|
2006 Journal Article Erratum: A sex-limited genome scan for body mass index in an unselected sample (Twin Research and Human Genetics (2005) 8, 6 (616-632))Cornes, B. K., Medland, S. E., Ferreira, M. A.R., Morley, K. I., Duffy, D. L., Heijmans, B. T., Montgomery, G. W. and Martin, N. G. (2006). Erratum: A sex-limited genome scan for body mass index in an unselected sample (Twin Research and Human Genetics (2005) 8, 6 (616-632)). Twin Research and Human Genetics, 9 (3) doi: 10.1375/twin.9.3.ii |
|
2006 Journal Article Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblingsVisscher, Peter M., Medland, Sarah E., Ferreira, Manuel A. R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006). Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. Plos Genetics, 2 (3), 316-325. doi: 10.1371/journal.pgen.0020041 |
|
2006 Journal Article Handedness in twins: Joint analysis of data from 35 samplesMedland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M. and Martin, Nicholas G. (2006). Handedness in twins: Joint analysis of data from 35 samples. Twin Research and Human Genetics, 9 (1), 46-53. doi: 10.1375/183242706776402885 |
|
2006 Journal Article A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin familiesMorley, Katherine I., Medland, Sarah E., Ferreira, Manuel A. R., Lynskey, Michael T., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2006). A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin families. Behavior Genetics, 36 (1), 87-99. doi: 10.1007/s10519-005-9004-0 |
|
2006 Journal Article Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory taskHansell, N. K., Medland, S. E., Ferreira, A. R., Geffen, G. M., Zhu, G., Montgomery, G. W., Duffy, D. L., Wright, M.J. and Martin, N. G. (2006). Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task. Behavior Genetics, 36 (1), 29-44. doi: 10.1007/s10519-005-9002-2 |
|
2006 Journal Article Population differences in finger-length ratios: Ethnicity or latitude?Loehlin, John C., McFadden, Dennis, Medland, Sarah E. and Martin, Nicholas G. (2006). Population differences in finger-length ratios: Ethnicity or latitude?. Archives of Sexual Behavior, 35 (6), 739-742. doi: 10.1007/s10508-006-9039-1 |
|
2006 Journal Article ViewPoint and ViewDist: Utilities for rapid graphing of linkage distributions and identification of outliersBeeby, Harry N., Medland, Sarah E. and Martin, Nicholas G. (2006). ViewPoint and ViewDist: Utilities for rapid graphing of linkage distributions and identification of outliers. Behavior Genetics, 36 (1), 7-11. doi: 10.1007/s10519-006-9045-z |
|
2005 Journal Article Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin familiesCornes, B.K., Medland, S.E., Ferreira, M.A.R., Morley, K.I., Duffy, D.L., Heijmans, B.T., Montgomery, G.W. and Martin, N.G. (2005). Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families. Twin Research and Human Genetics, 8 (6), 616-632. doi: 10.1375/183242705774860240 |
|
2005 Journal Article Parameterization of sex-limited autosomal linkage analysis for MxMedland, Sarah E. (2005). Parameterization of sex-limited autosomal linkage analysis for Mx. Twin Research and Human Genetics, 8 (6), 569-573. doi: 10.1375/183242705774860213 |
|
2005 Journal Article Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and femalesMedland, Sarah E., Duffy, David L., Spurdle, Amanda B., Wright, Margaret J., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2005). Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females. Behavior Genetics, 35 (6), 735-744. doi: 10.1007/s10519-005-6187-3 |
|
2005 Journal Article Genomewide significant linkage to migrainous Hheadache on chromosome 5q21Nyholt, Dale R., Morley, Katherine I., Ferreira, Manual A. R., Medland, Sarah E., Boomsma, Dorret I., Heath, Andrew C., Merikangas, Kathleen R., Montgomery, Grant W. and Martin, Nicholas G. (2005). Genomewide significant linkage to migrainous Hheadache on chromosome 5q21. American Journal Of Human Genetics, 77 (3), 500-512. doi: 10.1086/444510 |
|
2005 Journal Article A survey of homozygous deletions in human cancer genomesCox, C, Bignell, G, Greenman, C, Stabenau, A, Warren, W, Stephens, P, Davies, H, Watt, S, Teague, J, Edkins, S, Birney, E, Easton, DF, Wooster, R, Futreal, PA and Stratton, MR (2005). A survey of homozygous deletions in human cancer genomes. Proceedings of the National Academy of Sciences of the United States of America, 102 (12), 4542-4547. doi: 10.1073/pnas.0408593102 |
|
2005 Other Outputs The genetic epidemiology of behavioural lateralityMedland, Sarah (2005). The genetic epidemiology of behavioural laterality. PhD Thesis, School of Psychology, The University of Queensland. doi: 10.14264/220151 |
|
2004 Journal Article Intragenic ERBB2 kinase mutations in tumoursStephens, P, Hunter, C, Bignell, G, Edkins, S, Davies, H, Teague, J, Stevens, C, O'Meara, S, Smith, R, Parker, A, Barthorpe, A, Blow, M, Brackenbury, L, Butler, A, Clarke, O, Cole, J, Dicks, E, Dike, A, Drozd, A, Edwards, K, Forbes, S, Foster, R, Gray, K, Greenman, C, Halliday, K, Hills, K, Kosmidou, , Lugg, R, Menzies, A ... Stratton, MR (2004). Intragenic ERBB2 kinase mutations in tumours. Nature, 431 (7008), 525-526. doi: 10.1038/431525b |
|
2004 Journal Article Alternate parameterization for scalar and non-scalar sex-limitation models in MxMedland, Sarah E. (2004). Alternate parameterization for scalar and non-scalar sex-limitation models in Mx. Twin Research, 7 (3), 299-305. doi: 10.1375/136905204774200587 |
|
2004 Journal Article A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalitiesYouings, S, Ellis, K, Ennis, S, Barber, J and Jacobs, P (2004). A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities. American Journal of Medical Genetics Part a, 126A (1), 46-60. doi: 10.1002/ajmg.a.20553 |
|
2004 Journal Article A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15qZhu, G., Evans, D. M., Duffy, D. L., Montgomery, G. W., Medland, S. E., Gillespie, N. A., Ewen, K. R., Jewell, M., Liew, Y. W., Hayward, N. K., Sturm, R. A., Trent, J. M. and Martin, N. G. (2004). A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q. Twin Research, 7 (2), 197-210. doi: 10.1375/136905204323016186 |
|
2004 Journal Article Gender diagnosticity and androgen receptor gene CAG repeat sequenceLoehlin, John C., Jonsson, Erik G., Gustavsson, J. Petter, Schalling, Martin, Medland, Sarah E., Montgomery, Grant W. and Martin, Nicholas G. (2004). Gender diagnosticity and androgen receptor gene CAG repeat sequence. Twin Research, 7 (5), 456-461. doi: 10.1375/1369052042335359 |
|
2004 Journal Article Effects of culture, sex, and age on the distribution of handedness: An evaluation of the sensitivity of three measures of handednessMedland, Sara E., Perelle, I., De Monte, V. and Ehrman, L. (2004). Effects of culture, sex, and age on the distribution of handedness: An evaluation of the sensitivity of three measures of handedness. Laterality, 9 (3), 287-297. doi: 10.1080/13576500342000040a |
|
2004 Journal Article Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationTarpey, Patrick, Parnau, Josep, Blow, Matthew, Woffendin, Hayley, Bignell, Graham, Cox, Charles, Cox, James, Davies, Helen, Edkins, Sarah, Holden, Simon, Korny, Angelique, Mallya, Uma, Moon, Jenny, O’Meara, Sarah, Parker, Adrian, Stephens, Philip, Stevens, Claire, Teague, Jon, Donnelly, Andrew, Mangelsdorf, Marie, Mulley, John, Partington, Michael, Turner, Gillian, Stevenson, Roger, Schwartz, Charles, Young, Ian, Easton, Douglas, Bobrow, Martin, Futreal, P. Andrew ... Raymond, F. Lucy (2004). Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation. American Journal of Human Genetics, 75 (2), 318-324. doi: 10.1086/422703 |
