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21.	Ganna, A, et al. (author) Genome studies must account for history-Response 2019 In: Science (New York, N.Y.). - : American Association for the Advancement of Science (AAAS). - 1095-9203 .- 0036-8075. ; 366:6472, s. 1461-1462 Journal article (other academic/artistic)
22.	Ganna, A, et al. (author) Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum 2018 In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 102:6, s. 1204-1211 Journal article (peer-reviewed)
23.	Ganna, A, et al. (author) Quantifying the impact of rare coding variation across the phenotypic spectrum 2018 In: EUROPEAN JOURNAL OF HUMAN GENETICS. - 1018-4813. ; 26, s. 5-6 Conference paper (other academic/artistic)
24.	Ganna, A, et al. (author) Ultra-rare disruptive and damaging mutations influence educational attainment in the general population 2016 In: Nature neuroscience. - : Springer Science and Business Media LLC. - 1546-1726 .- 1097-6256. ; 19:12, s. 1563-1565 Journal article (peer-reviewed)
25.	Goldstein, JI, et al. (author) Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles 2014 In: Nature communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 5, s. 4757- Journal article (peer-reviewed)
26.	Gormley, P, et al. (author) Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families 2018 In: Neuron. - : Elsevier BV. - 1097-4199 .- 0896-6273. ; 98:4, s. 743- Journal article (peer-reviewed)
27.	Gormley, P, et al. (author) Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine 2016 In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 48:8, s. 856- Journal article (peer-reviewed)
28.	Grove, J, et al. (author) Identification of common genetic risk variants for autism spectrum disorder 2019 In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 51:3, s. 431- Journal article (peer-reviewed)
29.	Gusev, A, et al. (author) Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases 2014 In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 95:5, s. 535-552 Journal article (peer-reviewed)
30.	Gusev, A, et al. (author) Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights 2018 In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 50:4, s. 538- Journal article (peer-reviewed)

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Result 21-30 of 76

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Type of publication: journal article (73); conference paper (1)

Type of content: peer-reviewed (66); other academic/artistic (8)

Author/Editor: Neale, BM (76); Daly, MJ (40); Sullivan, PF (39); Ripke, S (31); O'Donovan, MC (28); Werge, T (27); show more...; Hultman, CM (26); Palotie, A (26); Borglum, AD (24); Sklar, P (23); Mortensen, PB (21); Mattheisen, M (21); Hougaard, DM (21); Esko, T (20); Smoller, JW (19); Mors, O (19); Metspalu, A (19); Wray, NR (18); Knowles, JA (18); Grove, J (18); Nordentoft, M (18); Stefansson, K (18); Gill, M. (18); Milani, L (18); Pato, MT (17); Stefansson, H. (17); Maier, W (17); Andreassen, OA (16); Rujescu, D (16); Muller-Myhsok, B (16); Nothen, MM (16); Kendler, KS (16); Bybjerg-Grauholm, J. (16); Breen, G (15); Craddock, N (15); Kirov, G (15); Ophoff, RA (15); Rietschel, M (15); Schulze, TG (15); Agerbo, E (15); Pato, CN (14); Cichon, S (14); Morris, DW (14); Martin, NG (14); Medland, SE (14); Degenhardt, F (14); Herms, S. (14); Bergen, SE (14); Frank, J (14); Witt, SH (14); show less...

University: Karolinska Institutet (75); Umeå University (5); University of Gothenburg (4); Uppsala University (2); Örebro University (1); Lund University (1); show more...; Stockholm School of Economics (1); show less...

Language: English (76)

Research subject (UKÄ/SCB): Medical and Health Sciences (14); Natural sciences (2)

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