| Year |
Citation |
Score |
| 2015 |
Pu X, Ajani JA, Gu J, Gu X, Ye Y, Wu X. Abstract 5587: Personalized risk prediction tool for esophageal adenocarcinoma in Caucasian population Cancer Research. 75: 5587-5587. DOI: 10.1158/1538-7445.Am2015-5587 |
0.343 |
|
| 2009 |
Shete S, Hosking FJ, Robertson LB, Dobbins SE, Sanson M, Malmer B, Simon M, Marie Y, Boisselier B, Delattre JY, Hoang-Xuan K, El Hallani S, Idbaih A, Zelenika D, Andersson U, ... ... Gu X, et al. Genome-wide association study identifies five susceptibility loci for glioma. Nature Genetics. 41: 899-904. PMID 19578367 DOI: 10.1038/Ng.407 |
0.37 |
|
| 2009 |
Hirschfield GM, Liu X, Xu C, Lu Y, Xie G, Lu Y, Gu X, Walker EJ, Jing K, Juran BD, Mason AL, Myers RP, Peltekian KM, Ghent CN, Coltescu C, et al. Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants. The New England Journal of Medicine. 360: 2544-55. PMID 19458352 DOI: 10.1056/Nejmoa0810440 |
0.366 |
|
| 2009 |
Gu X, Frankowski RF, Rosner GL, Relling M, Peng B, Amos CI. A modified forward multiple regression in high-density genome-wide association studies for complex traits. Genetic Epidemiology. 33: 518-25. PMID 19365845 DOI: 10.1002/Gepi.20404 |
0.552 |
|
| 2008 |
Wang Y, Broderick P, Webb E, Wu X, Vijayakrishnan J, Matakidou A, Qureshi M, Dong Q, Gu X, Chen WV, Spitz MR, Eisen T, Amos CI, Houlston RS. Common 5p15.33 and 6p21.33 variants influence lung cancer risk. Nature Genetics. 40: 1407-9. PMID 18978787 DOI: 10.1038/Ng.273 |
0.373 |
|
| 2008 |
Amos CI, Wu X, Broderick P, Gorlov IP, Gu J, Eisen T, Dong Q, Zhang Q, Gu X, Vijayakrishnan J, Sullivan K, Matakidou A, Wang Y, Mills G, Doheny K, et al. Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nature Genetics. 40: 616-22. PMID 18385676 DOI: 10.1038/Ng.109 |
0.382 |
|
| 2007 |
Criswell LA, Chen WV, Jawaheer D, Lum RF, Wener MH, Gu X, Gregersen PK, Amos CI. Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits. Arthritis and Rheumatism. 56: 58-68. PMID 17195208 DOI: 10.1002/Art.22325 |
0.324 |
|
| 2006 |
Jones JS, Amos CI, Pande M, Gu X, Chen J, Campos IM, Wei Q, Rodriguez-Bigas M, Lynch PM, Frazier ML. DNMT3b polymorphism and hereditary nonpolyposis colorectal cancer age of onset. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 15: 886-91. PMID 16702365 DOI: 10.1158/1055-9965.Epi-05-0644 |
0.391 |
|
| 2006 |
Newman WG, Gu X, Wintle RF, Liu X, van Oene M, Amos CI, Siminovitch KA. DLG5 variants contribute to Crohn disease risk in a Canadian population. Human Mutation. 27: 353-8. PMID 16450402 DOI: 10.1002/Humu.20301 |
0.373 |
|
| 2006 |
Zecevic M, Amos CI, Gu X, Campos IM, Jones JS, Lynch PM, Rodriguez-Bigas MA, Frazier ML. IGF1 gene polymorphism and risk for hereditary nonpolyposis colorectal cancer. Journal of the National Cancer Institute. 98: 139-43. PMID 16418517 DOI: 10.1093/Jnci/Djj016 |
0.338 |
|
| 2005 |
Jones JS, Gu X, Lynch PM, Rodriguez-Bigas M, Amos CI, Frazier ML. ATM polymorphism and hereditary nonpolyposis colorectal cancer (HNPCC) age of onset (United States). Cancer Causes & Control : Ccc. 16: 749-53. PMID 16049814 DOI: 10.1007/S10552-005-1540-7 |
0.333 |
|
| 2005 |
van Oene M, Wintle RF, Liu X, Yazdanpanah M, Gu X, Newman B, Kwan A, Johnson B, Owen J, Greer W, Mosher D, Maksymowych W, Keystone E, Rubin LA, Amos CI, et al. Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations. Arthritis and Rheumatism. 52: 1993-8. PMID 15986374 DOI: 10.1002/Art.21123 |
0.34 |
|
| 2005 |
Newman B, Wintle RF, van Oene M, Yazdanpanah M, Owen J, Johnson B, Gu X, Amos CI, Keystone E, Rubin LA, Siminovitch KA. SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population. Arthritis and Rheumatism. 52: 425-9. PMID 15693005 DOI: 10.1002/Art.20854 |
0.335 |
|
| 2005 |
Newman B, Gu X, Wintle R, Cescon D, Yazdanpanah M, Liu X, Peltekova V, Van Oene M, Amos CI, Siminovitch KA. A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease. Gastroenterology. 128: 260-9. PMID 15685536 DOI: 10.1053/J.Gastro.2004.11.056 |
0.361 |
|
| 2004 |
Jones JS, Chi X, Gu X, Lynch PM, Amos CI, Frazier ML. p53 polymorphism and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 10: 5845-9. PMID 15355915 DOI: 10.1158/1078-0432.Ccr-03-0590 |
0.4 |
|
| 2004 |
Evans SC, Liang M, Amos C, Gu X, Lozano G. A novel genetic modifier of p53, mop1, results in embryonic lethality. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 415-23. PMID 15181534 DOI: 10.1007/S00335-004-2327-Y |
0.366 |
|
| 2004 |
Peltekova VD, Wintle RF, Rubin LA, Amos CI, Huang Q, Gu X, Newman B, Van Oene M, Cescon D, Greenberg G, Griffiths AM, St George-Hyslop PH, Siminovitch KA. Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nature Genetics. 36: 471-5. PMID 15107849 DOI: 10.1038/Ng1339 |
0.317 |
|
| 2004 |
Newman B, Silverberg MS, Gu X, Zhang Q, Lazaro A, Steinhart AH, Greenberg GR, Griffiths AM, McLeod RS, Cohen Z, Fernández-Viña M, Amos CI, Siminovitch K. CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease. The American Journal of Gastroenterology. 99: 306-15. PMID 15046222 DOI: 10.1111/J.1572-0241.2004.04038.X |
0.341 |
|
| 2001 |
Amos CI, Shete S, Gu X. Variance components analysis for genetic linkage of time to onset for disease. Genetic Epidemiology. 21. PMID 11793775 DOI: 10.1002/Gepi.2001.21.S1.S768 |
0.331 |
|
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