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Journal of Statistical Software, ISSN 1548-7660, 2012, Volume 46, Issue 2, pp. 1 - 39
This paper discusses a Fortran 90 program referred to as BIEMS (Bayesian inequality and equality constrained model selection) that can be used for calculating... 
Fortran 90 | Gibbs sampler | Bayes factors | Equality and inequality constrained models | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | equality and inequality constrained models | STATISTICS & PROBABILITY | SELECTION
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S1123 - S1124
Journal Article
PLoS Computational Biology, ISSN 1553-7358, 2015, Volume 11, Issue 4, pp. e1004219 - e1004219
Journal Article
Psychological Medicine, ISSN 0033-2917, 07/2019, pp. 1 - 11
BACKGROUNDMounting evidence shows genetic overlap between multiple psychiatric disorders. However, the biological underpinnings of shared risk for psychiatric... 
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S1282 - S1283
Journal Article
PLoS Computational Biology, ISSN 1553-734X, 04/2015, Volume 11, Issue 4
  By aggregating data for complex traits in a biologically meaningful way, gene and gene-set analysis constitute a valuable addition to single-marker analysis.... 
Competition | Simulation | Genes | Statistics | Magma | Methods | Crohns disease
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S728 - S729
Genome-wide association studies (GWAS) have successfully identified many novel loci for psychiatric traits. At the same time the results of GWAS showed that... 
PHARMACOLOGY & PHARMACY | PSYCHIATRY | NEUROSCIENCES | CLINICAL NEUROLOGY | Genetic research | Genes | Analysis
Journal Article
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K. E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Levinson, Douglas F and Gejman, Pablo V and Laurent, Claudine and Mowry, Bryan J and O'Donovan, Michael C and Pulver, Ann E and Schwab, Sibylle G and Wildenauer, Dieter B and Dudbridge, Frank and Shi, Jianxin and Albus, Margot and Alexander, Madeline and Campion, Dominique and Cohen, David and Dikeos, Dimitris and Duan, Jubao and Eichhammer, Peter and Godard, Stephanie and Hansen, Mark and Lerer, F. Bernard and Liang, Kung-Yee and Maier, Wolfgang and Mallet, Jacques and Nertney, Deborah A and Nestadt, Gerald and Norton, Nadine and Papadimitriou, George N and Ribble, Robert and Sanders, Alan R and Silverman, Jeremy M and Walsh, Dermot and Williams, Nigel M and Wormley, Brandon and Arranz, Maria J and Bakker, Steven and Bender, Stephan and Bramon, Elvira and Collier, David and Crespo-Facorro, Benedicto and Hall, Jeremy and Iyegbe, Conrad and Jablensky, Assen and Kahn, Rene S and Kalaydjieva, Luba and Lawrie, Stephen and Lewis, Cathryn M and ... and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 10, pp. 1150 - 1159
Journal Article
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 11, pp. 1584 - 1592
Persistent insomnia is among the most frequent complaints in general practice. To identify genetic factors for insomnia complaints, we performed a genome-wide... 
SLEEP DISTURBANCE | HUMAN HEIGHT | POPULATION | METAANALYSIS | RESTLESS LEGS SYNDROME | MYOCARDIAL-INFARCTION | VARIANTS | GENETICS & HEREDITY | SEX-DIFFERENCES | PERSISTENT INSOMNIA | EPIDEMIOLOGY | Humans | Type D Personality | Male | Educational Status | Genetic Loci | Gene Regulatory Networks | Restless Legs Syndrome - genetics | Restless Legs Syndrome - metabolism | Adult | Female | Quality of Life - psychology | Neoplasm Proteins - genetics | Sleep Initiation and Maintenance Disorders - metabolism | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Restless Legs Syndrome - physiopathology | Gene Frequency | Chromosome Mapping | Homeodomain Proteins - genetics | Protein Interaction Mapping | Restless Legs Syndrome - psychology | Alleles | Sex Factors | Sleep Initiation and Maintenance Disorders - genetics | Sleep Initiation and Maintenance Disorders - physiopathology | Polymorphism, Single Nucleotide | Myeloid Ecotropic Viral Integration Site 1 Protein | Genome, Human | Sleep Initiation and Maintenance Disorders - psychology | Care and treatment | Genome-wide association studies | Insomnia | Development and progression | Genotype | Genetic aspects | Health aspects | Methods | Legs | Psychological factors | Genes | Association analysis | Gender differences | Genomes | Metabolism | Loci | Independent sample | Studies | Restless legs syndrome | Sleep disorders | Pleiotropy | Sexes | Genetic factors | Bioinformatics | Index Medicus
Journal Article
by Cornelius A. Rietveld and Sarah E. Medland and Jaime Derringer and Jian Yang and Tõnu Esko and Nicolas W. Martin and Harm-Jan Westra and Konstantin Shakhbazov and Abdel Abdellaoui and Arpana Agrawal and Eva Albrecht and Behrooz Z. Alizadeh and Najaf Amin and John Barnard and Sebastian E. Baumeister and Kelly S. Benke and Lawrence F. Bielak and Jeffrey A. Boatman and Patricia A. Boyle and Gail Davies and Christiaan de Leeuw and Niina Eklund and Daniel S. Evans and Rudolf Ferhmann and Krista Fischer and Christian Gieger and Håkon K. Gjessing and Sara Hägg and Jennifer R. Harris and Caroline Hayward and Christina Holzapfel and Carla A. Ibrahim-Verbaas and Erik Ingelsson and Bo Jacobsson and Peter K. Joshi and Astanand Jugessur and Marika Kaakinen and Stavroula Kanoni and Juha Karjalainen and Ivana Kolcic and Kati Kristiansson and Zoltán Kutalik and Jari Lahti and Sang H. Lee and Peng Lin and Penelope A. Lind and Yongmei Liu and Kurt Lohman and Marisa Loitfelder and George McMahon and Pedro Marques Vidal and Osorio Meirelles and Lili Milani and Ronny Myhre and Marja-Liisa Nuotio and Christopher J. Oldmeadow and Katja E. Petrovic and Wouter J. Peyrot and Ozren Polašek and Lydia Quaye and Eva Reinmaa and John P. Rice and Thais S. Rizzi and Helena Schmidt and Reinhold Schmidt and Albert V. Smith and Jennifer A. Smith and Toshiko Tanaka and Antonio Terracciano and Matthijs J. H. M. van der Loos and Veronique Vitart and Henry Völzke and Jürgen Wellmann and Lei Yu and Wei Zhao and Jüri Allik and John R. Attia and Stefania Bandinelli and François Bastardot and Jonathan Beauchamp and David A. Bennett and Klaus Berger and Laura J. Bierut and Dorret I. Boomsma and Ute Bültmann and Harry Campbell and Christopher F. Chabris and Lynn Cherkas and Mina K. Chung and Francesco Cueca and Mariza de Andrade and Philip L. De Jager and Jan-Emmanuel De Neve and Ian J. Deary and George V. Dedoussis and Panos Deloukas and Maria Dimitriou and Guðný Eiríksdóttir and Martin F. Elderson and Johan G. Eriksson and ... and LifeLines Cohort Study and The LifeLines Cohort Study and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper
Science, ISSN 0036-8075, 6/2013, Volume 340, Issue 6139, pp. 1467 - 1471
Journal Article
by Savage, Jeanne E and Jansen, Philip R and Stringer, Sven and Watanabe, Kyoko and Bryois, Julien and De Leeuw, Christiaan A and Nagel, Mats and Awasthi, Swapnil and Barr, Peter B and Coleman, Jonathan R. I and Grasby, Katrina L and Hammerschlag, Anke R and Kaminski, Jakob A and Karlsson, Robert and Krapohl, Eva and Lam, Max and Nygaard, Marianne and Reynolds, Chandra A and Trampush, Joey W and Young, Hannah and Zabaneh, Delilah and Hägg, Sara and Hansell, Narelle K and Karlsson, Ida K and Linnarsson, Sten and Montgomery, Grant W and Muñoz-Manchado, Ana B and Quinlan, Erin B and Schumann, Gunter and Skene, Nathan G and Webb, Bradley T and White, Tonya and Arking, Dan E and Avramopoulos, Dimitrios and Bilder, Robert M and Bitsios, Panos and Burdick, Katherine E and Cannon, Tyrone D and Chiba-Falek, Ornit and Christoforou, Andrea and Cirulli, Elizabeth T and Congdon, Eliza and Corvin, Aiden and Davies, Gail and Deary, Ian J and Derosse, Pamela and Dickinson, Dwight and Djurovic, Srdjan and Donohoe, Gary and Conley, Emily Drabant and Eriksson, Johan G and Espeseth, Thomas and Freimer, Nelson A and Giakoumaki, Stella and Giegling, Ina and Gill, Michael and Glahn, David C and Hariri, Ahmad R and Hatzimanolis, Alex and Keller, Matthew C and Knowles, Emma and Koltai, Deborah and Konte, Bettina and Lahti, Jari and Le Hellard, Stephanie and Lencz, Todd and Liewald, David C and London, Edythe and Lundervold, Astri J and Malhotra, Anil K and Melle, Ingrid and Morris, Derek and Need, Anna C and Ollier, William and Palotie, Aarno and Payton, Antony and Pendleton, Neil and Poldrack, Russell A and Räikkönen, Katri and Reinvang, Ivar and Roussos, Panos and Rujescu, Dan and Sabb, Fred W and Scult, Matthew A and Smeland, Olav B and Smyrnis, Nikolaos and Starr, John M and Steen, Vidar M and Stefanis, Nikos C and Straub, Richard E and Sundet, Kjetil and Tiemeier, Henning and Voineskos, Aristotle N and Weinberger, Daniel R and Widen, Elisabeth and Yu, Jin and Abecasis, Goncalo and Andreassen, Ole A and Breen, Gerome and Christiansen, Lene and ...
Nature Genetics, ISSN 1061-4036, 07/2018, Volume 50, Issue 7, pp. 912 - 919
Intelligence is highly heritable(1) and a major determinant of human health and well-being(2). Recent genome-wide meta-analyses have identified 24 genomic loci... 
GENERAL COGNITIVE FUNCTION | CONSORTIUM | TEST BATTERIES | GWAS | ANNOTATION | GENETICS & HEREDITY | RISK | LOCI | EDUCATIONAL-ATTAINMENT | TRAITS | HERITABILITY | Genetic Predisposition to Disease | Humans | Middle Aged | Adolescent | Female | Male | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Intelligence - genetics | Quantitative Trait Loci | Brain - physiology | Brain | Chromatin | Neurosciences | Intelligence | Synaptogenesis | Mental disorders | Genomics | Genes | Cognitive ability | Schizophrenia | Association analysis | Nervous system | Identification | Mapping | Genomes | Genetic effects | Annotations | Coding | Genetic analysis | Neostriatum | Alzheimer's disease | Bioinformatics | Neurodegenerative diseases | Neurons | Attention deficit hyperactivity disorder | Causation | Gene expression | Spiny neurons | Loci | Educational attainment | Meta-analysis | Quantitative trait loci | Neurological diseases | Studies | Pyramidal cells | Gene loci | Gene mapping | Alzheimers disease | Hippocampus | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap | Alzheimer disease | Article | nervous system development | genetic association | gene location | schizophrenia | Klinisk medicin | pleiotropy | gene mapping | genetic correlation | priority journal | human | Neurologi | corpus striatum | hippocampus | synapse | chromatin | heredity | genetic variability | intelligence | pyramidal nerve cell | gene locus | Mendelian randomization analysis | Clinical Medicine | Neurology | expression quantitative trait locus | medium spiny neuron | genome-wide association study | attention deficit disorder | exon | conserved sequence | gene expression
Journal Article