Browse By Publication: American Journal of Human Genetics

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Number of items: 28.

Anttila, V., Kallela, M., Oswell, G., Kaunisto, M.A., Nyholt, D.R., Hamalainen, E., et al. (2006) Trait components provide tools to dissect the genetic susceptibility of migraine. American Journal of Human Genetics, 79(1), pp. 85-99.
Number of citations in Scopus 51
Number of citations in Web of Science® 46

Anttila, V., Nyholt, Dale R., Kallela, M., Artto, V., Vepsalainen, S., Jakkula, E., et al. (2008) Consistently replicating locus linked to migraine on 10q22-q23. American Journal of Human Genetics, 82(5), pp. 1051-63.
Number of citations in Scopus 28
Number of citations in Web of Science® 26

Bodea, C. A., Neale, B. M., Ripke, S., Barclay, M., Peyrin-Biroulet, L., Chamaillard, M., et al. (2016) A method to exploit the structure of genetic ancestry space to enhance case-control studies. American Journal of Human Genetics, 98(5), pp. 857-868.

Eggert, Stacy L., Huyck, Karen L., Somasundaram, Priya, Kavalla, Raghava, Stewart, Elizabeth A., Lu, Ake T., et al. (2012) Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata. American Journal of Human Genetics, 91(4), pp. 621-628.
Number of citations in Scopus 32
Number of citations in Web of Science® 29

Ferreira, M. A., Hottenga, J. J., Warrington, N. M., Medland, S. E., Willemsen, G., Lawrence, R. W., et al. (2009) Sequence variants in three loci influence monocyte counts and erythrocyte volume. American Journal of Human Genetics, 85(5), pp. 745-749.
Number of citations in Scopus 46
Number of citations in Web of Science® 44

Ferreira, Manuel A.R., Mangino, Massimo, Brumme, Chanson J., Zhao, Zhen Zhen, Medland, Sarah E., Wright, Margaret J., et al. (2010) Quantitative Trait Loci for CD4:CD8 Lymphocyte Ratio Are Associated with Risk of Type 1 Diabetes and HIV-1 Immune Control. American Journal of Human Genetics, 86(1), pp. 88-92.
Number of citations in Scopus 51
Number of citations in Web of Science® 47

Griffiths, Lyn R., Zwi, M. B., McLeod, J. G., & Nicholson, G. A. (1988) Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I. American Journal of Human Genetics, 42(5), pp. 756-771.
Number of citations in Scopus 26
Number of citations in Web of Science® 37

Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, et al. (2013) Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans. American Journal of Human Genetics, 93(5), pp. 915-925.
Number of citations in Scopus 62
Number of citations in Web of Science® 60

Hemani, G., Yang, J., Vinkhuyzen, A., Powell, J. E., Willemsen, G., Hottenga, J. J., et al. (2013) Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs. American Journal of Human Genetics, 93(5), pp. 865-875.
Number of citations in Scopus 28
Number of citations in Web of Science® 26

Laval, S.H., Timms, A., Edwards, S., Bradbury, L.A., Brophy, S., Milicic, A., et al. (2001) Whole-genome screening in ankylosing spondylitis: Evidence of non-MHC genetic-susceptibility loci. American Journal of Human Genetics, 68(4), pp. 918-926.
Number of citations in Scopus 201
Number of citations in Web of Science® 174

Liu, J. Z., McRae, A. F., Nyholt, D.R., Medland, S. E., Wray, N. R., Brown, K. M., et al. (2010) A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87(1), pp. 139-145.
Number of citations in Scopus 380
Number of citations in Web of Science® 372

Liu, J.*, Nyholt, D.R., Magnussen, P., Parano, E., Pavone, P., Geschwind, D., et al. (2001) A genomewide screen for autism susceptibility loci. American Journal of Human Genetics, 69(2), pp. 327-40.
Number of citations in Scopus 237
Number of citations in Web of Science® 228

Mayes, M. D., Bossini-Castillo, L., Gorlova, O., Martin, J. E., Zhou, X., Chen, W. V., et al. (2014) Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. American Journal of Human Genetics, 94(1), pp. 47-61.
Number of citations in Scopus 61
Number of citations in Web of Science® 55

McInerney-Leo, Aideen M., Schmidts, Miriam, Cortés, Claudio R., Leo, Paul J., Gener, Blanca, Courtney, Andrew D., et al. (2013) Short-rib polydactyly and jeune syndromes are caused by mutations in WDR60. American Journal of Human Genetics, 93(3), pp. 515-523.
Number of citations in Scopus 42
Number of citations in Web of Science® 38

Medland, S. E., Nyholt, D.R., Painter, J. N., McEvoy, B. P., McRae, A. F., Zhu, G., et al. (2009) Common variants in the trichohyalin gene are associated with straight hair in Europeans. American Journal of Human Genetics, 85(5), pp. 750-5.
Number of citations in Scopus 127
Number of citations in Web of Science® 122

Medland, S. E., Zayats, T., Glaser, B., Nyholt, D.R., Gordon, S. D., Wright, M. J., et al. (2010) A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. American Journal of Human Genetics, 86(4), pp. 519-525.
Number of citations in Scopus 58
Number of citations in Web of Science® 50

Nyholt, D.R. (2000) All LODs are not created equal. American Journal of Human Genetics, 67(2), pp. 282-8.
Number of citations in Scopus 87
Number of citations in Web of Science® 86

Nyholt, D.R., Morley, K. I., Ferreira, M. A., Medland, S. E., Boomsma, D. I., Heath, A. C., et al. (2005) Genomewide significant linkage to migrainous headache on chromosome 5q21. American Journal of Human Genetics, 77(3), pp. 500-12.
Number of citations in Scopus 74
Number of citations in Web of Science® 63

Painter, Jodie N., Kaufmann, Susanne, O’Mara, Tracy A., Hillman, Kristine M., Sivakumaran, Haran, Darabi, Hatef, et al. (2016) A common variant at the 14q32 endometrial cancer risk locus activates AKT1 through YY1 binding. American Journal of Human Genetics, 98(6), pp. 1159-1169.
Number of full-text downloads 6

Rautanen, Anna, Pirinen, Matti, Mills, Tara C., Rockett, Kirk A., Strange, Amy, Ndungu, Anne W., et al. (2016) Polymorphism in a lincRNA associates with a doubled risk of pneumococcal bacteremia in Kenyan children. American Journal of Human Genetics, 98(6), pp. 1092-1100.
Number of citations in Scopus 2
Number of citations in Web of Science® 3

Schmidts, Miriam, Vodopiutz, Julia, Christou-Savina, Sonia, Cortés, Claudio R., McInerney-Leo, Aideen M., Emes, Richard D., et al. (2013) Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy. American Journal of Human Genetics, 93(5), pp. 932-944.
Number of citations in Scopus 32
Number of citations in Web of Science® 30

Timms, A. E., Crane, A. M., Sims, A. M., Cordell, H. J., Bradbury, L. A., Abbott, A., et al. (2004) The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis. American Journal of Human Genetics, 75(4), pp. 587-595.
Number of citations in Scopus 105
Number of citations in Web of Science® 90

Timms, Andrew E., Crane, Alison M., Sims, Anne-Marie, Cordell, Heather J., Bradbury, Linda A., Abbott, Aaron, et al. (2004) The Interleukin 1 Gene Cluster Contains a Major Susceptibility Locus for Ankylosing Spondylitis. American Journal of Human Genetics, 75(4), pp. 587-595.
Number of citations in Scopus 105
Number of citations in Web of Science® 91

Treloar, S. A., Wicks, J., Nyholt, D. R., Montgomery, G. W., Bahlo, M., Smith, V., et al. (2005) Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. American Journal of Human Genetics, 77(3), pp. 365-376.
Number of citations in Scopus 117
Number of citations in Web of Science® 92

Visscher, P. M., Brown, Matthew A., McCarthy, M. I., & Yang, J. (2012) Five years of GWAS discovery. American Journal of Human Genetics, 90(1), pp. 7-24.
Number of citations in Scopus 800
Number of citations in Web of Science® 740

Williams, C. J., Zhang, Y., Timms, A., Bonavita, G., Caeiro, F., Broxholme, J., et al. (2002) Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH. American Journal of Human Genetics, 71(4), pp. 985-991.
Number of citations in Scopus 84
Number of citations in Web of Science® 68

Zankl, A., Duncan, Emma L., Leo, P. J., Clark, G. R., Glazov, E. A., Addor, M. C., et al. (2012) Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB. American Journal of Human Genetics, 90(3), pp. 494-501.
Number of citations in Scopus 33
Number of citations in Web of Science® 28

Zankl, Andreas, Duncan, Emma L., Leo, Paul J., Clark, Graeme R., Glazov, Evgeny A., Addor, Marie-Claud, et al. (2014) Erratum: Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB. American Journal of Human Genetics, 94(4), p. 643.
Number of citations in Scopus 1
Number of citations in Web of Science® 1

This list was generated on Sun Jun 25 12:57:59 2017 AEST.