Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness von Homann, O R, Misura, K, Lamas, E, Sandrock, R W, Nelson, P, McDonough, S I, DeLisi, L E

Volltext

Speech disorder in schizophrenia: Review of the literature and exploration of its relation to the uniquely human capacity for language von DELISI, Lynn E

Volltext

The Concept of Progressive Brain Change in Schizophrenia: Implications for Understanding Schizophrenia von DeLisi, Lynn E.

Volltext

A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder von Sachs, N A, Sawa, A, Holmes, S E, Ross, C A, DeLisi, L E, Margolis, R L

Volltext

Language as a biomarker in those at high-risk for psychosis von Rosenstein, M, Foltz, P.W, DeLisi, L.E, Elvevåg, B

Volltext

Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia von Tarabeux, J, Kebir, O, Gauthier, J, Hamdan, F F, Xiong, L, Piton, A, Spiegelman, D, Henrion, É, Millet, B, Fathalli, F, Joober, R, Rapoport, J L, DeLisi, L E, Fombonne, É, Mottron, L, Forget-Dubois, N, Boivin, M, Michaud, J L, Drapeau, P, Lafrenière, R G, Rouleau, G A, Krebs, M-O

Volltext

Patterns in adolescent cannabis use predict the onset and symptom structure of schizophrenia-spectrum disorder von Shahzade, C., Chun, J., DeLisi, L.E., Manschreck, T.C.

Volltext

Decreased axial diffusivity within language connections: A possible biomarker of schizophrenia risk von Kubicki, M, Shenton, M.E, Maciejewski, P.K, Pelavin, P.E, Hawley, K.J, Ballinger, T, Swisher, T, Jabbar, G.A, Thermenos, H.W, Keshavan, M.S, Seidman, L.J, DeLisi, L.E

Volltext

Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia von 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

Volltext

Altered language network activity in young people at familial high-risk for schizophrenia von Thermenos, H.W, Whitfield-Gabrieli, S, Seidman, L.J, Kuperberg, G, Juelich, R.J, Divatia, S, Riley, C, Jabbar, G.A, Shenton, M.E, Kubicki, M, Manschreck, T, Keshavan, M.S, DeLisi, L.E

Volltext

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia von Piton, A, Gauthier, J, Hamdan, F F, Lafrenière, R G, Yang, Y, Henrion, E, Laurent, S, Noreau, A, Thibodeau, P, Karemera, L, Spiegelman, D, Kuku, F, Duguay, J, Destroismaisons, L, Jolivet, P, Côté, M, Lachapelle, K, Diallo, O, Raymond, A, Marineau, C, Champagne, N, Xiong, L, Gaspar, C, Rivière, J-B, Tarabeux, J, Cossette, P, Krebs, M-O, Rapoport, J L, Addington, A, DeLisi, L E, Mottron, L, Joober, R, Fombonne, E, Drapeau, P, Rouleau, G A

Volltext

Rapid telomere erosion in schizophrenia von Kao, H-T, Cawthon, R M, DeLisi, L E, Bertisch, H C, Ji, F, Gordon, D, Li, P, Benedict, M M, Greenberg, W M, Porton, B

Volltext

Frequency of normative word associations in the speech of individuals at familial high-risk for schizophrenia von Manschreck, T.C, Merrill, A.M, Jabbar, G, Chun, J, DeLisi, L.E

Volltext

Longitudinal Neuropsychological Follow-Up Study of Patients With First-Episode Schizophrenia von Hoff, Anne L., Sakuma, Michael, Wieneke, Mary, Horon, Robert, Kushner, Maureen, DeLisi, Lynn E.

Volltext

fMRI study of language activation in schizophrenia, schizoaffective disorder and in individuals genetically at high risk von Li, Xiaobo, Branch, Craig A, Ardekani, Babak A, Bertisch, Hilary, Hicks, Chindo, DeLisi, Lynn E

Volltext

A mutation in NPAS3 segregates with mental illness in a small family von Yu, L, Arbez, N, Nucifora, L G, Sell, G L, DeLisi, L E, Ross, C A, Margolis, R L, Nucifora, F C

Volltext

Schizophrenia as a chronic active brain process: a study of progressive brain structural change subsequent to the onset of schizophrenia von DeLisi, Lynn E., Sakuma, Michael, Tew, William, Kushner, Maureen, Hoff, Anne L., Grimson, Roger

Volltext

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia von Francks, C, Maegawa, S, Laurén, J, Abrahams, B S, Velayos-Baeza, A, Medland, S E, Colella, S, Groszer, M, McAuley, E Z, Caffrey, T M, Timmusk, T, Pruunsild, P, Koppel, I, Lind, P A, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, A J, Riley, B P, Martin, N G, Strittmatter, S M, Möller, H-J, Rujescu, D, St Clair, D, Muglia, P, Roos, J L, Fisher, S E, Wade-Martins, R, Rouleau, G A, Stein, J F, Karayiorgou, M, Geschwind, D H, Ragoussis, J, Kendler, K S, Airaksinen, M S, Oshimura, M, DeLisi, L E, Monaco, A P

Volltext

Encouraging a new generation of researchers in a time of limited resources von DeLisi, L.E, Fleischhacker, W.W

Volltext

Lack of Association Between Duration of Untreated Illness and Severity of Cognitive and Structural Brain Deficits at the First Episode of Schizophrenia von Hoff, Anne L., Sakuma, Michael, Razi, Kamran, Heydebrand, Gitry, Csernansky, John G., DeLisi, Lynn E.

Volltext