Browse By Publication: Human Molecular Genetics

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Number of items: 33.

Amin Al Olama, A., Kote-Jarai, Z., Schumacher, F.R., Wiklund, F., Berndt, S.I., Benlloch, S., et al. (2012) A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease. Human Molecular Genetics, 22(2), pp. 408-415.
Number of citations in Scopus 51
Number of citations in Web of Science® 15

Amin Al Olama, Ali, Dadaev, Tokhir, Hazelett, Dennis J., Li, Qiuyan, Leongamornlert, Daniel, Saunders, Edward J., et al. (2015) Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans. Human Molecular Genetics, 24(19), pp. 5589-5602.
Number of citations in Scopus 13
Number of citations in Web of Science® 12

Benyamin, Beben, Middelberg, Rita P., Lind, Penelope A., Valle, Anne M., Gordon, Scott, Nyholt, Dale R., et al. (2011) GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Human Molecular Genetics, 20(22), pp. 4504-4514.
Number of citations in Scopus 23
Number of citations in Web of Science® 22

Bolderson, Emma, Scorah, Jennifer, Helleday, Thomas, Smythe, Carl, & Meuth, Mark (2004) ATM is required for the cellular response to thymidine induced replication fork stress. Human Molecular Genetics, 13(23), pp. 2937-2945.
Number of citations in Scopus 68
Number of citations in Web of Science® 65

Boraska, V., Jeroncic, A., Colonna, V., Southam, L., Nyholt, D.R., Rayner, N.W., et al. (2012) Genome-wide meta-analysis of common variant differences between men and women. Human Molecular Genetics, 21(21), pp. 4805-4815.
Number of citations in Scopus 7
Number of citations in Web of Science® 9

Briggs, F. B. S., Bartlett, S. E., Goldstein, B. A., Wang, J., McCauley, J. L., Zuvich, R. L., et al. (2010) Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals. Human Molecular Genetics, 19(21), pp. 4286-4295.
Number of citations in Scopus 11
Number of citations in Web of Science® 8

Brown, Matthew A., Edwards, S., Hoyle, E., Campbell, S., Laval, S., Daly, A. K., et al. (2000) Polymorphisms of the CYP2D6 gene increase susceptibility to ankylosing spondylitis. Human Molecular Genetics, 9(11), pp. 1563-1566.
Number of citations in Scopus 72
Number of citations in Web of Science® 56

Cortes, A., Field, J., Glazov, E. A., Hadler, J., Stankovich, J., Brown, M. A., et al. (2013) Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes. Human Molecular Genetics, 22(11), pp. 2283-2292.
Number of citations in Scopus 12
Number of citations in Web of Science® 10

Esposito, T., Lea, R.A., Maher, B.H., Moses, D., Cox, H.C., Magliocca, S., et al. (2013) Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. Human Molecular Genetics, 22(18), pp. 3654-3666.
Number of full-text downloads 28
Number of citations in Scopus 2
Number of citations in Web of Science® 3

Gandhi, K. S., McKay, F. C., Cox, M., Riveros, C., Armstrong, N., Heard, R. N., et al. (2010) The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. Human Molecular Genetics, 19(11), pp. 2134-2143.
Number of citations in Scopus 53
Number of citations in Web of Science® 50

Gu, Ben J., Field, Judith, Dutertre, Sébastien, Ou, Amber, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, et al. (2015) A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis. Human Molecular Genetics, 24(19), pp. 5644-5654.
Number of citations in Scopus 4
Number of citations in Web of Science® 6

Harvey, D., Pointon, J. J., Evans, D. M., Karaderi, T., Farrar, C., Appleton, L. H., et al. (2009) Investigating the genetic association between ERAP1 and ankylosing spondylitis. Human Molecular Genetics, 18(21), pp. 4204-4212.
Number of citations in Scopus 71
Number of citations in Web of Science® 74

Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simón-Sánchez, J., et al. (2012) Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics, 21(22), pp. 4996-5009.
Number of citations in Scopus 57
Number of citations in Web of Science® 55

Kote-Jarai, Z., Saunders, E., Leongamornlert, D.A., Tymrakiewicz, M., Dadaev, T., Jugurnath-Little, S., et al. (2013) Fine-mapping identifies multiple prostate cancer risk loci on 5p15 some associating with TERT expression. Human Molecular Genetics, 22(12), pp. 2520-2528.
Number of full-text downloads 30
Number of citations in Scopus 54
Number of citations in Web of Science® 57

Lee, S.H., Harold, D., Nyholt, D.R., Goddard, M.E., Zondervan, K.T., Williams, J., et al. (2013) Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Human Molecular Genetics, 22(4), pp. 832-841.
Number of full-text downloads 6
Number of citations in Scopus 69
Number of citations in Web of Science® 65

Lu, Y., Cuellar-Partida, G., Painter, J.N., Nyholt, D.R., Morris, A.P., Fasching, P.A., et al. (2015) Shared genetics underlying epidemiological association between endometriosis and ovarian cancer. Human Molecular Genetics, 24(20), pp. 5955-5964.
Number of citations in Scopus 8
Number of citations in Web of Science® 3

McInerney-Leo, A.M., Sparrow, D.B., Harris, J.E., Gardiner, B.B., Marshall, M.S., O'Reilly, V.C., et al. (2015) Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects. Human Molecular Genetics, 24(5), pp. 1234-1242.
Number of citations in Scopus 1
Number of citations in Web of Science® 1

Middelberg, Rita P., Benyamin, Beben, de Moor, Marleen H.M., Warrington, Nichole M., Gordon, Scott, Henders, Anjali K., et al. (2012) Loci affecting gamma-glutamyl transferase in adults and adolescents show age x SNP interaction and cardiometabolic disease associations. Human Molecular Genetics, 21(2), pp. 446-455.
Number of citations in Scopus 16
Number of citations in Web of Science® 13

Milevskiy, Michael J.G., Al-Ejeh, Fares, Saunus, Jodi M., Northwood, Korinne S., Bailey, Peter J., Betts, Joshua A., et al. (2016) Long-range regulators of the lncRNA HOTAIR enhance its prognostic potential in breast cancer. Human Molecular Genetics. (In Press)

Moayyeri, A., Hsu, Y.H., Karasik, D., Estrada, K., Xiao, S.M., Nielson, C., et al. (2014) Genetic determinants of heel bone properties: Genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Human Molecular Genetics, 23(11), pp. 3054-3068.
Number of citations in Scopus 27
Number of citations in Web of Science® 25

Mohindra, Atul, Bolderson, Emma, Stone, Jason, Wells, Michael, Helleday, Thomas, & Meuth, Mark (2004) A tumour-derived mutant allele of XRCC2 preferentially suppresses homologous recombination at DNA replication forks. Human Molecular Genetics, 13(2), pp. 203-212.
Number of citations in Scopus 17
Number of citations in Web of Science® 16

Niu, Tianhua, Liu, Ning, Zhao, Ming, Xie, Guie, Zhang, Lei, Li, Jian, et al. (2015) Identification of a novel FGFRL1 MicroRNA target site polymorphism for bone mineral density in meta-analyses of genome-wide association studies. Human Molecular Genetics, 24(16), pp. 4710-4727.
Number of citations in Scopus 4
Number of citations in Web of Science® 3

Nyholt, D. R., Dawkins, J. L., Brimage, P. J., Goadsby, P. J., Nicholson, G. A., & Griffiths, L. R. (1998) Evidence for an X-linked genetic component in familial typical migraine. Human Molecular Genetics, 7(3), pp. 459-463.
Number of citations in Scopus 83
Number of citations in Web of Science® 69

Nyholt, Dale R., Dawkins, Jennifer L., Brimage, Peter J., Goadsby, Peter J., Nicholson, Garth A., & Griffiths, Lyn R. (1998) Evidence for an X-linked genetic component in familial typical migraine. Human Molecular Genetics, 7(3), pp. 459-463.
Number of citations in Scopus 83
Number of citations in Web of Science® 69

Nyholt, Dale R., LaForge, K. S., Kallela, M., Alakurtti, K., Anttila, V., Farkkila, M., et al. (2008) A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics, 17(21), pp. 3318-3331.
Number of citations in Scopus 53
Number of citations in Web of Science® 48

Painter, J.N., O'Mara, T.A., Batra, J., Cheng, T., Lose, F.A., Dennis, J., et al. (2014) Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24(5), pp. 1478-1492.
Number of full-text downloads 7
Number of citations in Scopus 11
Number of citations in Web of Science® 10

Rahmioglu, Nilufer, Macgregor, Stuart, Drong, Alexander W., Hedman, Åsa K., Harris, Holly R., Randall, Joshua C., et al. (2015) Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci. Human Molecular Genetics, 24(4), pp. 1185-1199.
Number of citations in Scopus 10
Number of citations in Web of Science® 7

Sparrow, Duncan B., McInerney-Leo, Aideen, Gucev, Zoran S., Gardiner, Brooke, Marshall, Mhairi, Leo, Paul J., et al. (2013) Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. Human Molecular Genetics, 22(8), pp. 1625-1631.
Number of citations in Scopus 24
Number of citations in Web of Science® 20

Spencer, C. C., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., et al. (2011) Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Human Molecular Genetics, 20(2), pp. 345-353.
Number of citations in Scopus 125
Number of citations in Web of Science® 112

Strange, A., Bellenguez, C., Sim, X., Luben, R., Hysi, P. G., Ramdas, W. D., et al. (2013) Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus. Human Molecular Genetics, 22(22), pp. 4653-4660.
Number of citations in Scopus 8
Number of citations in Web of Science® 5

Suraweera, Amila, Lim, YiChieh, Woods, Rick, Birrell, Geoff W., Nasim, Talat, Becherel , Olivier J., et al. (2009) Functional role for senataxin, defective in ataxia oculomotor apraxia type 2, in transcriptional regulation. Human Molecular Genetics, 18(18), pp. 3384-3396.
Number of citations in Scopus 66
Number of citations in Web of Science® 60

Timpson, N. J., Tobias, J. H., Richards, J. B., Soranzo, N., Duncan, Emma L., Sims, A. M., et al. (2009) Common variants in the region around Osterix are associated with bone mineral density and growth in childhood. Human Molecular Genetics, 18(8), pp. 1510-1517.
Number of citations in Scopus 72
Number of citations in Web of Science® 70

Zhang, L., Choi, H.J., Estrada, K., Leo, P.J., Li, J., Pei, Y.F., et al. (2013) Multistage genome-wide association meta-analyses identified two new loci for bone mineral density. Human Molecular Genetics, 23(7), pp. 1923-1933.
Number of citations in Scopus 42
Number of citations in Web of Science® 41

This list was generated on Sun Mar 19 23:09:12 2017 AEST.