The Oklahoma State Health Department Mobile Multiphasic Screening Program for Chronic Disease. I.

Por Adler, J J, Bloss, C M, Mosley, K T
Publicado em 1966

The Oklahoma State Department of Health Mobile Multiphasic Screening Program for Chronic Disease. II.

Por Adler, J J, Bloss, C M, Mosley, K T
Publicado em 1966

Influence of individual differences in disease perception on consumer response to direct-to-consumer genomic testing

Por Boeldt, D.L., Schork, N.J., Topol, E.J., Bloss, C.S.
Publicado no Clin Genet (2014)

Schizophrenia-risk variant rs6994992 in the neuregulin-1 gene on brain developmental trajectories in typically developing children

Por Douet, V, Chang, L, Pritchett, A, Lee, K, Keating, B, Bartsch, H, Jernigan, T L, Dale, A, Akshoomoff, N, Murray, S, Bloss, C, Kennedy, D N, Amaral, D, Gruen, J, Kaufmann, W E, Casey, B J, Sowell, E, Ernst, T
Publicado em 2014

Differences in Neurocognitive Impairment among HIV-infected Latinos in the United States

Por Marquine, María J., Heaton, Anne, Johnson, Neco, Rivera-Mindt, Monica, Cherner, Mariana, Bloss, C., Hulgan, T., Umlauf, Anya, Moore, David J., Fazeli, Pariya, Morgello, Susan, Franklin, Donald, Letendre, Scott, Ellis, Ron, Collier, Ann C., Marra, Christina M., Clifford, David. B., Gelman, Benjamin B., Sacktor, Ned, Simpson, David, McCutchan, J. Allen, Grant, Igor, Heaton, Robert K.
Publicado no J Int Neuropsychol Soc (2017)

Apolipoprotein E4 Genotype Does Not Increase Risk of HIV-associated Neurocognitive Disorders

Por Morgan, E.E., Woods, S.P., Letendre, S.L., Franklin, D.R., Bloss, C., Goate, A., Heaton, R.K., Collier, A.C., Marra, C.M., Gelman, B.B., McArthur, J.C., Morgello, S., Simpson, D.M., McCutchan, J.A., Ellis, R.J., Abramson, I., Gamst, A., Fennema-Notestine, C., Smith, D.M., Grant, I., Vaida, F., Clifford, D.B.
Publicado em 2013

Genome-wide association study of shared components of reading disability and language impairment

Por Eicher, J D, Powers, N R, Miller, L L, Akshoomoff, N, Amaral, D G, Bloss, C S, Libiger, O, Schork, N J, Darst, B F, Casey, B J, Chang, L, Ernst, T, Frazier, J, Kaufmann, W E, Keating, B, Kenet, T, Kennedy, D, Mostofsky, S, Murray, S S, Sowell, E R, Bartsch, H, Kuperman, J M, Brown, T T, Hagler, D J, Dale, A M, Jernigan, T L, St Pourcain, B, Davey Smith, G, Ring, S M, Gruen, J R
Publicado em 2013

Evidence for the role of EPHX2 gene variants in anorexia nervosa

Por Scott-Van Zeeland, A A, Bloss, C S, Tewhey, R, Bansal, V, Torkamani, A, Libiger, O, Duvvuri, V, Wineinger, N, Galvez, L, Darst, B F, Smith, E N, Carson, A, Pham, P, Phillips, T, Villarasa, N, Tisch, R, Zhang, G, Levy, S, Murray, S, Chen, W, Srinivasan, S, Berenson, G, Brandt, H, Crawford, S, Crow, S, Fichter, M M, Halmi, K A, Johnson, C, Kaplan, A S, La Via, M, Mitchell, J E, Strober, M, Rotondo, A, Treasure, J, Woodside, D B, Bulik, C M, Keel, P, Klump, K L, Lilenfeld, L, Plotnicov, K, Topol, E J, Shih, P B, Magistretti, P, Bergen, A W, Berrettini, W, Kaye, W, Schork, N J
Publicado em 2014