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

Por Amos, C. I.
Publicado em 1994

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

Por Page, G P, Amos, C I
Publicado em 1999

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

Por Amos, C I, Williamson, J A
Publicado em 1993

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

Por Amos, C I, Martinez, M, Bale, S J
Publicado em 1991

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

Por Page, G P, Amos, C I, Boerwinkle, E
Publicado em 1998

DNA pooling in mutation detection with reference to sequence analysis.

Por Amos, C I, Frazier, M L, Wang, W
Publicado em 2000

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

Por Amos, C I, Dawson, D V, Elston, R C
Publicado em 1990

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

Por Spitz, Margaret R., Amos, C. I., D'amelio, A., Dong, Q., Etzel, C.
Publicado em 2009

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

Por Amos, C I, Elston, R C, Bonney, G E, Keats, B J, Berenson, G S
Publicado em 1990

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

Por Allison, D B, Neale, M C, Zannolli, R, Schork, N J, Amos, C I, Blangero, J
Publicado em 1999

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

Por Wu, X, Kemp, B, Amos, C I, Honn, S E, Zhang, W, Walsh, G L, Spitz, M R
Publicado em 1999

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

Por 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.
Publicado em 1996

Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients

Por 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
Publicado em 2001

Linkage of familial Hibernian fever to chromosome 12p13.

Por 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
Publicado em 1998

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

Por 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.
Publicado em 2010

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

Por 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.
Publicado em 2004

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

Por 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
Publicado no Transl Psychiatry (2015)

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

Por 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
Publicado em 2010