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

Year Number of Results
1850 1
1859 1
1864 1
1865 1
1868 2
1871 4
1872 1
1873 3
1874 5
1875 2
1877 1
1881 1
1882 1
1883 6
1884 4
1885 1
1887 2
1888 3
1889 2
1890 1
1891 2
1892 3
1895 1
1899 1
1900 1
1901 5
1902 5
1903 2
1904 4
1905 3
1906 1
1907 1
1911 1
1912 1
1919 1
1925 1
1928 1
1933 1
1934 1
1935 1
1940 1
1945 6
1946 14
1947 8
1948 3
1949 12
1950 8
1951 11
1952 3
1953 12
1954 9
1955 7
1956 10
1957 4
1958 3
1959 6
1960 7
1961 5
1962 5
1963 4
1964 4
1965 6
1966 10
1967 10
1968 9
1969 11
1970 5
1971 14
1972 20
1973 24
1974 22
1975 27
1976 18
1977 26
1978 20
1979 32
1980 36
1981 44
1982 25
1983 44
1984 51
1985 46
1986 52
1987 60
1988 53
1989 56
1990 59
1991 55
1992 44
1993 51
1994 53
1995 64
1996 89
1997 70
1998 72
1999 65
2000 71
2001 75
2002 89
2003 68
2004 82
2005 121
2006 106
2007 114
2008 146
2009 140
2010 141
2011 218
2012 200
2013 195
2014 206
2015 199
2016 218
2017 271
2018 238
2019 234
2020 242
2021 291
2022 256
2023 259
2024 255
2025 194

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5,622 results

Results by year

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Page 1
Patient-Specific In Vivo Gene Editing to Treat a Rare Genetic Disease.
Musunuru K, Grandinette SA, Wang X, Hudson TR, Briseno K, Berry AM, Hacker JL, Hsu A, Silverstein RA, Hille LT, Ogul AN, Robinson-Garvin NA, Small JC, McCague S, Burke SM, Wright CM, Bick S, Indurthi V, Sharma S, Jepperson M, Vakulskas CA, Collingwood M, Keogh K, Jacobi A, Sturgeon M, Brommel C, Schmaljohn E, Kurgan G, Osborne T, Zhang H, Kinney K, Rettig G, Barbosa CJ, Semple SC, Tam YK, Lutz C, George LA, Kleinstiver BP, Liu DR, Ng K, Kassim SH, Giannikopoulos P, Alameh MG, Urnov FD, Ahrens-Nicklas RC. Musunuru K, et al. Among authors: wright cm. N Engl J Med. 2025 Jun 12;392(22):2235-2243. doi: 10.1056/NEJMoa2504747. Epub 2025 May 15. N Engl J Med. 2025. PMID: 40373211
Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts.
Mirshahi UL, Colclough K, Wright CF, Wood AR, Beaumont RN, Tyrrell J, Laver TW, Stahl R, Golden A, Goehringer JM; Geisinger-Regeneron DiscovEHR Collaboration; Frayling TF, Hattersley AT, Carey DJ, Weedon MN, Patel KA. Mirshahi UL, et al. Among authors: wright cf. Am J Hum Genet. 2022 Nov 3;109(11):2018-2028. doi: 10.1016/j.ajhg.2022.09.014. Epub 2022 Oct 17. Am J Hum Genet. 2022. PMID: 36257325 Free PMC article.
Overview.
Bradshaw D, Pillay van-Wyk V, Neethling I, Roomaney RA, Cois A, Joubert JD, Nannan N, Abdelatief N, Awotiwon OF, Turawa EB, Nojilana B, Groenewald P, Matzopoulos R, Prinsloo M, Cairncross E, Wright CY, Peer N, Pacella R; The Sacra Collaborative Group. Bradshaw D, et al. Among authors: wright cy. S Afr Med J. 2022 Sep 30;112(8b):556-570. doi: 10.7196/SAMJ.2022.v112i8b.16648. S Afr Med J. 2022. PMID: 36458357
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.
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height.
Hawkes G, Beaumont RN, Li Z, Mandla R, Li X, Albert CM, Arnett DK, Ashley-Koch AE, Ashrani AA, Barnes KC, Boerwinkle E, Brody JA, Carson AP, Chami N, Chen YI, Chung MK, Curran JE, Darbar D, Ellinor PT, Fornage M, Gordeuk VR, Guo X, He J, Hwu CM, Kalyani RR, Kaplan R, Kardia SLR, Kooperberg C, Loos RJF, Lubitz SA, Minster RL, Naseri T, Viali S, Mitchell BD, Murabito JM, Palmer ND, Psaty BM, Redline S, Shoemaker MB, Silverman EK, Telen MJ, Weiss ST, Yanek LR, Zhou H; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; Liu CT, North KE, Justice AE, Locke JM, Owens N, Murray A, Patel K, Frayling TM, Wright CF, Wood AR, Lin X, Manning A, Weedon MN. Hawkes G, et al. Among authors: wright cf. Nat Commun. 2024 Oct 3;15(1):8549. doi: 10.1038/s41467-024-52579-w. Nat Commun. 2024. PMID: 39362880 Free PMC article.
Acetaminophen for Patent Ductus Arteriosus and Risk of Mortality and Pulmonary Morbidity.
Jensen EA, DeMauro SB, Rysavy MA, Patel RM, Laughon MM, Eichenwald EC, Do BT, Das A, Wright CJ; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Jensen EA, et al. Among authors: wright cj. Pediatrics. 2024 Aug 1;154(2):e2023065056. doi: 10.1542/peds.2023-065056. Pediatrics. 2024. PMID: 39011550 Free PMC article.
Use of a Novel Artificial Intelligence System Leads to the Detection of Significantly Higher Number of Adenomas During Screening and Surveillance Colonoscopy: Results From a Large, Prospective, US Multicenter, Randomized Clinical Trial.
Desai M, Ausk K, Brannan D, Chhabra R, Chan W, Chiorean M, Gross SA, Girotra M, Haber G, Hogan RB, Jacob B, Jonnalagadda S, Iles-Shih L, Kumar N, Law J, Lee L, Lin O, Mizrahi M, Pacheco P, Parasa S, Phan J, Reeves V, Sethi A, Snell D, Underwood J, Venu N, Visrodia K, Wong A, Winn J, Wright CH, Sharma P. Desai M, et al. Among authors: wright ch. Am J Gastroenterol. 2024 Jul 1;119(7):1383-1391. doi: 10.14309/ajg.0000000000002664. Epub 2024 Jan 18. Am J Gastroenterol. 2024. PMID: 38235741 Clinical Trial.
5,622 results