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index medicus (21) 21
humans (17) 17
schizophrenia (17) 17
anorexia nervosa (13) 13
genomes (13) 13
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genes (11) 11
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eating disorders (9) 9
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anorexia (7) 7
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quantitative trait loci (7) 7
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article (6) 6
gene mapping (6) 6
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genetic variation (5) 5
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polygenic risk (5) 5
polymorphism, single nucleotide (5) 5
population (5) 5
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anorèxia nerviosa (2) 2
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1. Full Text Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
by Barbeira, Alvaro N and Dickinson, Scott P and Bonazzola, Rodrigo and Zheng, Jiamao and Wheeler, Heather E and Torres, Jason M and Torstenson, Eric S and Shah, Kaanan P and Garcia, Tzintzuni and Edwards, Todd L and Stahl, Eli A and Huckins, Laura M and Aguet, François and Ardlie, Kristin G and Cummings, Beryl B and Gelfand, Ellen T and Getz, Gad and Hadley, Kane and Handsaker, Robert E and Huang, Katherine H and Kashin, Seva and Karczewski, Konrad J and Lek, Monkol and Li, Xiao and MacArthur, Daniel G and Nedzel, Jared L and Nguyen, Duyen T and Noble, Michael S and Segrè, Ayellet V and Trowbridge, Casandra A and Tukiainen, Taru and Abell, Nathan S and Balliu, Brunilda and Barshir, Ruth and Basha, Omer and Battle, Alexis and Bogu, Gireesh K and Brown, Andrew and Brown, Christopher D and Castel, Stephane E and Chen, Lin S and Chiang, Colby and Conrad, Donald F and Damani, Farhan N and Davis, Joe R and Delaneau, Olivier and Dermitzakis, Emmanouil T and Engelhardt, Barbara E and Eskin, Eleazar and Ferreira, Pedro G and Frésard, Laure and Gamazon, Eric R and Garrido-Martín, Diego and Gewirtz, Ariel D. H and Gliner, Genna and Gloudemans, Michael J and Guigo, Roderic and Hall, Ira M and Han, Buhm and He, Yuan and Hormozdiari, Farhad and Howald, Cedric and Jo, Brian and Kang, Eun Yong and Kim, Yungil and Kim-Hellmuth, Sarah and Lappalainen, Tuuli and Li, Gen and Li, Xin and Liu, Boxiang and Mangul, Serghei and McCarthy, Mark I and McDowell, Ian C and Mohammadi, Pejman and Monlong, Jean and Montgomery, Stephen B and Muñoz-Aguirre, Manuel and Ndungu, Anne W and Nobel, Andrew B and Oliva, Meritxell and Ongen, Halit and Palowitch, John J and Panousis, Nikolaos and Papasaikas, Panagiotis and Park, YoSon and Parsana, Princy and Payne, Anthony J and Peterson, Christine B and Quan, Jie and Reverter, Ferran and Sabatti, Chiara and Saha, Ashis and Sammeth, Michael and Scott, Alexandra J and Shabalin, Andrey A and Sodaei, Reza and Stephens, Matthew and Stranger, Barbara E and Strober, Benjamin J and Sul, Jae Hoon and ... and GTEx Consortium
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1825 - 20
Scalable, integrative methods to understand mechanisms that link genetic variants with phenotypes are needed. Here we derive a mathematical expression to... 
RISK LOCI | TRANSCRIPTOME | VARIANTS | GENOTYPE IMPUTATION | MULTIDISCIPLINARY SCIENCES | COMMON DISEASES | DISEASE ASSOCIATIONS | IDENTIFICATION | COMPLEX TRAITS | DATASETS | GENOME-WIDE ASSOCIATION | Genetic Variation | Gene Expression | Meta-Analysis as Topic | Phenotype | Chromosome Mapping - methods | Computer Simulation | Humans | Models, Genetic | Polymorphism, Single Nucleotide | Genome-Wide Association Study - statistics & numerical data | Organ Specificity | Quantitative Trait Loci | Genetic variance | Statistical analysis | Robustness (mathematics) | Etiology | Genes | Phenotypic variations | Regulatory mechanisms (biology) | Statistical methods | Gene expression | Tissues | Gene mapping | Genome-wide association studies | Data integration
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2. Full Text Analysis of shared heritability in common disorders of the brain
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
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3. Full Text F112IDENTIFICATION AND CHARACTERIZATION OF SHARED AND DISTINCT ASSOCIATIONS UNDERLYING SCHIZOPHRENIA AND BIPOLAR DISORDER USING TRANSCRIPTOMIC IMPUTATION APPROACHES
by Huckins, Laura
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S1170 - S1171
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4. Full Text Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa
by Duncan, Laramie and Yilmaz, Zeynep and Gaspar, Helena and Walters, Raymond and Goldstein, Jackie and Anttila, Verneri and Bulik-Sullivan, Brendan and Ripke, Stephan and Thornton, Laura and Hinney, Anke and Daly, Mark and Sullivan, Patrick F and Zeggini, Eleftheria and Breen, Gerome and Bulik, Cynthia M and Gaspar, Héléna and Adan, Roger and Alfredsson, Lars and Ando, Tetsuya and Andreassen, Ole and Aschauer, Harald and Baker, Jessica and Barrett, Jeffrey and Bencko, Vladimir and Bergen, Andrew and Berrettini, Wade and Birgegård, Andreas and Boni, Claudette and Perica, Vesna Boraska and Brandt, Harry and Burghardt, Roland and Carlberg, Laura and Cassina, Matteo and Cesta, Carolyn and Cichon, Sven and Clementi, Maurizio and Cohen-Woods, Sarah and Coleman, Joni and Cone, Roger and Courtet, Philippe and Crawford, Steven and Crow, Scott and Crowley, Jim and Danner, Unna and Davis, Oliver and de Zwaan, Martina and Dedoussis, George and Degortes, Daniela and DeSocio, Janiece and Dick, Danielle and Dikeos, Dimitris and Dina, Christian and Ding, Bo and Dmitrzak-Weglarz, Monika and Docampo, Elisa and Egberts, Karin and Ehrlich, Stefan and Escaramís, Geòrgia and Esko, Tõnu and Espeseth, Thomas and Estivill, Xavier and Favaro, Angela and Fernández-Aranda, Fernando and Fichter, Manfred and Finan, Chris and Fischer, Krista and Floyd, James and Föcker, Manuel and Foretova, Lenka and Forzan, Monica and Fox, Caroline and Franklin, Christopher and Gaborieau, Valerie and Gallinger, Steven and Gambaro, Giovanni and Giegling, Ina and Gonidakis, Fragiskos and Gorwood, Philip and Gratacos, Monica and Guillaume, Sébastien and Guo, Yiran and Hakonarson, Hakon and Halmi, Katherine and Harrison, Rebecca and Hatzikotoulas, Konstantinos and Hauser, Joanna and Hebebrand, Johannes and Helder, Sietske and Hendriks, Judith and Herms, Stefan and Herpertz-Dahlmann, Beate and Herzog, Wolfgang and Hilliard, Christopher and Huckins, Laura and Hudson, James and Huemer, Julia and Imgart, Hartmut and Inoko, Hidetoshi and Jall, Sigrid and Jamain, Stephane and ... and Eatint Disorders Working Grp and Eating Disorders Working Group of the Psychiatric Genomics Consortium and Institute of Neuroscience and Physiology and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institutionen för neurovetenskap och fysiologi
American Journal of Psychiatry, ISSN 0002-953X, 09/2017, Volume 174, Issue 9, pp. 850 - 858
Objective:The authors conducted a genome-wide association study of anorexia nervosa and calculated genetic correlations with a series of psychiatric,... 
PSYCHIATRIC-DISORDERS | RISK | METAANALYSIS | PSYCHIATRY | Anorexia Nervosa - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Phenotype | Humans | Linkage Disequilibrium - genetics | Polymorphism, Single Nucleotide - genetics | Case-Control Studies | Genotype | Development and progression | Genetic aspects | Anorexia nervosa | Metabolism | Health aspects | Anorèxia nerviosa | Genetics | Genètica | Metabolisme | Life Sciences | Clinical Medicine | Psykiatri | Klinisk medicin | Psychiatry
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5. Full Text A genome-wide association study of anorexia nervosa
by Boraska, V and Franklin, C S and Floyd, J A B and Thornton, L M and Huckins, L M and Southam, L and Rayner, N W and Tachmazidou, I and Klump, K L and Treasure, J and Lewis, C M and Schmidt, U and Tozzi, F and Kiezebrink, K and Hebebrand, J and Gorwood, P and Adan, R A H and Kas, M J H and Favaro, A and Santonastaso, P and Fernández-Aranda, F and Gratacos, M and Rybakowski, F and Dmitrzak-Weglarz, M and Kaprio, J and Keski-Rahkonen, A and Raevuori, A and Van Furth, E F and Slof-Op 't Landt, M C T and Hudson, J I and Reichborn-Kjennerud, T and Knudsen, G P S and Monteleone, P and Kaplan, A S and Karwautz, A and Hakonarson, H and Berrettini, W H and Guo, Y|info:eu-repo/dai/nl/369207084 and Li, D and Schork, N J and Komaki, G and Ando, T and Inoko, H and Esko, T and Fischer, K and Männik, K and Metspalu, A and Baker, J H and Cone, R D and Dackor, J and DeSocio, J E and Hilliard, C E and O'Toole, J K and Pantel, J and Szatkiewicz, J P and Taico, C and Zerwas, S and Trace, S E and Davis, O S P and Helder, S and Bühren, K and Burghardt, R and de Zwaan, M and Egberts, K and Ehrlich, S and Herpertz-Dahlmann, B and Herzog, W and Imgart, H and Scherag, A and Scherag, S and Zipfel, S and Boni, C and Ramoz, N and Versini, A and Brandys, M K and Danner, U N and de Kovel, C and Heniks, J and Koeleman, B P C and Ophoff, R A and Strengman, E and van Elburg, Annemarie|info:eu-repo/dai/nl/191430129 and Bruson, A and Clementi, M and Degortes, D and Forzan, M and Tenconi, E and Docampo, E and Escaramís, G and Jiménez-Murcia, S and Lissowska, J and Rajewski, A and Szeszenia-Dabrowska, N and Slopien, A and Hauser, J and Karhunen, L and Meulenbelt, I and Slagboom, P E and Tortorella, A and Maj, M and ... and Wellcome Trust Case Control Conso and Wellcome Trust Case Control Consortium 3 and The Wellcome Trust Case Control Consortium 322
Molecular Psychiatry, ISSN 1359-4184, 2014, Volume 19, Issue 10, pp. 1085 - 1094
Anorexia nervosa (AN) is a complex and heritable eating disorder characterized by dangerously low body weight. Neither candidate gene studies nor an initial... 
Body mass index | Metabolic | GWAS | Anorexia nervosa | Genome-wide association study | Eating disorders | MEDICAL COMPLICATIONS | POPULATION-BASED TWIN | RISK-FACTORS | PSYCHIATRY | body mass index | BIOCHEMISTRY & MOLECULAR BIOLOGY | BULIMIA-NERVOSA | eating disorders | EATING-DISORDERS | anorexia nervosa | NEUROSCIENCES | genome-wide association study | BODY-MASS INDEX | LINKAGE ANALYSIS | ANXIETY DISORDERS | OF-THE-LITERATURE | CONTROLLED FAMILY | metabolic | Anorexia Nervosa - genetics | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Guanine Nucleotide Exchange Factors - genetics | Meta-Analysis as Topic | Humans | Japan | Asian Continental Ancestry Group - genetics | Male | Case-Control Studies | Cullin Proteins - genetics | Carrier Proteins - genetics | Calcineurin - genetics | Female | Polymorphism, Single Nucleotide | Nuclear Proteins - genetics | Psychological aspects | Genetic aspects | Research | Epidemiology | Patient outcomes
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6. Full Text A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
by Li, Xiang-Dong and Chang, Xiao and Connolly, John J and Tian, Lifeng and Liu, Yichuan and Bhoj, Elizabeth J and Robinson, Nora and Abrams, Debra and Li, Yun R and Bradfield, Jonathan P and Kim, Cecilia E and Li, Jin and Wang, Fengxiang and Snyder, James and Lemma, Maria and Hou, Cuiping and Wei, Zhi and Guo, Yiran and Qiu, Haijun and Mentch, Frank D and Thomas, Kelly A and Chiavacci, Rosetta M and Cone, Roger and Li, Bingshan and Sleiman, Patrick M. A and Hakonarson, Hakon and Kas, Martien J.H and Psychiat Genomics Consortium and Price Fdn Collaborative Grp and Eating Disorders Working Group of the Psychiatric Genomics Consortium and Price Foundation Collaborative Group
Scientific Reports, ISSN 2045-2322, 06/2017, Volume 7, Issue 1, pp. 3847 - 8
We conducted a genome-wide association study (GWAS) of anorexia nervosa (AN) using a stringently defined phenotype. Analysis of phenotypic variability led to... 
PRESSURE | VARIANTS | GENETICS | MULTIDISCIPLINARY SCIENCES | EBF1 | EATING-DISORDERS | PARAMETERS | B-CELL-FACTOR | OBSESSIVE-COMPULSIVE DISORDER | CHILDREN | Early B-cell factor | Anorexia | Typing | Lymphocytes B | Leptin | Eating disorders | Genomes | Single-nucleotide polymorphism | Anorexia nervosa | Anorèxia nerviosa | Genomics | Genòmica
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7. Full Text Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches
by Yao, Shuyang and Kuja-Halkola, Ralf and Martin, Nicholas and Martin, Joanna and Lu, Yi and Lichtenstein, Paul and Norring, Claes and Birgegård, Andreas and Yilmaz, Zeynep and Hübel, Christopher and Watson, Hunna and Baker, Jessica and Almqvist, Catarina and Adan, Roger and Ando, Tetsuya and Bergen, Andrew and Berrettini, Wade and Boni, Claudette and Boraska Perica, Vesna and Brandt, Harry and Burghardt, Roland and Cassina, Matteo and Cesta, Carolyn and Clementi, Maurizio and Coleman, Joni and Cone, Roger and Courtet, Philippe and Crawford, Steven and Crow, Scott and Crowley, James and Danner, Unna and Davis, Oliver and de Zwaan, Martina and Dedoussis, George and Degortes, Daniela and DeSocio, Janiece and Dick, Danielle and Dikeos, Dimitris and Dmitrzak-Weglarz, Monika and Docampo, Elisa and Egberts, Karin and Ehrlich, Stefan and Escaramís, Geòrgia and Esko, Tõnu and Estivill, Xavier and Favaro, Angela and Fernández-Aranda, Fernando and Fichter, Manfred and Finan, Chris and Fischer, Krista and Föcker, Manuel and Foretova, Lenka and Forzan, Monica and Franklin, Christopher and Gaspar, Héléna and Gonidakis, Fragiskos and Gorwood, Philip and Gratacos, Monica and Guillaume, Sébastien and Guo, Yiran and Hakonarson, Hakon and Halmi, Katherine and Hatzikotoulas, Konstantinos and Hauser, Joanna and Hebebrand, Johannes and Helder, Sietske and Hendriks, Judith and Herpertz-Dahlmann, Beate and Herzog, Wolfgang and Hilliard, Christopher and Hinney, Anke and Huckins, Laura and Hudson, James and Huemer, Julia and Imgart, Hartmut and Inoko, Hidetoshi and Jiménez-Murcia, Susana and Johnson, Craig and Jordan, Jenny and Juréus, Anders and Kalsi, Gursharan and Kaminska, Debora and Kaplan, Allan and Kaprio, Jaakko and Karhunen, Leila and Karwautz, Andreas and Kas, Martien and Kaye, Walter and Kennedy, Martin and Kennedy, James and Keski-Rahkonen, Anna and Kiezebrink, Kirsty and Kim, Youl-Ri and Klump, Kelly and Knudsen, Gun Peggy and Koeleman, Bobby and Koubek, Doris and La Via, Maria and Landén, Mikael and Levitan, Robert and ... and Eating Disorders Working Group of the Psychiatric Genomics Consortium and Psychiat Genomics Consortium
Biological Psychiatry, ISSN 0006-3223, 10/2019, Volume 86, Issue 8, pp. 577 - 586
Although attention-deficit/hyperactivity disorder (ADHD) and eating disorders (EDs) frequently co-occur, little is known about the shared etiology. In this... 
Polygenic risk score | ADHD | Anorexia nervosa | Genetic epidemiology | Bulimia nervosa | Eating disorders | MORTALITY | ADULTS | LIABILITY | SYMPTOMS | OVERWEIGHT/OBESITY | CHILDHOOD | NEUROSCIENCES | COMORBIDITY | ANOREXIA-NERVOSA | LISDEXAMFETAMINE
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