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Schizophrenia Research, ISSN 0920-9964, 09/2018, Volume 199, p. 181
Recent results imply that rare variants contribute to the risk of schizophrenia. Exome sequence data from the UK10K project was used to identify three rare,... 
Medical colleges | Genes | Genetic research | Schizophrenia | Amino acids | Bipolar disorder | Rankings
Journal Article
by Hollingworth, P and Harold, D and Sims, R and Gerrish, A and Lambert, J.C and Carrasquillo, M.M and Abraham, R and Hamshere, M.L and Pahwa, J.S and Moskvina, V and Dowzell, K and Jones, N and Stretton, A and Thomas, C and Richards, A and Ivanov, D and Widdowson, C and Chapman, J and Lovestone, S and Powell, J and Proitsi, P and Lupton, M.K and Brayne, C and Rubinsztein, D.C and Gill, M and Lawlor, B and Lynch, A and Brown, K.S and Passmore, P.A and Craig, D and McGuinness, B and Todd, S and Holmes, C and Mann, D and Smith, A.D and Beaumont, H and Warden, D and Wilcock, G and Love, S and Kehoe, P.G and Hooper, N.M and Vardy, E.R.L.C and Hardy, J and Mead, S and Fox, N.C and Rossor, M and Collinge, J and Maier, W and Jessen, F and Ruther, E and Schurmann, B and Heun, R and Kolsch, H and van den Bussche, H and Heuser, I and Kornhuber, J and Wiltfang, J and Dichgans, M and Frolich, L and Hampel, H and Gallacher, J and Hull, M and Rujescu, D and Giegling, I and Goate, A.M and Kauwe, J.S.K and Cruchaga, C and Nowotny, P and Morris, J.C and Mayo, K and Sleegers, K and Bettens, K and Engelborghs, S and de Deyn, P.P and Van Broeckhoven, C and Livingston, G and Bass, N.J and Gurling, H and McQuillin, A and Gwilliam, R and Deloukas, P and Al-Chalabi, A and Shaw, C.E and Tsolaki, M and Singleton, A.B and Guerreiro, R and Muhleisen, T. W and Nothen, M. M and Moebus, S and Jockel, K.H and Klopp, N and Wichmann, H. E and Pankratz, V.S and Sando, S.B and Aasly, J.O and Barcikowska, M and Wszolek, Z.K and Dickson, D.W and Graff-Radford, N.R. and others and Alzheimer's Dis Neuroimaging and EADI1 Consortium and CHARGE Consortium and Alzheimer's Disease Neuroimaging Initiative and EADI1 consortium and CHARGE consortium and the Alzheimer's Disease Neuroimaging Initiative
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 5, pp. 429 - 435
Journal Article
Lancet, The, ISSN 0140-6736, 2011, Volume 378, Issue 9793, pp. 771 - 784
Journal Article
Schizophrenia Research, ISSN 0920-9964, 09/2018, Volume 199, pp. 181 - 188
Recent results imply that rare variants contribute to the risk of schizophrenia. Exome sequence data from the UK10K project was used to identify three rare,... 
Psychosis | Genetic risk | Genotyping | Sequencing | Index Medicus
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 06/2008, Volume 13, Issue 6, pp. 558 - 569
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 10/2016, Volume 26, pp. S575 - S576
Journal Article
Journal Article
International Journal of Radiation Oncology, Biology, Physics, ISSN 0360-3016, 11/2018, Volume 102, Issue 3, pp. e469 - e470
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 2012, Volume 17, Issue 12, pp. 1316 - 1327
Psychotic symptoms occur in similar to 40% of subjects with Alzheimer's disease (AD) and are associated with more rapid cognitive decline and increased... 
genetic | behavioural symptoms | genome-wide associationstudy | Alzheimer's disease | psychosis | COMMON VARIANTS | PSYCHIATRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | COGNITIVE IMPAIRMENT | BIPOLAR DISORDER | CEREBROSPINAL-FLUID | NEUROSCIENCES | INCREASED FAMILIAL RISK | NEUROPSYCHIATRIC INVENTORY | IDENTIFIES VARIANTS | NATIONAL INSTITUTE | genome-wide association study | COMPLEMENT RECEPTOR 1 | URIC-ACID | Psychiatric Status Rating Scales - statistics & numerical data | Psychotic Disorders - diagnosis | Genetic Predisposition to Disease - genetics | Alzheimer Disease - complications | Psychotic Disorders - complications | Humans | Middle Aged | Male | Genome-Wide Association Study - statistics & numerical data | Chromosomes, Human, Pair 4 - genetics | DNA, Intergenic - genetics | Case-Control Studies | Psychotic Disorders - genetics | Apolipoproteins E - genetics | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Female | Aged | Glucose Transport Proteins, Facilitative - genetics | Neurocalcin - genetics | Alzheimer Disease - genetics | Genome-Wide Association Study - methods | Alzheimer Disease - psychology | Psychoses | Genomics | Physiological aspects | Development and progression | Genetic aspects | Research | Psychosis | chromosome 4 | Neurodegenerative diseases | Apolipoprotein E | Cognitive ability | Aging | Family studies | Data processing | Heritability | Single-nucleotide polymorphism | Gene mapping | Index Medicus | Life Sciences | Human health and pathology | Psychiatrics and mental health
Journal Article