ST_refs
References from Statistical Genetics: Gene Mapping Through Linkage and Association
A-C D-F G-K L-N O-R S-T U-Z Online Material
S.A.G.E. (2006). v5.2 Statistical Analysis for Genetic Epidemiology. http://darwin.cwru.edu/sage/.
Saccone, S. F., Rice, J. P., & Saccone, N. L. (2006). Power-based, phase-informed selection of single nucleotide polymorphisms for disease association screens. Genet Epidemiol, 30(6), 459-470 Abstract
Sachidanandam, R., Weissman, D., Schmidt, S. C., Kakol, J. M., Stein, L. D., Marth, G., Sherry, S., Mullikin, J. C., Mortimore, B. J., Willey, D. L., Hunt, S. E., Cole, C. G., Coggill, C., Rice, C. M., Ning, Z., Rogers, J., Bentley, D. R., Kwok, Y., Mardis, E. R., Yeh, R. T., Schultz, B., Cook, L., Davenport, R., Dante, M., Fulton, L., Hillier, L., Waterston, R. H., McPherson, J. D., Gilman, B., Schaffner, S., Van Etten, W. J., Reich, D., Higgins, J., Daly, M. J., Blumenstiel, B., Baldwin, J., Stange-Thomann, N., Zody, M. C., Linton, L., Lander, E. S., & Altshuler, D. (2001). A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature, 409(6822), 928-933 Abstract
Saiki, R. K., Gelfand, D. H., Stoffel, S., Scharf, S. J., Higuchi, R., Horn, G. T., Mullis, K. B., & Erlich, H. A. (1988). Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science, 239(4839), 487-491 Abstract
Saris, W. E., & Satorra, A. (1993). Power evaluations in structural equation models. In Bollen, K. A. & Long, J. S. (Eds.), Testing Structural Equation Models (p181-204). Newbury Park, CA: Sage.
Sasieni, D. (1997). From genotypes to genes: doubling the sample size. Biometrics, 53(4), 1253-1261 Abstract
Satagopan, J. M., Verbel, D. A., Venkatraman, E. S., Offit, K. E., & Begg, C. B. (2002). Two-stage designs for gene-disease association studies. Biometrics, 58(1), 163-170 Abstract
Satagopan, J. M., & Elston, R. C. (2003). Optimal two-stage genotyping in population-based association studies. Genet Epidemiol, 25(2), 149-157 Abstract
Satagopan, J. M., Venkatraman, E. S., & Begg, C. B. (2004). Two-stage designs for gene-disease association studies with sample size constraints. Biometrics, 60(3), 589-597 Abstract
Satorra, A., & Saris, W. E. (1985). The power of the likelihood ratio test in covariance structure analysis. _Psychometrika _, 50, 83-90
Satten, G. A., Flanders, W. D., & Yang, Q. (2001). Accounting for unmeasured population substructure in case-control studies of genetic association using a novel latent-class model. Am J Hum Genet, 68(2), 466-477 Abstract
Sawcer, S., Jones, H. B., Judge, D., Visser, F., Compston, A., Goodfellow, N., & Clayton, D. (1997). Empirical genomewide significance levels established by whole genome simulations. Genet Epidemiol, 14(3), 223-229 Abstract
Saxena, R., de Bakker, I., Singer, K., Mootha, V., Burtt, N., Hirschhorn, J. N., Gaudet, D., Isomaa, B., Daly, M. J., Groop, L., Ardlie, K. G., & Altshuler, D. (2006). Comprehensive association testing of common mitochondrial DNA variation in metabolic disease. Am J Hum Genet, 79(1), 54-61 Abstract
Schafer, J. L. (1997). Analysis of Incomplete Multivariate Data. London: Chapman and Hall.
Schafer, J. L. (1999). Multiple imputation: a primer. Stat. Methods Med. Res, 8, 3-15
Schafer, J. L., & Graham, J. W. (2002). Missing data: our view of the state of the art. Psychol Methods, 7(2), 147-177 Abstract
Schaffner, S. F., Foo, C., Gabriel, S., Reich, D., Daly, M. J., & Altshuler, D. (2005). Calibrating a coalescent simulation of human genome sequence variation. Genome Res, 15(11), 1576-1583 Abstract
Schaid, D. J., & Sommer, S. S. (1994). Comparison of statistics for candidate-gene association studies using cases and parents. Am J Hum Genet, 55(2), 402-409 Abstract
Schaid, D. J., Rowland, C. M., Tines, D. E., Jacobson, R. M., & Poland, G. A. (2002). Score tests for association between traits and haplotypes when linkage phase is ambiguous. Am J Hum Genet, 70(2), 425-434
Schlesselman, J. J. (1982). Case-Control Studies: Design, Conduct, Analysis.. New York, NY.: Oxford University Press.
Schmitz, S., Cherny, S. S., & Fulker, D. W. (1998). Increase in power through multivariate analyses. Behav Genet, 28(5), 357-363 Abstract
Schork, N. J. (1993). Extended multipoint identity-by-descent analysis of human quantitative traits: efficiency, power, and modeling considerations. Am J Hum Genet, 53(6), 1306-1319 Abstract
Schork, N. J., Allison, D. B., & Thiel, B. (1996). Mixture distributions in human genetics research. Stat Methods Med Res, 5(2), 155-178 Abstract
Schuit, S. C., van Meurs, J. B., Bergink, A. P., van der Klift, M., Fang, Y., Leusink, G., Hofman, A., van Leeuwen, J. P., Uitterlinden, A. G., & Pols, H. A. (2004). Height in pre- and postmenopausal women is influenced by estrogen receptor alpha gene polymorphisms. J Clin Endocrinol Metab, 89(1), 303-309 Abstract
Schulze, T. G., Buervenich, S., Badner, J. A., Steele, C. J., Detera-Wadleigh, S. D., Dick, D., Foroud, T., Cox, N. J., MacKinnon, D. F., Potash, J. B., Berrettini, W. H., Byerley, W., Coryell, W., DePaulo, J. R., Jr., Gershon, E. S., Kelsoe, J. R., McInnis, M. G., Murphy, D. L., Reich, T., Scheftner, W., Nurnberger, J. I., Jr., & McMahon, F. J. (2004). Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees. Biol Psychiatry, 56(1), 18-23 Abstract
Schymick, J. C., Scholz, S. W., Fung, H. C., Britton, A., Arepalli, S., Gibbs, J. R., Lombardo, F., Matarin, M., Kasperaviciute, D., Hernandez, D. G., Crews, C., Bruijn, L., Rothstein, J., Mora, G., Restagno, G., Chio, A., Singleton, A., Hardy, J., & Traynor, B. J. (2007). Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol, 6(4), 322-328 Abstract
Searle, S. R. (1982). Matrix Algebra Useful for Statistics. New York, NY.: Wiley-Interscience.
Sebastiani, P., Lazarus, R., Weiss, S. T., Kunkel, L. M., Kohane, I. S., & Ramoni, M. F. (2003). Minimal haplotype tagging. Proc Natl Acad Sci U S A, 100(17), 9900-9905 Abstract
Sebat, J., Lakshmi, B., Troge, J., Alexander, J., Young, J., Lundin, P., Maner, S., Massa, H., Walker, M., Chi, M., Navin, N., Lucito, R., Healy, J., Hicks, J., Ye, K., Reiner, A., Gilliam, T. C., Trask, B., Patterson, N., Zetterberg, A., & Wigler, M. (2004). Large-scale copy number polymorphism in the human genome. Science, 305(5683), 525-528 Abstract
Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., Leotta, A., Pai, D., Zhang, R., Lee, Y. H., Hicks, J., Spence, S. J., Lee, A. T., Puura, K., Lehtimaki, T., Ledbetter, D., Gregersen, K., Bregman, J., Sutcliffe, J. S., Jobanputra, V., Chung, W., Warburton, D., King, M. C., Skuse, D., Geschwind, D. H., Gilliam, T. C., Ye, K., & Wigler, M. (2007). Strong association of de novo copy number mutations with autism. Science, 316(5823), 445-449 Abstract
Seldin, M. F., Shigeta, R., Villoslada, P., Selmi, C., Tuomilehto, J., Silva, G., Belmont, J. W., Klareskog, L., & Gregersen, K. (2006). European population substructure: clustering of northern and southern populations. PLoS Genet, 2(9), e143 Abstract
Self, S. G., & Liang, K. Y. (1987). Asymptotic properties of maximum
likelihood estimators and likelihood ratio tests under nonstandard conditions. J. Am. Stat. Assoc, 82, 605-610
Sham, C. (1998). Statistics in Human Genetics. London: Arnold.
Sham, C., Cherny, S. S., Purcell, S., & Hewitt, J. K. (2000). Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data. Am J Hum Genet, 66(5), 1616-1630 Abstract
Sham, C., Zhao, J. H., Cherny, S. S., & Hewitt, J. K. (2000). Variance-Components QTL linkage analysis of selected and non-normal samples: conditioning on trait values. Genet Epidemiol, 19 Suppl 1, S22-28 Abstract
Sham, C., & Purcell, S. (2001). Equivalence between Haseman-Elston and variance-components linkage analyses for sib pairs. Am J Hum Genet, 68(6), 1527-1532 Abstract
Sham, C., Purcell, S., Cherny, S. S., & Abecasis, G. R. (2002). Powerful regression-based quantitative-trait linkage analysis of general pedigrees. Am J Hum Genet, 71(2), 238-253 Abstract
Sham, C., Rijsdijk, F. V., Knight, J., Makoff, A., North, B., & Curtis, D. (2004). Haplotype association analysis of discrete and continuous traits using mixture of regression models. Behav Genet, 34(2), 207-214
Shaw, F. H., & Geyer, C. J. (1997). Estimation and testing in constrained covariance component models. Biometrika, 84, 95-102
Shete, S., & Amos, C. I. (2002). Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprinting. Am J Hum Genet, 70(3), 751-757 Abstract
Shete, S., & Zhou, X. (2005). Parametric approach to genomic imprinting analysis with applications to Angelman’s syndrome. Hum Hered, 59(1), 26-33 Abstract
Skol, A. D., Scott, L. J., Abecasis, G. R., & Boehnke, M. (2006a). Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nat Genet, 38(2), 209-213 Abstract
Skol, A. D., Scott, L. J., Abecasis, G. R., & Boehnke, M. (2006b). Corrigendum: Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nat Genet, 38, 390 Abstract
Sladek, R., Rocheleau, G., Rung, J., Dina, C., Shen, L., Serre, D., Boutin, P., Vincent, D., Belisle, A., Hadjadj, S., Balkau, B., Heude, B., Charpentier, G., Hudson, T. J., Montpetit, A., Pshezhetsky, A. V., Prentki, M., Posner, B. I., Balding, D. J., Meyre, D., Polychronakos, C., & Froguel, (2007). A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature, 445(7130), 881-885 Abstract
Smith, C. A. (1963). Testing for Heterogeneity of Recombination Fraction Values in Human Genetics. Ann Hum Genet, 27, 175-182 Abstract
Smith, F. M., Garfield, A. S., & Ward, A. (2006). Regulation of growth and metabolism by imprinted genes. Cytogenet Genome Res, 113(1-4), 279-291 Abstract
Snieder, H., van Doornen, L. J. P., & Boomsma, D. I. (1995). Developmental genetic trends in blood pressure levels and blood pressure reactivity to stress. In Turner, J. R., Cardon, L. R. & Hewitt, J. K. (Eds.), Behavior Genetic Approaches in Behavioral Medicine (p105-130). New York, NY: Plenum Press.
Snieder, H., van Doornen, L. J., & Boomsma, D. I. (1997). The age dependency of gene expression for plasma lipids, lipoproteins, and apolipoproteins. Am J Hum Genet, 60(3), 638-650 Abstract
Sobel, E., & Lange, K. (1996). Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet, 58(6), 1323-1337 Abstract
Sobel, E., Sengul, H., & Weeks, D. E. (2001). Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees. Hum Hered, 52(3), 121-131 Abstract
Sobel, E., Papp, J. C., & Lange, K. (2002). Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet, 70(2), 496-508 Abstract
Sobell, J. L., Heston, L. L., & Sommer, S. S. (1993). Novel association approach for determining the genetic predisposition to schizophrenia: case-control resource and testing of a candidate gene. Am J Med Genet, 48(1), 28-35 Abstract
Sorensen, D., & Gianola, D. (2002). Likelihood, Bayesian, and MCMC Methods in Quantitative Genetics.. New York, NY: Springer.
Spielman, R. S., McGinnis, R. E., & Ewens, W. J. (1993). Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet, 52(3), 506-516 Abstract
Spielman, R. S., & Ewens, W. J. (1998). A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test. Am J Hum Genet, 62(2), 450-458 Abstract
Stefansson, H., Helgason, A., Thorleifsson, G., Steinthorsdottir, V., Masson, G., Barnard, J., Baker, A., Jonasdottir, A., Ingason, A., Gudnadottir, V. G., Desnica, N., Hicks, A., Gylfason, A., Gudbjartsson, D. F., Jonsdottir, G. M., Sainz, J., Agnarsson, K., Birgisdottir, B., Ghosh, S., Olafsdottir, A., Cazier, J. B., Kristjansson, K., Frigge, M. L., Thorgeirsson, T. E., Gulcher, J. R., Kong, A., & Stefansson, K. (2005). A common inversion under selection in Europeans. Nat Genet, 37(2), 129-137 Abstract
Stephens, M., & Donnelly, (2000). Inference in molecular population genetics. J. R. Stat. Soc. Ser. B, 62, 605-655
Stephens, M., Smith, N. J., & Donnelly, (2001). A new statistical method for haplotype reconstruction from population data. Am J Hum Genet, 68(4), 978-989 Abstract
Stephens, M., & Donnelly, (2003). A comparison of bayesian methods for haplotype reconstruction from population genotype data. Am J Hum Genet, 73(5), 1162-1169 Abstract
Stephens, M., & Scheet, (2005). Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. Am J Hum Genet, 76(3), 449-462 Abstract
Stine, O. C., Xu, J., Koskela, R., McMahon, F. J., Gschwend, M., Friddle, C., Clark, C. D., McInnis, M. G., Simpson, S. G., Breschel, T. S., Vishio, E., Riskin, K., Feilotter, H., Chen, E., Shen, S., Folstein, S., Meyers, D. A., Botstein, D., Marr, T. G., & DePaulo, J. R. (1995). Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect. Am J Hum Genet, 57(6), 1384-1394 Abstract
Storey, J. D., & Tibshirani, R. (2003). Statistical significance for genomewide studies. Proc Natl Acad Sci U S A, 100(16), 9440-9445 Abstract
Strachan, T., & Read, A. (1999). Human Molecular Genetics 2 (2nd ed.). Oxford: BIOS Scientific Publishers Ltd.
Stram, D. O., & Lee, J. W. (1994). Variance components testing in the longitudinal mixed effects model. Biometrics, 50(4), 1171-1177 Abstract
Stram, D. O., Haiman, C. A., Hirschhorn, J. N., Altshuler, D., Kolonel, L. N., Henderson, B. E., & Pike, M. C. (2003). Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study. Hum Hered, 55(1), 27-36 Abstract
Stram, D. O., Leigh Pearce, C., Bretsky, P., Freedman, M., Hirschhorn, J. N., Altshuler, D., Kolonel, L. N., Henderson, B. E., & Thomas, D. C. (2003). Modeling and E-M estimation of haplotype-specific relative risks from genotype data for a case-control study of unrelated individuals. Hum Hered, 55(4), 179-190
Stram, D. O. (2004). Tag SNP selection for association studies. Genet Epidemiol, 27(4), 365-374
Stranger, B. E., Forrest, M. S., Clark, A. G., Minichiello, M. J., Deutsch, S., Lyle, R., Hunt, S., Kahl, B., Antonarakis, S. E., Tavare, S., Deloukas, P., & Dermitzakis, E. T. (2005). Genome-wide associations of gene expression variation in humans. PLoS Genet, 1(6), e78 Abstract
Strauch, K., Fimmers, R., Windemuth, C., Hahn, A., Wienker, T. F., & Baur, M. (1999). Linkage analysis with adequate modeling of a parent-of-origin effect. Genet Epidemiol, 17 Suppl 1, S331-336 Abstract
Strauch, K., Fimmers, R., Kurz, T., Deichmann, K. A., Wienker, T. F., & Baur, M. (2000). Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization. Am J Hum Genet, 66(6), 1945-1957 Abstract
Strauch, K., & Baur, M. (2005). Parent-of-origin, imprinting, mitochondrial, and X-linked effects in traits related to alcohol dependence: presentation Group 18 of Genetic Analysis Workshop 14. Genet Epidemiol, 29 Suppl 1, S125-132 Abstract
Stringham, H. M., & Boehnke, M. (1996). Identifying marker typing incompatibilities in linkage analysis. Am J Hum Genet, 59(4), 946-950 Abstract
Stringham, H. M., & Boehnke, M. (2001). Lod scores for gene mapping in the presence of marker map uncertainty. Genet Epidemiol, 21(1), 31-39 Abstract
Stumpf, M. P., & McVean, G. A. (2003). Estimating recombination rates from population-genetic data. Nat Rev Genet, 4(12), 959-968 Abstract
Suarez, B. K., Rice, J., & Reich, T. (1978). The generalized sib pair IBD distribution: its use in the detection of linkage. Ann Hum Genet, 42(1), 87-94 Abstract
Suarez, B. K., & Hodge, S. E. (1979). A simple method to detect linkage for rare recessive diseases: an application to juvenile diabetes. Clin Genet, 15(2), 126-136 Abstract
Sullivan, F., Eaves, L. J., Kendler, K. S., & Neale, M. C. (2001). Genetic case-control association studies in neuropsychiatry. Arch Gen Psychiatry, 58(11), 1015-1024 Abstract
Sullivan, F., Neale, B. M., Neale, M. C., van den Oord, E., & Kendler, K. S. (2003). Multipoint and single point non-parametric linkage analysis with imperfect data. Am J Med Genet B Neuropsychiatr Genet, 121(1), 89-94 Abstract
Surani, M. A., Barton, S. C., & Norris, M. L. (1984). Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature, 308(5959), 548-550 Abstract
Sved, J. A. (1971). Linkage disequilibrium and homozygosity of chromosome segments in finite populations. Theor Popul Biol, 2(2), 125-141 Abstract
Szatmari, P., Paterson, A. D., Zwaigenbaum, L., Roberts, W., Brian, J., Liu, X. Q., Vincent, J. B., Skaug, J. L., Thompson, A. P., Senman, L., Feuk, L., Qian, C., Bryson, S. E., Jones, M. B., Marshall, C. R., Scherer, S. W., Vieland, V. J., Bartlett, C., Mangin, L. V., Goedken, R., Segre, A., Pericak-Vance, M. A., Cuccaro, M. L., Gilbert, J. R., Wright, H. H., Abramson, R. K., Betancur, C., Bourgeron, T., Gillberg, C., Leboyer, M., Buxbaum, J. D., Davis, K. L., Hollander, E., Silverman, J. M., Hallmayer, J., Lotspeich, L., Sutcliffe, J. S., Haines, J. L., Folstein, S. E., Piven, J., Wassink, T. H., Sheffield, V., Geschwind, D. H., Bucan, M., Brown, W. T., Cantor, R. M., Constantino, J. N., Gilliam, T. C., Herbert, M., Lajonchere, C., Ledbetter, D. H., Lese-Martin, C., Miller, J., Nelson, S., Samango-Sprouse, C. A., Spence, S., State, M., Tanzi, R. E., Coon, H., Dawson, G., Devlin, B., Estes, A., Flodman, P., Klei, L., McMahon, W. M., Minshew, N., Munson, J., Korvatska, E., Rodier, M., Schellenberg, G. D., Smith, M., Spence, M. A., Stodgell, C., Tepper, G., Wijsman, E. M., Yu, C. E., Roge, B., Mantoulan, C., Wittemeyer, K., Poustka, A., Felder, B., Klauck, S. M., Schuster, C., Poustka, F., Bolte, S., Feineis-Matthews, S., Herbrecht, E., Schmotzer, G., Tsiantis, J., Papanikolaou, K., Maestrini, E., Bacchelli, E., Blasi, F., Carone, S., Toma, C., Van Engeland, H., de Jonge, M., Kemner, C., Koop, F., Langemeijer, M., Hijimans, C., Staal, W. G., Baird, G., Bolton, F., Rutter, M. L., Weisblatt, E., Green, J., Aldred, C., Wilkinson, J. A., Pickles, A., Le Couteur, A., Berney, T., McConachie, H., Bailey, A. J., Francis, K., Honeyman, G., Hutchinson, A., Parr, J. R., Wallace, S., Monaco, A. P., Barnby, G., Kobayashi, K., Lamb, J. A., Sousa, I., Sykes, N., Cook, E. H., Guter, S. J., Leventhal, B. L., Salt, J., Lord, C., Corsello, C., Hus, V., Weeks, D. E., Volkmar, F., Tauber, M., Fombonne, E., & Shih, A. (2007). Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet, 39(3), 319-328 Abstract
Tabachnik, B. G., & Fidell, L. S. (2001). Using Multivariate Statistics. Boston, MA.: Allyn and Bacon.
Tanck, M. W., Klerkx, A. H., Jukema, J. W., De Knijff, P., Kastelein, J. J., & Zwinderman, A. H. (2003). Estimation of multilocus haplotype effects using weighted penalised log-likelihood: analysis of five sequence variations at the cholesteryl ester transfer protein gene locus. Ann Hum Genet, 67(Pt 2), 175-184 Abstract
Tapper, W., Collins, A., Gibson, J., Maniatis, N., Ennis, S., & Morton, N. E. (2005). A map of the human genome in linkage disequilibrium units. Proc Natl Acad Sci U S A, 102(33), 11835-11839 Abstract
Tavtigian, S. V., Simard, J., Teng, D. H., Abtin, V., Baumgard, M., Beck, A., Camp, N. J., Carillo, A. R., Chen, Y., Dayananth, P., Desrochers, M., Dumont, M., Farnham, J. M., Frank, D., Frye, C., Ghaffari, S., Gupte, J. S., Hu, R., Iliev, D., Janecki, T., Kort, E. N., Laity, K. E., Leavitt, A., Leblanc, G., McArthur-Morrison, J., Pederson, A., Penn, B., Peterson, K. T., Reid, J. E., Richards, S., Schroeder, M., Smith, R., Snyder, S. C., Swedlund, B., Swensen, J., Thomas, A., Tranchant, M., Woodland, A. M., Labrie, F., Skolnick, M. H., Neuhausen, S., Rommens, J., & Cannon-Albright, L. A. (2001). A candidate prostate cancer susceptibility gene at chromosome 17 Nat Genet, 27(2), 172-180 Abstract
Templeton, A. (2002). Out of Africa again and again. Nature, 416(6876), 45-51 Abstract
Templeton, A. R., Boerwinkle, E., & Sing, C. F. (1987). A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. I. Basic theory and an analysis of alcohol dehydrogenase activity in Drosophila. Genetics, 117(2), 343-351
Templeton, A. R., Sing, C. F., Kessling, A., & Humphries, S. (1988). A cladistic analysis of phenotype associations with haplotypes inferred from restriction endonuclease mapping. II. The analysis of natural populations. Genetics, 120(4), 1145-1154 Abstract
Templeton, A. R., Crandall, K. A., & Sing, C. F. (1992). A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation. Genetics, 132(2), 619-633 Abstract
Templeton, A. R., & Sing, C. F. (1993). A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. IV. Nested analyses with cladogram uncertainty and recombination. Genetics, 134(2), 659-669 Abstract
Templeton, A. R., Weiss, K. M., Nickerson, D. A., Boerwinkle, E., & Sing, C. F. (2000). Cladistic structure within the human Lipoprotein lipase gene and its implications for phenotypic association studies. Genetics, 156(3), 1259-1275 Abstract
Terwilliger, J. D., Ding, Y., & Ott, J. (1992). On the relative importance of marker heterozygosity and intermarker distance in gene mapping. Genomics, 13(4), 951-956 Abstract
Terwilliger, J. D., & Ott, J. (1994). Handbook of Human Genetic Linkage. In (p237-238). Baltimore, MD: Johns Hopkins University Press.
Terwilliger, J. D. (1996). SIBPAIR: sibpair analysis on nuclear families. http://www.helsinki.fi/~tsjuntun/linkage/analyze/..
Thomas, D. C., Haile, R. W., & Duggan, D. (2005). Recent developments in genomewide association scans: a workshop summary and review. Am J Hum Genet, 77(3), 337-345 Abstract
Thompson, W. R. (1966). Multivariate experiment in Behavior Genetics. . In Cattell, R. B. (Ed.), Handbook of Multivariate Experimental Psychology (p711-731). Chicago, IL: Rand McNally.
Tikhonoff, V., Kuznetsova, T., Stolarz, K., Bianchi, G., Casiglia, E., Kawecka-Jaszcz, K., Nikitin, Y., Tizzone, L., Wang, J. G., & Staessen, J. A. (2003). beta-Adducin polymorphisms, blood pressure, and sodium excretion in three European populations. Am J Hypertens, 16(10), 840-846 Abstract
Tishkoff, S. A., Reed, F. A., Ranciaro, A., Voight, B. F., Babbitt, C. C., Silverman, J. S., Powell, K., Mortensen, H. M., Hirbo, J. B., Osman, M., Ibrahim, M., Omar, S. A., Lema, G., Nyambo, T. B., Ghori, J., Bumpstead, S., Pritchard, J. K., Wray, G. A., & Deloukas, (2007). Convergent adaptation of human lactase persistence in Africa and Europe. Nat Genet, 39(1), 31-40 Abstract
Trikalinos, T. A., Salanti, G., Khoury, M. J., & Ioannidis, J. (2006). Impact of violations and deviations in Hardy-Weinberg equilibrium on postulated gene-disease associations. Am J Epidemiol, 163(4), 300-309 Abstract
Tsai, S. J., Wang, Y. C., & Hong, C. J. (2001). Allelic variants of the alpha1a adrenoceptor and the promoter region of the alpha2a adrenoceptor and temperament factors. Am J Med Genet, 105(1), 96-98 Abstract
Tsai, S. J., Wang, Y. C., Chen, J. Y., & Hong, C. J. (2003). Allelic variants of the tryptophan hydroxylase (A218C) and serotonin 1B receptor (A-161T) and personality traits. Neuropsychobiology, 48(2), 68-71 Abstract
Tu, I. P., & Whittemore, A. S. (1999). Power of association and linkage tests when the disease alleles are unobserved. Am J Hum Genet, 64(2), 641-649 Abstract
Tukey, J. W. (1951). Components in regression. Biometrics, 7, 33-69
Turkheimer, E., & Gottesman, I. I. (1991). Is H2 = 0 a null hypothesis anymore? Behav. Brain Sci, 14, 410-411
Turkheimer, E., Haley, A., Waldron, M., D’Onofrio, B., & Gottesman, II. (2003). Socioeconomic status modifies heritability of IQ in young children. Psychol Sci, 14(6), 623-628 Abstract
Tzeng, J. Y., Wang, C. H., Kao, J. T., & Hsiao, C. K. (2006). Regression-Based Association Analysis with Clustered Haplotypes through Use of Genotypes. Am J Hum Genet, 78(2), 231-242 Abstract