Search Results - Melton, P.

Genome-wide association study of autistic-like traits in a general population study of young adults by Jones, R., Cadby, G., Melton, P., Abraham, L., Whitehouse, A., Moses, Eric

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Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns by McCarthy, N., Melton, P., Cadby, G., Yazar, S., Franchina, M., Moses, Eric, Mackey, D., Hewitt, A.

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Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes by Yong, H., Melton, P., Johnson, M., Freed, K., Kalionis, B., Murthi, P., Brennecke, S., Keogh, R., Moses, Eric

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The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia by Thomsen, L., Mccarthy, N., Melton, P., Cadby, G., Austgulen, R., Nygård, O., Johnson, M., Brennecke, S., Moses, Eric, Bjørge, L., Iversen, A.

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Exome array analysis suggests an increased variant burden in families with schizophrenia by McCarthy, N., Melton, P., Ward, S., Allan, S., Dragovic, M., Clark, M., Morar, B., Rubio, J., Blangero, J., Badcock, J., Morgan, V., Moses, Eric, Jablensky, A.

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Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma by Sneddon, S., Leon, J., Dick, I., Cadby, G., Olsen, N., Brims, F., Allcock, R., Moses, Eric, Melton, P., de Klerk, N., Musk, A., Robinson, B., Creaney, J.

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Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort by Thomsen, L., Melton, P., Tollaksen, K., Lyslo, I., Roten, L., Odland, M., Strand, K., Nygard, O., Sun, C., Iversen, A., Austgulen, R., Moses, Eric, Bjørge, L.

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Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22 by Løset, M., Johnson, M., Melton, P., Ang, W., Huang, R., Mori, T., Beilin, L., Pennell, C., Roten, L., Iversen, A., Austgulen, R., East, C., Blangero, J., Brennecke, S., Moses, Eric

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Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study by Cadby, G., Melton, P., McCarthy, N., Almeida, M., Williams-Blangero, S., Curran, J., VandeBerg, J., Hui, J., Beilby, J., Musk, A., James, A., Hung, J., Blangero, J., Moses, Eric

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Serum marker of inflammasome activity correlates with liver injury in nonalcoholic fatty liver disease and is influenced by genetic polymorphisms by Adams, L., Wree, A., Melton, P., Jeffrey, G., Ching, H., de Boer, B., Olynyk, J., Ayonrinde, O., Mori, T., Beilin, L., Price, Patricia, Pennell, C., Eslam, M., George, J., Feldstein, A.

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Genetic architecture of carotid artery intima-media thickness in Mexican Americans by Melton, P., Carless, M., Curran, J., Dyer, T., Göring, H., Kent, J., Drigalenko, E., Johnson, M., MacCluer, J., Moses, Eric, Comuzzie, A., Mahaney, M., O'Leary, D., Blangero, J., Almasy, L.

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A Genome-Wide Integrative Genomic Study Localizes Genetic Factors Influencing Antibodies against Epstein-Barr Virus Nuclear Antigen 1 (EBNA-1) by Rubicz, R., Yolken, R., Drigalenko, E., Carless, M., Dyer, T., Bauman, L., Melton, P., Kent, J., Harley, J., Curran, J., Johnson, M., Cole, S., Almasy, L., Moses, Eric, Dhurandhar, N., Kraig, E., Blangero, J., Leach, C., Göring, H.

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A genome-wide association study for malignant mesothelioma risk by Cadby, G., Mukherjee, S., Musk, A., Reid, A., Garlepp, Michael, Dick I., Robinson, C., Hui, J., Fiorito, G., Guarrera, S., Beilby, J., Melton, P., Moses, E., Ugolini, D., Mirabelli, D., Bonassi, S., Magnani, C., Dianzani, I., Matullo, G., Robinson, B., Creaney, J., Palmer, L.

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Bivariate genetic association of KIAA1797 with heart rate in American Indians: The Strong Heart Family Study by Melton, P., Rutherford, S., Voruganti, V., Göring, H., Laston, S., Haack, K., Comuzzie, A., Dyer, T., Johnson, M., Kent, J., Curran, J., Moses, Eric, Blangero, J., Barac, A., Lee, E., Best, L., Fabsitz, R., Devereux, R., Okin, P., Bella, J., Broeckel, U., Howard, B., MacCluer, J., Cole, S., Almasy, L.

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Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease by Johnson, M., Brennecke, S., East, C., Dyer, T., Roten, L., Proffitt, J., Melton, P., Fenstad, M., Aalto-Viljakainen, T., Mäkikallio, K., Heinonen, S., Kajantie, E., Kere, J., Laivuori, H., Austgulen, R., Blangero, J., Moses, Eric, Pouta, A., Kivinen, K., Ekholm, E., Hietala, R., Sainio, S., Saisto, T., Uotila, J., Klemetti, M., Lokki, A., Georgiadis, L.

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