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Methods in Molecular Biology, ISSN 1064-3745, 2015, Volume 1326, pp. 35 - 44
Since the breakthrough of genome-wide association studies and genetic studies of common complex diseases like celiac disease have been able to finally identify... 
LOD score | Transmission disequilibrium test | Association | Genetic linkage | Nonparametric linkage | Sib-pairs | Genome-wide | Complex inheritance | Genome-Wide Association Study | Celiac Disease - genetics | Humans | Age of Onset | Adult | HLA Antigens - genetics | Child | Genetic Linkage
Journal Article
Rhinology, ISSN 0300-0729, 03/2015, Volume 53, Issue 1, pp. 25 - 28
Background: Nasal polyps is a common disease but little is known about its' pathogenesis. Our hypothesis was that there are genetic factors involved in the... 
nasal polyps | genetics | humans | OTORHINOLARYNGOLOGY | adults | sex | Genetic Predisposition to Disease | Prevalence | Humans | Middle Aged | Nasal Polyps - genetics | Adult | Female | Male | Aged | Nasal Polyps - epidemiology | Sweden - epidemiology
Journal Article
Journal Article
Lakartidningen, ISSN 0023-7205, 2017, Volume 114, Issue 12
Journal Article
Scandinavian Journal of Gastroenterology, ISSN 1502-7708, 2016, Volume 51, Issue 4, p. 427
Objective Histological evaluation of intestinal biopsies for the diagnosis of coeliac disease can be challenging and compatible with risk of misdiagnosis. The... 
Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Gastroenterologi | Klinisk medicin | Gastroenterology and Hepatology
Journal Article
PLoS ONE, ISSN 1932-6203, 2018, Volume 13, Issue 3
Background: We have previously performed a Genome Wide Association and linkage study that indicated a new disease triggering mechanism involving amino acid... 
Pediatrics | Näringslära | Pediatrik | Gastroenterologi | Gastroenterology and Hepatology | Nutrition and Dietetics
Journal Article
Nutrients, ISSN 2072-6643, 12/2015, Volume 7, Issue 12, pp. 10100 - 10115
Exposure to polyunsaturated fatty acids (PUFA) influences immune function and may affect the risk of allergy development. Long chain PUFAs are produced from... 
Allergy | ELOVL2 | Respiratory allergy | Elongase | FADS | Phospholipids | Umbilical cord serum | Long chain polyunsaturated fatty acids | Arachidonic acid | Atopic eczema | Nutrigenetics | Fatty acid desaturase | Single nucleotide polymorphism | BAS birth cohort | single nucleotide polymorphism | phospholipids | umbilical cord serum | LYMPHOCYTE-PROLIFERATION | NO ASSOCIATION | elongase | EXTRACTION | NUTRITION & DIETETICS | respiratory allergy | METABOLISM | ATOPIC DISEASES | BLOOD | arachidonic acid | VARIANTS | allergy | atopic eczema | nutrigenetics | INFLAMMATION | fatty acid desaturase | long chain polyunsaturated fatty acids | DELTA-5 | EXPRESSION | Haplotypes | Acetyltransferases - metabolism | Dermatitis, Atopic - genetics | Multigene Family | Humans | Male | Genotyping Techniques | Acetyltransferases - genetics | Sweden | Fetal Blood - chemistry | Female | Hypersensitivity - genetics | Phospholipids - blood | Body Mass Index | Fatty Acid Desaturases - genetics | Fatty Acid Desaturases - metabolism | Linear Models | Logistic Models | Fatty Acids, Unsaturated - blood | Adolescent | Alleles | Dermatitis, Atopic - blood | Polymorphism, Single Nucleotide | Cohort Studies | Hypersensitivity - blood | Composition | Immune response | Polyunsaturated fatty acids | Hypersensitivity | Risk reduction | Chains | Risk | Single-nucleotide polymorphism | Desaturase | Fatty acids | Atopy | Carriers | Fatty acid composition | Diet | Eczema | Clusters | Skin diseases | Age | Medical and Health Sciences | Medicin och hälsovetenskap | Hälsovetenskaper | Näringslära | Nutrition and Dietetics | Health Sciences
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2013, Volume 8, Issue 8, p. e70174
Celiac disease is a common autoimmune disorder characterized by an intestinal inflammation triggered by gluten, a storage protein found in wheat, rye and... 
COMPLEX HUMAN-DISEASES | ACTIVATION | DISEQUILIBRIUM | METABOLISM | PHOSPHATASE | MULTIDISCIPLINARY SCIENCES | RISK VARIANTS | STRESS | MAPK | TISSUE TRANSGLUTAMINASE | APPL1 | Mitogen-Activated Protein Kinase Phosphatases - immunology | Humans | Autoimmunity - genetics | Nuclear Family | Male | Case-Control Studies | HLA-DQ Antigens - immunology | Intestines - immunology | Autoimmune Diseases - genetics | Autoimmunity - immunology | Celiac Disease - immunology | Dual-Specificity Phosphatases - genetics | Immune System - immunology | Female | Autoimmune Diseases - pathology | Child | Genetic Linkage | Genome-Wide Association Study | Intestines - pathology | Celiac Disease - genetics | Autoimmune Diseases - immunology | Dual-Specificity Phosphatases - immunology | Immune System - pathology | Mitogen-Activated Protein Kinase Phosphatases - genetics | Celiac Disease - pathology | HLA-DQ Antigens - genetics | Polymorphism, Single Nucleotide - genetics | Genome, Human | Type 2 diabetes | Autoimmunity | Genes | Genomics | HLA histocompatibility antigens | Genomes | Disease susceptibility | Epidemiology | Celiac disease | Rheumatoid factor | Histocompatibility antigens | Physiological aspects | Family | Genetic aspects | Pediatrics | Disease | Mucosa | Disorders | Association analysis | Smooth muscle | Risk factors | DUSP10 gene | Genetics | Genetic factors | Chromosomes | Antigens | Autoantibodies | Heredity | Gene expression | Metabolism | Patients | Diseases | Studies | Energy balance | Hospitals | Rheumatoid arthritis | Wheat | Adaptive systems | Epithelial cells | Homeostasis | Proline | Arthritis | Intestine | Polarity | Extracellular matrix | Gluten | Rye | Immune system | Linkage analysis | Barley | Immune response | Psoriasis | Diabetes mellitus | Health risks | Muscles | Autoantigens | Loci | Histocompatibility antigen HLA | Diabetes | Autoimmune diseases | Glutamine | Naturvetenskap | Natural Sciences
Journal Article
Molecular Immunology, ISSN 0161-5890, 03/2015, Volume 64, Issue 1, pp. 190 - 194
Journal Article
Rhinology, ISSN 0300-0729, 2015, Volume 53, Issue 1, pp. 25 - 28
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 06/2015, Volume 16, Issue 1, p. 44
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 03/2012, Volume 49, Issue 3, pp. 200 - 205
Journal Article
by Kähönen, Mika and Albrecht, Eva and Obeidat, Ma'en and Mustelin, Linda and Froguel, Philippe and Burton, Paul R and Johansson, Åsa and Jankovic, Stipan and Grallert, Harald and Imboden, Medea and Hartikainen, Anna-Liisa and Delplanque, Jérôme and Porteous, David J and Olin, Anna-Carin and Schnabel, Eva and Holloway, John W and Ebrahim, Shah and Zgaga, Lina and MacLeod, Andrew K and Sayers, Ian and Rudan, Igor and Tobin, Martin D and Ripatti, Samuli and Wain, Louise V and McArdle, Wendy L and Evans, David M and Cooper, Matthew N and Smith, George Davey and Spector, Tim D and Völzke, Henry and Deloukas, Panos and Jarvelin, Marjo-Riitta and Blakey, John D and Strachan, David P and Cooper, Cyrus and Schulz, Holger and Campbell, Harry and Huffman, Jennifer E and Hall, Ian P and Rudnicka, Alicja R and James, Alan L and Rantanen, Taina and Lawlor, Debbie A and Morris, Andrew D and Nyberg, Fredrik and Ramasamy, Adaikalavan and Wright, Alan F and Karrasch, Stefan and Palmer, Lyle J and Wild, Sarah H and Repapi, Emmanouela and Hui, Jennie and Morris, Richard W and Elliott, Paul and Polašek, Ozren and Shaheen, Seif and Britton, John R and Igl, Wilmar and Heliövaara, Markku and Johnson, Toby and Bouatia-Naji, Nabila and Homuth, Georg and Dennison, Elaine and McKeever, Tricia M and Granell, Raquel and Pouta, Anneli and Gyllensten, Ulf and Zaboli, Ghazal and Soranzo, Nicole and Hingorani, Aroon D and Vitart, Veronique and Koch, Beate and Zhao, Jing Hua and Barroso, Inês and Wilson, James F and Kaprio, Jaakko and Jackson, Cathy and Wareham, Nicholas J and Loos, Ruth J F and Grkovic, Ivica and Peltonen, Leena and Torén, Kjell and Probst-Hensch, Nicole M and Wannamethee, S Goya and Pavord, Ian D and Gläser, Sven and Naluai, Åsa Torinsson and Henderson, John and Wichmann, H Erich and Surakka, Ida and Mangino, Massimo and Whincup, Peter H and Zhai, Guangju and Hayward, Caroline and Wellcome Trust Case Control Consor and NSHD Resp Study Team and Wellcome Trust Case Control Consortium and NSHD Respiratory Study Team and The NSHD Respiratory Study Team and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 01/2010, Volume 42, Issue 1, pp. 36 - 44
Journal Article
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