scholarly journals Oncogene-induced replication stress preferentially targets common fragile sites in preneoplastic lesions. A genome-wide study

Oncogene ◽  
2007 ◽  
Vol 27 (23) ◽  
pp. 3256-3264 ◽  
Author(s):  
P K Tsantoulis ◽  
A Kotsinas ◽  
P P Sfikakis ◽  
K Evangelou ◽  
M Sideridou ◽  
...  
Keyword(s):  
Replication Stress ◽  
Fragile Sites ◽  
Preneoplastic Lesions ◽  
Common Fragile Sites ◽  
Genome Wide ◽  
A Genome ◽  
Genome Wide Study

scholarly journals Corrigendum: A genome-wide analysis of common fragile sites: What features determine chromosomal instability in the human genome?

2016 ◽  
Vol 26 (10) ◽  
pp. 1451-1451
Author(s):  
Arkarachai Fungtammasan ◽  
Erin Walsh ◽  
Francesca Chiaromonte ◽  
Kristin A. Eckert ◽  
Kateryna D. Makova
Keyword(s):  
Human Genome ◽  
Chromosomal Instability ◽  
Fragile Sites ◽  
Common Fragile Sites ◽  
Genome Wide Analysis ◽  
Genome Wide ◽  
A Genome

scholarly journals A genome-wide analysis of common fragile sites: What features determine chromosomal instability in the human genome?

2012 ◽  
Vol 22 (6) ◽  
pp. 993-1005 ◽  
Author(s):  
Arkarachai Fungtammasan ◽  
Erin Walsh ◽  
Francesca Chiaromonte ◽  
Kristin A. Eckert ◽  
Kateryna D. Makova
Keyword(s):  
Human Genome ◽  
Chromosomal Instability ◽  
Fragile Sites ◽  
Common Fragile Sites ◽  
Genome Wide Analysis ◽  
Genome Wide ◽  
A Genome

scholarly journals Genome-wide study of methotrexate clearance replicates SLCO1B1

Blood ◽  
2013 ◽  
Vol 121 (6) ◽  
pp. 898-904 ◽  
Author(s):  
Laura B. Ramsey ◽  
John C. Panetta ◽  
Colton Smith ◽  
Wenjian Yang ◽  
Yiping Fan ◽  
...  
Keyword(s):  
Genetic Variations ◽  
Genome Wide ◽  
A Genome ◽  
Key Points ◽  
Genome Wide Study

Key Points A genome-wide study of the association of over 5 million SNPs with methotrexate clearance in 1279 patients treated with HDMTX in multicenter COG trials 9904 and 9905. We replicated the finding that inherited variations in SLCO1B1 are the most important genetic variations influencing methotrexate clearance.

scholarly journals A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

BMC Genetics ◽  
2014 ◽  
Vol 15 (1) ◽  
pp. 24 ◽  
Author(s):  
Samuel G Younkin ◽  
Robert B Scharpf ◽  
Holger Schwender ◽  
Margaret M Parker ◽  
Alan F Scott ◽  
...  
Keyword(s):  
Cleft Lip ◽  
De Novo ◽  
Candidate Locus ◽  
Genome Wide ◽  
A Genome ◽  
Cleft Lip Palate ◽  
Genome Wide Study

scholarly journals Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome

2011 ◽  
Vol 12 (1) ◽  
Author(s):  
Thomas M Morgan ◽  
John A House ◽  
Sharon Cresci ◽  
Philip Jones ◽  
Hooman Allayee ◽  
...  
Keyword(s):  
Acute Coronary Syndrome ◽  
Coronary Syndrome ◽  
Genome Wide ◽  
A Genome ◽  
Genome Wide Study

scholarly journals A Genome-Wide Study of Cytogenetic Changes in Colorectal Cancer Using SNP Microarrays: Opportunities for Future Personalized Treatment

PLoS ONE ◽  
2012 ◽  
Vol 7 (2) ◽  
pp. e31968 ◽  
Author(s):  
Farzana Jasmine ◽  
Ronald Rahaman ◽  
Charlotte Dodsworth ◽  
Shantanu Roy ◽  
Rupash Paul ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Personalized Treatment ◽  
Genome Wide ◽  
A Genome ◽  
Snp Microarrays ◽  
Cytogenetic Changes ◽  
Genome Wide Study
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