Phenomics: the systematic study of phenotypes on a genome-wide scale
Bilder, R.M, Sabb, F.W, Cannon, T.D, London, E.D, Jentsch, J.D, Parker, D. Stott, Poldrack, R.A, Evans, C, Freimer, N.B
Published in Neuroscience (24.11.2009)
Published in Neuroscience (24.11.2009)
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Challenges in phenotype definition in the whole-genome era: multivariate models of memory and intelligence
Sabb, F.W, Burggren, A.C, Higier, R.G, Fox, J, He, J, Parker, D.S, Poldrack, R.A, Chu, W, Cannon, T.D, Freimer, N.B, Bilder, R.M
Published in Neuroscience (24.11.2009)
Published in Neuroscience (24.11.2009)
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Adult age confounds estimates of static allometric slopes in a vertebrate
Rodríguez, R.L., Cramer, J.D., Schmitt, C.A., Gaetano, T.J., Grobler, J.P., Freimer, N.B., Turner, T.R.
Published in Ethology, ecology & evolution (02.10.2015)
Published in Ethology, ecology & evolution (02.10.2015)
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Genome-Wide Linkage Scan of Bipolar Disorder in a Colombian Population Isolate Replicates Loci on Chromosomes 7p21–22, 1p31, 16p12 and 21q21–22 and Identifies a Novel Locus on Chromosome 12q
Kremeyer, B., García, J., Müller, H., Burley, M.W., Herzberg, I., Parra, M.V., Duque, C., Vega, J., Montoya, P., López, M.C., Bedoya, G., Reus, V., Palacio, C., López, C., Ospina-Duque, J., Freimer, N.B., Ruiz-Linares, A.
Published in Human heredity (01.01.2010)
Published in Human heredity (01.01.2010)
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99 – Predicting schizophrenia spectrum disorders with psychological scales – The Northern Finland 1966 Birth Cohort
Miettunen, J, Veijola, J, Isohanni, M.K, Paunio, T, Freimer, N.B, Lauronen, E, Ekelund, J, Peltonen, L, Joukamaa, M, Lichtermann, D
Published in Schizophrenia research (01.02.2008)
Published in Schizophrenia research (01.02.2008)
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A phenome-wide examination of neural and cognitive function
Poldrack, R A, Congdon, E, Triplett, W, Gorgolewski, K J, Karlsgodt, K H, Mumford, J A, Sabb, F W, Freimer, N B, London, E D, Cannon, T D, Bilder, R M
Published in Scientific data (06.12.2016)
Published in Scientific data (06.12.2016)
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Polygenic Hyperlipidemia Increases Coronary Artery Disease Risk In The Uk Biobank
Ripatti, P., Rämö, J.T., Söderlund, S., Surakka, I., Havulinna, A.S., Widén, E., Palta, P., Freimer, N.B., Salomaa, V., Pirinen, M., Palotie, A., Taskinen, M.R., Ripatti, S.
Published in Atherosclerosis (01.08.2019)
Published in Atherosclerosis (01.08.2019)
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A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees
Jasinska, A.J., Service, S., Jawaheer, D., DeYoung, J., Levinson, M., Zhang, Z., Kremeyer, B., Muller, H., Aldana, I., Garcia, J., Restrepo, G., Lopez, C., Palacio, C., Duque, C., Parra, M., Vega, J., Ortiz, D., Bedoya, G., Mathews, C., Davanzo, P., Fournier, E., Bejarano, J., Ramirez, M., Araya Ortiz, C., Araya, X., Molina, J., Sabatti, C., Reus, V., Ospina, J., Macaya, G., Ruiz-Linares, A., Freimer, N.B.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2009)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2009)
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A Minimalist Approach to Gene Mapping: Locating the Gene for Acheiropodia, by Homozygosity Analysis
Escamilla, M.A., DeMille, M.C., Benavides, E., Roche, E., Almasy, L., Pittman, S., Hauser, J., Lew, D.F., Freimer, N.B., Whittle, M.R.
Published in American journal of human genetics (01.06.2000)
Published in American journal of human genetics (01.06.2000)
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Incorrect specification of marker allele frequencies : effects on linkage analysis
FREIMER, N. B, SANDKUIJL, L. A, BLOWER, S. M
Published in American journal of human genetics (01.06.1993)
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Published in American journal of human genetics (01.06.1993)
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Results of a genome-wide genetic screen for panic disorder
Knowles, J A, Fyer, A J, Vieland, V J, Weissman, M M, Hodge, S E, Heiman, G A, Haghighi, F, de Jesus, G M, Rassnick, H, Preud'homme-Rivelli, X, Austin, T, Cunjak, J, Mick, S, Fine, L D, Woodley, K A, Das, K, Maier, W, Adams, P B, Freimer, N B, Klein, D F, Gilliam, T C
Published in American journal of medical genetics (28.03.1998)
Published in American journal of medical genetics (28.03.1998)
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