Variability in Working Memory Performance Explained by Epistasis vs Polygenic Scores in the ZNF804A Pathway

Autor: Nicodemus, Kk, Hargreaves, A, Morris, D, Anney, R, Gill, M, Corvin, A, Donohoe, G, Ripke, S, Sanders, Ar, Kendler, Ks, Levinson, Df, Sklar, P, Holmans, Pa, Lin, Dy, Duan, J, Ophoff, Ra, Andreassen, Oa, Scolnick, E, Cichon, S, Clair, St, D, Gurling, H, Werge, T, Rujescu, D, Blackwood, Dh, Pato, Cn, Malhotra, Ak, Purcell, S, Dudbridge, F, Neale, Bm, Rossin, L, Visscher, Pm, Posthuma, D, Ruderfer, Dm, Fanous, A, Stefansson, H, Steinberg, S, Mowry, Bj, Golimbet, V, Hert, De, M, Jönsson, Eg, Bitter, I, Pietiläinen, Op, Collier, Da, Tosato, Sarah, Agartz, I, Albus, M, Alexander, M, Amdur, Rl, Amin, F, Bass, N, Bergen, Se, Black, Dw, Børglum, Ad, Brown, Ma, Bruggeman, R, Buccola, Ng, Byerley, Wf, Cahn, W, Cantor, Rm, Carr, Vj, Catts, Sv, Choudhury, K, Cloninger, C, Cormican, P, Craddock, N, Danoy, Pa, Datta, S, Haan, De, L, Demontis, D, Dikeos, D, Djurovic, S, Donnelly, P, Duong, L, Dwyer, S, Fink Jensen, A, Freedman, R, Freimer, Nb, Friedl, M, Georgieva, L, Giegling, I, Glenthøj, B, Godard, S, Hamshere, M, Hansen, M, Hansen, T, Hartmann, Am, Henskens, Fa, Hougaard, Dm, Hultman, Cm, Ingason, A, Jablensky, Av, Jakobsen, Kd, Jay, M, Jürgens, G, Kahn, Rs, Keller, Mc, Kenis, G, Kenny, E, Kim, Y, Kirov, Gk, Konnerth, H, Konte, B, Krabbendam, L, Krasucki, R, Lasseter, Vk, Laurent, C, Lawrence, J, Lencz, T, Lerer, F, Liang, Ky, Lichtenstein, P, Lieberman, Ja, Linszen, Dh, Lönnqvist, J, Loughland, Cm, Maclean, Aw, Maher, Bs, Maier, W, Mallet, J, Malloy, P, Mattheisen, M, Mattingsdal, M, Mcghee, Ka, Mcgrath, Jj, Mcintosh, A, Mclean, De, Mcquillin, A, Melle, I, Michie, Pt, Milanova, V, Morris, Dw, Mors, O, Mortensen, Pb, Moskvina, V, Muglia, P, Myin Germeys, I, Nertney, Da, Nestadt, G, Nielsen, J, Nikolov, I, Nordentoft, M, Norton, N, Nöthen, Mm, O'Dushlaine, Ct, Olincy, A, Olsen, L, O'Neill, F, Ørntoft, Tf, Owen, Mj, Pantelis, C, Papadimitriou, G, Pato, Mt, Peltonen, L, Petursson, H, Pickard, B, Pimm, J, Pulver, Ae, Puri, V, Quested, D, Quinn, Em, Rasmussen, Hb, Réthelyi, Jm, Ribble, R, Rietschel, M, Riley, Bp, Ruggeri, Mirella, Schall, U, Schulze, Tg, Schwab, Sg, Scott, Rj, Shi, J, Sigurdsson, E, Silverman, Jm, Spencer, Cc, Stefansson, K, Strange, A, Strengman, E, Stroup, T, Suvisaari, J, Terenius, L, Thirumalai, S, Thygesen, Jh, Timm, S, Toncheva, D, Van, Den, Oord, E, Van, Os, Van, J, Winkel, R, Veldink, J, Walsh, D, Wang, Ag, Wiersma, D, Wildenauer, Db, Williams, Hj, Williams, Nm, Wormley, B, Zammit, S, Sullivan, Pf, O'Donovan, Mc, Daly, Mj, Gejman, P.

Publikováno v: Journal of the American Academy of Child and Adolescent Psychiatry, 71(7), 778-785. Elsevier Limited
Nicodemus, K K, Hargreaves, A, Morris, D, Anney, R, Gill, M, Corvin, A, Donohoe, G & Schizophrenia Psychiatric Genome-wide Association Study (GWAS) Consortium 2014, ' Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway ', J A M A Psychiatry, vol. 71, no. 7, pp. 778-85 . https://doi.org/10.1001/jamapsychiatry.2014.528
JAMA psychiatry, vol 71, iss 7
Nicodemus, K K, Hargreaves, A, Morris, D, Anney, R, Gill, M, Corvin, A, Posthuma, D & Donohoe, G 2014, ' Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. ', Journal of the American Academy of Child and Adolescent Psychiatry, vol. 71, no. 7, pp. 778-785 . https://doi.org/10.1001/jamapsychiatry.2014.528
JAMA Psychiatry, 71(7), 778-785. American Medical Association
JAMA psychiatry, 71(7), 778-785. American Medical Association

IMPORTANCE We investigated the variation in neuropsychological function explained by risk alleles at the psychosis susceptibility gene ZNF804A and its interacting partners using single nucleotide polymorphisms (SNPs), polygenic scores, and epistatic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1e597267adcf8243757fe951af9a47a
https://doi.org/10.1001/jamapsychiatry.2014.528

Large recurrent microdeletions associated with schizophrenia

Autor: Toulopoulou, T, Franke, B, Crombie, C, Fossdal, R, Sigmundsson, T, BuizerVoskamp, JE, Hansen, T, Jakobsen, KD, Muglia, P, Francks, C, Matthews, PM, Murray, R, Ruggeri, M, Sabatti, C, Gylfason, A, Halldorsson, BV, Vassos, E, Tosato, S, Walshe, M, Freimer, NB, Gulcher, JR, Gudbjartsson, D, Thorsteinsdottir, U, Kong, A, Thorgeirsson, TE, Olesen, J, Vasilescu, C, Andreassen, OA, Melle, I, Mühleisen, TW, Wang, AG, Ullum, H, Need, AC, Sigurdsson, A, Jonasdottir, A, Djurovic, S, Ophoff, RA, Georgi, A, Rietschel, M, Werge, T, Bjornsson, A, Mattiasdottir, S, Blondal, T, Haraldsson, M, Petursson, H, MyinGermeys, I, Krabbendam, L, De Haan, L, Cahn, W, Bruggeman, R, Wiersma, D, Goldstein, DB, Nöthen, MM, Peltonen, L, Van Os, J, Linszen, DH, Kahn, RS, Stefansson, K, Magnusdottir, BB, Di Forti, M, Bramon, E, Paunio, T, TuulioHenriksson, A, Giegling, I, Möller, HJ, Suvisaari, J, Hartmann, A, Shianna, KV, Ge, D, Lonnqvist, J, Collier, DA, Walker, N, Li, T, Fraser, G, Ingason, A, Steinberg, S, Sigurdsson, E, St Clair, D, Kiemeney, LA, Stefansson, H, Rujescu, D, Cichon, S, Pietiläinen, OPH

Publikováno v: Nature, 455, 7210, pp. 232-6
Nature, 455, 232-6
Nature, 455(7210), 232-236. Nature Publishing Group

Reduced fecundity, associated with severe mental disorders, places negative selection pressure on risk alleles and may explain, in part, why common variants have not been found that confer risk of disorders such as autism, schizophrenia and mental re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abe93dab86948eaa9355e125d23ef45b
http://hdl.handle.net/10722/141844

Association to markers in the 19p13 region in panic disorder samples from the genetic isolate of Faroe Islands

Autor: Dahl, HA, Wang, AG, Wang, M, Ewald, H, Mors, Ole, Kruse, TA

Publikováno v: Dahl, HA, Wang, AG, Wang, M, Ewald, H, Mors, O & Kruse, TA 2005, ' Association to markers in the 19p13 region in panic disorder samples from the genetic isolate of Faroe Islands ' Association to markers in the 19p13 region in panic disorder samples from the genetic isolate of Faroe Islands, 17/12/2010, .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::96329be67a722b7e1c829b19018194a4
https://pure.au.dk/portal/da/publications/association-to-markers-in-the-19p13-region-in-panic-disorder-samples-from-the-genetic-isolate-of-faroe-islands(322e6180-ba63-11da-bee9-02004c4f4f50).html

The glutamate decarboxylase gene 1 as a potential candidate gene for autism

Autor: Buttenschøn, Henriette Nørmølle, Als, Thomas Damm, Daoud, Agata El, Foldager, Leslie, Wang, AG, Børglum, Anders, Kruse, TA, Lauritsen, MB, Mors, Ole

Publikováno v: Buttenschøn, H N, Als, T D, Daoud, A E, Foldager, L, Wang, AG, Børglum, A, Kruse, TA, Lauritsen, MB & Mors, O 2005, ' The glutamate decarboxylase gene 1 as a potential candidate gene for autism. ', 17/12/2010, .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::f9561d602ba799aab7c1b7525cfeffa0
https://pure.au.dk/portal/da/publications/the-glutamate-decarboxylase-gene-1-as-a-potential-candidate-gene-for-autism(36483930-85fb-11db-bee9-02004c4f4f50).html

Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation

Autor: Wang Ag, May-Yung Yen, Yau-Huei Wei, Chen Cs

Publikováno v: The British journal of ophthalmology. 86(9)

Aims: To investigate the change of mitochondrial DNA (mtDNA) content in Leber’s hereditary optic neuropathy (LHON) with 11778 mutation. Methods: Mitochondrial DNA content in 27 LHON patients with 11778 mutation, 26 asymptomatic maternal relatives,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbc136600333786fa1fe24d1490cbcfb
https://pubmed.ncbi.nlm.nih.gov/12185132