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index medicus (24) 24
humans (22) 22
genetics & heredity (17) 17
spondylitis, ankylosing - genetics (12) 12
case-control studies (11) 11
genetic aspects (11) 11
genome-wide association (11) 11
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female (10) 10
genetics (10) 10
polymorphism, single nucleotide (10) 10
body mass index (9) 9
genome-wide association study (9) 9
male (9) 9
ankylosing spondylitis (8) 8
article (8) 8
genomes (8) 8
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rheumatology (8) 8
stability constants (8) 8
chemistry, analytical (7) 7
creatinine (7) 7
gene frequency (7) 7
genetic predisposition to disease (7) 7
obesity (7) 7
phenotype (7) 7
risk factors (7) 7
studies (7) 7
body height - genetics (6) 6
gene expression (6) 6
variants (6) 6
association (5) 5
genotype (5) 5
immunology (5) 5
l-asparagine (5) 5
ligand (5) 5
polymorphism (5) 5
risk (5) 5
susceptibility loci (5) 5
adult (4) 4
bioinformatics (4) 4
cohort studies (4) 4
crystal (4) 4
epidemiology (4) 4
genetic association (4) 4
genome, human - genetics (4) 4
health aspects (4) 4
identification (4) 4
l-glutamic acid (4) 4
linkage disequilibrium (4) 4
medical and health sciences (4) 4
medical research (4) 4
medicin och hälsovetenskap (4) 4
metabolism (4) 4
mixed complex (4) 4
molecular-structure (4) 4
multidisciplinary sciences (4) 4
polymorphism, single nucleotide - genetics (4) 4
single nucleotide polymorphisms (4) 4
adiponectin (3) 3
adipose-tissue (3) 3
alleles (3) 3
aminopeptidases - genetics (3) 3
animals (3) 3
arthritis (3) 3
biochemistry & molecular biology (3) 3
biomedical research (3) 3
body mass (3) 3
body size (3) 3
cardiovascular disease (3) 3
complex (3) 3
consortia (3) 3
deoxyribonucleic acid--dna (3) 3
energy intake (3) 3
expression (3) 3
gene frequency - genetics (3) 3
genes (3) 3
genetic variation (3) 3
genomics (3) 3
inflammation (3) 3
insulin-resistance (3) 3
metaanalysis (3) 3
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phenotypes (3) 3
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population (3) 3
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proteins (3) 3
psoriasis (3) 3
receptor (3) 3
spondyloarthropathy (3) 3
stability constant (3) 3
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abridged index medicus (2) 2
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Nature Communications, ISSN 2041-1723, 08/2015, Volume 6, Issue 1, p. 7502
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2010, Volume 42, Issue 2, pp. 123 - 127
Journal Article
by Marouli, Eirini and Graff, Mariaelisa and Medina-Gomez, Carolina and Lo, Ken Sin and Wood, Anew R and Kjaer, Troels R and Fine, Rebecca S and Lu, Yingchang and Schurmann, Claudia and Highland, Heather M and Rüeger, Sina and Thorleifsson, Gudmar and Justice, Anne E and Lamparter, David and Stirrups, Kathleen E and Turcot, Valérie and Young, Kristin L and Winkler, Thomas W and Esko, Tõnu and Karaderi, Tugce and Locke, Adam E and Masca, Nicholas G. D and Ng, Maggie C. Y and Mudgal, Poorva and Rivas, Manuel A and Vedantam, Sailaja and Mahajan, Anubha and Guo, Xiuqing and Abecasis, Goncalo and Aben, Katja K and Adair, Linda S and Alam, Dewan S and Albrecht, Eva and Allin, Kristine H and Allison, Matthew and Amouyel, Philippe and Appel, Emil V and Arveiler, Dominique and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Banas, Bernhard and Bang, Lia E and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bonnycastle, Lori L and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Burt, Amber A and Butterworth, Adam S and Carey, David J and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Auey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Galbany, Jordi Corominas and Cox, Amanda J and Cuellar-Partida, Gabriel and Danesh, John and Davies, Gail and de Bakker, Paul I. W and de Borst, Gert J and de Denus, Simon and de Groot, Mark C. H and de Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and den Hollander, Anneke I and Dennis, Joe G and Di Angelantonio, Emanuele and nos, Fotios and Du, Mengmeng and Dunning, Alison M and Easton, Douglas F and Ebeling, Tapani and Edwards, Todd L and Ellinor, Patrick T and Elliott, Paul and Evangelou, Evangelos and Farmaki, Aliki-Eleni and Faul, Jessica D and ... and EPIC-CVD Consortium and GoT2D Genes Consortium and MAGIC Investigators and Global Lipids Genetics Consortium and EPIC-InterAct Consortium and ReproGen Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and The EPIC-InterAct Consortium and CHD Exome+ Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature, ISSN 0028-0836, 2017, Volume 542, Issue 7640, pp. 186 - 190
Journal Article
by Turcot, Valérie and Lu, Yingchang and Highland, Heather M and Schurmann, Claudia and Justice, Anne E and Fine, Rebecca S and Bradfield, Jonathan P and Esko, Tõnu and Giri, Ayush and Graff, Mariaelisa and Guo, Xiuqing and Hendricks, Audrey E and Karaderi, Tugce and Lempradl, Adelheid and Locke, Adam E and Mahajan, Anubha and Marouli, Eirini and Sivapalaratnam, Suthesh and Young, Kristin L and Alfred, Tamuno and Feitosa, Mary F and Masca, Nicholas G. D and Manning, Alisa K and Medina-Gomez, Carolina and Mudgal, Poorva and Ng, Maggie C. Y and Reiner, Alex P and Vedantam, Sailaja and Willems, Sara M and Winkler, Thomas W and Abecasis, Gonçalo and Aben, Katja K and Alam, Dewan S and Alharthi, Sameer E and Allison, Matthew and Amouyel, Philippe and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Bang, Lia E and Barroso, Inês and Bastarache, Lisa and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boehnke, Michael and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Brumat, Marco and Burt, Amber A and Butterworth, Adam S and Campbell, Peter T and Cappellani, Stefania and Carey, David J and Catamo, Eulalia and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der I and Chowdhury, Rajiv and Christensen, Cramer and Chu, Audrey Y and Cocca, Massimiliano and Cook, James P and Corley, Janie and Corominas Galbany, Jordi and Cox, Amanda J and Crosslin, David S and Cuellar-Partida, Gabriel and D'Eustacchio, Angela and Danesh, John and Davies, Gail and Bakker, Paul I. W and Groot, Mark C. H and Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and Heijer, Martin and Hollander, Anneke I and Ruijter, Hester M and Dennis, Joe G and Denny, Josh C and Angelantonio, Emanuele and Drenos, Fotios and Du, Mengmeng and Dubé, Marie-Pierre and Dunning, Alison M and Easton, Douglas F and Edwards, Todd L and ... and Chd Exome Consortium and EPIC InterAct Consortium and Global Lipids Genetic Consortium and GoT2D Genes Consortium and MAGIC Investigators and Understanding Soc Sci Grp and ReproGen Consortium and Interval Study and Epic-Cvd Consortium and ExomeBP Consortium and T2D-Genes Consortium and INTERVAL Study and EPIC-CVD Consortium and EPIC InterAct Consortium and CHD Exome+ Consortium and Understanding Society Scientific Group and The MAGIC Investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature Genetics, ISSN 1061-4036, 01/2018, Volume 50, Issue 1, pp. 26 - 35
Journal Article
by Cortes, Adrian and Hadler, Johanna and Pointon, Jenny P and Robinson, Philip C and Karaderi, Tugce and Leo, Paul and Cremin, Katie and Pryce, Karena and Harris, Jessica and Lee, Seunghun and Joo, Kyung Bin and Shim, Seung-Cheol and Weisman, Michael and Ward, Michael and Zhou, Xiaodong and Garchon, Henri-Jean and Chiocchia, Gilles and Nossent, Johannes and Lie, Benedicte A and Førre, Øystein and Tuomilehto, Jaakko and Laiho, Kari and Jiang, Lei and Liu, Yu and Wu, Xin and Bradbury, Linda A and Elewaut, Dirk and Burgos-Vargas, Ruben and Stebbings, Simon and Appleton, Louise and Farrah, Claire and Lau, Jonathan and Kenna, Tony J and Haroon, Nigil and Ferreira, Manuel A and Yang, Jian and Mulero, Juan and Fernandez-Sueiro, Jose Luis and Gonzalez-Gay, Miguel A and Lopez-Larrea, Carlos and Deloukas, Panos and Donnelly, Peter and Bowness, Paul and Gafney, Karl and Gaston, Hill and Gladman, Dafna D and Rahman, Proton and Maksymowych, Walter P and Xu, Huji and Crusius, J Bart A and Van Der Horst-Bruinsma, Irene E and Chou, Chung-Tei and Valle-Oñate, Raphael and Romero-Sánchez, Consuelo and Hansen, Inger Myrnes and Pimentel-Santos, Fernando M and Inman, Robert D and Videm, Vibeke and Martin, Javier and Breban, Maxime and Reveille, John D and Evans, David M and Kim, Tae-Hwan and Wordsworth, Bryan Paul and Brown, Matthew A and Australo-Anglo-Amer and GFEGS and Spondyloarthrit Res Consortium and Int Genetics Ankylosing and WTCCC2 and Nord-Trondelag Hlth Study HUNT and Groupe Française d'Etude Génétique des Spondylarthrites (GFEGS) and Nord-Trøndelag Health Study (HUNT) and Spondyloarthritis Research Consortium of Canada (SPARCC) and Australo-Anglo-American Spondyloarthritis Consortium (TASC) and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International Genetics of Ankylosing Spondylitis Consortium (IGAS)
Nature Genetics, ISSN 1061-4036, 07/2013, Volume 45, Issue 7, pp. 730 - 738
Journal Article
by Joshi, Peter and Esko, Tõnu and Mattsson, Hannele and Eklund, Niina and Gandin, Ilaria and Nutile, T and Jackson, Anne and Schurmann, Claudia and Smith, G.D and Zhang, Weihua and Okada, Yukinori and Stancáková, Alena and Faul, Jessica D and Zhao, Wei and Bartz, Traci M and Concas, M.P and Franceschini, Nora and Enroth, Stefan and Vitart, Veronique and Trompet, Stella and Guo, Xiuqing and Chasman, Daniel and O'Connel, Jeffrey R and Corre, Tanguy and Nongmaithem, Suraj S and Chen, Yuning and Mangino, Massimo and Ruggiero, D and Traglia, Michela and Farmaki, Aliki-Eleni and Kacprowski, Tim and Bjonnes, Anew and Spek, Ashley and Wu, Ying and Giri, Anil K and Yanek, Lisa and Wang, Lihua and Hofer, Edith and Rietveld, Niels and McLeod, Olga and Cornelis, Marilyn and Pattaro, Cristian and Verweij, Niek and Baumbach, Clemens and Abdellaoui, Abdel and Warren, Helen and Vuckovic, gana and Mei, Hao and Bouchard, Claude and Perry, John and Cappellani, Stefania and Mirza, Saira and Benton, Miles C and Broeckel, Ulrich and Medland, Sarah Elizabeth and Lind, Penelope and Malerba, Giovanni and ng, Alexander and Yengo, Loic and Bielak, Lawrence F and Zhi, Degui and Most, Peter and Shriner, Daniel and Mägi, Reedik and Hemani, G and Karaderi, Tugce and Wang, Zhaoming and Liu, Tian and Demuth, Ilja and Zhao, Jing Hua and Meng, Weihua and Lataniotis, Lazaros and Van Der Laan, Sander W and Bradfield, Jonathan and Wood, Anew and Bonnefond, Amélie and Ahluwalia, Tarunveer Singh and Hall, Leanne M and Salvi, Erika and Yazar, Seyhan and Carstensen, Lisbeth and De Haan, Hugoline G and Abney, Mark and Afzal, Uzma and Allison, Matthew and Amin, Najaf and Asselbergs, Folkert W and Bakker, Stephan and Barr, Graham and Baumeister, Sebastian and Benjamin, Daniel J and Bergmann, Sven and Boerwinkle, Eric and Bottinger, Erwin P and Campbell, Archie and Chakravarti, Aravinda and Chan, Yingleong and Chanock, Stephen and Chen, Constance and Chen, Y.-D. Ida and ... and BioBank Japan Project and The BioBank Japan Project and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinsk genetik och genomik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi
Nature: international weekly journal of science, ISSN 0028-0836, 07/2015, Volume 523, Issue 7561, pp. 459 - 462
textabstractHomozygosity has long been associated with rare, often devastating, Mendelian disorders, and Darwin was one of the first to recognize that... 
INTELLIGENCE | HOMOZYGOSITY | MULTIDISCIPLINARY SCIENCES | ARCHITECTURE | GENETIC-VARIANTS | TRAITS | ASSOCIATION | BLOOD-PRESSURE | Studies | Cognition & reasoning | Disease | Genomics | Cognitive ability | Genomes | Educational attainment | Medical and Health Sciences | Medicin och hälsovetenskap
Journal Article
by Evans, David M and Spencer, Chris C. A and Pointon, Jennifer J and Su, Zhan and Harvey, David and Kochan, Grazyna and Opperman, Udo and Dilthey, Alexander and Pirinen, Matti and Stone, Millicent A and Appleton, Louise and Moutsianis, Loukas and Leslie, Stephen and Wordsworth, Tom and Kenna, Tony J and Karaderi, Tugce and Thomas, Gethin P and Ward, Michael M and Weisman, Michael H and Farrar, Claire and Bradbury, Linda A and Danoy, Patrick and Inman, Robert D and Maksymowych, Walter and Gladman, Dafna and Rahman, Proton and Morgan, Ann and Marzo-Ortega, Helena and Bowness, Paul and Gaffney, Karl and Gaston, J. S. Hill and Smith, Malcolm and Bruges-Armas, Jacome and Couto, Ana-Rita and Sorrentino, Rosa and Paladini, Fabiana and Ferreira, Manuel A and Xu, Huji and Liu, Yu and Jiang, Lei and Lopez-Larrea, Carlos and Díaz-Peña, Roberto and Lóepez-Vázquez, Antonio and Zayats, Tetyana and Band, Gavin and Bellenguez, Céline and Blackburn, Hannah and Blackwell, Jenefer M and Bramon, Elvira and Bumpstead, Suzannah J and Casas, Juan P and Corvin, Aiden and Craddock, Nicholas and Deloukas, Panos and Dronov, Serge and Duncanson, Audrey and Edkins, Sarah and Freeman, Colin and Gillman, Matthew and Gray, Emma and Gwilliam, Rhian and Hammond, Naomi and Hunt, Sarah E and Jankowski, Janusz and Jayakumar, Alagurevathi and Langford, Cordelia and Liddle, Jennifer and Markus, Hugh S and Mathew, Christopher G and McCann, Owen T and McCarthy, Mark I and Palmer, Colin N. A and Peltonen, Leena and Plomin, Robert and Potter, Simon C and Rautanen, Anna and Ravindrarajah, Radhi and Ricketts, Michelle and Samani, Nilesh and Sawcer, Stephen J and Strange, Amy and Trembath, Richard C and Viswanathan, Ananth C and Waller, Matthew and Weston, Paul and Whittaker, Pamela and Widaa, Sara and Wood, Nicholas W and McVean, Gilean and Reveille, John D and Wordsworth, B. Paul and Brown, Matthew A and Donnelly, Peter and Australo-Anglo-Amer Spondyloarthri and Wellcome Trust Case Control Consor and Spondyloarthrit Res Consortium Can and Wellcome Trust Case Control Consortium 2 (WTCCC2) and Spondyloarthritis Research Consortium of Canada (SPARCC) and Australo-Anglo-American Spondyloarthritis Consortium (TASC) and The Australo-Anglo-American Spondyloarthritis Consortium (TASC) and the Wellcome Trust Case Control Consortium 2 (WTCCC2)
Nature Genetics, ISSN 1061-4036, 08/2011, Volume 43, Issue 8, pp. 761 - 767
Ankylosing spondylitis is a common form of inflammatory arthritis predominantly affecting the spine and pelvis that occurs in approximately 5 out of 1,000... 
POPULATION | CELLS | INFLAMMATORY-BOWEL-DISEASE | GENETIC ASSOCIATION | GENETICS & HEREDITY | RISK | TRIMS PRECURSORS | AMINOPEPTIDASE | HLA | PROMOTES | GENOME-WIDE ASSOCIATION | Receptors, Prostaglandin E, EP4 Subtype - genetics | Interleukin-12 Subunit p40 - genetics | Aminopeptidases - genetics | Genome-Wide Association Study | Meta-Analysis as Topic | Peptide Fragments - metabolism | Disease Susceptibility | Spondylitis, Ankylosing - genetics | Membrane Proteins - genetics | Minor Histocompatibility Antigens | Humans | European Continental Ancestry Group | Receptors, Tumor Necrosis Factor, Type I - genetics | Spondylitis, Ankylosing - metabolism | Case-Control Studies | CARD Signaling Adaptor Proteins - genetics | Latent TGF-beta Binding Proteins - genetics | Receptors, Peptide | CD8-Positive T-Lymphocytes - metabolism | Core Binding Factor Alpha 3 Subunit - genetics | Polymorphism, Genetic - genetics | Aminopeptidases - metabolism | HLA-B27 Antigen - genetics | Histocompatibility antigens | HLA histocompatibility antigens | Physiological aspects | Disease susceptibility | Genetic aspects | Research | Single nucleotide polymorphisms | Ankylosing spondylitis | Risk factors | Inflammatory bowel disease | Medical research | Biomedical research | Lymphocytes | Immunotherapy | Quality control | Genomes | Gene expression | Deoxyribonucleic acid--DNA
Journal Article