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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1944 1
1946 1
1947 1
1950 1
1951 1
1952 2
1954 1
1955 1
1956 3
1957 1
1958 2
1959 5
1960 6
1962 1
1963 2
1964 11
1965 1
1966 1
1967 1
1968 6
1969 2
1970 5
1971 2
1972 2
1973 3
1974 3
1975 4
1976 5
1977 6
1978 5
1979 2
1980 7
1981 5
1982 4
1983 4
1984 3
1985 2
1986 1
1987 3
1988 5
1990 2
1991 3
1992 3
1993 8
1994 5
1995 12
1996 2
1997 5
1998 12
1999 4
2000 2
2001 4
2002 6
2003 4
2004 3
2006 2
2007 3
2008 4
2009 2
2010 6
2011 10
2012 15
2013 16
2014 24
2015 24
2016 29
2017 16
2018 15
2019 28
2020 39
2021 30
2022 20
2023 12
2024 20

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472 results

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Page 1
Artificial intelligence for natural product drug discovery.
Mullowney MW, Duncan KR, Elsayed SS, Garg N, van der Hooft JJJ, Martin NI, Meijer D, Terlouw BR, Biermann F, Blin K, Durairaj J, Gorostiola González M, Helfrich EJN, Huber F, Leopold-Messer S, Rajan K, de Rond T, van Santen JA, Sorokina M, Balunas MJ, Beniddir MA, van Bergeijk DA, Carroll LM, Clark CM, Clevert DA, Dejong CA, Du C, Ferrinho S, Grisoni F, Hofstetter A, Jespers W, Kalinina OV, Kautsar SA, Kim H, Leao TF, Masschelein J, Rees ER, Reher R, Reker D, Schwaller P, Segler M, Skinnider MA, Walker AS, Willighagen EL, Zdrazil B, Ziemert N, Goss RJM, Guyomard P, Volkamer A, Gerwick WH, Kim HU, Müller R, van Wezel GP, van Westen GJP, Hirsch AKH, Linington RG, Robinson SL, Medema MH. Mullowney MW, et al. Among authors: rees er. Nat Rev Drug Discov. 2023 Nov;22(11):895-916. doi: 10.1038/s41573-023-00774-7. Epub 2023 Sep 11. Nat Rev Drug Discov. 2023. PMID: 37697042 Free article. Review.
Genomic findings in schizophrenia and their implications.
Owen MJ, Legge SE, Rees E, Walters JTR, O'Donovan MC. Owen MJ, et al. Among authors: rees e. Mol Psychiatry. 2023 Sep;28(9):3638-3647. doi: 10.1038/s41380-023-02293-8. Epub 2023 Oct 18. Mol Psychiatry. 2023. PMID: 37853064 Free PMC article. Review.
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T; GERAD1 Consortium; CRESTAR Consortium; Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR. Pardiñas AF, et al. Among authors: rees e. Nat Genet. 2018 Mar;50(3):381-389. doi: 10.1038/s41588-018-0059-2. Epub 2018 Feb 26. Nat Genet. 2018. PMID: 29483656 Free PMC article.
Rare coding variants in ten genes confer substantial risk for schizophrenia.
Singh T, Poterba T, Curtis D, Akil H, Al Eissa M, Barchas JD, Bass N, Bigdeli TB, Breen G, Bromet EJ, Buckley PF, Bunney WE, Bybjerg-Grauholm J, Byerley WF, Chapman SB, Chen WJ, Churchhouse C, Craddock N, Cusick CM, DeLisi L, Dodge S, Escamilla MA, Eskelinen S, Fanous AH, Faraone SV, Fiorentino A, Francioli L, Gabriel SB, Gage D, Gagliano Taliun SA, Ganna A, Genovese G, Glahn DC, Grove J, Hall MH, Hämäläinen E, Heyne HO, Holi M, Hougaard DM, Howrigan DP, Huang H, Hwu HG, Kahn RS, Kang HM, Karczewski KJ, Kirov G, Knowles JA, Lee FS, Lehrer DS, Lescai F, Malaspina D, Marder SR, McCarroll SA, McIntosh AM, Medeiros H, Milani L, Morley CP, Morris DW, Mortensen PB, Myers RM, Nordentoft M, O'Brien NL, Olivares AM, Ongur D, Ouwehand WH, Palmer DS, Paunio T, Quested D, Rapaport MH, Rees E, Rollins B, Satterstrom FK, Schatzberg A, Scolnick E, Scott LJ, Sharp SI, Sklar P, Smoller JW, Sobell JL, Solomonson M, Stahl EA, Stevens CR, Suvisaari J, Tiao G, Watson SJ, Watts NA, Blackwood DH, Børglum AD, Cohen BM, Corvin AP, Esko T, Freimer NB, Glatt SJ, Hultman CM, McQuillin A, Palotie A, Pato CN, Pato MT, Pulver AE, St Clair D, Tsuang MT, Vawter MP, Walters JT, Werge TM, Ophoff RA, Sullivan… See abstract for full author list ➔ Singh T, et al. Among authors: rees e. Nature. 2022 Apr;604(7906):509-516. doi: 10.1038/s41586-022-04556-w. Epub 2022 Apr 8. Nature. 2022. PMID: 35396579 Free PMC article.
Uncommon low-grade brain tumors.
Ajithkumar T, Imbulgoda N, Rees E, Harris F, Horan G, Burke A, Jefferies S, Price S, Cross J, Allinson K. Ajithkumar T, et al. Among authors: rees e. Neuro Oncol. 2019 Feb 14;21(2):151-166. doi: 10.1093/neuonc/noy151. Neuro Oncol. 2019. PMID: 30239861 Free PMC article. Review.
Copy number variation and neuropsychiatric illness.
Rees E, Kirov G. Rees E, et al. Curr Opin Genet Dev. 2021 Jun;68:57-63. doi: 10.1016/j.gde.2021.02.014. Epub 2021 Mar 19. Curr Opin Genet Dev. 2021. PMID: 33752146 Free PMC article. Review.
Tooling-up for infectious disease transmission modelling.
Baguelin M, Medley GF, Nightingale ES, O'Reilly KM, Rees EM, Waterlow NR, Wagner M. Baguelin M, et al. Among authors: rees em. Epidemics. 2020 Sep;32:100395. doi: 10.1016/j.epidem.2020.100395. Epub 2020 May 13. Epidemics. 2020. PMID: 32405321 Free PMC article. Review.
Subfemtowatt Laser Phase Tracking.
Sambridge CS, Roberts LE, Wade AR, Valliyakalayil JT, Rees ER, Chabbra N, Zhang J, Sutton AJ, Shaddock DA, McKenzie K. Sambridge CS, et al. Among authors: rees er. Phys Rev Lett. 2023 Nov 10;131(19):193804. doi: 10.1103/PhysRevLett.131.193804. Phys Rev Lett. 2023. PMID: 38000398
472 results