X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (118) 118
index medicus (90) 90
genetics & heredity (63) 63
male (57) 57
female (56) 56
genotype (47) 47
polymorphism, single nucleotide (45) 45
lung cancer (41) 41
lung neoplasms - genetics (40) 40
genetic predisposition to disease (39) 39
genome-wide association study (39) 39
middle aged (38) 38
genome-wide association (33) 33
public, environmental & occupational health (33) 33
risk (32) 32
risk factors (32) 32
adult (31) 31
cancer (31) 31
genomics (31) 31
case-control studies (30) 30
phenotype (30) 30
oncology (29) 29
article (28) 28
genetics (28) 28
association (24) 24
genes (23) 23
genetic aspects (23) 23
smoking (23) 23
aged (22) 22
genomes (22) 22
epidemiology (21) 21
research (21) 21
genetic research (20) 20
variants (20) 20
linkage disequilibrium (19) 19
models, genetic (18) 18
analysis (17) 17
genetic variation (16) 16
lung neoplasms - epidemiology (16) 16
susceptibility locus (16) 16
medicine (15) 15
polymorphism, single nucleotide - genetics (15) 15
single nucleotide polymorphisms (15) 15
alleles (14) 14
medical and health sciences (14) 14
medicin och hälsovetenskap (14) 14
single-nucleotide polymorphism (14) 14
susceptibility loci (14) 14
adolescent (13) 13
blood pressure - genetics (13) 13
gene frequency (13) 13
genetic association studies (13) 13
health aspects (13) 13
models (13) 13
pedigree (13) 13
gene expression (12) 12
genetic linkage (12) 12
metaanalysis (12) 12
proceedings (12) 12
biochemistry & molecular biology (11) 11
european continental ancestry group - genetics (11) 11
linkage (11) 11
lung neoplasms - pathology (11) 11
odds ratio (11) 11
adenocarcinoma (10) 10
age of onset (10) 10
aged, 80 and over (10) 10
animals (10) 10
clinical medicine (10) 10
genetic predisposition to disease - genetics (10) 10
genome-wide association study - methods (10) 10
klinisk medicin (10) 10
multidisciplinary sciences (10) 10
polymorphism (10) 10
research article (10) 10
science (10) 10
studies (10) 10
young adult (10) 10
breast-cancer (9) 9
cancer and oncology (9) 9
cancer och onkologi (9) 9
expression (9) 9
genotype & phenotype (9) 9
haplotypes (9) 9
high-throughput nucleotide sequencing (9) 9
lung neoplasms - etiology (9) 9
lung-cancer (9) 9
oncology, experimental (9) 9
polymorphism, genetic (9) 9
population (9) 9
quantitative trait loci (9) 9
sequence analysis, dna (9) 9
chromosome mapping (8) 8
gene-environment interaction (8) 8
genetic markers (8) 8
health risks (8) 8
human genetics (8) 8
immunology (8) 8
mathematical & computational biology (8) 8
mice (8) 8
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


Journal of the National Cancer Institute, ISSN 0027-8874, 2010, Volume 102, Issue 13, pp. 959 - 971
BACKGROUND: Genome-wide association studies have identified three chromosomal regions at 15q25, 5p15, and 6p21 as being associated with the risk of lung... 
Smoking - adverse effects | Japan - epidemiology | Lung Neoplasms - ethnology | Tobacco Use Disorder - ethnology | United States - epidemiology | Carcinoma, Small Cell - genetics | Carcinoma, Squamous Cell - genetics | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Male | Carcinoma, Large Cell - ethnology | Case-Control Studies | Carcinoma, Squamous Cell - ethnology | Canada - epidemiology | Carcinoma, Small Cell - ethnology | Lung Neoplasms - etiology | Aged, 80 and over | Adult | Female | Tobacco Use Disorder - genetics | Adenocarcinoma - genetics | Carcinoma, Large Cell - genetics | Adenocarcinoma - ethnology | Korea - epidemiology | Odds Ratio | Quality Control | Lung Neoplasms - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Genetic Association Studies | Risk Assessment | Europe | Gene Frequency | Risk Factors | Linkage Disequilibrium - genetics | Genotype | Smoking - genetics | International Cooperation | Chromosomes, Human, Pair 6 | Chromosomes, Human, Pair 5 | Homozygote | Singapore - epidemiology | Chromosomes, Human, Pair 15 | Aged | Polymorphism, Single Nucleotide | NICOTINE DEPENDENCE | POLYMORPHISMS | ONCOLOGY | PROGNOSTIC MARKER | SEQUENCE VARIANTS | RISK | GENETIC-VARIANTS | SMOKING | DNA-REPAIR | GENOME-WIDE ASSOCIATION | TELOMERE LENGTH | Quantitative trait loci | Genetic aspects | Research | Genetic susceptibility | Lung cancer | Risk factors | Genotype & phenotype | Chromosomes | Genomics
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2009, Volume 85, Issue 5, pp. 679 - 691
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2008, Volume 3, Issue 7, pp. e2622 - e2622
Journal Article
by Amos, Christopher I and Dennis, Joe and Wang, Zhaoming and Byun, Jinyoung and Schumacher, Fredrick R and Gayther, Simon A and Casey, Graham and Hunter, David J and Sellers, Thomas A and Gruber, Stephen B and Dunning, Alison M and Michailidou, Kyriaki and Fachal, Laura and Doheny, Kimberly and Spurdle, Amanda B and Li, Yafang and Xiao, Xiangjun and Romm, Jane and Pugh, Elizabeth and Coetzee, Gerhard A and Hazelett, Dennis J and Bojesen, Stig E and Caga-Anan, Charlisse and Haiman, Christopher A and Kamal, Ahsan and Luccarini, Craig and Tessier, Daniel and Vincent, Daniel and Bacot, Francois and Van Den Berg, David J and Nelson, Stefanie and Demetriades, Stephen and Goldgar, David E and Couch, Fergus J and Forman, Judith L and Giles, Graham G and Conti, David V and Bickeboller, Heike and Risch, Angela and Waldenberger, Melanie and Bruske-Hohlfeld, Irene and Hicks, Belynda D and Ling, Hua and McGuffog, Lesley and Lee, Andrew and Kuchenbaecker, Karoline and Soucy, Penny and Manz, Judith and Cunningham, Julie M and Butterbach, Katja and Kote-Jarai, Zsofia and Kraft, Peter and FitzGerald, Liesel and Lindstrom, Sara and Adams, Marcia and McKay, James D and Phelan, Catherine M and Benlloch, Sara and Kelemen, Linda E and Brennan, Paul and Riggan, Marjorie and O'Mara, Tracy A and Shen, Hongbing and Shi, Yongyong and Thompson, Deborah J and Goodman, Marc T and Nielsen, Sune F and Berchuck, Andrew and Laboissiere, Sylvie and Schmit, Stephanie L and Shelford, Tameka and Edlund, Christopher K and Taylor, Jack A and Field, John K and Park, Sue K and Offit, Kenneth and Thomassen, Mads and Schmutzler, Rita and Ottini, Laura and Hung, Rayjean J and Marchini, Jonathan and Olama, Ali Amin Al and Peters, Ulrike and Eeles, Rosalind A and Seldin, Michael F and Gillanders, Elizabeth and Seminara, Daniela and Antoniou, Antonis C and Pharoah, Paul D.P and Chenevix-Trench, Georgia and Chanock, Stephen J and Simard, Jacques and Easton, Douglas F
Cancer Epidemiology Biomarkers and Prevention, ISSN 1055-9965, 01/2017, Volume 26, Issue 1, pp. 126 - 135
Journal Article
Human Heredity, ISSN 0001-5652, 06/2018, Volume 83, Issue 1, p. 26
The OncoArray by Illumina includes approximately 570K SNPs with a genome wide backbone of 275K tag SNPs. Additional SNPs on the chip associated with five... 
Disequilibrium | Lung cancer | Linkage disequilibrium | Oncology | Genomes | Single-nucleotide polymorphism | Inflammation | Colon cancer | Rectum | Colon | Gene mapping | Prostate | Prostate cancer
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2012, Volume 21, Issue 22, pp. 4980 - 4995
Journal Article
2007, Statistik und ihre Anwendungen, ISBN 9783540256168
Die speziellen Strukturen des menschlichen Genoms und die Regeln der Vererbung erfordern spezielle statistische Methoden zur Analyse genetischer und... 
Medicine | Epidemiology | Statistics | Human genetics
Web Resource
EMBO Molecular Medicine, ISSN 1757-4676, 11/2015, Volume 7, Issue 11, pp. 1480 - 1502
The MHC class I chain‐related molecule A (MICA) is a highly polymorphic ligand for the activating natural killer (NK)‐cell receptor NKG2D. A single nucleotide... 
graft‐versus‐host disease | NK cells | cytotoxic T cells | single nucleotide polymorphism | NK‐cell receptors | Graft-versus-host disease | Single nucleotide polymorphism | NK-cell receptors | Cytotoxic T cells | CHRONIC MYELOGENOUS LEUKEMIA | MEDICINE, RESEARCH & EXPERIMENTAL | LIGAND EXPRESSION | I-RELATED CHAIN | BONE-MARROW-TRANSPLANTATION | NATURAL CYTOTOXICITY | VERSUS-HOST-DISEASE | CD8(+) T-CELLS | ACTIVATING IMMUNORECEPTOR NKG2D | CHAIN-RELATED GENE | graft-versus-host disease | Humans | Middle Aged | Child, Preschool | Infant | Male | Mutation, Missense | Young Adult | Graft vs Host Disease - mortality | NK Cell Lectin-Like Receptor Subfamily K - metabolism | Aged, 80 and over | Killer Cells, Natural - immunology | Adult | Female | Child | Signal Transduction | Interferon-gamma - secretion | Mutant Proteins - genetics | Hematopoietic Stem Cell Transplantation | Treatment Outcome | Histocompatibility Antigens Class I - genetics | Graft vs Host Disease - pathology | Adolescent | Survival Analysis | Aged | CD8-Positive T-Lymphocytes - immunology | Cytotoxicity, Immunologic | Transplantation | Single nucleotide polymorphisms | Biological response modifiers | T cells | Hematopoietic stem cells | Stem cells | Transplants & implants | Disease | CD8 antigen | Leukemia | Stem cell transplantation | Cytotoxicity | Lymphocytes T | Dimorphism | Single-nucleotide polymorphism | Gene polymorphism | Cell surface | Genotype & phenotype | Lymphocytes | Tumor necrosis factor-TNF | Natural killer cells | Cell survival | Hematology | Mortality | Methionine | Hemopoiesis | Major histocompatibility complex | Globulins | Valine | Ligands | Lymphomas | Interferon | Polymorphism
Journal Article
by Khankari, Nikhil K and Shu, Xiao Ou and Wen, Wanqing and Kraft, Peter and Lindström, Sara and Peters, Ulrike and Schildkraut, Joellen and Schumacher, Freick and Bofetta, Paolo and Risch, Angela and Bickeböller, Heike and Amos, Christopher I and Easton, Douglas and Eeles, Rosalind A and Gruber, Stephen B and Haiman, Christopher A and Hunter, David J and Chanock, Stephen J and Pierce, Brandon L and Zheng, Wei and Blalock, Kena and Campbell, Peter T and Casey, Graham and Conti, David V and Edlund, Christopher K and Figueiredo, Jane and James Gauderman, W and Gong, Jian and Green, Roger C and Harju, John F and Harrison, Tabitha A and Jacobs, Eric J and Jenkins, Mark A and Jiao, Shuo and Li, Li and Lin, Yi and Manion, Frank J and Moreno, Victor and Mukherjee, Bhramar and Raskin, Leon and Schumacher, Freick R and Seminara, Daniela and Severi, Gianluca and Stenzel, Stephanie L and Thomas, Duncan C and Hopper, John L and Southey, Melissa C and Makalic, Enes and Schmidt, Daniel F and Fletcher, Olivia and Peto, Julian and Gibson, Lorna and dos Santos Silva, Isabel and Ahsan, Habib and Whittemore, Alice and Waisfisz, Quinten and Meijers-Heijboer, Hanne and Adank, Muriel and van der Luijt, Rob B and Uitterlinden, Ane G and Hofman, Albert and Meindl, Alfons and Schmutzler, Rita K and Müller-Myhsok, Bertram and Lichtner, Peter and Nevanlinna, Heli and Muranen, Taru A and Aittomäki, Kristiina and Blomqvist, Carl and Chang-Claude, Jenny and Hein, Rebecca and Dahmen, Norbert and Beckman, Lars and Crisponi, Laura and Hall, Per and Czene, Kamila and Irwanto, Astrid and Liu, Jianjun and Easton, Douglas F and Turnbull, Clare and Rahman, Nazneen and Eeles, Rosalind and Kote-Jarai, Zsofia and Muir, Kenneth and Giles, Graham and Neal, David and Donovan, Jenny L and Hamdy, Freddie C and Wiklund, Freik and Gronberg, Henrik and Haiman, Christopher and Schumacher, Fred and Travis, Ruth and Riboli, Elio and Hunter, David and Gapstur, Susan and Berndt, Sonja and Chanock, Stephen and Han, Younghun and Su, Li and ... and Colorectal Transdisciplinary Study and Elucidating Loci Involved Prostate and Transdisciplinary Res Canc Lung TR and Discovery Biol Risk Inherited Vari and Colorectal Transdisciplinary Study (CORECT) and Elucidating Loci Involved in Prostate Cancer Susceptibility (ELLIPSE) and Transdisciplinary Research in Cancer of the Lung (TRICL) and Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) and on behalf of the Colorectal Transdisciplinary Study (CORECT)
PLoS medicine, ISSN 1549-1277, 09/2016, Volume 13, Issue 9, p. e1002118
Journal Article