X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (33) 33
humans (23) 23
risk (18) 18
genomes (16) 16
article (13) 13
medical and health sciences (13) 13
medicin och hälsovetenskap (13) 13
cancer (12) 12
glioma (11) 11
risk factors (11) 11
variants (11) 11
female (10) 10
genetic predisposition to disease (10) 10
genome-wide association (10) 10
genome-wide association study (10) 10
male (10) 10
multidisciplinary sciences (10) 10
breast-cancer (9) 9
tumors (9) 9
clinical medicine (8) 8
colorectal neoplasms - genetics (8) 8
epidemiology (8) 8
genetic aspects (8) 8
klinisk medicin (8) 8
oncology (8) 8
basic medicine (7) 7
cancer and oncology (7) 7
cancer och onkologi (7) 7
central-nervous-system (7) 7
genetics & heredity (7) 7
glioblastoma (7) 7
medical genetics (7) 7
medicinsk genetik (7) 7
medicinska och farmaceutiska grundvetenskaper (7) 7
polymorphism, single nucleotide (7) 7
alleles (6) 6
case-control studies (6) 6
glioma - genetics (6) 6
life sciences (6) 6
metaanalysis (6) 6
middle aged (6) 6
susceptibility loci (6) 6
expression (5) 5
genetics (5) 5
mutation (5) 5
mutations (5) 5
single-nucleotide polymorphism (5) 5
susceptibility (5) 5
association (4) 4
brain neoplasms - genetics (4) 4
brain tumors (4) 4
colorectal cancer (4) 4
framework (4) 4
genetic research (4) 4
genome-wide association studies (4) 4
genotype (4) 4
germline mutations (4) 4
loci (4) 4
medical research (4) 4
medicine (4) 4
polymorphism, single nucleotide - genetics (4) 4
prognosis (4) 4
science (4) 4
abridged index medicus (3) 3
adult glioma (3) 3
bioaerosols (3) 3
biochemistry & molecular biology (3) 3
brain (3) 3
brain cancer (3) 3
brca2 protein - genetics (3) 3
colorectal carcinoma (3) 3
colorectal neoplasms (3) 3
common variation (3) 3
digestive system diseases (3) 3
disease (3) 3
disease susceptibility (3) 3
etiology (3) 3
european continental ancestry group - genetics (3) 3
genes (3) 3
genetic variance (3) 3
genomics (3) 3
genotype & phenotype (3) 3
health (3) 3
health risk assessment (3) 3
health sciences (3) 3
hälsovetenskaper (3) 3
lighting (3) 3
microsatellite instability (3) 3
neoplasms (3) 3
odds ratio (3) 3
polymorphism (3) 3
protein (3) 3
proteins (3) 3
research (3) 3
single nucleotide polymorphisms (3) 3
statistical analysis (3) 3
studies (3) 3
telomere length (3) 3
[sdv.can]life sciences [q-bio]/cancer (2) 2
acidemia type-ii (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Cancer Epidemiology Biomarkers and Prevention, ISSN 1055-9965, 04/2018, Volume 27, Issue 4, pp. 418 - 428
Since the first reports in 2009, genome-wide association studies (GWAS) have been successful in identifying germline variants associated with glioma... 
BREAST-CANCER | IDENTIFIES 5 | NERVOUS-SYSTEM | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | ONCOLOGY | ELECTRON-TRANSFER FLAVOPROTEIN | P53 GENE-MUTATIONS | ACIDEMIA TYPE-II | COLORECTAL-CANCER | GERMLINE MUTATIONS | CANCER SUSCEPTIBILITY LOCI | TELOMERE LENGTH | Glioma | Etiology | Biomarkers | Risk | Genomes | Epidemiology | Subgroups | Tumors | Cancer | Polymorphism
Journal Article
by Wang, Yufei and McKay, James D and Rafnar, Thorunn and Wang, Zhaoming and Timofeeva, Maria N and Broderick, Peter and Zong, Xuchen and Laplana, Marina and Wei, Yongyue and Han, Younghun and Lloyd, Amy and Delahaye-Sourdeix, Manon and Chubb, Daniel and Gaborieau, Valerie and Wheeler, William and Chatterjee, Nilanjan and Thorleifsson, Gudmar and Sulem, Patrick and Liu, Geoffrey and Kaaks, Rudolf and Henrion, Marc and Kinnersley, Ben and Vallée, Maxime and Lecalvez-Kelm, Florence and Stevens, Victoria L and Gapstur, Susan M and Chen, Wei V and Zaridze, David and Szeszenia-Dabrowska, Neonilia and Lissowska, Jolanta and Rudnai, Peter and Fabianova, Eleonora and Mates, Dana and Bencko, Vladimir and Foretova, Lenka and Janout, Vladimir and Krokan, Hans E and Gabrielsen, Maiken Elvestad and Skorpen, Frank and Vatten, Lars and Njølstad, Inger and Chen, Chu and Goodman, Gary and Benhamou, Simone and Vooder, Tonu and Välk, Kristjan and Nelis, Mari and Metspalu, Andres and Lener, Marcin and Lubiński, Jan and Johansson, Mattias and Vineis, Paolo and Agudo, Antonio and Clavel-Chapelon, Francoise and Bueno-De-Mesquita, H. Bas and Trichopoulos, Dimitrios and Khaw, Kay-Tee and Johansson, Mikael and Weiderpass, Elisabete and Tjønneland, Anne and Riboli, Elio and Lathrop, Mark and Scelo, Ghislaine and Albanes, Demetrius and Caporaso, Neil E and Ye, Yuanqing and Gu, Jian and Wu, Xifeng and Spitz, Margaret R and Dienemann, Hendrik and Rosenberger, Albert and Su, Li and Matakidou, Athena and Eisen, Timothy and Stefansson, Kari and Risch, Angela and Chanock, Stephen J and Christiani, David C and Hung, Rayjean J and Brennan, Paul and Landi, Maria Teresa and Houlston, Richard S and Amos, Christopher I and Medicinska fakulteten and Institutionen för strålningsvetenskaper and Onkologi and Umeå universitet
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 7, pp. 736 - 741
Journal Article
by Melin, Beatrice S and Barnholtz-Sloan, Jill S and Wrensch, Margaret R and Johansen, Christoffer and Il'yasova, Dora and Kinnersley, Ben and Ostrom, Quinn T and Labreche, Karim and Chen, Yanwen and Armstrong, Georgina and Liu, Yanhong and Eckel-Passow, Jeanette E and Decker, Paul A and Labussière, Marianne and Idbaih, Ahmed and Hoang-Xuan, Khe and Di Stefano, Anna-Luisa and Mokhtari, Karima and Delattre, Jean-Yves and Broderick, Peter and Galan, Pilar and Gousias, Konstantinos and Schramm, Johannes and Schoemaker, Minouk J and Fleming, Sarah J and Herms, Stefan and Heilmann, Stefanie and Nöthen, Markus M and Wichmann, Heinz-Erich and Schreiber, Stefan and Swerdlow, Anthony and Lathrop, Mark and Simon, Matthias and Sanson, Marc and Andersson, Ulrika and Rajaraman, Preetha and Chanock, Stephen and Linet, Martha and Wang, Zhaoming and Yeager, Meredith and Wiencke, John K and Hansen, Helen and McCoy, Lucie and Rice, Terri and Kosel, Matthew L and Sicotte, Hugues and Amos, Christopher I and Bernstein, Jonine L and Davis, Faith and Lachance, Dan and Lau, Ching and Merrell, Ryan T and Shildkraut, Joellen and Ali-Osman, Francis and Sadetzki, Siegal and Scheurer, Michael and Shete, Sanjay and Lai, Rose K and Claus, Elizabeth B and Olson, Sara H and Jenkins, Robert B and Houlston, Richard S and Bondy, Melissa L and Freeman, L.E.B and Koutros, S and Albanes, D and Visvanathan, K and Stevens, V.L and Henriksson, R and Michaud, D.S and Feychting, M and Ahlbom, A and Giles, G.G and Milne, R and McKean-Cowdin, R and Le Marchand, L and Stampfer, M and Ruder, A.M and Carreon, T and Hallmans, G and Zeleniuch-Jacquotte, A and Gaziano, J.M and Sesso, H.D and Purdue, M.P and White, E and Buring, J and GliomaScan Consortium and Medicinska fakulteten and Umeå universitet and Institutionen för strålningsvetenskaper
Nature Genetics, ISSN 1061-4036, 05/2017, Volume 49, Issue 5, pp. 789 - 794
Journal Article
Nature Communications, ISSN 2041-1723, 06/2016, Volume 7, Issue 1, p. 11883
Colorectal cancer (CRC) displays a complex pattern of inheritance. It is postulated that much of the missing heritability of CRC is enshrined in high-impact... 
METAANALYSIS | VARIANTS | GENE | MULTIDISCIPLINARY SCIENCES | GERMLINE MUTATIONS | ARCHITECTURE | FRAMEWORK | PREDISPOSE | EXPRESSION | POLE | ADENOMAS
Journal Article
Current Protocols in Human Genetics, ISSN 1934-8266, 07/2018, Volume 98, Issue 1, p. e63
Chromosome conformation capture (3C), coupled with next-generation sequencing (Hi-C), provides a means for deciphering not only the principles underlying... 
gene expression regulation | di-tags | promoter-enhancer contacts | Capture Hi-C (CHi-C)
Journal Article
Scientific Reports, ISSN 2045-2322, 05/2015, Volume 5, Issue 1, p. 10442
Journal Article
by Schmidt, Amand F and Holmes, Michael V and Preiss, David and Swerdlow, Daniel I and Denaxas, Spiros and Fatemifar, Ghazaleh and Faraway, Rupert and Finan, Chris and Valentine, Dennis and Fairhurst-Hunter, Zammy and Hartwig, Fernando Pires and Horta, Bernardo Lessa and Hypponen, Elina and Power, Christine and Moldovan, Max and van Iperen, Erik and Hovingh, Kees and Demuth, Ilja and Norman, Kristina and Steinhagen-Thiessen, Elisabeth and Demuth, Juri and Bertram, Lars and Lill, Christina M and Coassin, Stefan and Willeit, Johann and Kiechl, Stefan and Willeit, Karin and Mason, Dan and Wright, John and Morris, Richard and Wanamethee, Goya and Whincup, Peter and Ben-Shlomo, Yoav and McLachlan, Stela and Price, Jackie F and Kivimaki, Mika and Welch, Catherine and Sanchez-Galvez, Adelaida and Marques-Vidal, Pedro and Nicolaides, Andrew and Panayiotou, Andrie G and Onland-Moret, N. Charlotte and van der Schouw, Yvonne T and Matullo, Giuseppe and Fiorito, Giovanni and Guarrera, Simonetta and Sacerdote, Carlotta and Wareham, Nicholas J and Langenberg, Claudia and Scott, Robert A and Luan, Jian’an and Bobak, Martin and Malyutina, Sofia and Pająk, Andrzej and Kubinova, Ruzena and Tamosiunas, Abdonas and Pikhart, Hynek and Grarup, Niels and Pedersen, Oluf and Hansen, Torben and Linneberg, Allan and Jess, Tine and Cooper, Jackie and Humphries, Steve E and Brilliant, Murray and Kitchner, Terrie and Hakonarson, Hakon and Carrell, David S and McCarty, Catherine A and Lester, Kirchner H and Larson, Eric B and Crosslin, David R and de Andrade, Mariza and Roden, Dan M and Denny, Joshua C and Carty, Cara and Hancock, Stephen and Attia, John and Holliday, Elizabeth and Scott, Rodney and Schofield, Peter and O’Donnell, Martin and Yusuf, Salim and Chong, Michael and Pare, Guillaume and van der Harst, Pim and Said, M. Abdullah and Eppinga, Ruben N and Verweij, Niek and Snieder, Harold and Christen, Tim and Mook-Kanamori, D. O and Gustafsson, Stefan and Lind, Lars and Ingelsson, Erik and Pazoki, Raha and Franco, Oscar and Hofman, Albert and Uitterlinden, Andre and Dehghan, Abbas and ... and the ICBP Consortium and the METASTROKE Consortium of the ISGC and Lifelines Cohort authors
BMC Cardiovascular Disorders, ISSN 1471-2261, 12/2019, Volume 19, Issue 1, pp. 1 - 10
Abstract Background We characterised the phenotypic consequence of genetic variation at the PCSK9 locus and compared findings with recent trials of... 
Genetic association studies | LDL-cholesterol | Phenome-wide association scan | Mendelian randomisation
Journal Article