X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (60) 60
humans (53) 53
gastroenterology & hepatology (32) 32
male (30) 30
female (29) 29
children (27) 27
pediatrics (27) 27
child (24) 24
research (23) 23
gastroenterology and hepatology (22) 22
genetics & heredity (21) 21
genetics (20) 20
ulcerative colitis (20) 20
risk factors (19) 19
adolescent (18) 18
crohns-disease (18) 18
genetic predisposition to disease (18) 18
genome-wide association (18) 18
inflammatory bowel disease (18) 18
inflammatory-bowel-disease (18) 18
article (17) 17
child, preschool (16) 16
polymorphism, single nucleotide (16) 16
wildlife management (15) 15
abridged index medicus (14) 14
bobwhites (14) 14
crohn disease - genetics (14) 14
ecology (13) 13
genetic aspects (13) 13
genome-wide association study (13) 13
crohn's disease (12) 12
risk (12) 12
susceptibility loci (12) 12
zoology (12) 12
case-control studies (11) 11
colinus virginianus (11) 11
infant (11) 11
medical research (11) 11
adult (10) 10
association (10) 10
birds (10) 10
genomics (10) 10
health aspects (10) 10
ulcerative-colitis (10) 10
diagnosis (9) 9
gene expression (9) 9
genotype (9) 9
inflammatory bowel diseases (9) 9
northern bobwhite (9) 9
quails (9) 9
studies (9) 9
susceptibility (9) 9
colitis, ulcerative - genetics (8) 8
disease (8) 8
gene (8) 8
genetic variation (8) 8
variants (8) 8
analysis (7) 7
animal populations (7) 7
diseases (7) 7
expression (7) 7
genes (7) 7
retrospective studies (7) 7
age (6) 6
alleles (6) 6
biochemistry & molecular biology (6) 6
cohort studies (6) 6
follow-up studies (6) 6
genomes (6) 6
haplotypes (6) 6
hospitals (6) 6
identification (6) 6
intestine (6) 6
medicin och hälsovetenskap (6) 6
medicine (6) 6
polymorphism, single nucleotide - genetics (6) 6
prognosis (6) 6
rheumatoid-arthritis (6) 6
transplantation (6) 6
wildlife conservation (6) 6
age of onset (5) 5
autoimmune diseases (5) 5
behavior (5) 5
bird nesting (5) 5
bobwhite (5) 5
data processing (5) 5
digestive system diseases (5) 5
gastroenterology (5) 5
genetic linkage (5) 5
genetics, population (5) 5
habitat (5) 5
immunology (5) 5
infants (5) 5
inflammatory bowel diseases - genetics (5) 5
liver transplantation (5) 5
medical and health sciences (5) 5
medicine, experimental (5) 5
physiological aspects (5) 5
polymorphism (5) 5
prospective studies (5) 5
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nucleic Acids Research, ISSN 0305-1048, 04/2018, Volume 46, Issue 6, pp. e32 - e32
Abstract High-throughput sequencing data are increasingly being made available to the research community for secondary analyses, providing new opportunities... 
RARE-VARIANT ASSOCIATION | GENETIC-VARIATION | HIGH-RISK | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUSCEPTIBILITY | GERMLINE MUTATIONS | OVARIAN-CANCER | BRCA2 | IDENTIFICATION | BREAST | GENOME-WIDE ASSOCIATION | Methods Online
Journal Article
Journal Article
Gastroenterology, ISSN 0016-5085, 06/2018, Volume 154, Issue 8, pp. 2097 - 2110
Journal Article
INFLAMMATORY BOWEL DISEASES, ISSN 1078-0998, 07/2019, Volume 25, Issue 7, pp. 1208 - 1217
Background Variation in care is common in medical practice. Reducing variation in care is shown to improve quality and increase favorable outcomes in chronic... 
QUALITY-OF-CARE | ASSOCIATION INSTITUTE GUIDELINE | ULCERATIVE-COLITIS | RISK | PREVALENCE | COMBINATION | pediatric | anti-TNF | THIOPURINES | INFLAMMATORY-BOWEL-DISEASE | THERAPY | quality improvement | OUTCOMES | GASTROENTEROLOGY & HEPATOLOGY | outcome
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2013, Volume 45, Issue 6, pp. 664 - 669
Journal Article
by Anderson, Carl A and Boucher, Gabrielle and Lees, Charlie W and Franke, Ane and D'Amato, Mauro and Taylor, Kent D and Lee, James C and Goyette, Philippe and Imielinski, Marcin and Latiano, Anna and Lagacé, Caroline and Scott, Regan and Amininejad, Leila and Bumpstead, Suzannah and Baidoo, Leonard and Baldassano, Robert N and Barclay, Murray and Bayless, Theodore M and Brand, Stephan and Büning, Carsten and Colombel, Jean-Frédéric and Denson, Lee A and de Vos, Martine and Dubinsky, Marla and Edwards, Cathryn and Ellinghaus, David and Fehrmann, Rudolf S. N and Floyd, James A. B and Florin, Timothy and Franchimont, Denis and Franke, Lude and Georges, Michel and Glas, Jürgen and Glazer, Nicole L and Guthery, Stephen L and Haritunians, Talin and Hayward, Nicholas K and Hugot, Jean-Pierre and Jobin, Gilles and Laukens, Debby and Lawrance, Ian and Lémann, Marc and Levine, Arie and Libioulle, Cecile and Louis, Edouard and McGovern, Dermot P and Milla, Monica and Montgomery, Grant W and Morley, Katherine I and Mowat, Craig and Ng, Aylwin and Newman, William and Ophoff, Roel A and Papi, Laura and Palmieri, Orazio and Peyrin-Biroulet, Laurent and Panés, Julián and Phillips, Anne and Prescott, Natalie J and Proctor, Deborah D and Roberts, Rebecca and Russell, Richard and Rutgeerts, Paul and Sanderson, Jeremy and Sans, Miquel and Schumm, Philip and Seibold, Frank and Sharma, Yashoda and Simms, Lisa A and Seielstad, Mark and Steinhart, A. Hillary and Targan, Stephan R and van den Berg, Leonard H and Vatn, Morten and Verspaget, Hein and Walters, Thomas and Wijmenga, Cisca and Wilson, David C and Westra, Harm-Jan and Xavier, Ramnik J and Zhao, Zhen Z and Ponsioen, Cyriel Y and Andersen, Vibeke and Torkvist, Leif and Gazouli, Maria and Anagnou, Nicholas P and Karlsen, Tom H and Kupcinskas, Limas and Sventoraityte, Jurgita and Mansfield, John C and Kugathasan, Subra and Silverberg, Mark S and Halfvarson, Jonas and Rotter, Jerome I and Mathew, Christopher G and Griffiths, Anne M and Gearry, Richard and Ahmad, Tariq and Brant, Steven R and Chamaillard, Mathias and ... and Hälsoakademin and Örebro universitet
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 3, pp. 246 - 252
Journal Article
by Tsoi, L.C and Spain, S.L and Knight, J and Ellinghaus, E and Stuart, P.E and Capon, F and Ding, J and Li, J and Tejasvi, T and Gudjonsson, J.E and Kang, H and Allen, M.H and McManus, R and Novelli, G and Samuelsson, L and Schalkwijk, J and Stahle, M and Burden, A.D and Smith, C.H and Cork, M.J and Estivill, X and Bowcock, A and Krueger, G.G and Weger, W and Worthington, J and Tazi-Ahnini, R and Nestle, F.O and Hayday, A and Hoffmann, P and Winkelmann, J and Wijmenga, C and Langford, C and Edkins, S and Anews, R and Blackburn, H and Strange, A and Band, G and Pearson, R and Vukcevic, D and Spencer, C.C and Deloukas, P and Mrowietz, U and Schreiber, S and Weidinger, S and Koks, S and Kingo, K and Esko, T and Metspalu, A and Lim, H.W and Voorhees, J.J and Weichenthal, M and Wichmann, H.E and Chanan, V and Rosen, C.F and Rahman, P and Gladman, D.D and Griffiths, C.E and Reis, A and Kere, J and Duffin, K.C and Helms, C and Goldgar, D and Li, Y and Paschall, J and Malloy, M.J and Pullinger, C.R and Kane, J.P and Gardner, J and Perlmutter, A and Miner, A and Feng, B.J and Hiremagalore, R and Ike, R.W and Christophers, E and Henseler, T and Ruether, A and Schrodi, S.J and Prahalad, S and Guthery, S.L and Hiregalore, R and Donnelly, P and Collaborative Assoc Study Psoriasi and Psoriasis Assoc Genetics Extension and Genetic Anal Psoriasis Consortium and Wellcome Trust Case Control Consor and Psoriasis Association Genetics Extension and Genetic Analysis of Psoriasis Consortium and Collaborative Association Study of Psoriasis (CASP) and Wellcome Trust Case Control Consortium 2 and Sahlgrenska akademin and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 12, pp. 1341 - 1348
To gain further insight into the genetic architecture of psoriasis, we conducted a meta-analysis of 3 genome-wide association studies (GWAS) and 2 independent... 
COMMON VARIANTS | SIGNALING PATHWAYS | MULTIPLE COMMON | INTERFERON-GAMMA | TH17 DIFFERENTIATION | GENETICS & HEREDITY | GENE-EXPRESSION | T-CELL DEVELOPMENT | GENOME-WIDE ASSOCIATION | CELIAC-DISEASE | NEGATIVE REGULATOR | Oligonucleotide Array Sequence Analysis | Humans | Immunity, Innate - genetics | Genetic Loci | CARD Signaling Adaptor Proteins - genetics | Psoriasis - genetics | Core Binding Factor Alpha 3 Subunit - immunology | STAT3 Transcription Factor - genetics | Skin - immunology | Psoriasis - immunology | CARD Signaling Adaptor Proteins - immunology | DEAD Box Protein 58 | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Guanylate Cyclase - immunology | Membrane Proteins - genetics | Membrane Proteins - immunology | GTPase-Activating Proteins - immunology | DEAD-box RNA Helicases - genetics | Core Binding Factor Alpha 3 Subunit - genetics | DEAD-box RNA Helicases - immunology | Guanylate Cyclase - genetics | T-Lymphocytes - immunology | Polymorphism, Single Nucleotide | GTPase-Activating Proteins - genetics | STAT3 Transcription Factor - immunology | Psoriasis | Physiological aspects | Disease susceptibility | Genetic aspects | Research | Autoimmune diseases | Gene expression | Chromosomes | Risk factors | Index Medicus | genetic analysis | innate immunity | Dermatologi och venereologi | Dermatology and Venereal Diseases | psoriasis
Journal Article