X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (13330) 13330
Book Chapter (45) 45
Dissertation (21) 21
Conference Proceeding (12) 12
Book / eBook (6) 6
Publication (5) 5
Magazine Article (4) 4
Government Document (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (9641) 9641
dna mutational analysis (8430) 8430
mutation (5928) 5928
female (5154) 5154
male (4772) 4772
genetic aspects (3180) 3180
adult (2848) 2848
middle aged (2626) 2626
genetics & heredity (2446) 2446
animals (2310) 2310
molecular sequence data (2148) 2148
analysis (1911) 1911
research (1909) 1909
biochemistry & molecular biology (1880) 1880
aged (1845) 1845
genes (1831) 1831
cancer (1827) 1827
oncology (1790) 1790
base sequence (1782) 1782
phenotype (1680) 1680
mutational analysis (1603) 1603
proteins (1538) 1538
gene (1524) 1524
dna mutational analysis - methods (1494) 1494
expression (1397) 1397
gene mutations (1388) 1388
genetics (1357) 1357
genotype (1330) 1330
child (1322) 1322
amino acid sequence (1321) 1321
adolescent (1304) 1304
mutations (1273) 1273
research article (1229) 1229
pedigree (1220) 1220
dna (1137) 1137
multidisciplinary sciences (1123) 1123
tumors (1123) 1123
cell biology (1085) 1085
genetic research (1071) 1071
genomics (1070) 1070
genetic predisposition to disease (1066) 1066
mutation - genetics (1037) 1037
polymerase chain reaction (1036) 1036
pathology (1032) 1032
deoxyribonucleic acid--dna (1004) 1004
genomes (1003) 1003
gene expression (974) 974
mice (932) 932
identification (919) 919
child, preschool (895) 895
neurosciences (822) 822
young adult (819) 819
aged, 80 and over (815) 815
protein (792) 792
microbiology (775) 775
risk factors (767) 767
clinical neurology (766) 766
medicine (750) 750
alleles (746) 746
diagnosis (732) 732
physiological aspects (728) 728
health aspects (714) 714
biology (694) 694
disease (692) 692
genetic testing (682) 682
models, molecular (656) 656
infant (654) 654
mutation, missense (653) 653
evolution (642) 642
point mutation (642) 642
prognosis (634) 634
protein binding (622) 622
biotechnology & applied microbiology (619) 619
gene frequency (618) 618
life sciences (610) 610
polymorphism, single nucleotide (608) 608
immunohistochemistry (596) 596
science (579) 579
medicine & public health (573) 573
mutagenesis (569) 569
patients (549) 549
hematology (533) 533
escherichia-coli (530) 530
exons (519) 519
cell line (515) 515
studies (513) 513
binding sites (494) 494
virology (492) 492
care and treatment (485) 485
mutational processes (482) 482
breast cancer (480) 480
signal transduction (478) 478
molecular biology (469) 469
dna - genetics (466) 466
sequence analysis, dna (465) 465
case-control studies (463) 463
immunology (463) 463
genetic association studies (461) 461
neoplasms - genetics (460) 460
enzymes (459) 459
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (13347) 13347
Japanese (43) 43
German (37) 37
French (12) 12
Chinese (11) 11
Russian (7) 7
Polish (6) 6
Spanish (4) 4
Dutch (3) 3
Czech (2) 2
Hungarian (1) 1
Korean (1) 1
Norwegian (1) 1
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Alexandrov, Ludmil B and Nik-Zainal, Serena and Wedge, David C and Aparicio, Samuel A. J. R and Behjati, Sam and Biankin, Andrew V and Bignell, Graham R and Bolli, Niccolò and Borg, Ake and Børresen-Dale, Anne-Lise and Boyault, Sandrine and Burkhardt, Birgit and Butler, Adam P and Caldas, Carlos and Davies, Helen R and Desmedt, Christine and Eils, Roland and Eyfjörd, Jórunn Erla and Foekens, John A and Greaves, Mel and Hosoda, Fumie and Hutter, Barbara and Ilicic, Tomislav and Imbeaud, Sandrine and Imielinski, Marcin and Jäger, Natalie and Jones, David T. W and Jones, David and Knappskog, Stian and Kool, Marcel and Lakhani, Sunil R and López-Otín, Carlos and Martin, Sancha and Munshi, Nikhil C and Nakamura, Hiromi and Northcott, Paul A and Pajic, Marina and Papaemmanuil, Elli and Paradiso, Angelo and Pearson, John V and Puente, Xose S and Raine, Keiran and Ramakrishna, Manasa and Richardson, Andrea L and Richter, Julia and Rosenstiel, Philip and Schlesner, Matthias and Schumacher, Ton N and Span, Paul N and Teague, Jon W and Totoki, Yasushi and Tutt, Andrew N. J and Valdés-Mas, Rafael and van Buuren, Marit M and van ’t Veer, Laura and Vincent-Salomon, Anne and Waddell, Nicola and Yates, Lucy R and Zucman-Rossi, Jessica and Andrew Futreal, P and McDermott, Ultan and Lichter, Peter and Meyerson, Matthew and Grimmond, Sean M and Siebert, Reiner and Campo, Elías and Shibata, Tatsuhiro and Pfister, Stefan M and Campbell, Peter J and Stratton, Michael R and ICGC MMML-Seq Consortium and ICGC PedBrain and ICGC Breast Cancer Consortium and Australian Pancreatic Cancer Genome Initiative and ICGC Breast Canc Consortium and Australian Pancreatic Canc Genome
Nature (London), ISSN 1476-4687, 2013, Volume 500, Issue 7463, pp. 415 - 421
Journal Article
Cell (Cambridge), ISSN 0092-8674, 05/2012, Volume 149, Issue 5, pp. 979 - 993
Journal Article
Genome medicine, ISSN 1756-994X, 2018, Volume 10, Issue 1, pp. 33 - 11
Journal Article
Nature (London), ISSN 1476-4687, 2012, Volume 486, Issue 7403, pp. 400 - 404
Journal Article
Science translational medicine, ISSN 1946-6242, 2015, Volume 7, Issue 283, pp. 283ra54 - 283ra54
Journal Article
Nature genetics, ISSN 1546-1718, 2018, Volume 50, Issue 10, pp. 1381 - 1387
Journal Article
Genome medicine, ISSN 1756-994X, 04/2018, Volume 10, Issue 1
BACKGROUND: Base substitution catalogues represent historical records of mutational processes that have been active in a cell... 
Base substitutions | Mutational processes | Somatic mutations | Mutational signatures | Replicative strand bias | Transcriptional strand bias
Journal Article
The Journal of Pathology, ISSN 0022-3417, 05/2014, Volume 233, Issue 1, pp. 39 - 50
Journal Article