Search Results - Blangero, J.
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Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity by Khan, F., Melton, Phillip, McCarthy, N., Morar, B., Blangero, J., Moses, Eric, Jablensky, A.
Published 2018Get full text
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Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study) by Roten, L., Johnson, M., Forsmo, S., Fitzpatrick, E., Dyer, T., Brennecke, S., Blangero, J., Moses, Eric, Austgulen, R.
Published 2009Get full text
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Genome wide association and pathway analysis of segment-specific carotid intima-media thickness phenotypes: The San Antonio Family Heart Study by Melton, Phillip, Curran, J., Carless, M., Johnson, M., Dyer, T., MacCluer, J., Moses, E., Goering, H., Blangero, J., Almasy, L.
Published 2011Get full text
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Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13q by Fenstad, M., Johnson, M., Roten, L., Aas, P., Forsmo, S., Klepper, K., East, C., Abraham, L., Blangero, J., Brennecke, S., Austgulen, R., Moses, Eric
Published 2010Get full text
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