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Year Number of Results
1987 1
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2007 1
2009 1
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2012 1
2014 1
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2019 5
2020 5
2021 3
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33 results

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Page 1
Evidence for 28 genetic disorders discovered by combining healthcare and research data.
Kaplanis J, Samocha KE, Wiel L, Zhang Z, Arvai KJ, Eberhardt RY, Gallone G, Lelieveld SH, Martin HC, McRae JF, Short PJ, Torene RI, de Boer E, Danecek P, Gardner EJ, Huang N, Lord J, Martincorena I, Pfundt R, Reijnders MRF, Yeung A, Yntema HG; Deciphering Developmental Disorders Study; Vissers LELM, Juusola J, Wright CF, Brunner HG, Firth HV, FitzPatrick DR, Barrett JC, Hurles ME, Gilissen C, Retterer K. Kaplanis J, et al. Nature. 2020 Oct;586(7831):757-762. doi: 10.1038/s41586-020-2832-5. Epub 2020 Oct 14. Nature. 2020. PMID: 33057194 Free PMC article.
The contribution of X-linked coding variation to severe developmental disorders.
Martin HC, Gardner EJ, Samocha KE, Kaplanis J, Akawi N, Sifrim A, Eberhardt RY, Tavares ALT, Neville MDC, Niemi MEK, Gallone G, McRae J; Deciphering Developmental Disorders Study; Wright CF, FitzPatrick DR, Firth HV, Hurles ME. Martin HC, et al. Nat Commun. 2021 Jan 27;12(1):627. doi: 10.1038/s41467-020-20852-3. Nat Commun. 2021. PMID: 33504798 Free PMC article.
Emergent order in hydrodynamic spin lattices.
Sáenz PJ, Pucci G, Turton SE, Goujon A, Rosales RR, Dunkel J, Bush JWM. Sáenz PJ, et al. Among authors: turton se. Nature. 2021 Aug;596(7870):58-62. doi: 10.1038/s41586-021-03682-1. Epub 2021 Aug 4. Nature. 2021. PMID: 34349289 Free article.
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Jeffries L, Mis EK, McWalter K, Donkervoort S, Brodsky NN, Carpier JM, Ji W, Ionita C, Roy B, Morrow JS, Darbinyan A, Iyer K, Aul RB, Banka S, Chao KR, Cobbold L, Cohen S, Custodio HM, Drummond-Borg M, Elmslie F, Finanger E, Hainline BE, Helbig I, Hewson S, Hu Y, Jackson A, Josifova D, Konstantino M, Leach ME, Mak B, McCormick D, McGee E, Nelson S, Nguyen J, Nugent K, Ortega L, Goodkin HP, Roeder E, Roy S, Sapp K, Saade D, Sisodiya SM, Stals K, Towner S, Wilson W; Deciphering Developmental Disorders; Genomics England Research Consortium; Undiagnosed Disease Network; Khokha MK, Bönnemann CG, Lucas CL, Lakhani SA. Jeffries L, et al. Genet Med. 2024 Feb;26(2):101023. doi: 10.1016/j.gim.2023.101023. Epub 2023 Nov 7. Genet Med. 2024. PMID: 37947183
Speed oscillations in classical pilot-wave dynamics.
Durey M, Turton SE, Bush JWM. Durey M, et al. Among authors: turton se. Proc Math Phys Eng Sci. 2020 Jul;476(2239):20190884. doi: 10.1098/rspa.2019.0884. Epub 2020 Jul 22. Proc Math Phys Eng Sci. 2020. PMID: 32831603 Free PMC article.
Neural correlates of the DMT experience assessed with multivariate EEG.
Timmermann C, Roseman L, Schartner M, Milliere R, Williams LTJ, Erritzoe D, Muthukumaraswamy S, Ashton M, Bendrioua A, Kaur O, Turton S, Nour MM, Day CM, Leech R, Nutt DJ, Carhart-Harris RL. Timmermann C, et al. Among authors: turton s. Sci Rep. 2019 Nov 19;9(1):16324. doi: 10.1038/s41598-019-51974-4. Sci Rep. 2019. PMID: 31745107 Free PMC article.
Auditory sequence analysis and phonological skill.
Grube M, Kumar S, Cooper FE, Turton S, Griffiths TD. Grube M, et al. Among authors: turton s. Proc Biol Sci. 2012 Nov 7;279(1746):4496-504. doi: 10.1098/rspb.2012.1817. Epub 2012 Sep 5. Proc Biol Sci. 2012. PMID: 22951739 Free PMC article.
Blunted endogenous opioid release following an oral dexamphetamine challenge in abstinent alcohol-dependent individuals.
Turton S, Myers JF, Mick I, Colasanti A, Venkataraman A, Durant C, Waldman A, Brailsford A, Parkin MC, Dawe G, Rabiner EA, Gunn RN, Lightman SL, Nutt DJ, Lingford-Hughes A. Turton S, et al. Mol Psychiatry. 2020 Aug;25(8):1749-1758. doi: 10.1038/s41380-018-0107-4. Epub 2018 Jun 25. Mol Psychiatry. 2020. PMID: 29942043 Free PMC article. Clinical Trial.
33 results