Jakob and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Robinson, Elise and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A.Jeremy and Wijsman, Ellen M and Werge, Thomas and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Vanengeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Sanders, Stephan J and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne Giørtz and Pedersen, Carsten Bøcker and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Nordentoft, Merete and Murtha, Michael T and Mouga, Susana and Mortensen, Preben Bo and Mors, Ole and Morrow, Eric M and Moreno-De-Luca, Daniel and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and McGrew, Susan G and Mattheisen, Manuel and Martsenkovsky, Igor and Martin, Donna M and Mane, Shrikant M and Magnusson, Pall and Magalhaes, Tiago and Maestrini, Elena and Lowe, Jennifer K and Lord, Catherine and Levitt, Pat and Martin, Christa Lese and Ledbetter, David H and Leboyer, Marion and Lecouteur, Ann S and Ladd-Acosta, Christine and Kolevzon, Alexander and Klauck, Sabine M and Jacob, Suma and Iliadou, Bozenna and Hultman, Christina M and Hougaard, David M and Hertz-Picciotto, Irva and Hendren, Robert and Hansen, Christine Søholm and Haines, Jonathan L and Guter, Stephen J and ... and Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Molecular Autism, ISSN 2040-2392, 05/2017, Volume 8, Issue 1, pp. 21 - 17
Background: Over the past decade genome-wide association studies (GWAS) have been applied to aid in the understanding of the biology of traits. The success of... 
Gene-set analysis | Genome-wide association study | Genetic correlation | Neurodevelopment | Schizophrenia | Heritability | Autism spectrum disorder | Meta-analysis | MENTAL-RETARDATION | NEUROSCIENCES | FOXP1 | INTELLECTUAL DISABILITY | RISK LOCI | GENETICS & HEREDITY | COMMON | SCAN | COPY NUMBER VARIATION | LINKAGE | GENOME-WIDE ASSOCIATION | REVEALS | Autism Spectrum Disorder - genetics | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Chromosomes, Human, Pair 10 - chemistry | Plasma Membrane Calcium-Transporting ATPases - genetics | Membrane Proteins - genetics | Humans | Repressor Proteins - genetics | Male | Genetic Loci | Transcription Factors - genetics | Forkhead Transcription Factors - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Carrier Proteins - genetics | Schizophrenia - genetics | Schizophrenia - diagnosis | Schizophrenia - physiopathology | Female | Autism Spectrum Disorder - diagnosis | Autism Spectrum Disorder - physiopathology | Genetic aspects | Research | Genetic susceptibility | Risk factors | Pervasive developmental disorders | Autism | Genomes | Gene expression | Life Sciences | Genetics | Autism spectrum disorder, Genome-wide association study, Meta-analysis, Genetic correlation, Heritability, Gene-set analysis, Schizophrenia, Neurodevelopment | genetic | Neurologi | asperger-syndrome | resource exchange | Genetics & Heredity | Neurosciences & Neurology | pervasive developmental disorders | Neurology | copy number variation | neuronal migration | risk loci | de-novo mutations | genome-wide association | mental-retardation | intellectual disability
Journal Article
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.