GK_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

Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., Liu-Cordero, S. N., Rotimi, C., Adeyemo, A., Cooper, R., Ward, R., Lander, E. S., Daly, M. J., & Altshuler, D. (2002). The structure of haplotype blocks in the human genome. Science, 296(5576), 2225-2229 Abstract

Galton, F. (1889). Natural Inheritance.. London: Macmillan.

Gauderman, W. J., Morrison, J. L., & Siegmund, K. D. (2001). Should we consider gene x environment interaction in the hunt for quantitative trait loci? Genet Epidemiol, 21 Suppl 1, S831-836 Abstract

Geiringer, H. (1944). On the probability theory of linkage in Mendelian heredity. Ann Math Stat, 15, 25-57

Gelman, A., Carlin, J. B., Stern, H. S., & Rubin, D. B. (2004). Bayesian Data Analysis, 2nd Edn.. London: Chapman and Hall.

Gentleman, R., Rossini, A. J., & Sudoit, S. (2006). Bioconductor.

Ghosh, S., Karanjawala, Z. E., Hauser, E. R., Ally, D., Knapp, J. I., Rayman, J. B., Musick, A., Tannenbaum, J., Te, C., Shapiro, S., Eldridge, W., Musick, T., Martin, C., Smith, J. R., Carpten, J. D., Brownstein, M. J., Powell, J. I., Whiten, R., Chines, P., Nylund, S. J., Magnuson, V. L., Boehnke, M., & Collins, F. S. (1997). Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group Genome Res, 7(2), 165-178 Abstract

Gilks, W. R., Richardson, S., & Spiegelhalter, D. J. (Eds.). (1996). Markov Chain Monte Carlo in practice.. London: Chapman and Hall.

Gill, E., Murray, W., & Wright, M. H. (1981). Practical Optimization.. London: Academic Press. .

Gillespie, N. A., & Neale, M. C. (2006). A finite mixture model for genotype and environment interactions: detecting latent population heterogeneity. Twin Res Hum Genet, 9(3), 412-423 Abstract

Glaser, R. L., Ramsay, J. P., & Morison, I. M. (2006). The imprinted gene and parent-of-origin effect database now includes parental origin of de novo mutations. Nucleic Acids Res, 34(Database issue), D29-31 Abstract

Gonick, L., & Smith, M. (1994). Cartoon Guide to Statistics.. New York, NY.: Harper Collins,.

Gonzalez-Neira, A., Ke, X., Lao, O., Calafell, F., Navarro, A., Comas, D., Cann, H., Bumpstead, S., Ghori, J., Hunt, S., Deloukas, P., Dunham, I., Cardon, L. R., & Bertranpetit, J. (2006). The portability of tagSNPs across populations: a worldwide survey. Genome Res, 16(3), 323-330 Abstract

Gordon, D., Heath, S. C., & Ott, J. (1999). True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms. Hum Hered, 49(2), 65-70 Abstract

Gordon, D., Heath, S. C., Liu, X., & Ott, J. (2001). A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. Am J Hum Genet, 69(2), 371-380 Abstract

Gordon, D., Finch, S., Nothnagel, M., & Ott, J. (2002). Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms. Human Heredity, 54, 22-33

Goring, H. H., & Ott, J. (1997). Relationship estimation in affected sib pair analysis of late-onset diseases. Eur J Hum Genet, 5(2), 69-77 Abstract

Goring, H. H., & Terwilliger, J. D. (2000a). Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters. Am J Hum Genet, 66(4), 1298-1309 Abstract

Goring, H. H., & Terwilliger, J. D. (2000b). Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions. Am J Hum Genet, 66(3), 1107-1118 Abstract

Gorlova, O. Y., Amos, C. I., Wang, N. W., Shete, S., Turner, S. T., & Boerwinkle, E. (2003). Genetic linkage and imprinting effects on body mass index in children and young adults. Eur J Hum Genet, 11(6), 425-432 Abstract

Gosso, M. F., van Belzen, M., de Geus, E. J., Polderman, J. C., Heutink, P., Boomsma, D. I., & Posthuma, D. (2006). Association between the CHRM2 gene and intelligence in a sample of 304 Dutch families. Genes Brain Behav, 5(8), 577-584 Abstract

Greenberg, D. A. (1989). Inferring mode of inheritance by comparison of lod scores. Am J Med Genet, 34(4), 480-486 Abstract

Greene, W. H. (1993). _ Econometric Analysis, 2nd Edn_. New York, NY.: Macmillan.

Gu, C., Todorov, A., & Rao, D. C. (1996). Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci. Genet Epidemiol, 13(6), 513-533 Abstract

Gudbjartsson, D. F., Jonasson, K., Frigge, M. L., & Kong, A. (2000). Allegro, a new computer program for multipoint linkage analysis. Nat Genet, 25(1), 12-13 Abstract

Guo, S. W., & Thompson, E. A. (1992). Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics, 48(2), 361-372 Abstract

Guo, S. W. (1997). Linkage disequilibrium measures for fine-scale mapping: a comparison. Hum Hered, 47(6), 301-314 Abstract

Guo, X., & Elston, R. C. (1999). Linkage information content of polymorphic genetic markers. Hum Hered, 49(2), 112-118 Abstract

Gusella, J. F., Keys, C., VarsanyiBreiner, A., Kao, F. T., Jones, C., Puck, T. T., & Housman, D. (1980). Isolation and localization of DNA segments from specific human chromosomes. Proc Natl Acad Sci U S A, 77(5), 2829-2833 Abstract

Gusella, J. F., Wexler, N. S., Conneally, M., Naylor, S. L., Anderson, M. A., Tanzi, R. E., Watkins, C., Ottina, K., Wallace, M. R., Sakaguchi, A. Y., & et al. (1983). A polymorphic DNA marker genetically linked to Huntington’s disease. Nature, 306(5940), 234-238 Abstract

Halpern, J., & Whittemore, A. S. (1999). Multipoint linkage analysis. A cautionary note. Hum Hered, 49(4), 194-196 Abstract

Hamer, D., & Sirota, L. (2000). Beware the chopsticks gene. Mol Psychiatry, 5(1), 11-13 Abstract

Hanson, R. L., Kobes, S., Lindsay, R. S., & Knowler, W. C. (2001). Assessment of parent-of-origin effects in linkage analysis of quantitative traits. Am J Hum Genet, 68(4), 951-962 Abstract

Hardy, G. H. (1908). Mendelian Proportions in a Mixed Population. Science, 28(706), 49-50 Abstract

Hartl, D. L., & Clark, A. G. (1997). Principles of Population Genetics.. Sunderland, MA.: Sinauer.

Haseman, J. K., & Elston, R. C. (1972). The investigation of linkage between a quantitative trait and a marker locus. Behav Genet, 2(1), 3-19 Abstract

Hauser, E. R., Watanabe, R. M., Duren, W. L., Bass, M. P., Langefeld, C. D., & Boehnke, M. (2004). Ordered subset analysis in genetic linkage mapping of complex traits. Genet Epidemiol, 27(1), 53-63 Abstract

Haviland, M. B., Kessling, A. M., Davignon, J., & Sing, C. F. (1995). Cladistic analysis of the apolipoprotein AI-CIII-AIV gene cluster using a healthy French Canadian sample. I. Haploid analysis. Ann Hum Genet, 59(Pt 2), 211-231 Abstract

Havill, L. M., Dyer, T. D., Richardson, D. K., Mahaney, M. C., & Blangero, J. (2005). The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification. BMC Genet, 6 Suppl 1, S91 Abstract

Hawley, M. E., & Kidd, K. K. (1995). HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. J Hered, 86(5), 409-411 Abstract

Hays, W. L. (1988). Statistics, 4th Edn.. New York, NY.: Holt, Rinehart and Winston.

Hazel, L. N. (1943). The Genetic Basis for Constructing Selection Indexes. Genetics, 28(6), 476-490 Abstract

Heath, A. C., & Eaves, L. J. (1985). Resolving the effects of phenotype and social background on mate selection. Behav Genet, 15(1), 15-30 Abstract

Heath, A. C., Kendler, K. S., Eaves, L. J., & Markell, D. (1985). The resolution of cultural and biological inheritance: informativeness of different relationships. Behav Genet, 15(5), 439-465 Abstract

Heath, A. C., Todorov, A. A., Nelson, E. C., Madden, A., Bucholz, K. K., & Martin, N. G. (2002). Gene-environment interaction effects on behavioral variation and risk of complex disorders: the example of alcoholism and other psychiatric disorders. Twin Res, 5(1), 30-37 Abstract

Heath, S. C. (1997). Markov chain Monte Carlo segregation and linkage analysis for oligogenic models. Am J Hum Genet, 61(3), 748-760 Abstract

Hedrick, W., & Thomson, G. (1986). A two-locus neutrality test: applications to humans, E. coli and lodgepole pine. Genetics, 112(1), 135-156 Abstract

Hedrick, W. (1987). Gametic disequilibrium measures: proceed with caution. Genetics, 117(2), 331-341 Abstract

Herbert, A., Gerry, N. P., McQueen, M. B., Heid, I. M., Pfeufer, A., Illig, T., Wichmann, H. E., Meitinger, T., Hunter, D., Hu, F. B., Colditz, G., Hinney, A., Hebebrand, J., Koberwitz, K., Zhu, X., Cooper, R., Ardlie, K., Lyon, H., Hirschhorn, J. N., Laird, N. M., Lenburg, M. E., Lange, C., & Christman, M. F. (2006). A common genetic variant is associated with adult and childhood obesity. Science, 312(5771), 279-283 Abstract

Heutink, P., van de Wetering, B. J., Pakstis, A. J., Kurlan, R., Sandor, P., Oostra, B. A., & Sandkuijl, L. A. (1995). Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice? Am J Hum Genet, 57(2), 465-473 Abstract

Hewitt, J. K., & Heath, A. C. (1988). A note on computing the chi-square noncentrality parameter for power analyses. Behav Genet, 18(1), 105-108 Abstract

Higuchi, S., Matsushita, S., Imazeki, H., Kinoshita, T., Takagi, S., & Kono, H. (1994). Aldehyde dehydrogenase genotypes in Japanese alcoholics. Lancet, 343(8899), 741-742 Abstract

Hill, A. B. (1965). The Environment and Disease: Association or Causation? Proc R Soc Med, 58, 295-300 Abstract

Hill, W. G., & Robertson, A. (1968). The effects of inbreeding at loci with heterozygote advantage. Genetics, 60(3), 615-628 Abstract

Hill, W. G. (1977). Correlation of gene frequencies between neutral linked genes in finite populations. Theor Popul Biol, 11(2), 239-248 Abstract

Hinds, D. A., & Risch, N. (1996). The ASPEX package: affected sib-pair exclusion mapping. http://aspex.sourceforge.net/..

Hinds, D. A., Stuve, L. L., Nilsen, G. B., Halperin, E., Eskin, E., Ballinger, D. G., Frazer, K. A., & Cox, D. R. (2005). Whole-genome patterns of common DNA variation in three human populations. Science, 307(5712), 1072-1079 Abstract

Hinrichs, A. S., Karolchik, D., Baertsch, R., Barber, G. P., Bejerano, G., Clawson, H., Diekhans, M., Furey, T. S., Harte, R. A., Hsu, F., Hillman-Jackson, J., Kuhn, R. M., Pedersen, J. S., Pohl, A., Raney, B. J., Rosenbloom, K. R., Siepel, A., Smith, K. E., Sugnet, C. W., Sultan-Qurraie, A., Thomas, D. J., Trumbower, H., Weber, R. J., Weirauch, M., Zweig, A. S., Haussler, D., & Kent, W. J. (2006). The UCSC Genome Browser Database: update 2006. Nucleic Acids Res, 34(Database issue), D590-598 Abstract

Hirschhorn, J. N., Lohmueller, K., Byrne, E., & Hirschhorn, K. (2002). A comprehensive review of genetic association studies. Genet Med, 4(2), 45-61 Abstract

Hirschhorn, J. N., & Daly, M. J. (2005). Genome-wide association studies for common diseases and complex traits. Nat Rev Genet, 6(2), 95-108 Abstract

Hodge, S. E., Abreu, C., & Greenberg, D. A. (1997). Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study. Am J Hum Genet, 60(1), 217-227 Abstract

Holliday, E., Mowry, B., Chant, D., & Nyholt, D. (2005). The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data. Hum Genet, 117(2-3), 160-167 Abstract

Holmans, (1993). Asymptotic properties of affected-sib-pair linkage analysis. Am J Hum Genet, 52(2), 362-374 Abstract

Holmans, P., & Clayton, D. (1995). Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers. Am J Hum Genet, 57(5), 1221-1232 Abstract

Hoppe, B., Haupl, T., Gruber, R., Kiesewetter, H., Burmester, G. R., Salama, A., & Dorner, T. (2006). Detailed analysis of the variability of peptidylarginine deiminase type 4 in German patients with rheumatoid arthritis: a case-control study. Arthritis Res Ther, 8(2), R34 Abstract

Hopper, J. L., & Mathews, J. D. (1982). Extensions to multivariate normal models for pedigree analysis. Ann Hum Genet, 46(Pt 4), 373-383 Abstract

Horsthemke, B., & Buiting, K. (2006). Imprinting defects on human chromosome 15. Cytogenet Genome Res, 113(1-4), 292-299 Abstract

Horvath, S., & Laird, N. M. (1998). A discordant-sibship test for disequilibrium and linkage: no need for parental data. Am J Hum Genet, 63(6), 1886-1897 Abstract

Horvath, S., Xu, X., Lake, S. L., Silverman, E. K., Weiss, S. T., & Laird, N. M. (2004). Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics. Genet Epidemiol, 26(1), 61-69 Abstract

Hottenga, J. J., Boomsma, D. I., Kupper, N., Posthuma, D., Snieder, H., Willemsen, G., & de Geus, E. J. (2005). Heritability and stability of resting blood pressure. Twin Res Hum Genet, 8(5), 499-508 Abstract

Huber, (1967). The behaviour of maximum likelihood estimates under nonstandard conditions. In Proceedings of the Fifth Berkeley Symposium in Mathematical Statistics and Probability, Vol 1 (p221-233). Berkeley, CA,: University of California Press,.

Hugot, J. P., Chamaillard, M., Zouali, H., Lesage, S., Cezard, J. P., Belaiche, J., Almer, S., Tysk, C., O’Morain, C. A., Gassull, M., Binder, V., Finkel, Y., Cortot, A., Modigliani, R., Laurent-Puig, P., Gower-Rousseau, C., Macry, J., Colombel, J. F., Sahbatou, M., & Thomas, G. (2001). Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease. Nature, 411(6837), 599-603 Abstract

Idury, R. M., & Cardon, L. R. (1997). A simple method for automated allele binning in microsatellite markers. Genome Res, 7(11), 1104-1109 Abstract

Idury, R. M., & Elston, R. C. (1997). A faster and more general hidden Markov model algorithm for multipoint likelihood calculations. Hum Hered, 47(4), 197-202 Abstract

International HapMap Consortium. (2005). A haplotype map of the human genome. Nature, 437(7063), 1299-1320 Abstract

Ioannidis, J. P., Rosenberg, S., Goedert, J. J., & O’Brien, T. R. (2002). Commentary: meta-analysis of individual participants’ data in genetic epidemiology. Am J Epidemiol, 156(3), 204-210 Abstract

Ioannidis, J. P., Trikalinos, T. A., Ntzani, E. E., & Contopoulos-Ioannidis, D. G. (2003). Genetic associations in large versus small studies: an empirical assessment. Lancet, 361(9357), 567-571 Abstract

Ioannidis, J. (2005). Why most published research findings are false. PLoS Med, 2(8), e124 Abstract

James, J. W. (1971). Frequency in relatives for an all-or-none trait. Ann Hum Genet, 35(1), 47-49 Abstract

Jardine, R., & Martin, N. G. (1984). No evidence for sex-linked or sex-limited gene expression influencing spatial orientation. Behav Genet, 14(4), 345-354 Abstract

Jeffreys, A. J., Kauppi, L., & Neumann, R. (2001). Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex. Nat Genet, 29(2), 217-222 Abstract

Jensen, F. V. (1996). An Introduction to Bayesian Networks.. London: University College Press, .

Jinks, J. L., & Fulker, D. W. (1970). Comparison of the biometrical genetical, MAVA, and classical approaches to the analysis of human behavior. Psychol Bull, 73(5), 311-349 Abstract

Johnson, G. C., Esposito, L., Barratt, B. J., Smith, A. N., Heward, J., Di Genova, G., Ueda, H., Cordell, H. J., Eaves, I. A., Dudbridge, F., Twells, R. C., Payne, F., Hughes, W., Nutland, S., Stevens, H., Carr, P., Tuomilehto-Wolf, E., Tuomilehto, J., Gough, S. C., Clayton, D. G., & Todd, J. A. (2001). Haplotype tagging for the identification of common disease genes. Nat Genet, 29(2), 233-237 Abstract

Johnson, R. A., & Wichern, D. W. (2002). Applied Multivariate Statistical Analysis. Upper Saddle River, NJ.: Prentice Hall,.

Jorde, L. B. (1995). Linkage disequilibrium as a gene-mapping tool. Am J Hum Genet, 56(1), 11-14 Abstract

Joreskog, K. G. (1966). Testing a simple structure hypothesis in factor analysis. Psychometrika, 31(2), 165-178 Abstract

Joreskog, K. G. (1967). Some Contributions to Maximum Likelihood Factor Analysis. Psychometrika, 32(4), 443

Joreskog, K. G., & Lawley, D. N. (1968). New Methods in Maximum Likelihood Factor Analysis. British Journal of Mathematical & Statistical Psychology, 21, 85-

Joreskog, K. G., & Sorbom, D. (1993). LISREL 8 User’s Reference Guide.. Chicago, IL: Scientific Software International.

Kang, S. J., Gordon, D., & Finch, S. J. (2004). What SNP genotyping errors are most costly for genetic association studies? Genet Epidemiol, 26(2), 132-141 Abstract

Karlin, S., & Piazza, A. (1981). Statistical methods for assessing linkage disequilibrium at the HLA-A, B, C loci. Ann Hum Genet, 45(Pt 1), 79-94 Abstract

Ke, X., Durrant, C., Morris, A. P., Hunt, S., Bentley, D. R., Deloukas, P., & Cardon, L. R. (2004). Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples. Hum Mol Genet, 13(21), 2557-2565 Abstract

Ke, X., Hunt, S., Tapper, W., Lawrence, R., Stavrides, G., Ghori, J., Whittaker, P., Collins, A., Morris, A. P., Bentley, D., Cardon, L. R., & Deloukas, (2004). The impact of SNP density on fine-scale patterns of linkage disequilibrium. Hum Mol Genet, 13(6), 577-588 Abstract

Ke, X., Miretti, M. M., Broxholme, J., Hunt, S., Beck, S., Bentley, D. R., Deloukas, P., & Cardon, L. R. (2005). A comparison of tagging methods and their tagging space. Hum Mol Genet, 14(18), 2757-2767 Abstract

Keavney, B., McKenzie, C. A., Connell, J. M., Julier, C., Ratcliffe, J., Sobel, E., Lathrop, M., & Farrall, M. (1998). Measured haplotype analysis of the angiotensin-I converting enzyme gene. Hum Mol Genet, 7(11), 1745-1751 Abstract

Kempthorne, O., & Osborne, R. H. (1961). The interpretation of twin data. Am J Hum Genet, 13, 320-339 Abstract

Kendall, M., & Stuart, A. (1979). The Advanced Theory of Statistics, Vol 2: Inference and Relationshi. New York, NY: John Wiley & Sons.

Kent, J. W., Dyer, T. D., & Blangero, J. (2005). Estimating the additive genetic effect of the X chromosome. Genet Epidemiol, 29(4), 377-388 Abstract

Kent, J. W., Jr., Lease, L. R., Mahaney, M. C., Dyer, T. D., Almasy, L., & Blangero, J. (2005). X chromosome effects and their interactions with mitochondrial effects. BMC Genet, 6 Suppl 1, S157 Abstract

Kerem, B., Rommens, J. M., Buchanan, J. A., Markiewicz, D., Cox, T. K., Chakravarti, A., Buchwald, M., & Tsui, L. C. (1989). Identification of the cystic fibrosis gene: genetic analysis. Science, 245(4922), 1073-1080 Abstract

Kidd, K. K., Pakstis, A. J., Speed, W. C., & Kidd, J. R. (2004). Understanding human DNA sequence variation. J Hered, 95(5), 406-420 Abstract

Kirk, R. E. (1994). Experimental Design: Procedures for the Behavioral Sciences (Psychology). Belmont, CA.: Wadsworth Publishing.

Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J. Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., Bracken, M. B., Ferris, F. L., Ott, J., Barnstable, C., & Hoh, J. (2005). Complement factor H polymorphism in age-related macular degeneration. Science, 308(5720), 385-389 Abstract

Knapp, M., Seuchter, S. A., & Baur, M. (1994). Linkage analysis in nuclear families. 2: Relationship between affected sib-pair tests and lod score analysis. Hum Hered, 44(1), 44-51 Abstract

Knapp, M. (1997). The affected sib pair method for linkage analysis. In Pawlowitzki, I. H., Edwards, J. H. & Thompson, E. A. (Eds.), Genetic Mapping of Disease Genes. (p150-151). London: Academic Press.

Knapp, M. (1999). A note on power approximations for the transmission/disequilibrium test. Am J Hum Genet, 64(4), 1177-1185 Abstract

Knapp, M., & Strauch, K. (2004). Affected-sib-pair test for linkage based on constraints for identical-by-descent distributions corresponding to disease models with imprinting. Genet Epidemiol, 26(4), 273-285 Abstract

Knorr-Held, L., & Rasser, G. (2000). Bayesian detection of clusters and discontinuities in disease maps. Biometrics, 56(1), 13-21 Abstract

Knowler, W. C., Williams, R. C., Pettitt, D. J., & Steinberg, A. G. (1988). Gm3;5,13,14 and type 2 diabetes mellitus: an association in American Indians with genetic admixture. Am J Hum Genet, 43(4), 520-526 Abstract

Koenig, M., Hoffman, E. P., Bertelson, C. J., Monaco, A. P., Feener, C., & Kunkel, L. M. (1987). Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell, 50(3), 509-517 Abstract

Kong, A., & Cox, N. J. (1997). Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet, 61(5), 1179-1188 Abstract

Kong, A., Gudbjartsson, D. F., Sainz, J., Jonsdottir, G. M., Gudjonsson, S. A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G., Shlien, A., Palsson, S. T., Frigge, M. L., Thorgeirsson, T. E., Gulcher, J. R., & Stefansson, K. (2002). A high-resolution recombination map of the human genome. Nat Genet, 31(3), 241-247 Abstract

Kong, X., Murphy, K., Raj, T., He, C., White, S., & Matise, T. C. (2004). A combined linkage-physical map of the human genome. Am J Hum Genet, 75(6), 1143-1148 Abstract

Kraemer, H. C. (1985). A strategy to teach the concept and application of power of statistical tests. J. Educat. Stat., 10, 173-195

Kraft, P., Cox, D. G., Paynter, R. A., Hunter, D., & De Vivo, I. (2005). Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques. Genet Epidemiol, 28(3), 261-272 Abstract

Kruglyak, L., & Lander, E. S. (1995). Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet, 57(2), 439-454 Abstract

Kruglyak, L., Daly, M. J., Reeve-Daly, M. P., & Lander, E. S. (1996). Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet, 58(6), 1347-1363 Abstract

Kruglyak, L. (1997). The use of a genetic map of biallelic markers in linkage studies. Nat Genet, 17(1), 21-24 Abstract

Kruglyak, L., & Daly, M. J. (1998). Linkage thresholds for two-stage genome scans. Am J Hum Genet, 62(4), 994-997 Abstract

Kruglyak, L., & Lander, E. S. (1998). Faster multipoint linkage analysis using Fourier transforms. J Comput Biol, 5(1), 1-7 Abstract

Kruglyak, L. (1999). Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nat Genet, 22(2), 139-144 Abstract

Kupper, N., Willemsen, G., Riese, H., Posthuma, D., Boomsma, D. I., & de Geus, E. J. (2005). Heritability of daytime ambulatory blood pressure in an extended twin design. Hypertension, 45(1), 80-85 Abstract

Kwok, Y. (2001). Methods for genotyping single nucleotide polymorphisms. Annu Rev Genomics Hum Genet, 2, 235-258 Abstract