SNP500V
HUMAN VARIATION PANEL
Description:
SNP500CANCER RESOURCE OF THE CANCER GENOME ANATOMY PROJECT IN THE NATIONAL CANCER INSTITUTE
Aliquot Size:
10 µg each
Sex:
Males: 42 Females: 68
| Talal AH, Ding Y, Venuto CS, Chakan LM, McLeod A, Dharia A, Morse GD, Brown LS, Markatou M, Kharasch ED, Toward precision prescribing for methadone: Determinants of methadone deposition PloS one15:e0231467 2019 |
| PubMed ID: 32302325 |
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| Huang CR, Schneider AM, Lu Y, Niranjan T, Shen P, Robinson MA, Steranka JP, Valle D, Civin CI, Wang T, Wheelan SJ, Ji H, Boeke JD, Burns KH, Mobile interspersed repeats are major structural variants in the human genome Cell141:1171-82 2010 |
| PubMed ID: 20602999 |
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| Canova C, Hashibe M, Simonato L, Nelis M, Metspalu A, Lagiou P, Trichopoulos D, Ahrens W, Pigeot I, Merletti F, Richiardi L, Talamini R, Barzan L, Macfarlane GJ, Macfarlane TV, Holcátová I, Bencko V, Benhamou S, Bouchardy C, Kjaerheim K, Lowry R, Agudo A, Castellsagué X, Conway DI, McKinney PA, Znaor A, McCartan BE, Healy CM, Marron M, Brennan P, Genetic associations of 115 polymorphisms with cancers of the upper aerodigestive tract across 10 European countries: the ARCAGE project Cancer research69:2956-65 2009 |
| PubMed ID: 19339270 |
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| Calado RT, Graf SA, Wilkerson KL, Kajigaya S, Ancliff PJ, Dror Y, Chanock SJ, Lansdorp PM, Young NS, Mutations in the SBDS gene in acquired aplastic anemia mutation69:2956-65 2007 |
| PubMed ID: 17478638 |
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| Fredman D, Sawyer SL, Strömqvist L, Mottagui-Tabar S, Kidd KK, Wahlestedt C, Chanock SJ, Brookes AJ, Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection Human mutation27:173-86 2006 |
| PubMed ID: 16429399 |
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| Pachkowski BF, Winkel S, Kubota Y, Swenberg JA, Millikan RC, Nakamura J, XRCC1 genotype and breast cancer: functional studies and epidemiologic data show interactions between XRCC1 codon 280 His and smoking Cancer research66:2860-8 2006 |
| PubMed ID: 16510609 |
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| Packer BR, Yeager M, Burdett L, Welch R, Beerman M, Qi L, Sicotte H, Staats B, Acharya M, Crenshaw A, Eckert A, Puri V, Gerhard DS, Chanock SJ, SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes. Nucleic Acids Res34(Database issue:D617-21 2006 |
| PubMed ID: 16381944 |
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| Hughes AL, Packer B, Welch R, Bergen AW, Chanock SJ, Yeager M, Effects of natural selection on interpopulation divergence at polymorphic sites in human protein-coding Loci Genetics170:1181-7 2005 |
| PubMed ID: 15911586 |
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| Hughes AL, Packer B, Welch R, Chanock SJ, Yeager M, High level of functional polymorphism indicates a unique role of natural selection at human immune system loci Immunogenetics57:821-7 2005 |
| PubMed ID: 16261383 |
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| Lightfoot TJ, Skibola CF, Willett EV, Skibola DR, Allan JM, Coppede F, Adamson PJ, Morgan GJ, Roman E, Smith MT, Risk of non-Hodgkin lymphoma associated with polymorphisms in folate-metabolizing genes Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology14:2999-3003 2005 |
| PubMed ID: 16365025 |
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| Millikan RC, Player JS, Decotret AR, Tse CK, Keku T, Polymorphisms in DNA repair genes, medical exposure to ionizing radiation, and breast cancer risk Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology14:2326-34 2005 |
| PubMed ID: 16214912 |
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| Yamaguchi H, Calado RT, Ly H, Kajigaya S, Baerlocher GM, Chanock SJ, Lansdorp PM, Young NS, Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. N Engl J Med352(14):1413-24 2005 |
| PubMed ID: 15814878 |
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| Kamangar F, Abnet CC, Hutchinson AA, Newschaffer CJ, Helzlsouer K, Shugart YY, Pietinen P, Dawsey SM, Albanes D, Virtamo J, Taylor PR, Polymorphisms in inflammation-related genes and risk of gastric cancer (Finland) Cancer causes & control : CCC17:117-25 2004 |
| PubMed ID: 16411061 |
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| Lei B, Morris DP, Smith MP, Svetkey LP, Newman MF, Rotter JI, Buchanan TA, Beckstrom-Sternberg SM, Green ED, Schwinn DA, Novel human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function Naunyn-Schmiedeberg's archives of pharmacology371:229-39 2004 |
| PubMed ID: 15900517 |
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| Mosse YP, Laudenslager M, Khazi D, Carlisle AJ, Winter CL, Rappaport E, Maris JM, Germline PHOX2B mutation in hereditary neuroblastoma. Am J Hum Genet75(4):727-30 2004 |
| PubMed ID: 15338462 |
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| Packer BR, Yeager M, Staats B, Welch R, Crenshaw A, Kiley M, Eckert A, Beerman M, Miller E, Bergen A, Rothman N, Strausberg R, Chanock SJ, SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes. Nucleic Acids Res32:D528-32 2004 |
| PubMed ID: 14681474 |
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| Landi S, Gemignani F, Gioia-Patricola L, Chabrier A, Canzian F, Evaluation of a microarray for genotyping polymorphisms related to xenobiotic metabolism and DNA repair. Biotechniques35(4):816-20, 822, 824-7 2003 |
| PubMed ID: 14579748 |
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