Robust variance-components approach for assessing genetic linkage in pedigrees.

بواسطة Amos, C. I.
منشور في 1994

Comparison of linkage-disequilibrium methods for localization of genes influencing quantitative traits in humans.

بواسطة Page, G P, Amos, C I
منشور في 1999

Robustness of the maximum-likelihood (LOD) method for detecting linkage.

بواسطة Amos, C I, Williamson, J A
منشور في 1993

Can a susceptibility locus for schizophrenia be excluded from chromosome 5q11-13?

بواسطة Amos, C I, Martinez, M, Bale, S J
منشور في 1991

The quantitative LOD score: test statistic and sample size for exclusion and linkage of quantitative traits in human sibships.

بواسطة Page, G P, Amos, C I, Boerwinkle, E
منشور في 1998

DNA pooling in mutation detection with reference to sequence analysis.

بواسطة Amos, C I, Frazier, M L, Wang, W
منشور في 2000

The probabilistic determination of identity-by-descent sharing for pairs of relatives from pedigrees.

بواسطة Amos, C I, Dawson, D V, Elston, R C
منشور في 1990

Re: Discriminatory Accuracy From Single-Nucleotide Polymorphisms in Models to Predict Breast Cancer Risk

بواسطة Spitz, Margaret R., Amos, C. I., D'amelio, A., Dong, Q., Etzel, C.
منشور في 2009

A multivariate method for detecting genetic linkage, with application to a pedigree with an adverse lipoprotein phenotype.

بواسطة Amos, C I, Elston, R C, Bonney, G E, Keats, B J, Berenson, G S
منشور في 1990

Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure.

بواسطة Allison, D B, Neale, M C, Zannolli, R, Schork, N J, Amos, C I, Blangero, J
منشور في 1999

Associations among telomerase activity, p53 protein overexpression, and genetic instability in lung cancer

بواسطة Wu, X, Kemp, B, Amos, C I, Honn, S E, Zhang, W, Walsh, G L, Spitz, M R
منشور في 1999

Genetic variants in the folate metabolic pathway genes predict melanoma-specific survival

بواسطة Dai, W., Liu, H., Liu, Y., Xu, X., Qian, D., Luo, S., Cho, E., Zhu, D., Amos, C. I., Fang, S., Lee, J. E., Li, X., Nan, H., Li, C., Wei, Q.
الحاوية / القاعدة Br J Dermatol (2020)

Genetic variability in the tumor necrosis factor-lymphotoxin region influences susceptibility to rheumatoid arthritis.

بواسطة Mulcahy, B., Waldron-Lynch, F., McDermott, M. F., Adams, C., Amos, C. I., Zhu, D. K., Ward, R. H., Clegg, D. O., Shanahan, F., Molloy, M. G., O'Gara, F.
منشور في 1996

Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients

بواسطة Soliman, A S, Bondy, M L, El-Badawy, S A, Mokhtar, N, Eissa, S, Bayoumy, S, Seifeldin, I A, Houlihan, P S, Lukish, J R, Watanabe, T, Chan, A On On, Zhu, D, Amos, C I, Levin, B, Hamilton, S R
منشور في 2001

Linkage of familial Hibernian fever to chromosome 12p13.

بواسطة McDermott, M F, Ogunkolade, B W, McDermott, E M, Jones, L C, Wan, Y, Quane, K A, McCarthy, J, Phelan, M, Molloy, M G, Powell, R J, Amos, C I, Hitman, G A
منشور في 1998

A susceptibility locus on chromosome 6q greatly increases risk lung cancer risk among light and never smokers

بواسطة Amos, C.I., Pinney, S. M., Li, Y., Kupert, E, Lee, J, de Andrade, M. A., Yang, P., Schwartz, A.G., Fain, P. R., Gazdar, A., Minna, J., Wiest, J.S., Zeng, D., Rothschild, H., Mandal, D., You, M., Coons, Teresa, Gaba, C., Bailey-Wilson, J.E., Anderson, M.W.
منشور في 2010

A Major Lung Cancer Susceptibility Locus Maps to Chromosome 6q23–25

بواسطة Bailey-Wilson, J. E., Amos, C. I., Pinney, S. M., Petersen, G. M., de Andrade, M., Wiest, J. S., Fain, P., Schwartz, A. G., You, M., Franklin, W., Klein, C., Gazdar, A., Rothschild, H., Mandal, D., Coons, T., Slusser, J., Lee, J., Gaba, C., Kupert, E., Perez, A., Zhou, X., Zeng, D., Liu, Q., Zhang, Q., Seminara, D., Minna, J., Anderson, M. W.
منشور في 2004

Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

بواسطة Hancock, D B, Reginsson, G W, Gaddis, N C, Chen, X, Saccone, N L, Lutz, S M, Qaiser, B, Sherva, R, Steinberg, S, Zink, F, Stacey, S N, Glasheen, C, Chen, J, Gu, F, Frederiksen, B N, Loukola, A, Gudbjartsson, D F, Brüske, I, Landi, M T, Bickeböller, H, Madden, P, Farrer, L, Kaprio, J, Kranzler, H R, Gelernter, J, Baker, T B, Kraft, P, Amos, C I, Caporaso, N E, Hokanson, J E, Bierut, L J, Thorgeirsson, T E, Johnson, E O, Stefansson, K
الحاوية / القاعدة Transl Psychiatry (2015)

Identification of novel genetic markers associated with the clinical phenotypes of systemic sclerosis through a genome wide association strategy

بواسطة Gorlova, O, Martin, J M, Rueda, B, Koeleman, BPC, Ying, J, Teruel, M, Diaz-Gallo, L M, Broen, J C, Vonk, M C, Simeon, C P, Alizadeh, B Z, Coenen, MJH, Voskuyl, A E, Schuerwegh, A J, van Riel, PLCM, Vanthuyne, M, van ‘t Slot, R, Italiaander, A, Ophoff, R A, Hunzelmann, N, Fonollosa, V, Ortego-Centeno, N, González-Gay, M A, García-Hernández, F J, González-Escribano, M F, Airo, P, van Laar, J, Worthington, J, Hesselstrand, R, Smith, V, De Keyser, F, Houssiau, F, Chee, M M, Madhok, R, Shiels, P, Westhovens, R, Kreuter, A, de Baere, E, Witte, T, Padyukov, L, Nordin, A, Scorza, R, Lunardi, C, Lie, B A, Hoffmann-Vold, A M, García de la Peña, P, Carreira, P, Varga, J, Hinchcliff, M, Lee, A T, Gourh, P, Amos, C I, Riemekasten, G, Herrick, A, Beretta, L, Fonseca, C, Denton, C P, Gregersen, P K, Agarwal, S, Assassi, S, Tan, F K, Arnett, F C, Radstake, TRDJ, Mayes, M D, Martin, J
منشور في 2010