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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
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) and Örebro universitet and Institutionen för medicinska vetenskaper
SCIENTIFIC REPORTS, ISSN 2045-2322, 07/2019, Volume 9, Issue 1, pp. 10351 - 18
Journal Article
Nature genetics, ISSN 1061-4036, 2010, Volume 42, Issue 4, pp. 332 - 337
Journal Article
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 ...
Scientific reports, ISSN 2045-2322, 2019, Volume 9, Issue 1, p. 10351
Journal Article
Gastroenterology, ISSN 0016-5085, 2016, Volume 150, Issue 5, pp. 1196 - 1207
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2010, Volume 5, Issue 1, pp. 24 - 24
Familial hypocholesterolemia, namely abetalipoproteinemia, hypobetalipoproteinemia and chylomicron retention disease (CRD), are rare genetic diseases that... 
TRIGLYCERIDE TRANSFER PROTEIN | VITAMIN-E-DEFICIENCY | MEDICINE, RESEARCH & EXPERIMENTAL | ANDERSON DISEASE | SAR1B GENE | X-RAY ABSORPTIOMETRY | APOPROTEIN-B | APOLIPOPROTEIN-B GENE | ENDOPLASMIC-RETICULUM | TRANSPORT VESICLE | ABETALIPOPROTEINEMIA | Malabsorption Syndromes - diagnosis | Lipid Metabolism Disorders - therapy | Anthropometry | Humans | Child, Preschool | Infant | Male | Lipid Metabolism Disorders - diagnosis | Malnutrition - complications | Lipid Metabolism Disorders - complications | Vitamin E Deficiency - complications | Adult | Female | Malabsorption Syndromes - therapy | Child | Diarrhea - complications | Fatty Acids - metabolism | Malabsorption Syndromes - complications | Monomeric GTP-Binding Proteins - genetics | Nervous System Diseases - complications | Malabsorption Syndromes - genetics | Chylomicrons - metabolism | Monomeric GTP-Binding Proteins - metabolism | Lipid Metabolism Disorders - genetics | Mutation | Cohort Studies | Growth Disorders - complications | Care and treatment | Usage | Genetic disorders | Gene mutations | Practice guidelines (Medicine) | Diagnosis | Health aspects | Risk factors | Proteins | Medical research | Nutrition | Cholesterol | Lipid Metabolism Disorders | Fatty Acids | Malabsorption Syndromes | Diarrhea | Chylomicrons | Monomeric GTP-Binding Proteins | Life Sciences | Vitamin E Deficiency | Genetics | Growth Disorders | Malnutrition | Nervous System Diseases
Journal Article
Journal Article
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 Milla, Monica and Montgomery, Grant W and Ng, Sok Meng Evelyn and Oikonomou, Ioannis and Peeters, Harald and Proctor, Deborah D and Rahier, Jean-Francois and Roberts, Rebecca 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, Andre and Vatn, Morten H 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 Roberts, Rebecca L 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 Van Gossum, André 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 Ng, Sok Meng 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, Regan and Sharma, Yashoda and Silverberg, Mark S and Spears, Denise and Steinhart, A. Hillary and Stempak, Joanne M and Swoger, Jason M and Tsagarelis, Constantina and ... and The International IBD Genetics Consortium 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 |