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by Hou, Liping, PhD and Heilbronner, Urs, PhD and Degenhardt, Franziska, MD and Adli, Mazda, MD and Akiyama, Kazufumi, MD and Akula, Nirmala, PhD and Ardau, Raffaella, MD and Arias, Bárbara, PhD and Backlund, Lena, MD and Banzato, Claudio E M, MD and Benabarre, Antoni, MD PhD and Bengesser, Susanne, MD and Bhattacharjee, Abesh Kumar, MD and Biernacka, Joanna M, PhD and Birner, Armin, MD and Brichant-Petitjean, Clara, MD and Bui, Elise T, MA and Cervantes, Pablo, MD and Chen, Guo-Bo, PhD and Chen, Hsi-Chung, MD and Chillotti, Caterina, MD and Cichon, Sven, PhD and Clark, Scott R, MBBS and Colom, Francesc, PhD and Cousins, David A, PhD and Cruceanu, Cristiana, BSc and Czerski, Piotr M, PhD and Dantas, Clarissa R, MD and Dayer, Alexandre, MD and Étain, Bruno, MD and Falkai, Peter, MD and Forstner, Andreas J, MD and Frisén, Louise, MD and Fullerton, Janice M, PhD and Gard, Sébastien, MD and Garnham, Julie S, BN and Goes, Fernando S, MD and Grof, Paul, MD and Gruber, Oliver, MD and Hashimoto, Ryota, MD and Hauser, Joanna, MD and Herms, Stefan, PhD and Hoffmann, Per, PhD and Hofmann, Andrea, PhD and Jamain, Stephane, PhD and Jiménez, Esther, PhD and Kahn, Jean-Pierre, MD Phd and Kassem, Layla, PhD and Kittel-Schneider, Sarah, MD and Kliwicki, Sebastian, MD and König, Barbara, MSc and Kusumi, Ichiro, MD and Lackner, Nina, MSc and Laje, Gonzalo, MD and Landén, Mikael, MD and Lavebratt, Catharina, PhD and Leboyer, Marion, MD and Leckband, Susan G, BS and Jaramillo, Carlos A López, MD and MacQueen, Glenda, MD and Manchia, Mirko, MD and Martinsson, Lina, MD and Mattheisen, Manuel, PhD and McCarthy, Michael J, MD and McElroy, Susan L, MD and Mitjans, Marina, PhD and Mondimore, Francis M, MD and Monteleone, Palmiero, MD and Nievergelt, Caroline M, PhD and Nöthen, Markus M, MD and Ösby, Urban, MD and Ozaki, Norio, MD and Perlis, Roy H, MD and Pfennig, Andrea, MD and Reich-Erkelenz, Daniela, MA and Rouleau, Guy A, MD and Schofield, Peter R, PhD DSc and Schubert, K Oliver, MD and Schweizer, Barbara W, RN and Seemüller, Florian, MD and Severino, Giovanni, MD and Shekhtman, Tatyana, MSc and Shilling, Paul D, MD and Shimoda, Kazutaka, MD and Simhandl, Christian, MD and Slaney, Claire M, RN and Smoller, Jordan W, MD and Squassina, Alessio, PhD and Stamm, Thomas, MD and Stopkova, Pavla, MD and Tighe, Sarah K, MD and Tortorella, Alfonso, MD and Turecki, Gustavo, MD and Volkert, Julia, PhD and Witt, Stephanie, PhD and Wright, Adam, MCP and Young, L Trevor, MD and Zandi, Peter P, PhD and Potash, James B, MD and DePaulo, J Raymond, MD and ... and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Lancet, The, ISSN 0140-6736, 2016, Volume 387, Issue 10023, pp. 1085 - 1093
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 137, Issue 1, pp. 130 - 136
Journal Article
by Direk, Nese, MD, MSc and Williams, Stephanie, ScM and Smith, Jennifer A., PhD, MPH and Ripke, Stephan, MD, PhD and Air, Tracy, BA(Hons , M.Biostatistics and Amare, Azmeraw T., MPH, MSc and Amin, Najaf, PhD and Baune, Bernhard T., MD, PhD, MPH and Bennett, David A., MD and Blackwood, Douglas H.R., MD, PhD and Boomsma, Dorret, PhD and Breen, Gerome, PhD and Buttenschøn, Henriette N., PhD and Byrne, Enda M., PhD and Børglum, Anders D., MD, PhD and Castelao, Enrique, MSc and Cichon, Sven, PhD and Clarke, Toni-Kim, PhD and Cornelis, Marilyn C., PhD and Dannlowski, Udo, MD, PhD and De Jager, Philip L., MD, PhD and Demirkan, Ayse, PhD and Domenici, Enrico, PhD and van Duijn, Cornelia M., PhD and Dunn, Erin C., ScD, MPH and Eriksson, Johan G., MD, DMSc and Esko, Tonu, PhD and Faul, Jessica D., PhD and Ferrucci, Luigi, MD, PhD and Fornage, Myriam, PhD and Geus, Eco de, PhD and Gill, Michael, MD and Gordon, Scott D., PhD and Grabe, Hans Jörgen, MD and Grootheest, Gerard van, MSc and Hamilton, Steven P., MD, PhD and Hartman, Catharina A., PhD and Heath, Andrew C., DPhil and Hek, Karin, PhD and Hofman, Albert, MD, PhD and Homuth, Georg, PhD and Horn, Carsten, PhD and Hottenga, Jouke Jan, PhD and Kardia, Sharon L.R., PhD and Kloiber, Stefan, MD and Koenen, Karestan, PhD and Kutalik, Zoltán, PhD and Ladwig, Karl-Heinz, MD, PhD and Lahti, Jari, PhD and Levinson, Douglas F., MD and Lewis, Cathryn M., PhD and Lewis, Glyn, PhD and Li, Qingqin S., PhD and Llewellyn, David J., PhD and Lucae, Susanne, MD, PhD and Lunetta, Kathryn L., PhD and MacIntyre, Donald J., MD and Madden, Pamela, PhD and Martin, Nicholas G., PhD and McIntosh, Andrew M., MD and Metspalu, Andres, MD, PhD and Milaneschi, Yuri, PhD and Montgomery, Grant W., PhD and Mors, Ole, PhD and Mosley, Thomas H., PhD and Murabito, Joanne M., MD, ScM and Müller-Myhsok, Bertram, MD and Nöthen, Markus M., MD, PhD and Nyholt, Dale R., PhD and O’Donovan, Michael C., MD, PhD and Penninx, Brenda W., PhD and Pergadia, Michele L., PhD and Perlis, Roy, MD, MSc and Potash, James B., MD and Preisig, Martin, MD and Purcell, Shaun M., PhD and Quiroz, Jorge A., MD and Räikkönen, Katri, PhD and Rice, John P., PhD and Rietschel, Marcella, MD, PhD and Rivera, Margarita, PhD and Schulze, Thomas G., MD and Shi, Jianxin, PhD and Shyn, Stanley, MD, PhD and Sinnamon, Grant C., PhD and Smit, Johannes H., PhD and Smoller, Jordan W., MD, ScD and Snieder, Harold, PhD and Tanaka, Toshiko, PhD and Tansey, Katherine E., PhD and Teumer, Alexander, PhD and Uher, Rudolf, MD, PhD and Umbricht, Daniel, MD and der Auwera, Sandra Van, Dipl. Biomathematikerin and Ware, Erin B., PhD and Weir, David R., PhD and Weissman, Myrna M., PhD and Willemsen, Gonneke, PhD and Yang, Jingyun, PhD and Zhao, Wei, PhD and ...
Biological Psychiatry, ISSN 0006-3223, 09/2017, Volume 82, Issue 5, pp. 322 - 329
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 132, Issue 2, pp. 371 - 377
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2007, Volume 120, Issue 4, pp. 975 - 977
  Most cases of HAE are attributable to mutations in the SERPING1 gene, resulting in defective serpin C1 inhibitor (C1Inh; HAE types I and II, Mendelian... 
Allergy and Immunology | ALLERGY | IMMUNOLOGY | Factor XII - genetics | Pedigree | Humans | Female | Male | Complement C1 Inhibitor Protein - genetics | Mutation | Angioedema - genetics | Families & family life | Plasma | Females | Womens health | Angioedema | Innate immunity | Complement C1 Inhibitor Protein | Factor XII | Life Sciences | Immunology | Genetics | Human genetics
Journal Article
Journal of Pediatrics, The, ISSN 0022-3476, 2011, Volume 159, Issue 5, pp. 825 - 831.e1
Objective To identify genetic and nongenetic risk factors that contribute to the severity of the bladder exstrophy-epispadias complex (BEEC). Study design... 
Pediatrics | European Study Cohort | In vitro fertilization | Bladder exstrophy-epispadias complex | North American Study Cohort | OEIS | Ventricular septal defect | Intracytoplasmic sperm injection | VSD | CBE | EUROCAT | Omphalocele, exstrophy, imperforate anus, and spinal defects complex | Classic bladder exstrophy | ES cohort | Cleft lip with or without cleft palate | ICSI | CL-P | NAS cohort | Cloacal exstrophy | Epispadias | IVF | European Surveillance of Congenital Malformations network | BEEC | RISK | PEDIATRICS | DEFECTS | CLOACAL EXSTROPHY | POSSIBLE ASSOCIATION | BIRTHS | Folic Acid - therapeutic use | Sperm Injections, Intracytoplasmic - statistics & numerical data | Paternal Age | Humans | Middle Aged | Male | Pregnancy Trimester, First | Antacids - therapeutic use | Maternal Age | Adult | Female | Surveys and Questionnaires | Fertilization in Vitro - statistics & numerical data | Severity of Illness Index | Cleft Lip - epidemiology | Vitamin B Complex - therapeutic use | Risk Factors | Europe - epidemiology | Bladder Exstrophy - epidemiology | Pregnancy | Radiography - utilization | Phenotype | Smoking - epidemiology | Sex Distribution | Epispadias - epidemiology | Cleft Palate - epidemiology | North America - epidemiology | Prenatal Care | Oncology, Experimental | Genetic research | Birth defects | Genetic aspects | Research | Universities and colleges | Risk factors | Cancer
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2010, Volume 64, Issue 4, pp. e45 - e50
Background In 1925, Dr Marie Unna described a rare form of hereditary hypotrichosis in a German multigenerational family. This was later termed “Marie Unna... 
Dermatology | U2HR | hypotrichosis | hair loss | alopecia | loss of function mutation | Point Mutation | Pedigree | Humans | Hypotrichosis - genetics | Family Health | Hypotrichosis - congenital | Transcription Factors - genetics | Germany | Family
Journal Article
by Gharahkhani, Puya, Dr and Fitzgerald, Rebecca C, MD and Vaughan, Thomas L, MD and Palles, Claire, PhD and Gockel, Ines, Prof and Tomlinson, Ian, MD and Buas, Matthew F, PhD and May, Andrea, MD and Gerges, Christian, MD and Anders, Mario, Prof and Becker, Jessica, PhD and Kreuser, Nicole, BSc and Noder, Tania, BN and Venerito, Marino, MD and Veits, Lothar, MD and Schmidt, Thomas, MD and Manner, Hendrik, MD and Schmidt, Claudia, MD and Hess, Timo, MSc and Böhmer, Anne C, PhD and Izbicki, Jakob R, Prof and Hölscher, Arnulf H, Prof and Lang, Hauke, Prof and Lorenz, Dietmar, MD and Schumacher, Brigitte, MD and Hackelsberger, Andreas, MD and Mayershofer, Rupert, MD and Pech, Oliver, MD and Vashist, Yogesh, MD and Ott, Katja, MD and Vieth, Michael, MD and Weismüller, Josef, MD and Nöthen, Markus M, Prof and Attwood, Stephen, MD and Barr, Hugh, MD and Chegwidden, Laura, MSc and de Caestecker, John, MD and Harrison, Rebecca, MD and Love, Sharon B, MSc and MacDonald, David, DDS and Moayyedi, Paul, MD and Prenen, Hans, MD and Watson, R G Peter, MD and Iyer, Prasad G, MD and Anderson, Lesley A, PhD and Bernstein, Leslie, PhD and Chow, Wong-Ho, PhD and Hardie, Laura J, PhD and Lagergren, Jesper, Prof and Liu, Geoffrey, MD and Risch, Harvey A, MD and Wu, Anna H, PhD and Ye, Weimin, Prof and Bird, Nigel C, MD and Shaheen, Nicholas J, MD and Gammon, Marilie D, PhD and Corley, Douglas A, MD and Caldas, Carlos, PhD and Moebus, Susanne, Prof and Knapp, Michael, PhD and Peters, Wilbert H M, MD and Neuhaus, Horst, MD and Rösch, Thomas, Prof and Ell, Christian, MD and MacGregor, Stuart, PhD and Pharoah, Paul, PhD and Whiteman, David C, Prof and Jankowski, Janusz, Prof and Schumacher, Johannes, MD and Esophageal Adenocarcinoma GenEtics and Wellcome Trust Case Control Consor and Barrett's Esophageal Adenocarcinom and Wellcome Trust Case Control Consortium 2 (WTCCC2) and Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) and Esophageal Adenocarcinoma GenEtics Consortium (EAGLE)
Lancet Oncology, The, ISSN 1470-2045, 2016, Volume 17, Issue 10, pp. 1363 - 1373
Journal Article
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
Journal Article
by Sims, Rebecca and Van Der Lee, Sven J and Naj, Adam C and Bellenguez, Céline and Badarinarayan, Nandini and Jakobsdottir, Johanna and Kunkle, Brian W and Boland, Anne and Raybould, Rachel and Bis, Joshua C and Martin, Eden R and Grenier-Boley, Benjamin and Heilmann-Heimbach, Stefanie and Chouraki, Vincent and Kuzma, Amanda B and Sleegers, Kristel and Vronskaya, Maria and Ruiz, Agustin and Graham, Robert R and Olaso, Robert and Hoffmann, Per and Grove, Megan L and Vardarajan, Badri N and Hiltunen, Mikko and Nöthen, Markus M and White, Charles C and Hamilton-Nelson, Kara L and Epelbaum, Jacques and Maier, Wolfgang and Choi, Seung-Hoan and Beecham, Gary W and Dulary, Cécile and Herms, Stefan and Smith, Albert V and Funk, Cory C and Derbois, Céline and Forstner, Andreas J and Ahmad, Shahzad and Li, Hongdong and Bacq, Delphine and Harold, Denise and Satizabal, Claudia L and Valladares, Otto and Squassina, Alessio and Thomas, Rhodri and Brody, Jennifer A and Qu, Liming and Sánchez-Juan, Pascual and Morgan, Taniesha and Wolters, Frank J and Zhao, Yi and Garcia, Florentino Sanchez and Denning, Nicola and Fornage, Myriam and Malamon, John and Naranjo, Maria Candida Deniz and Majounie, Elisa and Mosley, Thomas H and Dombroski, Beth and Wallon, David and Lupton, Michelle K and Dupuis, Josée and Whitehead, Patrice and Fratiglioni, Laura and Medway, Christopher and Jian, Xueqiu and Mukherjee, Shubhabrata and Keller, Lina and Brown, Kristelle and Lin, Honghuang and Cantwell, Laura B and Panza, Francesco and McGuinness, Bernadette and Moreno-Grau, Sonia and Burgess, Jeremy D and Solfrizzi, Vincenzo and Proitsi, Petra and Adams, Hieab H and Allen, Mariet and Seripa, Davide and Pastor, Pau and Cupples, L Adrienne and Price, Nathan D and Hannequin, Didier and Frank-García, Ana and Levy, Daniel and Chakrabarty, Paramita and Caffarra, Paolo and Giegling, Ina and Beiser, Alexa S and Giedraitis, Vilmantas and Hampel, Harald and Garcia, Melissa E and Wang, Xue and Lannfelt, Lars and Mecocci, Patrizia and Eiriksdottir, Gudny and Crane, Paul K and Pasquier, Florence and Boccardi, Virginia and ... and EADI and GERAD PERADES and ARUKConsortium and CHARGE and ADGC and GERAD/PERADES, CHARGE, ADGC, EADI and ARUK Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 09/2017, Volume 49, Issue 9, pp. 1373 - 1384
We identified rare coding variant