Zobrazeno 1 - 10
of 63
pro vyhledávání: '"T.J. Flint"'
Autor:
T.J. Flint, Henriette N. Buttenschøn, Ingrid Bayer Kristensen, Søren Christoffersen, Leslie Foldager, Anders D. Børglum, Nikolaj Friis Hansen, Ole Mors, Ping Qin, Preben Bo Mortensen
Publikováno v:
Zacharov, T F, Qin, P, Buttenschøn, H N, Kristensen, I B, Friis Hansen, N, Christoffersen, S, Foldager, L, Mortensen, P B, Børglum, A & Mors, O 2010, ' An association study of suicide and candidate genes in the serotonergic system ', XVIIIth World Congress on Psychiatric Genetics. Book of abstracts., pp. 231-232 .
Aarhus University
Zacharov, T F, Qin, P, Buttenschøn, H N, Kristensen, I B, Christoffersen, S, Hansen, N F, Foldager, L, Mortensen, P B, Børglum, A & Mors, O 2010, ' An association study of suicide and candidate genes in the serotonergic system ', Risskov, Denmark, 11/11/2010-11/11/2010, .
Buttenschøn, H N, Flint, T J, Foldager, L, Qin, P, Christoffersen, S, Hansen, N F, Kristensen, I B, Mortensen, P B, Børglum, A D & Mors, O 2013, ' An association study of suicide and candidate genes in the serotonergic system ', Journal of Affective Disorders, vol. 148, no. 2-3, pp. 291-8 . https://doi.org/10.1016/j.jad.2012.12.011
Buttenschon, H N, Flint, T J, Foldager, L, Qin, P, Christoffersen, S, Hansen, N F, Kristensen, I B, Mortensen, P B, Borglum, A D & Mors, O 2013, ' An association study of suicide and candidate genes in the serotonergic system ', Journal of Affective Disorders, vol. 148, no. 2-3, pp. 291-298 . https://doi.org/10.1016/j.jad.2012.12.011
Aarhus University
Zacharov, T F, Qin, P, Buttenschøn, H N, Kristensen, I B, Christoffersen, S, Hansen, N F, Foldager, L, Mortensen, P B, Børglum, A & Mors, O 2010, ' An association study of suicide and candidate genes in the serotonergic system ', Risskov, Denmark, 11/11/2010-11/11/2010, .
Buttenschøn, H N, Flint, T J, Foldager, L, Qin, P, Christoffersen, S, Hansen, N F, Kristensen, I B, Mortensen, P B, Børglum, A D & Mors, O 2013, ' An association study of suicide and candidate genes in the serotonergic system ', Journal of Affective Disorders, vol. 148, no. 2-3, pp. 291-8 . https://doi.org/10.1016/j.jad.2012.12.011
Buttenschon, H N, Flint, T J, Foldager, L, Qin, P, Christoffersen, S, Hansen, N F, Kristensen, I B, Mortensen, P B, Borglum, A D & Mors, O 2013, ' An association study of suicide and candidate genes in the serotonergic system ', Journal of Affective Disorders, vol. 148, no. 2-3, pp. 291-298 . https://doi.org/10.1016/j.jad.2012.12.011
Introduction: Strong evidence demonstrates a genetic susceptibility to suicidal behaviour and a relationship between suicide and mental disorders. The aim of this study was to test for association between suicide and five selected genetic variants, w
Autor:
U. Froster-Iskenius, Samantha J. L. Knight, A. Roche, Kay E. Davies, J. Holland, Y. Nakahori, S Wong, Mark C. Hirst, Jack Tarleton, T.J. Flint, Charles E. Schwartz, David Bentley
The fragile X syndrome is an X-linked disorder which has been shown to be associated with the length variation of a DNA fragment containing a CGG trinucleotide repeat element at or close to the fragile site. Phenotypically normal carriers of the diso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2198d2837b953cbd2ea522b9596a7217
https://doi.org/10.1093/nar/19.16.4355
https://doi.org/10.1093/nar/19.16.4355
Autor:
L. Blanco, A. El Daoud, Torben A Kruse, Torben F. Ørntoft, F. Wikman, Ole Mors, Tove H. Jorgensen, Henriette N. Buttenschøn, Henrik Ewald, Thomas Damm Als, M. Torralba, B.M. Teruel, T.J. Flint
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :25-30
Homozygosity mapping is a very powerful method for finding rare recessive disease genes in monogenic disorders and may also be useful for locating risk genes in complex disorders, late onset disorders where parents often are not available, and for ra
Autor:
Tove H. Jorgensen, M. Pinaud, Henrik Ewald, Maria Vang, A.G. Wang, Torben A Kruse, Anders D. Børglum, Ole Mors, Hans Atli Dahl, T.J. Flint
Publikováno v:
American Journal of Medical Genetics. 114:245-252
Chromosome 22q may harbor risk genes for schizophrenia and bipolar affective disorder. This is evidenced through genetic mapping studies, investigations of cytogenetic abnormalities, and direct examination of candidate genes. Patients with schizophre
Publikováno v:
Ewald, H, Zacharov, T F, Degn, B, Mors, O & Kruse, T A 1998, ' A functional variant of the serotonin transporter gene in families with bipolar affective disorder ', Journal of Affective Disorders, vol. 48, no. 2-3, pp. 135-44 .
Background: The serotonin transporter protein (SERT) reuptakes serotonin from synapses and has been implied as the site of therapeutic action of many antidepressant drugs. SERT is one of the most relevant candidate genes for bipolar affective disorde
Publikováno v:
Psychiatric Genetics. 5:161-170
Dopa decarboxylase (DDC) is involved directly in the synthesis of dopamine and serotonin and indirectly in the synthesis of noradrenaline. The present study investigated two Danish families for linkage between manic depressive illness, a marker at th
Publikováno v:
Human Heredity. 44:287-294
Cooccurrence of Prader-Willi syndrome and psychosis has been reported in a few cases. Prader-Willi syndrome is most often associated with interstitial deletion or uniparental disomy of chromosome 15ql
Autor:
Carsten Bøcker Pedersen, Ditte Demontis, Thomas Werge, Jakob Grove, Preben Bo Mortensen, Karina Meden Sørensen, Mette Nyegaard, T.J. Flint, Anders D. Børglum, Anne Hedemand, Henriette N. Buttenschøn, Robert H. Yolken, Ole Mors, David M. Hougaard, Merete Nordentoft
Publikováno v:
Demontis, D, Nyegaard, M, Buttenschøn, H N, Hedemand, A, Pedersen, C B, Grove, J, Flint, T J, Nordentoft, M, Werge, T, Hougaard, D M, Sørensen, K M, Yolken, R H, Mors, O, Børglum, A D & Mortensen, P B 2011, ' Association of GRIN1 and GRIN2A-D With schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk ', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 156, no. 8, pp. 913-922 . https://doi.org/10.1002/ajmg.b.31234
N-methyl-D-aspartate (NMDA) receptors are very important for proper brain development and several lines of evidence support that hypofunction of the NMDA receptors are involved in the pathophysiology of schizophrenia. Gene variation and gene-environm
Autor:
Niclas Tue Hansen, Anders D. Børglum, Kasper Lage, Ole Mors, Torben Hansen, Shaun Purcell, Tune H. Pers, Henrik Dam, T.J. Flint, Erling T. Mellerup, Manuel A. R. Ferreira, Irene Kouskoumvekaki, Piotr Dworzynski, Christopher T. Workman, Ingrid Melle, Pernille Koefoed, Ole A. Andreassen, Søren Brunak, Srdjan Djurovic, Martin L. Miller, Thomas Werge
Publikováno v:
Pers, T H, Hansen, N T, Hansen, K L, Koefoed, P, Dworzynski, P, Miller, M L, Zacharov, T F, Mellerup, E T, Dam, H F, Andreassen, O A, Djurovic, S, Melle, I, Børglum, A D, Werge, T, Purcell, S, Ferreira, M A, Kouskoumvekaki, I, Workman, C, Hansen, T, Mors, O & Brunak, S 2011, ' Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes ', Genetic Epidemiology, vol. 35, no. 5, pp. 318-32 . https://doi.org/10.1002/gepi.20580
To access publisher's full text version of this article click on the hyperlink at the bottom of the page Meta-analyses of large-scale association studies typically proceed solely within one data type and do not exploit the potential complementarities
Autor:
Merete Nordentoft, David M. Hougaard, Paal Skytt Andersen, Karina Meden Sørensen, Thomas Werge, Carsten Bøcker Pedersen, Preben Bo Mortensen, Anne Hedemand, Mette Nyegaard, Leslie Foldager, Ditte Demontis, Ole Mors, Anders D. Børglum, T.J. Flint
Publikováno v:
Nyegaard, M, Demontis, D, Foldager, L, Hedemand, A, Flint, T J, Sørensen, K M, Andersen, P S, Nordentoft, M, Werge, T, Pedersen, C B, Hougaard, D M, Mortensen, P B, Mors, O & Børglum, A D 2010, ' CACNA1C (rs1006737) is associated with schizophrenia ', Molecular Psychiatry, vol. 15, no. 2, pp. 119-21 . https://doi.org/10.1038/mp.2009.69
Udgivelsesdato: 2010-Feb