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Genetic architecture of cancer and other complex diseases: lessons learned and future directionsHINDORFF, Lucia A; GILLANDERS, Elizabeth M; MANOLIO, Teri A et al.Carcinogenesis (New York. Print). 2011, Vol 32, Num 7, pp 945-954, issn 0143-3334, 10 p.Article

Detectable clonal mosaicism and its relationship to aging and cancerJACOBS, Kevin B; YEAGER, Meredith; CULLEN, Michael et al.Nature genetics. 2012, Vol 44, Num 6, pp 651-658, issn 1061-4036, 8 p.Article

Combined genome-wide scan for prostate cancer susceptibility genesGILLANDERS, Elizabeth M; JIANFENG XU; ALBERTUS, Julie et al.Journal of the National Cancer Institute. 2004, Vol 96, Num 16, pp 1240-1247, issn 0027-8874, 8 p.Article

Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1LANGE, Ethan M; GILLANDERS, Elizabeth M; MARKEY, Carol et al.The Prostate. 2003, Vol 57, Num 4, pp 326-334, issn 0270-4137, 9 p.Article

Common sequence variants on 20qll.22 confer melanoma susceptibilityBROWN, Kevin M; MACGREGOR, Stuart; THOMAS, Shane et al.Nature genetics. 2008, Vol 40, Num 7, pp 838-840, issn 1061-4036, 3 p.Article

Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease : significant evidence for linkage at chromosome 15q12LANGE, Ethan M; HO, Lindsey A; BEEBE-DIMMER, Jennifer L et al.Human genetics. 2006, Vol 119, Num 4, pp 400-407, issn 0340-6717, 8 p.Article

Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13TRANEBJAERG, Lisbeth; TESLOVICH, Tanya M; JONES, Marypat et al.Human genetics. 2003, Vol 113, Num 3, pp 293-295, issn 0340-6717, 3 p.Article

Physical and transcript Map of the hereditary prostate cancer region at Xq27STEPHAN, Dietrich A; HOWELL, Gareth R; SCHLEUTKER, Johanna et al.Genomics (San Diego, Calif.). 2002, Vol 79, Num 1, pp 41-50, issn 0888-7543Article

Population Sciences, Translational Research, and the Opportunities and Challenges for Genomics to Reduce the Burden of Cancer in the 21st CenturyKHOURY, Muin J; CLAUSER, Steven B; FREEDMAN, Andrew N et al.Cancer epidemiology, biomarkers & prevention. 2011, Vol 20, Num 10, pp 2105-2114, issn 1055-9965, 10 p.Article

Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysisLANGE, Ethan M; ROBBINS, Christiane M; CARPTEN, John D et al.Human genetics. 2007, Vol 121, Num 1, pp 49-55, issn 0340-6717, 7 p.Article

Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkageJIANFENG XU; LANGEFELD, Carl D; WALSH, Patrick C et al.Human genetics. 2004, Vol 115, Num 3, pp 255-262, issn 0340-6717, 8 p.Article

Genome-wide scan of swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3WIKLUND, Fredrik; GILLANDERS, Elizabeth M; JONSSON, Björn-Anders et al.The Prostate. 2003, Vol 57, Num 4, pp 290-297, issn 0270-4137, 8 p.Article

The landscape of recombination in African AmericansHINCH, Anjali G; TANDON, Arti; ALDRICH, Melinda C et al.Nature (London). 2011, Vol 476, Num 7359, pp 170-175, issn 0028-0836, 6 p.Article

Genome-wide association study identifies three loci associated with melanoma riskBISHOP, D. Timothy; DEMENAIS, Florence; BAKKER, Bert et al.Nature genetics. 2009, Vol 41, Num 8, pp 920-925, issn 1061-4036, 6 p.Article

Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma familiesDE SNOO, Femke A; HOTTENGA, Jouke-Jan; FRANTS, Rune R et al.European journal of human genetics. 2008, Vol 16, Num 9, pp 1135-1141, issn 1018-4813, 7 p.Article

Features associated with germline CDKN2A mutations : a GenoMEL study of melanoma-prone families from three continentsGOLDSTEIN, Alisa M; CHAN, May; CALISTA, Donato et al.Journal of medical genetics. 2007, Vol 44, Num 2, pp 99-106, issn 0022-2593, 8 p.Article

A major locus for hereditary prostate cancer in Finland : localization by linkage disequilibrium of a haplotype in the HPCX regionBAFFOE-BONNIE, Agnes B; SMITH, Jeffrey R; SOOD, Raman et al.Human genetics. 2005, Vol 117, Num 4, pp 307-316, issn 0340-6717, 10 p.Article

The Effect on Melanoma Risk of Genes Previously Associated With Telomere LengthILES, Mark M; BISHOP, D. Timothy; ANDRESEN, Per A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 10, issn 0027-8874, 267.1-267.5Article

A Review of NCI's Extramural Grant Portfolio: Identifying Opportunities for Future Research in Genes and Environment in Cancer : EPIDEMIOLOGY IN THE 21ST CENTURYGHAZARIAN, Armen A; SIMONDS, Naoko I; BENNETT, Kelly et al.Cancer epidemiology, biomarkers & prevention. 2013, Vol 22, Num 4, pp 501-507, issn 1055-9965, 7 p.Article

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairmentRENDTORFF, Nanna D; MEI ZHU; FRIDERICI, Karen H et al.European journal of human genetics. 2006, Vol 14, Num 10, pp 1097-1105, issn 1018-4813, 9 p.Article

High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMELGOLDSTEIN, Alisa M; CHAN, May; BRUNO, William et al.Cancer research (Baltimore). 2006, Vol 66, Num 20, pp 9818-9828, issn 0008-5472, 11 p.Article

Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effectCHANG, Bao-Li; LANGE, Ethan M; LANGEFELD, Carl D et al.Human genetics. 2006, Vol 118, Num 6, pp 716-724, issn 0340-6717, 9 p.Article

Genome-wide screen for prostate cancer susceptibility genes in men with clinically significant diseaseCHANG, Bao-Li; ISAACS, Sarah D; WILEY, Kathy E et al.The Prostate. 2005, Vol 64, Num 4, pp 356-361, issn 0270-4137, 6 p.Article

Genome-wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer familiesJIANFENG XU; GILLANDERS, Elizabeth M; FREAS-LUTZ, Diana et al.The Prostate. 2003, Vol 57, Num 4, pp 320-325, issn 0270-4137, 6 p.Article

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