X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (50) 50
humans (46) 46
female (32) 32
male (32) 32
abridged index medicus (24) 24
polymorphism, single nucleotide (23) 23
genomics (21) 21
article (17) 17
genome-wide association (16) 16
genomes (16) 16
genome-wide association study (14) 14
genotype (14) 14
adolescent (13) 13
genetics (13) 13
adult (12) 12
case-control studies (12) 12
gene (12) 12
genes (12) 12
genetic aspects (12) 12
risk (12) 12
child (11) 11
children (11) 11
genetic predisposition to disease (11) 11
mutation (11) 11
risk factors (11) 11
studies (11) 11
allergy and immunology (10) 10
child, preschool (10) 10
disease (10) 10
genetic research (10) 10
middle aged (10) 10
phenotype (10) 10
allergy (9) 9
analysis (9) 9
cohort studies (9) 9
genetics & heredity (9) 9
immunology (9) 9
medical colleges (9) 9
common variants (8) 8
endocrinology & metabolism (8) 8
expression (8) 8
infant (8) 8
medical research (8) 8
pediatrics (8) 8
association (7) 7
protein (7) 7
variants (7) 7
aged (6) 6
diagnosis (6) 6
epidemiology (6) 6
genetic testing (6) 6
genetic variation (6) 6
medical and health sciences (6) 6
medicin och hälsovetenskap (6) 6
medicine, experimental (6) 6
metaanalysis (6) 6
mutations (6) 6
neurosciences (6) 6
polymorphism, single nucleotide - genetics (6) 6
alleles (5) 5
biochemistry & molecular biology (5) 5
cardiac & cardiovascular systems (5) 5
clinical medicine (5) 5
diabetes mellitus, type 2 - genetics (5) 5
european continental ancestry group - genetics (5) 5
genetic disorders (5) 5
genetic loci (5) 5
genotype & phenotype (5) 5
internal medicine (5) 5
klinisk medicin (5) 5
loci (5) 5
polymorphism (5) 5
population (5) 5
psychiatry (5) 5
research (5) 5
single-nucleotide polymorphism (5) 5
susceptibility (5) 5
young adult (5) 5
adolescence (4) 4
african americans (4) 4
alzheimer's disease (4) 4
asthma (4) 4
asthma - genetics (4) 4
cardiovascular (4) 4
consortia (4) 4
deoxyribonucleic acid--dna (4) 4
gene expression (4) 4
genetic association studies (4) 4
genetic markers (4) 4
health aspects (4) 4
patients (4) 4
pedigree (4) 4
quantitative trait loci (4) 4
respiratory system (4) 4
single nucleotide polymorphisms (4) 4
surgery (4) 4
african americans - genetics (3) 3
algorithms (3) 3
alzheimer disease - genetics (3) 3
apolipoprotein-e genotype (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2010, Volume 125, Issue 2, pp. 336 - 346.e4
Journal Article
by Assimes, Themistocles L., MD, PhD and Hólm, Hilma, MD and Kathiresan, Sekar, MD and Reilly, Muredach P., MB and Thorleifsson, Gudmar, PhD and Voight, Benjamin F., PhD and Erdmann, Jeanette, PhD and Willenborg, Christina, MSc and Vaidya, Dhananjay, MBBS, PhD, MPH and Xie, Changchun, PhD and Patterson, Chris C., PhD and Morgan, Thomas M., MD and Burnett, Mary Susan, PhD and Li, Mingyao, PhD and Hlatky, Mark A., MD and Knowles, Joshua W., MD, PhD and Thompson, John R., PhD and Absher, Devin, PhD and Iribarren, Carlos, MD, MPH, PhD and Go, Alan, MD and Fortmann, Stephen P., MD and Sidney, Stephen, MD, MPH and Risch, Neil, PhD and Tang, Hua, PhD and Myers, Richard M., PhD and Berger, Klaus, MD and Stoll, Monika, PhD and Shah, Svati H., MD, MHS and Thorgeirsson, Gudmundur, MD, PhD and Andersen, Karl, MD, PhD and Havulinna, Aki S., MSc and Herrera, J. Enrique, MS and Faraday, Nauder, MD and Kim, Yoonhee, PhD and Kral, Brian G., MD, MPH and Mathias, Rasika A., ScD and Ruczinski, Ingo, PhD and Suktitipat, Bhoom, MD and Wilson, Alexander F., PhD and Yanek, Lisa R., MPH and Becker, Lewis C., MD and Linsel-Nitschke, Patrick, MD and Lieb, Wolfgang, MD and König, Inke R., PhD and Hengstenberg, Christian, MD and Fischer, Marcus, MD and Stark, Klaus, PhD and Reinhard, Wibke, MD and Winogradow, Janina, MD and Grassl, Martina, MD and Grosshennig, Anika, MSc and Preuss, Michael, MSc and Schreiber, Stefan, MD and Wichmann, H.-Erich, MD and Meisinger, Christa, MD, MPH and Yee, Jean, BS and Friedlander, Yechiel, PhD and Do, Ron, MSc and Meigs, James B., MD, MPH and Williams, Gordon, MD and Nathan, David M., MD and MacRae, Calum A., MD, PhD and Qu, Liming, MS and Wilensky, Robert L., MD and Matthai, William H., MD and Qasim, Atif N., MD and Hakonarson, Hakon, MD, PhD and Pichard, Augusto D., MD and Kent, Kenneth M., MD, PhD and Satler, Lowell, MD and Lindsay, Joseph M., MD and Waksman, Ron, MD and Knouff, Christopher W., MD, PhD and Waterworth, Dawn M., PhD and Walker, Max C., BSc and Mooser, Vincent E., MD and Marrugat, Jaume, MD, PhD and Lucas, Gavin, PhD and Subirana, Isaac, MSc and Sala, Joan, MD and Ramos, Rafael, MD, PhD and Martinelli, Nicola, MD and Olivieri, Oliviero, MD and Trabetti, Elisabetta, PhD and Malerba, Giovanni, PhD and Pignatti, Pier Franco, MD and Guiducci, Candace, BS and Mirel, Daniel, PhD and Parkin, Melissa, BS and Hirschhorn, Joel N., MD, PhD and Asselta, Rosanna, PhD and Duga, Stefano, PhD and Musunuru, Kiran, MD, PhD, MPH and Daly, Mark J., PhD and Purcell, Shaun, PhD and Eifert, Sandra, MD and Braund, Peter S., MSc and Wright, Benjamin J., PhD and Balmforth, Anthony J., PhD and Ball, Stephen G., PhD and ... and Cardiogenics and Wellcome Trust Case Control and Myocardial Infarction Genet and Wellcome Trust Case Control Consortium and Myocardial Infarction Genetics Consortium and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and EpiHealth: Epidemiology for Health and Lund University and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2010, Volume 56, Issue 19, pp. 1552 - 1563
Objectives We sought to replicate the association between the kinesin-like protein 6 (KIF6) Trp719Arg polymorphism (rs20455), and clinical coronary artery... 
Cardiovascular | Internal Medicine | coronary artery disease | polymorphism | KIF6 | kinesin-like protein 6 | myocardial infarction | OR | single nucleotide polymorphism | CI | CAD | Abbreviations and Acronyms | HR | odds ratio | SNP | hazard ratio | confidence interval | MI | POPULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | RISK-FACTORS | GENOMEWIDE ASSOCIATION | GENOTYPE DATA | HEART-DISEASE | GENE VARIANTS | CHROMOSOME 9P21.3 | CARDIOVASCULAR-DISEASE | NONFATAL MYOCARDIAL-INFARCTION | HEALTH | Humans | Middle Aged | Risk Factors | Tryptophan - genetics | Male | Coronary Artery Disease - enzymology | Case-Control Studies | Internationality | Arginine - genetics | Coronary Artery Disease - genetics | Kinesin - genetics | Polymorphism, Single Nucleotide - genetics | Female | Coronary Artery Disease - epidemiology | Genome-Wide Association Study - methods | Hypertension | Medical colleges | Medical research | Genetic disorders | Environmental health | Chronic diseases | Family medicine | Coronary heart disease | Population genetics | Biometry | Anopheles | Medicine, Experimental | Genetic aspects | Diabetes | Cardiology | Public health | Medical informatics | Kinesin | Heart | Heart attacks | African Americans | Cardiovascular disease | Genomes | Proteins | Studies | Confidence intervals | Consortia | International organizations | Ischemia | Womens health | Atherosclerosis | Age | Hispanics | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | myocardial | Medicin och hälsovetenskap | infarction | Klinisk medicin
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2011, Volume 127, Issue 6, pp. 1360 - 1367.e6
Journal Article
Journal Article
by van der Valk, Ralf J.P., PhD and Duijts, Liesbeth, MD, PhD and Timpson, Nicolas J., MD, PhD and Salam, Muhammad T., MD, PhD and Standl, Marie, MSc and Curtin, John A., PhD and Genuneit, Jon, MD, MSc and Kerhof, Marjan, MD, PhD and Kreiner-Møller, Eskil, MD and Cáceres, Alejandro, MD, PhD and Gref, Anna, MSc and Liang, Liming L., MD, PhD and Taal, H. Rob, MD, PhD and Bouzigon, Emmanuelle, MD, PhD and Demenais, Florence, MD and Nadif, Rachel, PhD and Ober, Carole, PhD and Thompson, Emma E., PhD and Estrada, Karol, PhD and Hofman, Albert, MD, PhD and Uitterlinden, André G., PhD and van Duijn, Cornélia, PhD and Rivadeneira, Fernando, MD, PhD and Li, Xia, MS and Eckel, Sandrah P., PhD and Berhane, Kiros, PhD and Gauderman, W. James, MD, PhD and Granell, Raquel, PhD and Evans, David M., PhD and St Pourcain, Beate, PhD and McArdle, Wendy, PhD and Kemp, John P., MSc and Smith, George Davey, MD, PhD and Tiesler, Carla M.T., MSc and Flexeder, Claudia, MSc and Simpson, Angela, MD, PhD and Murray, Clare S., MD, PhD and Fuchs, Oliver, MD, PhD and Postma, Dirkje S., MD, PhD and Bønnelykke, Klaus, MD, PhD and Torrent, Maties, MD, PhD and Andersson, Martin, MD, PhD and Sleiman, Patrick, MD, PhD and Hakonarson, Hakon, MD, PhD and Cookson, William O., MD, PhD and Moffatt, Miriam F., PhD and Paternoster, Lavinia, PhD and Melén, Erik, MD, PhD and Sunyer, Jordi, MD, PhD and Bisgaard, Hans, MD, DMSci and Koppelman, Gerard H., MD, PhD and Ege, Markus, MD, PhD and Custovic, Adnan, MD, PhD and Heinrich, Joachim, PhD and Gilliland, Frank D., MD, PhD and Henderson, Alexander J., MD and Jaddoe, Vincent W.V and de Jongste, Johan C., MD, PhD and EAGLE Consortium and EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 134, Issue 1, pp. 46 - 55
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 138, Issue 2, pp. 544 - 550.e4
Background Genome-wide association studies have shown a pattern of rare copy number variations and single nucleotide polymorphisms in patients with common... 
Allergy and Immunology | IRF2BP2 | Common variable immunodeficiency | primary antibody deficiency | immunoglobulin | machine learning | GENE | ALLERGY | DISEASE | IMMUNE-DEFICIENCY | SUPPORT VECTOR MACHINE | IMMUNOLOGY | T-Lymphocyte Subsets - immunology | Common Variable Immunodeficiency - immunology | Humans | Middle Aged | Male | Common Variable Immunodeficiency - diagnosis | Exome | Young Adult | Cell Differentiation - genetics | Adult | B-Lymphocyte Subsets - immunology | Female | Nuclear Proteins - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Common Variable Immunodeficiency - genetics | Genotype | Immunophenotyping | Nuclear Proteins - metabolism | Carrier Proteins - genetics | Cell Differentiation - immunology | Immunoglobulin Isotypes - blood | Phenotype | Carrier Proteins - metabolism | B-Lymphocyte Subsets - metabolism | Pedigree | T-Lymphocyte Subsets - metabolism | Adolescent | Biomarkers | Family | Immunoglobulin Isotypes - immunology | Aged | High-Throughput Nucleotide Sequencing | Mutation | Allergy | Medical colleges | Communicable diseases | Genomics | Allergic reaction | Diseases | Algorithms | Genetic research | Immunological deficiency syndromes | Immunological deficiency syndromes in children | Children | Single nucleotide polymorphisms | Chromosomes | Genetic polymorphisms | Machine learning | Studies | Flow cytometry | Immunoglobulins | Lymphocytes | Genes | Classification | Genetic testing | Patients | Deoxyribonucleic acid--DNA
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 135, Issue 6, pp. 1569 - 1577
Background Common variable immunodeficiency (CVID) is characterized clinically by inadequate quantity and quality of serum immunoglobulins with increased... 
Allergy and Immunology | rare variants | immunogenetics | ITGAM | Immunodeficiency | genome-wide association study | SYSTEMIC-LUPUS-ERYTHEMATOSUS | COMPLEMENT RECEPTOR-3 | AMYOTROPHIC-LATERAL-SCLEROSIS | IGA DEFICIENCY | IMMUNOLOGY | ANTIBODY-DEFICIENCY SYNDROME | ALLERGY | AUTOIMMUNE-DISEASES | LEUKOCYTE ADHESION | NF-KAPPA-B | T-CELLS | GENOME-WIDE ASSOCIATION | Common Variable Immunodeficiency - immunology | Humans | Child, Preschool | Male | Genetic Loci | Case-Control Studies | RNA-Binding Protein FUS - immunology | Common Variable Immunodeficiency - diagnosis | CD11b Antigen - genetics | Adult | Female | B-Lymphocytes - pathology | B-Lymphocytes - metabolism | Promoter Regions, Genetic | Genetic Predisposition to Disease | CD11b Antigen - immunology | Common Variable Immunodeficiency - pathology | RNA-Binding Protein FUS - genetics | Common Variable Immunodeficiency - genetics | Linkage Disequilibrium | B-Lymphocytes - immunology | Enhancer Elements, Genetic | Chromosomes, Human, Pair 16 | Immunologic Memory | Polymorphism, Single Nucleotide | Cohort Studies | Computer science | Medical colleges | Immunological deficiency syndromes | Health aspects | Mortality | Risk factors | Studies | Immunology | Disease | Genes | Quality control | Principal components analysis | Genomes | Chromosomes | Patients | Inflammatory diseases | Meta-analysis | immunodeficiency
Journal Article