Browse By Publication: Human Genetics

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Number of items: 13.

Bellis, C., Cox, H. C., Dyer, T. D., Charlesworth, J. C., Begley, K. N., Quinlan, S., et al. (2008) Linkage mapping of CVD risk traits in the isolated Norfolk Island population. Human Genetics, 124(5), pp. 543-552.
Number of citations in Scopus 17
Number of citations in Web of Science® 16

Chen, Carla C.M., Mengersen, Kerrie L., Keith, Jonathan M., Martin, Nicholas G., & Nyholt, Dale R. (2009) Linkage and heritability analysis of migraine symptom groupings: A comparison of three different clustering methods on twin data. Human Genetics, 125(5-6), pp. 591-604.
Number of citations in Scopus 3
Number of citations in Web of Science® 3

Chen, Carla Chia Ming, Keith, Jonathan M., Nyholt, Dale R., Martin, Nicholas , & Mengersen, Kerrie (2009) Bayesian latent trait modeling of migraine symptom data. Human Genetics, 126(2), pp. 277-288.
Number of citations in Scopus 6
Number of citations in Web of Science® 5

Holliday, E., Mowry, B., Chant, D., & Nyholt, D.R. (2005) The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data. Human Genetics, 117(2-3), pp. 160-167.
Number of citations in Scopus 7
Number of citations in Web of Science® 8

Kote-Jarai, Zsofia, Olama, Ali Amin Al, Leongamornlert, Daniel, Tymrakiewicz, Malgorzata, Saunders, E., Guy, Michelle, et al. (2011) Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript. Human Genetics, 129(6), pp. 687-694.
Number of citations in Scopus 46
Number of citations in Web of Science® 45

Ligthart, L., Hottenga, J.-J., Lewis, C.M., Farmer, A.E., Craig, I.W., Breen, G., et al. (2014) Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders. Human Genetics, 133(2), pp. 173-186.
Number of full-text downloads 10
Number of citations in Scopus 18
Number of citations in Web of Science® 16

Nyholt, D.R. (2001) Genetic case-control association studies--correcting for multiple testing. Human Genetics, 109(5), pp. 564-567.
Number of citations in Scopus 76
Number of citations in Web of Science® 74

Nyholt, Dale R., Curtain, Robert P., & Griffiths, Lyn R. (2000) Familial typical migraine: Significant linkage and localization of a gene to Xq24-28. Human Genetics, 107(1), pp. 18-23.
Number of citations in Scopus 89
Number of citations in Web of Science® 46

Piret, Sian E., Danoy, Patrick, Dahan, Karin, Reed, Anita A. C., Pryce, Karena, Wong, William, et al. (2011) Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21. Human Genetics, 129(1), pp. 51-58.
Number of citations in Scopus 16
Number of citations in Web of Science® 13

Rodriguez-Acevedo, Astrid J., Ferreira, Manuel A., Benton, Miles C., Carless, Melanie A., Göring, Harald H., Curran, Joanne E., et al. (2015) Common polygenic variation contributes to risk of migraine in the Norfolk Island population. Human Genetics, 134(10), pp. 1079-1087.
Number of full-text downloads 5
Number of citations in Scopus 2
Number of citations in Web of Science® 1

Rutherford, Sue, Johnson, Matthew, Curtain, Robert, & Griffiths, Lyn R. (2001) Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension. Human Genetics, 109(4), pp. 408-415.
Number of citations in Scopus 34
Number of citations in Web of Science® 27

Souter, Vivienne L., Parisi, Melissa A., Nyholt, Dale R., Kapur, Raj P., Henders, Anjali K., Opheim, Kent E., et al. (2007) A case of true hermaphroditism reveals an unusual mechanism of twinning. Human Genetics, 121(2), pp. 179-185.
Number of citations in Scopus 25
Number of citations in Web of Science® 24

This list was generated on Sun Apr 16 15:25:01 2017 AEST.