Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (25) 25
male (15) 15
female (13) 13
gastroenterology & hepatology (12) 12
index medicus (11) 11
adult (10) 10
inflammatory-bowel-disease (10) 10
medicine, general & internal (9) 9
middle aged (9) 9
crohns-disease (8) 8
genotype (7) 7
inflammatory bowel disease (7) 7
article (6) 6
crohn disease - genetics (6) 6
genetics (6) 6
medicin och hälsovetenskap (6) 6
polymorphism, single nucleotide (6) 6
animals (5) 5
colitis, ulcerative - genetics (5) 5
genetic predisposition to disease (5) 5
genome-wide association (5) 5
medical and health sciences (5) 5
aged (4) 4
canada (4) 4
efficacy (4) 4
genetics & heredity (4) 4
gut microbiota (4) 4
infliximab (4) 4
klinisk medicin (4) 4
phenotype (4) 4
therapy (4) 4
5-aminosalicylic acid (3) 3
aged, 80 and over (3) 3
aspergillus-nidulans (3) 3
cell cycle proteins (3) 3
clinical medicine (3) 3
cohort studies (3) 3
colitis, ulcerative - drug therapy (3) 3
dyneins - metabolism (3) 3
expression (3) 3
gastroenterologi (3) 3
gastroenterology and hepatology (3) 3
gene expression (3) 3
genome-wide association study (3) 3
genomes (3) 3
inflammatory bowel diseases (3) 3
inflammatory bowel diseases - genetics (3) 3
medicine (3) 3
medicinsk genetik (3) 3
medicinska och farmaceutiska grundvetenskaper (3) 3
metaanalysis (3) 3
microbiota (3) 3
multidisciplinary sciences (3) 3
nudc (3) 3
susceptibility (3) 3
susceptibility loci (3) 3
ulcerative colitis (3) 3
young adult (3) 3
abo antigen (2) 2
activation (2) 2
activity index (2) 2
adalimumab (2) 2
adenoviridae - genetics (2) 2
adolescent (2) 2
alleles (2) 2
anti-inflammatory agents - administration & dosage (2) 2
antibodies, monoclonal - therapeutic use (2) 2
association (2) 2
bacteria (2) 2
bacteria - classification (2) 2
basic medicine (2) 2
biochemistry & molecular biology (2) 2
biological availability (2) 2
biopsy (2) 2
blood group antigens (2) 2
card signaling adaptor proteins - genetics (2) 2
case-control studies (2) 2
cell biology (2) 2
cell division (2) 2
colitis, ulcerative - immunology (2) 2
colitis, ulcerative - microbiology (2) 2
colitis, ulcerative - pathology (2) 2
cos cells (2) 2
crohn disease - immunology (2) 2
crohn disease - microbiology (2) 2
crohn disease - pathology (2) 2
crohn's disease (2) 2
cytoplasmic dynein (2) 2
deglutition disorders - etiology (2) 2
determinants (2) 2
disease (2) 2
double-blind (2) 2
drug-treatment (2) 2
dynein (2) 2
endoscopy, gastrointestinal - standards (2) 2
esophageal carcinoma (2) 2
esophageal neoplasms - complications (2) 2
esophageal neoplasms - mortality (2) 2
ethnic groups (2) 2
fecal microbiota (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Ustekinumab as induction and maintenance therapy for Crohn's disease
by Feagan, Brian G and Sandborn, William J and Gasink, Christopher and Jacobstein, Douglas and Lang, Yinghua and Friedman, Joshua R and Blank, Marion A and Johanns, Jewel and Gao, Long-Long and Miao, Ye and Adedokun, Omoniyi J and Sands, Bruce E and Hanauer, Stephen B and Vermeire, Severine and Targan, Stephan and Ghosh, Subrata and De Villiers, Willem J and Colombel, Jean-Frederic and Tulassay, Zsolt and Seidler, Ursula and Salzberg, Bruce A and Desreumaux, Pierre and Lee, Scott D and Loftus, Edward V and Dieleman, Levinus A and Katz, Seymour and Rutgeerts, Paul and Bampton, P and Chung, A and Connor, S and Debinski, H and Leong, R and Macrae, F and Pavli, P and Sorrentino, D and van den Bogaerde, J and Vogel, W and Vogelsang, H and Louis, E and Mana, F and Zaltman, C and Aumais, G and Bernstein, C and Bressler, B and Dhalla, S and Marshall, J and Panaccione, R and Ropeleski, M and Stehlik, J and Volfova, M and Brynskov, J and Glerup, H and Abitbol-Selinger, V and Allez, M and Beaugerie, L and Bourreille, A and Cadiot, G and Dupas, J and Grimaud, J and Laharie, D and Lerebours, E and Moreau, J and Baumgart, D and Brand, S and Ebert, M and Ehehalt, R and Hasselblatt, P and Howaldt, S and Klaus, J and Krummenerl, P and Kucharzik, T and Lügering, A and Mudter, J and Preiss, J and Schreiber, S and Stallmach, A and Stein, J and Strauch, U and Salamon, A and Patchett, S and Lahat-Zok, A and Rachmilewitz, D and Annese, V and Bossa, F and Guidi, L and Kohn, A and Rocca, R and Ando, A and Ashida, T and Hanai, H and Ishida, T and Ito, H and Matsumoto, T and Motoya, S and Nakamura, S and Sameshima, Y and Suzuki, Y and Watanabe, K and Yamagami, H and Yamamoto, T and ... and UNITI-IM-UNITI Study Grp and UNITI–IM-UNITI Study Group
New England Journal of Medicine, ISSN 0028-4793, 11/2016, Volume 375, Issue 20, pp. 1946 - 1960
BACKGROUND Ustekinumab, a monoclonal antibody to the p40 subunit of interleukin-12 and interleukin-23, was evaluated as an intravenous induction therapy in two... 
MEDICINE, GENERAL & INTERNAL | INFECTIONS | ARTICLE | INFLAMMATORY-BOWEL-DISEASE | ADALIMUMAB | EFFICACY | SAFETY | RANDOMIZED-TRIAL | MONOCLONAL-ANTIBODY | INFLIXIMAB | Humans | Middle Aged | Induction Chemotherapy | Male | Remission Induction | Ustekinumab - therapeutic use | Ustekinumab - adverse effects | Ustekinumab - pharmacokinetics | Crohn Disease - drug therapy | Ustekinumab - immunology | Adult | Female | Maintenance Chemotherapy | Infusions, Intravenous
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data
by Romagnoni, A and Jegou, S and Van Steen, K and Wainrib, G and Hugot, JP and Peyrin-Biroulet, L and Chamaillard, M and Colombel, JF and Cottone, M and D'Amato, M and D'Inca, R and Halfvarson, J and Henderson, P and Karban, A and Kennedy, NA and Khan, MA and Lemann, M and Levine, A and Massey, D and Milla, M and Ng, SME and Oikonomou, I and Peeters, H and Proctor, DD and Rahier, JF and Rutgeerts, P and Seibold, F and Stronati, L and Taylor, KM and Torkvist, L and Ublick, K and Van Limbergen, J and Van Gossum, A and Vatn, MH and Zhang, H and Zhang, W and Andrews, JM and Bampton, PA and Barclay, M and Florin, TH and Gearry, R and Krishnaprasad, K and Lawrance, IC and Mahy, G and Montgomery, GW and Radford-Smith, G and Roberts, RL and Simms, LA and Hanigan, K and Croft, A and Amininijad, L and Cleynen, I and Dewit, O and Franchimont, D and Georges, M and Laukens, D and Theatre, E and Vermeire, S and Aumais, G and Baidoo, L and Barrie, AM and Beck, K and Bernard, EJ and Binion, DG and Bitton, A and Brant, SR and Cho, JH and Cohen, A and Croitoru, K and Daly, MJ and Datta, LW and Deslandres, C and Duerr, RH and Dutridge, D and Ferguson, J and Fultz, J and Goyette, P and Greenberg, GR and Haritunians, T and Jobin, G and Katz, S and Lahaie, RG and McGovern, DP and Nelson, L and Ng, SM and Ning, K and Pare, P and Regueiro, MD and Rioux, JD and Ruggiero, E and Schumm, LP and Schwartz, M and Scott, R and Sharma, Y and Silverberg, MS and Spears, D and Steinhart, AH and Stempak, JM and Swoger, JM and Tsagarelis, C and ... and Int Inflammatory Bowel Dis Genetic and International Inflammatory Bowel Disease Genetics Consortium (IIBDGC)
SCIENTIFIC REPORTS, ISSN 2045-2322, 07/2019, Volume 9, Issue 1, pp. 10351 - 18
Crohn Disease (CD) is a complex genetic disorder for which more than 140 genes have been identified using genome wide association studies (GWAS). However, the... 
LOCI | INFLAMMATORY-BOWEL-DISEASE | RISK PREDICTION | ASSOCIATION | MULTIDISCIPLINARY SCIENCES | Inflammatory bowel diseases | Complementarity | Epistasis | Genomes | Genetic variance | Learning algorithms | Genetic markers | Genotyping | Intestine | Neural networks | Machine learning | Quality control | Artificial intelligence | Genotypes
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
by Jostins, Luke and Ripke, Stephan and Weersma, Rinse K and Duerr, Richard H and McGovern, Dermot P and Hui, Ken Y and Lee, James C and Schumm, L. Philip and Sharma, Yashoda and Anderson, Carl A and Essers, Jonah and Mitrovic, Mitja and Ning, Kaida and Cleynen, Isabelle and Theatre, Emilie and Spain, Sarah L and Raychaudhuri, Soumya and Goyette, Philippe and Wei, Zhi and Abraham, Clara and Achkar, Jean-Paul and Ahmad, Tariq and Amininejad, Leila and Ananthakrishnan, Ashwin N and Andersen, Vibeke and Anews, Jane M and Baidoo, Leonard and Balschun, Tobias and Bampton, Peter A and Bitton, Alain and Boucher, Gabrielle and Brand, Stephan and Büning, Carsten and Cohain, Ariella and Cichon, Sven and D'Amato, Mauro and de Jong, Dirk and Devaney, Kathy L and Dubinsky, Marla and Edwards, Cathryn and Ellinghaus, David and Ferguson, Lynnette R and Franchimont, Denis and Fransen, Karin and Gearry, Richard and Georges, Michel and Gieger, Christian and Glas, Jürgen and Haritunians, Talin and Hart, Ailsa and Hawkey, Chris and Hedl, Matija and Hu, Xinli and Karlsen, Tom H and Kupcinskas, Limas and Kugathasan, Subra and Latiano, Anna and Laukens, Debby and Lawrance, Ian C and Lees, Charlie W and Louis, Edouard and Mahy, Gillian and Mansfield, John and Morgan, Angharad R and Mowat, Craig and Newman, William and Palmieri, Orazio and Ponsioen, Cyriel Y and Potocnik, Uros and Prescott, Natalie J and Regueiro, Miguel and Rotter, Jerome I and Russell, Richard K and Sanderson, Jeremy D and Sans, Miquel and Satsangi, Jack and Schreiber, Stefan and Simms, Lisa A and Sventoraityte, Jurgita and Targan, Stephan R and Taylor, Kent D and Tremelling, Mark and Verspaget, Hein W and de Vos, Martine and Wijmenga, Cisca and Wilson, David C and Winkelmann, Juliane and Xavier, Ramnik J and Zeissig, Sebastian and Zhang, Bin and Zhang, Clarence K and Zhao, Hongyu and Silverberg, Mark S and Annese, Vito and Hakonarson, Hakon and Brant, Steven R and Radford-Smith, Graham and Mathew, Christopher G and Rioux, John D and Schadt, Eric E and ... and Int IBD Genetics Consortium IIBDGC and International IBD Genetics Consortium (IIBDGC) and The International IBD Genetics Consortium (IIBDGC) and Region Örebro län and Örebro universitet and Institutionen för medicinska vetenskaper
Nature, ISSN 0028-0836, 2012, Volume 491, Issue 7422, pp. 119 - 124
Crohn's disease and ulcerative colitis, the two common forms of inflammatory bowel disease (IBD), affect over 2.5 million people of European ancestry, with... 
HYPER-IGE SYNDROME | RISK LOCI | NETWORK | NUMBER | METAANALYSIS | TUBERCULOSIS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | MUTATIONS | EXPRESSION | Crohn Disease - genetics | Humans | Inflammatory Bowel Diseases - immunology | Colitis, Ulcerative - genetics | Mycobacterium tuberculosis - immunology | Inflammatory Bowel Diseases - physiopathology | Colitis, Ulcerative - immunology | Host-Pathogen Interactions - immunology | Mycobacterium tuberculosis - pathogenicity | Haplotypes - genetics | Mycobacterium - pathogenicity | Mycobacterium Infections - genetics | Inflammatory Bowel Diseases - genetics | Crohn Disease - microbiology | Mycobacterium Infections - microbiology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Reproducibility of Results | Mycobacterium - immunology | Crohn Disease - immunology | Genome, Human - genetics | Phenotype | Colitis, Ulcerative - microbiology | Host-Pathogen Interactions - genetics | Polymorphism, Single Nucleotide - genetics | Inflammatory Bowel Diseases - microbiology | Crohn Disease - physiopathology | Colitis, Ulcerative - physiopathology | Inflammatory bowel disease | Candidates | Tuberculosis | Architecture | Genetics | Genomes | Diabetes | Gene expression | Health risk assessment | Immune system | Rheumatology and Autoimmunity | Basic Medicine | Medical Genetics | Medicinsk genetik | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Reumatologi och inflammation | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes
by Momozawa, Yukihide and Dmitrieva, Julia and Théâtre, Emilie and Deffontaine, Valérie and Rahmouni, Souad and Charloteaux, Benoît and Crins, François and Docampo, Elisa and Elansary, Mahmoud and Gori, Ann-Stephan and Lecut, Christelle and Mariman, Rob and Mni, Myriam and Oury, Cécile and Altukhov, Ilya and Alexeev, Dmitry and Aulchenko, Yuri and Amininejad, Leila and Bouma, Gerd and Hoentjen, Frank and Löwenberg, Mark and Oldenburg, Bas and Pierik, Marieke J and Vander Meulen-De Jong, Andrea E and Van Der Woude, C. Janneke and Visschedijk, Marijn C and Lathrop, Mark and Hugot, Jean-Pierre and Weersma, Rinse K and De Vos, Martine and Franchimont, Denis and Vermeire, Severine and Kubo, Michiaki and Louis, Edouard and Georges, Michel and Abraham, Clara and Achkar, Jean-Paul and Ahmad, Tariq and Ananthakrishnan, Ashwin N and Andersen, Vibeke and Anderson, Carl A and Andrews, Jane M and Annese, Vito and Aumais, Guy and Baidoo, Leonard and Baldassano, Robert N and Bampton, Peter A and Barclay, Murray and Barrett, Jeffrey C and Bayless, Theodore M and Bethge, Johannes and Bitton, Alain and Boucher, Gabrielle and Brand, Stephan and Brandt, Berenice and Brant, Steven R and Büning, Carsten and Chew, Angela and Cho, Judy H and Cleynen, Isabelle and Cohain, Ariella and Croft, Anthony and Daly, Mark J and D'Amato, Mauro and Danese, Silvio and De Jong, Dirk and Denapiene, Goda and Denson, Lee A and Devaney, Kathy L and Dewit, Olivier and D'Inca, Renata and Dubinsky, Marla and Duerr, Richard H and Edwards, Cathryn and Ellinghaus, David and Essers, Jonah and Ferguson, Lynnette R and Festen, Eleonora A and Fleshner, Philip and Florin, Tim and Franke, Andre and Fransen, Karin and Gearry, Richard and Gieger, Christian and Glas, Jürgen and Goyette, Philippe and Green, Todd and Griffiths, Anne M and Guthery, Stephen L and Hakonarson, Hakon and Halfvarson, Jonas and Hanigan, Katherine and Haritunians, Talin and Hart, Ailsa and Hawkey, Chris and Hayward, Nicholas K and Hedl, Matija and Henderson, Paul and Hu, Xinli and Huang, Hailiang and ... and Int IBD Genetics Consortium and The International IBD Genetics Consortium and Örebro universitet and Institutionen för medicinska vetenskaper
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1 - 18
GWAS have identified >200 risk loci for Inflammatory Bowel Disease (IBD). The majority of disease associations are known to be driven by regulatory variants.... 
INFLAMMATORY-BOWEL-DISEASE | RARE VARIANTS | CROHNS-DISEASE | LOW-FREQUENCY | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | QUANTITATIVE TRAIT LOCUS | SEQUENCING DATA | CODING VARIANTS | COMPLEX TRAITS | GENOME-WIDE ASSOCIATION | Inflammatory bowel disease | Inflammatory bowel diseases | Intestine | Modules | Genes | Health risks | Risk | Gene expression | Loci | Disease control | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies
by Bodea, Corneliu A and Neale, Benjamin M and Ripke, Stephan and Barclay, Murray and Peyrin-Biroulet, Laurent and Chamaillard, Mathias and Colombel, Jean-Frederick and Cottone, Mario and Croft, Anthony and D’Incà, Renata and Halfvarson, Jonas and Hanigan, Katherine and Henderson, Paul and Hugot, Jean-Pierre and Karban, Amir and Kennedy, Nicholas A and Khan, Mohammed Azam and Lémann, Marc and Levine, Arie and Massey, Dunecan and Massey, Dunecan C.O and Milla, Monica and Montgomery, Grant W and Ng, Sok Meng and Ng, Sok Meng Evelyn and Oikonomou, Ioannis and Peeters, Harald and Proctor, Deborah D and Rahier, Jean-Francois and Roberts, Rebecca and Roberts, Rebecca L and Rutgeerts, Paul and Seibold, Frank and Stronati, Laura and Taylor, Kirstin M and Törkvist, Leif and Ublick, Kullak and Van Limbergen, Johan and Van Gossum, André and Van Gossum, Andre and Vatn, Morten H and Zhang, Clarence and Zhang, Hu and Zhang, Wei and Andrews, Jane M and Bampton, Peter A and Florin, Timothy H and Gearry, Richard and Krishnaprasad, Krupa and Lawrance, Ian C and Mahy, Gillian and Radford-Smith, Graham and Simms, Lisa A and Amininijad, Leila and Cleynen, Isabelle and Dewit, Olivier and Franchimont, Denis and Georges, Michel and Laukens, Debby and Theatre, Emilie and Vermeire, Severine and Aumais, Guy and Baidoo, Leonard and Barrie, Arthur M and Beck, Karen and Bernard, Edmond-Jean and Binion, David G and Bitton, Alain and Brant, Steve R and Cho, Judy H and Cohen, Albert and Croitoru, Kenneth and Daly, Mark J and Datta, Lisa W and Deslandres, Colette and Duerr, Richard H and Dutridge, Debra and Ferguson, John and Fultz, Joann and Goyette, Philippe and Greenberg, Gordon R and Haritunians, Talin and Jobin, Gilles and Katz, Seymour and Lahaie, Raymond G and McGovern, Dermot P and Nelson, Linda and Ning, Kaida and Paré, Pierre and Regueiro, Miguel D and Rioux, John D and Ruggiero, Elizabeth and Schumm, L. Philip and Schwartz, Marc and Scott, Carol E and Scott, Richard and Scott, Regan and Sharma, Yashoda and Silverberg, Mark S and Spears, Denise and ... and International IBD Genetics Consortium
The American Journal of Human Genetics, ISSN 0002-9297, 05/2016, Volume 98, Issue 5, pp. 857 - 868
One goal of human genetics is to understand the genetic basis of disease, a challenge for diseases of complex inheritance because risk alleles are few relative... 
Genetics, Population | Genetic Predisposition to Disease | Disease - genetics | Gene Frequency | Humans | Bayes Theorem | Heredity - genetics | Polymorphism, Single Nucleotide - genetics | Genotype | Software | Case-Control Studies | Genetic Linkage | Genetic research | Usage | Methods | Gaussian processes | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Gastroenterology and Hepatology | Gastroenterologi
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes
by Momozawa, Yukihide and Dmitrieva, Julia and Théâtre, Emilie and Deffontaine, Valérie and Rahmouni, Souad and Charloteaux, Benoît and Crins, François and Docampo, Elisa and Elansary, Mahmoud and Gori, Ann-Stephan and Lecut, Christelle and Mariman, Rob and Mni, Myriam and Oury, Cécile and Altukhov, Ilya and Alexeev, Dmitry and Aulchenko, Yuri and Amininejad, Leila and Bouma, Gerd and Hoentjen, Frank and Löwenberg, Mark and Oldenburg, Bas and Pierik, Marieke J and Vander Meulen-de Jong, Andrea E and Janneke van der Woude, C and Visschedijk, Marijn C and Lathrop, Mark and Hugot, Jean-Pierre and Weersma, Rinse K and De Vos, Martine and Franchimont, Denis and Vermeire, Severine and Kubo, Michiaki and Louis, Edouard and Georges, Michel and International IBD Genetics Consortium
Nature communications, ISSN 2041-1723, 06/2018, Volume 9, Issue 1, p. 2427
GWAS have identified >200 risk loci for Inflammatory Bowel Disease (IBD). The majority of disease associations are known to be driven by regulatory variants.... 
Crohn Disease - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Middle Aged | Genotype | Male | Gene Expression Profiling | Multifactorial Inheritance | Sequence Analysis, DNA | Inflammatory Bowel Diseases - genetics | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Cohort Studies
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights