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

Year Number of Results
1920 1
1936 1
1938 1
1945 2
1946 5
1947 7
1948 4
1949 4
1950 1
1951 1
1952 1
1953 1
1954 1
1955 1
1958 2
1959 6
1961 4
1962 2
1964 1
1977 2
1978 1
1979 1
1981 2
1983 1
1994 1
1996 2
2000 4
2001 5
2002 2
2003 8
2004 2
2005 2
2006 5
2007 2
2008 6
2009 1
2010 4
2011 4
2012 7
2013 8
2014 12
2015 8
2016 6
2017 11
2018 11
2019 17
2020 12
2021 23
2022 31
2023 23
2024 20
2025 29
2026 4

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292 results

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Page 1
The Lancet Commission on ending stigma and discrimination in mental health.
Thornicroft G, Sunkel C, Alikhon Aliev A, Baker S, Brohan E, El Chammay R, Davies K, Demissie M, Duncan J, Fekadu W, Gronholm PC, Guerrero Z, Gurung D, Habtamu K, Hanlon C, Heim E, Henderson C, Hijazi Z, Hoffman C, Hosny N, Huang FX, Kline S, Kohrt BA, Lempp H, Li J, London E, Ma N, Mak WWS, Makhmud A, Maulik PK, Milenova M, Morales Cano G, Ouali U, Parry S, Rangaswamy T, Rüsch N, Sabri T, Sartorius N, Schulze M, Stuart H, Taylor Salisbury T, Vera San Juan N, Votruba N, Winkler P. Thornicroft G, et al. Among authors: stuart h. Lancet. 2022 Oct 22;400(10361):1438-1480. doi: 10.1016/S0140-6736(22)01470-2. Epub 2022 Oct 9. Lancet. 2022. PMID: 36223799 Review. No abstract available.
ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.
Cuvertino S, Stuart HM, Chandler KE, Roberts NA, Armstrong R, Bernardini L, Bhaskar S, Callewaert B, Clayton-Smith J, Davalillo CH, Deshpande C, Devriendt K, Digilio MC, Dixit A, Edwards M, Friedman JM, Gonzalez-Meneses A, Joss S, Kerr B, Lampe AK, Langlois S, Lennon R, Loget P, Ma DYT, McGowan R, Des Medt M, O'Sullivan J, Odent S, Parker MJ, Pebrel-Richard C, Petit F, Stark Z, Stockler-Ipsiroglu S, Tinschert S, Vasudevan P, Villa O, White SM, Zahir FR; DDD Study; Woolf AS, Banka S. Cuvertino S, et al. Among authors: stuart hm. Am J Hum Genet. 2017 Dec 7;101(6):1021-1033. doi: 10.1016/j.ajhg.2017.11.006. Am J Hum Genet. 2017. PMID: 29220674 Free PMC article.
Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
Wright CF, Campbell P, Eberhardt RY, Aitken S, Perrett D, Brent S, Danecek P, Gardner EJ, Chundru VK, Lindsay SJ, Andrews K, Hampstead J, Kaplanis J, Samocha KE, Middleton A, Foreman J, Hobson RJ, Parker MJ, Martin HC, FitzPatrick DR, Hurles ME, Firth HV; DDD Study. Wright CF, et al. N Engl J Med. 2023 Apr 27;388(17):1559-1571. doi: 10.1056/NEJMoa2209046. Epub 2023 Apr 12. N Engl J Med. 2023. PMID: 37043637 Free PMC article.
Conceptualizing belonging.
Mahar AL, Cobigo V, Stuart H. Mahar AL, et al. Among authors: stuart h. Disabil Rehabil. 2013 Jun;35(12):1026-32. doi: 10.3109/09638288.2012.717584. Epub 2012 Oct 1. Disabil Rehabil. 2013. PMID: 23020179 Review.
In vitro generation of mouse morula-like cells.
Li H, Chang L, Wu J, Huang J, Guan W, Bates LE, Stuart HT, Guo M, Zhang P, Huang B, Chen C, Zhang M, Chen J, Min M, Wu G, Hutchins AP, Silva JCR. Li H, et al. Among authors: stuart ht. Dev Cell. 2023 Nov 20;58(22):2510-2527.e7. doi: 10.1016/j.devcel.2023.09.013. Epub 2023 Oct 23. Dev Cell. 2023. PMID: 37875119 Free article.
Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders.
Molina-Ramírez LP, Kyle C, Ellingford JM, Wright R, Taylor A, Bhaskar SS, Campbell C, Jackson H, Fairclough A, Rousseau A, Burghel GJ, Dutton L, Banka S, Briggs TA, Clayton-Smith J, Douzgou S, Jones EA, Kingston HM, Kerr B, Ealing J, Somarathi S, Chandler KE, Stuart HM, Burkitt-Wright EM, Newman WG, Bruce IA, Black GC, Gokhale D. Molina-Ramírez LP, et al. Among authors: stuart hm. J Med Genet. 2022 Apr;59(4):393-398. doi: 10.1136/jmedgenet-2020-107303. Epub 2021 Apr 20. J Med Genet. 2022. PMID: 33879512 Free PMC article.
2024 Canadian Surgery Forum: Sept. 25-28, 2024.
Li C, Guo M, Karimuddin A, Guo M, Li C, Karimuddin A, Sutherland J, Huo B, McKechnie T, Ortenzi M, Lee Y, Antoniou S, Mayol J, Ahmed H, Boudreau V, Ramji K, Eskicioglu C, de Jager P, Urbach D, Poole M, Abbad A, Al-Shamali H, Al-Faraj Z, Wen C, Pescarus R, Bechara R, Hong D, Park LJ, Marcucci M, Ofori S, Bogach J, Serrano PE, Simunovic M, Yang I, Cadeddu M, Marcaccio MJ, Borges FK, Nenshi R, Devereaux PJ, Urbanellis P, Douglas J, Nemeth E, Ellsmere J, Spence R, Cunningham J, Falk R, Skinner T, Ebert N, Galbraith L, Prins M, Joharifard S, Joos E, Orovec A, Lethbridge L, Spence R, Hoogerboord M, Stuart H, Bergeron AM, Yang I, Bogach J, Nguyen L, Reade C, Eiriksson L, Morais M, Hanley G, Mah S, Brar K, Seymour KA, Eckhouse SR, Sudan R, Greenberg JA, Portenier D, Jung JJ, Light A, Dingley B, Delisle M, Apte S, Mallick R, Hamilton T, Stuart H, Talbot M, McKinnon G, Jost E, Thiboutot E, Nessim C, Katote N, Drohan A, Spence R, Neumann K, Shi G, Leung R, Lim C, Van Oirschot M, Grant A, Knowles S, Van Koughnett JA, Brousseau K, Monette L, McIsaac D, Wherrett C, Mallick R, Workneh A, Ramsay T, Tinmouth A, Shaw J, Carrier FM, Fergusson D, Martel G, Cornacchia M, Ivankovic V, Mam… See abstract for full author list ➔ Li C, et al. Among authors: stuart h. Can J Surg. 2024 Nov 28;67(6suppl2):S77-S108. doi: 10.1503/cjs.012624. Print 2024 Nov-Dec. Can J Surg. 2024. PMID: 39609036 Free PMC article. No abstract available.
Cellular population dynamics shape the route to human pluripotency.
Panariello F, Gagliano O, Luni C, Grimaldi A, Angiolillo S, Qin W, Manfredi A, Annunziata P, Slovin S, Vaccaro L, Riccardo S, Bouche V, Dionisi M, Salvi M, Martewicz S, Hu M, Cui M, Stuart H, Laterza C, Baruzzo G, Schiebinger G, Di Camillo B, Cacchiarelli D, Elvassore N. Panariello F, et al. Among authors: stuart h. Nat Commun. 2023 May 17;14(1):2829. doi: 10.1038/s41467-023-37270-w. Nat Commun. 2023. PMID: 37198156 Free PMC article.
292 results