Foto på William Hennah

William Hennah

Docent

  • PL 20 (Tukholmankatu 8)

    00014

    Finland

20032019
Om du gjort några ändringar i Pure kommer de visas här snart.

Publikationer 2003 2019

Filter
Artikel
2019

Gene expression changes related to immune processes associate with cognitive endophenotypes of schizophrenia

Ukkola-Vuoti, L., Torniainen-Holm, M., Ortega-Alonso, A., Sinha, V., Tuulio-Henriksson, A., Paunio, T., Lönnqvist, J., Suvisaari, J. & Hennah, W., 10 jan 2019, I : Progress in Neuro-Psychopharmacology & Biological Psychiatry. 88, s. 159-167 9 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Öppen tillgång
Fil

Variants in regulatory elements of PDE4D associate with major mental illness in the Finnish population

Sinha, V., Ukkola-Vuoti, L., Ortega-Alonso, A., Torniainen-Holm, M., Therman, S., Tuulio-Henriksson, A., Jylhä, P., Kaprio, J., Hovatta, I., Isometsä, E., Cannon, T. D., Lonnqvist, J., Paunio, T., Suvisaari, J. & Hennah, W., 2019, (!!Accepted/In press) I : Molecular Psychiatry. https://www.nature.com/articles/s41380-019-0429-x.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2018

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia

Teng, S., Thomson, P. A., McCarthy, S., Kramer, M., Muller, S., Lihm, J., Morris, S., Soares, D. C., Hennah, W., Harris, S., Camargo, L. M., Malkov, V., McIntosh, A. M., Millar, J. K., Blackwood, D. H., Evans, K. L., Deary, I. J., Porteous, D. J. & McCombie, W. R., maj 2018, I : Molecular Psychiatry. 23, 5, s. 1270-1277 8 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Öppen tillgång
Fil

The effect of the DISC1 Ser704Cys polymorphism on striatal dopamine synthesis capacity: an [F-18]-DOPA PET study

Dahoun, T., Pardinas, A. F., Veronese, M., Bloomfield, M. A. P., Jauhar, S., Bonoldi, I., Froudist-Walsh, S., Nosarti, C., Korth, C., Hennah, W., Walters, J., Prata, D. & Howes, O. D., 15 okt 2018, I : Human Molecular Genetics. 27, 20, s. 3498-3506 9 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Öppen tillgång
Fil
2017

Genome-Wide Association Study of Psychosis Proneness in the Finnish Population

Ortega-Alonso, A., Ekelund, J., Sarin, A-P., Miettunen, J., Veijola, J., Jarvelin, M-R. & Hennah, W., nov 2017, I : Schizophrenia bulletin. 43, 6, s. 1304-1314 11 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Öppen tillgång

The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to microRNA-484

Bradshaw, N. J., Ukkola-Vuoti, L., Pankakoski, M., Zheutlin, A. B., Ortega-Alonso, A., Torniainen-Holm, M., Sinha, V., Therman, S., Paunio, T., Suvisaari, J., Lonnqvist, J., Cannon, T. D., Haukka, J. & Hennah, W., nov 2017, I : Open biology. 7, 11, 11 s., 170153.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Öppen tillgång
Fil
2015

An interaction between NDE1 and high birth weight increases schizophrenia susceptibility

Wegelius, A., Pankakoski, M., Tomppo, L., Lehto, U., Lonnqvist, J., Suvisaari, J., Paunio, T. & Hennah, W., 15 dec 2015, I : Psychiatry Research. 230, 2, s. 194-199 6 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Öppen tillgång
Fil
2014

708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits

Thomson, P. A., Parla, J. S., McRae, A. F., Kramer, M., Ramakrishnan, K., Yao, J., Soares, D. C., McCarthy, S., Morris, S. W., Cardone, L., Cass, S., Ghiban, E., Hennah, W., Evans, K. L., Rebolini, D., Millar, J. K., Harris, S. E., Starr, J. M., MacIntyre, D. J., McIntosh, A. M. & 7 andra, Watson, J. D., Deary, I. J., Visscher, P. M., Blackwood, D. H., McCombie, W. R., Porteous, D. J. & Generation Scotland, jun 2014, I : Molecular Psychiatry. 19, 6, s. 668-675 8 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Allele-specific regulation of DISC1 expression by miR-135b-5p

Rossi, M., Kilpinen, L. H., Muona, M., Surakka, I., Ingle, C., Lahtinen, J., Hennah, W., Ripatti, S. & Hovatta, I., jun 2014, I : European Journal of Human Genetics. 22, 6, s. 840-843 4 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan

Porteous, D. J., Thomson, P. A., Millar, J. K., Evans, K. L., Hennah, W., Soares, D. C., McCarthy, S., McCombie, W. R., Clapcote, S. J., Korth, C., Brandon, N. J., Sawa, A., Kamiya, A., Roder, J. C., Lawrie, S. M., McIntosh, A. M., St Clair, D. & Blackwood, D. H., feb 2014, I : Molecular Psychiatry. 19, 2, s. 141-143 3 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskaplig

Neuropeptide precursor VGF is genetically associated with social anhedonia and underrepresented in the brain of major mental illness: its downregulation by DISC1

Ramos, A., Rodriguez-Seoane, C., Rosa, I., Trossbach, S. V., Ortega-Alonso, A., Tomppo, L., Ekelund, J., Veijola, J., Jarvelin, M-R., Alonso, J., Veiga, S., Sawa, A., Hennah, W., Garcia, A., Korth, C. & Requena, J. R., 15 nov 2014, I : Human Molecular Genetics. 23, 22, s. 5859-5865 7 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2013

Deletion of TOP3 beta, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

Stoll, G., Pietiläinen, O., Linder, B., Suvisaari, J., Brosi, C., Hennah, W., Leppä, V. M., Torniainen, M., Ripatti, S., Ala-Mello, S., Plottner, O., Rehnstrom, K., Tuulio-Henriksson, A., Varilo, T., Tallila, J., Kristiansson, K., Isohanni, M., Kaprio, J., Eriksson, J. G., Raitakari, O. T. & 13 andra, Lehtimaki, T., Jarvelin, M-R., Salomaa, V., Hurles, M., Stefansson, H., Palotie, L., Sullivan, P. F., Paunio, T., Lönnqvist, J., Daly, M. J., Fischer, U., Freimer, N. B. & Palotie, A., sep 2013, I : Nature Neuroscience. 16, 9, s. 1228-U99 13 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2012

DISC1 Conditioned GWAS for Psychosis Proneness in a Large Finnish Birth Cohort

Tomppo, L., Ekelund, J., Lichtermann, D., Veijola, J., Järvelin, M-R. & Hennah, W., 2012, I : PLoS One. 7, 2, s. e30643 5 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Öppen tillgång
Fil

Proteomic, genomic and translational approaches identify CRMP1 for a role in schizophrenia and its underlying traits

Bader, V., Tomppo, L., Trossbach, S. V., Bradshaw, N. J., Prikulis, I., Leliveld, S. R., Lin, C-Y., Ishizuka, K., Sawa, A., Ramos, A., Rosa, I., Garcia, A., Requena, J. R., Hipolito, M., Rai, N., Nwulia, E., Henning, U., Ferrea, S., Luckhaus, C., Ekelund, J. & 4 andra, Veijola, J., Jarvelin, M-R., Hennah, W. & Korth, C., 15 okt 2012, I : Human Molecular Genetics. 21, 20, s. 4406-4418 13 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2011

The effects of DISC1 risk variants on brain activation in controls, patients with bipolar disorder and patients with schizophrenia

Chakirova, G., Whalley, H. C., Thomson, P. A., Hennah, W., Moorhead, T. W. J., Welch, K. A., Giles, S., Hall, J., Johnstone, E. C., Lawrie, S. M., Porteous, D. J., Brown, V. J. & McIntosh, A. M., 2011, I : Psychiatry Research. Neuroimaging. 192, 1, s. 20-28 9 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2010

Variation in DISC1 is associated with anxiety, depression and emotional stability in elderly women

Harris, S. E., Hennah, W., Thomson, P. A., Luciano, M., Starr, J. M., Porteous, D. J. & Deary, I. J., 2010, I : Molecular Psychiatry. 15, s. 232-234 4 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2009

A NEW APPROACH FOR INVESTIGATING THE ROLE OF THE DYSTROBREVIN-BINDING PROTEIN (DTNBP1) IN PSYCHOSIS

Willhite, R., van Erp, T. G., Hennah, W., Thompson, P. M., Toga, A. W., Huttunen, M., Kaprio, J., Peltonen, L., Lonnqvist, J. & Cannon, T. D., 2009, I : Schizophrenia bulletin. 35, s. 103-104 2 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Association between genes of disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses

Tomppo, L., Hennah, W., Lahermo, P., Loukola, A., Tuulio-Henriksson, A., Suvisaari, J., Partonen, T., Ekelund, J., Lönnqvist, J. & Peltonen, L., 2009, I : Biological Psychiatry. 65, 12, s. 1055-1062 8 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Association of variants in DISC1 with psychosis-related traits in a large population cohort

Tomppo, L., Hennah, W., Miettunen, J., Jarvelin, M-R., Veijola, J., Ripatti, S., Lahermo, P., Lichtermann, D., Peltonen, L. & Ekelund, J., 2009, I : Archives of General Psychiatry. 66, 2, s. 134-141 8 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder

Hennah, W., Thomson, P., McQuillin, A., Bass, N., Loukola, A., Anjorin, A., Blackwood, D., Curtis, D., Deary, I. J., Harris, S. E., Isometsa, E. T., Lawrence, J., Lonnqvist, J., Muir, W., Palotie, A., Partonen, T., Paunio, T., Pylkko, E., Robinson, M., Soronen, P. & 7 andra, Suominen, K., Suvisaari, J., Thirumalai, S., St Clair, D., Gurling, H., Peltonen, L. & Porteous, D., 2009, I : Molecular Psychiatry. 14, 9, s. 865-873 9 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

The DISC1 pathway modulates expression of neurodevelopmental, synaptogenic and sensory perception genes

Hennah, W. & Porteous, D., 2009, I : PLoS One. 4, 3, s. e4906, [7 s.] 7 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2008

Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample

Soronen, P., Silander, K., Antila, M., Palo, O., Tuulio-Henriksson, A., Kieseppä, T., Ellonen, P., Wedenoja, J., Turunen, J., Pietiläinen, O., Hennah, W., Lönnqvist, J., Peltonen, L., Partonen, T., Paunio, T. & Turunen, J. A., 2008, I : Biological Psychiatry. 64, 5, s. 438-442 5 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Association of DISC1 with autism and Asperger syndrome

Kilpinen, H., Ylisaukko-oja, T., Hennah, W., Palo, O., Varilo, T., Vanhala, R., Nieminen- von Wendt, T., Wendt, L. V., Paunio, T. & Peltonen, L., 2008, I : Molecular Psychiatry. 13, 2, s. 187-196 10 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2007

Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments

Palo, O., Antila, M., Silander, K., Hennah, W., Kilpinen, H., Soronen, P., Tuulio-Henriksson, A., Kieseppä, T., Partonen, T., Lönnqvist, J., Peltonen, L. & Paunio, T., 2007, I : Human Molecular Genetics. 16, 20, s. 3517-3528 12 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1

Hennah, W., Tomppo, L., Hiekkalinna, T., Palo, O., Kilpinen, H., Ekelund, J., Tuulio-Henriksson, A., Silander, K., Partonen, T., Paunio, T., Terwilliger, J. D., Lönnqvist, J. & Peltonen, L., 2007, I : Human Molecular Genetics. 16, 5, s. 453-462 10 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Specific developmental disruption of disrupted-in-schizophrenia-1 function results in schizophrenia-related phenotypes in mice

Li, W., Zhou, Y., Jentsch, J. D., Brown, R. A. M., Tian, X., Ehninger, D., Hennah, W., Peltonen, L., Lonnqvist, J., Huttunen, M. O., Kaprio, J., Trachtenberg, J. T., Silva, A. J. & Cannon, T. D., 2007, I : Proceedings of the National Academy of Sciences of the United States of America. 104, 46, s. 18280-18285 6 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland

Turunen, J. A., Peltonen, J., Pietiläinen, O., Hennah, W., Loukola, A., Paunio, T., Silander, K., Ekelund, J., Varilo, T., Partonen, T., Lönnqvist, J. & Peltonen, L., 2007, I : Schizophrenia Research. 91, 1-3, s. 27-36 10 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2005

A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia

Hennah, W., Tuulio-Henriksson, A., Paunio, T., Ekelund, J., Varilo, T., Partonen, T., Cannon, T., Lönnqvist, J. & Peltonen, L., 2005, I : Molecular Psychiatry. 10, s. 1097-1103 7 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory

Cannon, T. D., Hennah, W., van Erp, T. G. M., Thompson, P. M., Lönnqvist, J., Huttunen, M., Gasperoni, T., Tuulio-Henriksson, A., Pirkola, T., Toga, A. W., Kaprio, J., Mazziotta, J. & Peltonen, L., 2005, I : Archives of General Psychiatry. 62, 11, s. 1205-1213 9 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2004

Replication of 1q42 linkage in Finnish schizophrenia pedigrees

Ekelund, J., Hennah, W., Hiekkalinna, T., Parker, A., Meyer, J., Lonnqvist, J. & Peltonen, L., 2004, I : Molecular Psychiatry. 9, s. 1037-1041 5 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

2003

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

Hennah, W., Varilo, T., Kestila, M., Paunio, T., Arajarvi, R., Haukka, J., Parker, A., Martin, R., Levitzky, S., Partonen, T., Meyer, J., Lonnqvist, J., Peltonen, L. & Ekelund, J., 2003, I : Human Molecular Genetics. 12, s. 3151-3159 9 s.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review