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Results: 1-10 |
Results: 10
On the validity of the TDT test in the presence of comorbidity and ascertainment bias
Authors: Robins, JM Smoller, JW Lunetta, KL
Citation: Jm. Robins et al., On the validity of the TDT test in the presence of comorbidity and ascertainment bias, GENET EPID, 21(4), 2001, pp. 326-336
HIN-1, a putative cytokine highly expressed in normal but not cancerous mammary epithelial cells
Authors: Krop, IE Sgroi, D Porter, DA Lunetta, KL LeVangie, R Seth, P Kaelin, CM Rhei, E Bosenberg, M Schnitt, S Marks, JR Pagon, Z Belina, D Razumovic, J Polyak, K
Citation: Ie. Krop et al., HIN-1, a putative cytokine highly expressed in normal but not cancerous mammary epithelial cells, P NAS US, 98(17), 2001, pp. 9796-9801
Abnormalities of bone marrow mesenchymal cells in multiple myeloma patients
Authors: Wallace, SR Oken, MM Lunetta, KL Panoskaitsis-Mortari, A Masellis, AM
Citation: Sr. Wallace et al., Abnormalities of bone marrow mesenchymal cells in multiple myeloma patients, CANCER, 91(7), 2001, pp. 1219-1230
Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours
Authors: Yeh, JJ Lunetta, KL van Orsouw, NJ Moore, FD Mutter, GL Vijg, J Dahia, PLM Eng, C
Citation: Jj. Yeh et al., Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours, ONCOGENE, 19(16), 2000, pp. 2060-2066
Implications of comorbidity and ascertainment bias for identifying diseasegenes
Authors: Smoller, JW Lunetta, KL Robins, J
Citation: Jw. Smoller et al., Implications of comorbidity and ascertainment bias for identifying diseasegenes, AM J MED G, 96(6), 2000, pp. 817-822
Phenol sulfotransferases: Hormonal regulation, polymorphism, and age of onset of breast cancer
Authors: Seth, P Lunetta, KL Bell, DW Gray, H Nasser, SM Rhei, E Kaelin, CM Iglehart, DJ Marks, JR Garber, JE Haber, DA Polyak, K
Citation: P. Seth et al., Phenol sulfotransferases: Hormonal regulation, polymorphism, and age of onset of breast cancer, CANCER RES, 60(24), 2000, pp. 6859-6863
Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions
Authors: Lunetta, KL Faraone, SV Biederman, J Laird, NM
Citation: Kl. Lunetta et al., Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions, AM J HU GEN, 66(2), 2000, pp. 605-614
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
Authors: Marsh, DJ Kum, JB Lunetta, KL Bennett, MJ Gorlin, RJ Ahmed, SF Bodurtha, J Crowe, C Curtis, MA Dasouki, M Dunn, T Feit, H Geraghty, MT Graham, JM Hodgson, SV Hunter, A Korf, BR Manchester, D Miesfeldt, S Murday, VA Nathanson, KL Parisi, M Pober, B Romano, C Tolmie, JL Trembath, R Winter, RM Zackai, EH Zori, RT Weng, LP Dahia, PLM Eng, C
Citation: Dj. Marsh et al., PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome, HUM MOL GEN, 8(8), 1999, pp. 1461-1472
Exploring linkage for alcoholism using affection status and quantitative event related potential phenotypes
Authors: Lunetta, KL Wilcox, M Smoller, J Neuberg, D
Citation: Kl. Lunetta et al., Exploring linkage for alcoholism using affection status and quantitative event related potential phenotypes, GENET EPID, 17, 1999, pp. S241-S246
Using recursive partitioning for exploration and follow-up of linkage and association analyses
Authors: Wilcox, MA Smoller, JW Lunetta, KL Neuberg, D
Citation: Ma. Wilcox et al., Using recursive partitioning for exploration and follow-up of linkage and association analyses, GENET EPID, 17, 1999, pp. S391-S396
Risultati: 1-10 |