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Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia
Mah, S, Nelson, M R, DeLisi, L E, Reneland, R H, Markward, N, James, M R, Nyholt, D R, Hayward, N, Handoko, H, Mowry, B, Kammerer, S, Braun, A
Published in Molecular psychiatry (01.05.2006)
Published in Molecular psychiatry (01.05.2006)
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Journal Article
The future for genetic studies in reproduction
Montgomery, G. W., Zondervan, K. T., Nyholt, D. R.
Published in Molecular human reproduction (01.01.2014)
Published in Molecular human reproduction (01.01.2014)
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Journal Article
Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G x E) interaction
Cornes, B.K, Lind, P.A, Medland, S.E, Montgomery, G.W, Nyholt, D.R, Martin, N.G
Published in International Journal of Obesity (01.01.2009)
Published in International Journal of Obesity (01.01.2009)
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Journal Article
Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine
Anttila, V., Kallela, M., Oswell, G., Kaunisto, M.A., Nyholt, D.R., Hämäläinen, E., Havanka, H., Ilmavirta, M., Terwilliger, J., Sobel, E., Peltonen, L., Kaprio, J., Färkkilä, M., Wessman, M., Palotie, A.
Published in American journal of human genetics (01.07.2006)
Published in American journal of human genetics (01.07.2006)
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Journal Article
Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia
Handoko, H Y, Nyholt, D R, Hayward, N K, Nertney, D A, Hannah, D E, Windus, L C, McCormack, C M, Smith, H J, Filippich, C, James, M R, Mowry, B J
Published in Molecular psychiatry (01.06.2005)
Published in Molecular psychiatry (01.06.2005)
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Journal Article
No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
Heilmann, S., Nyholt, D.R., Brockschmidt, F.F., Hillmer, A.M., Herold, C., Becker, T., Martin, N.G., Nöthen, M.M.
Published in British journal of dermatology (1951) (01.07.2013)
Published in British journal of dermatology (1951) (01.07.2013)
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Journal Article
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.
Published in Nature communications (24.10.2019)
Published in Nature communications (24.10.2019)
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Journal Article
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis
Lee, S. H., Harold, D., Nyholt, D. R., Goddard, M. E., Zondervan, K. T., Williams, J., Montgomery, G. W., Wray, N. R., Visscher, P. M.
Published in Human molecular genetics (15.02.2013)
Published in Human molecular genetics (15.02.2013)
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Journal Article
A reanalysis of 409 European-Ancestry and African American schizophrenia pedigrees reveals significant linkage to 8p23.3 with evidence of locus heterogeneity
Holliday, E.G., Mowry, B.J., Nyholt, D.R.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2008)
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Journal Article
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort
Maher, B. H., Kerr, M., Cox, H. C., MacMillan, J. C., Brimage, P. J., Esposito, T., Gianfrancesco, F., Haupt, L. M., Nyholt, D. R., Lea, R. A., Griffiths, L. R.
Published in Neurogenetics (01.02.2012)
Published in Neurogenetics (01.02.2012)
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Journal Article
Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3–14
Warner, J V, Nyholt, D R, Busfield, F, Epstein, M, Burgess, J, Stranks, S, Hill, P, Perry-Keene, D, Learoyd, D, Robinson, B, Teh, B T, Prins, J B, Cardinal, J W
Published in Journal of medical genetics (01.03.2006)
Published in Journal of medical genetics (01.03.2006)
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Journal Article
Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.
Published in Nature communications (21.09.2022)
Published in Nature communications (21.09.2022)
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Journal Article
Teenage acne is influenced by genetic factors
Evans, D.M., Kirk, K.M., Nyholt, D.R., Novac, C., Martin, N.G.
Published in British journal of dermatology (1951) (01.03.2005)
Published in British journal of dermatology (1951) (01.03.2005)
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Journal Article
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine
Lea, R. A., Nyholt, D. R., Curtain, R. P., Ovcaric, M., Sciascia, R., Bellis, C., MacMillan, J., Quinlan, S., Gibson, R. A., McCarthy, L. C., Riley, J. H., Smithies, Y. J., Kinrade, S., Griffiths, L. R.
Published in Neurogenetics (01.05.2005)
Published in Neurogenetics (01.05.2005)
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Journal Article