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Results by year

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

Year Number of Results
1828 1
1844 2
1845 10
1873 1
1874 2
1883 2
1897 2
1904 1
1906 1
1908 1
1909 2
1910 2
1912 1
1913 1
1929 1
1932 1
1946 1
1947 3
1948 2
1949 2
1950 3
1951 4
1952 2
1953 6
1954 3
1956 3
1957 2
1958 6
1959 4
1960 3
1961 5
1962 2
1963 4
1964 5
1965 4
1966 8
1967 8
1968 7
1969 7
1970 10
1971 5
1972 6
1973 12
1974 17
1975 22
1976 22
1977 15
1978 18
1979 29
1980 30
1981 30
1982 31
1983 36
1984 39
1985 41
1986 40
1987 42
1988 62
1989 59
1990 60
1991 63
1992 89
1993 92
1994 80
1995 90
1996 87
1997 68
1998 81
1999 94
2000 110
2001 126
2002 96
2003 103
2004 95
2005 153
2006 161
2007 155
2008 140
2009 175
2010 176
2011 193
2012 244
2013 245
2014 266
2015 264
2016 293
2017 251
2018 279
2019 327
2020 347
2021 336
2022 300
2023 303
2024 283
2025 102

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Search Results

6,339 results

Results by year

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Page 1
Treatment of Metastatic Colorectal Cancer: ASCO Guideline.
Morris VK, Kennedy EB, Baxter NN, Benson AB 3rd, Cercek A, Cho M, Ciombor KK, Cremolini C, Davis A, Deming DA, Fakih MG, Gholami S, Hong TS, Jaiyesimi I, Klute K, Lieu C, Sanoff H, Strickler JH, White S, Willis JA, Eng C. Morris VK, et al. Among authors: white s. J Clin Oncol. 2023 Jan 20;41(3):678-700. doi: 10.1200/JCO.22.01690. Epub 2022 Oct 17. J Clin Oncol. 2023. PMID: 36252154 Free PMC article.
Antidepressants for pain management in adults with chronic pain: a network meta-analysis.
Birkinshaw H, Friedrich CM, Cole P, Eccleston C, Serfaty M, Stewart G, White S, Moore RA, Phillippo D, Pincus T. Birkinshaw H, et al. Among authors: white s. Cochrane Database Syst Rev. 2023 May 10;5(5):CD014682. doi: 10.1002/14651858.CD014682.pub2. Cochrane Database Syst Rev. 2023. PMID: 37160297 Free PMC article. Review.
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.
Chen Y, Dawes R, Kim HC, Ljungdahl A, Stenton SL, Walker S, Lord J, Lemire G, Martin-Geary AC, Ganesh VS, Ma J, Ellingford JM, Delage E, D'Souza EN, Dong S, Adams DR, Allan K, Bakshi M, Baldwin EE, Berger SI, Bernstein JA, Bhatnagar I, Blair E, Brown NJ, Burrage LC, Chapman K, Coman DJ, Compton AG, Cunningham CA, D'Souza P, Danecek P, Délot EC, Dias KR, Elias ER, Elmslie F, Evans CA, Ewans L, Ezell K, Fraser JL, Gallacher L, Genetti CA, Goriely A, Grant CL, Haack T, Higgs JE, Hinch AG, Hurles ME, Kuechler A, Lachlan KL, Lalani SR, Lecoquierre F, Leitão E, Fevre AL, Leventer RJ, Liebelt JE, Lindsay S, Lockhart PJ, Ma AS, Macnamara EF, Mansour S, Maurer TM, Mendez HR, Metcalfe K, Montgomery SB, Moosajee M, Nassogne MC, Neumann S, O'Donoghue M, O'Leary M, Palmer EE, Pattani N, Phillips J, Pitsava G, Pysar R, Rehm HL, Reuter CM, Revencu N, Riess A, Rius R, Rodan L, Roscioli T, Rosenfeld JA, Sachdev R, Shaw-Smith CJ, Simons C, Sisodiya SM, Snell P, St Clair L, Stark Z, Stewart HS, Tan TY, Tan NB, Temple SEL, Thorburn DR, Tifft CJ, Uebergang E, VanNoy GE, Vasudevan P, Vilain E, Viskochil DH, Wedd L, Wheeler MT, White SM, Wojcik M, Wolfe LA, Wolfenson Z, Wright CF, Xiao C, Zocche … See abstract for full author list ➔ Chen Y, et al. Among authors: white sm. Nature. 2024 Aug;632(8026):832-840. doi: 10.1038/s41586-024-07773-7. Epub 2024 Jul 11. Nature. 2024. PMID: 38991538 Free PMC article.
Rabbit Dermatology.
White SD. White SD. Vet Clin North Am Exot Anim Pract. 2023 May;26(2):347-357. doi: 10.1016/j.cvex.2022.12.002. Vet Clin North Am Exot Anim Pract. 2023. PMID: 36965875 Review.
Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder.
Cuinat S, Nizon M, Isidor B, Stegmann A, van Jaarsveld RH, van Gassen KL, van der Smagt JJ, Volker-Touw CML, Holwerda SJB, Terhal PA, Schuhmann S, Vasileiou G, Khalifa M, Nugud AA, Yasaei H, Ousager LB, Brasch-Andersen C, Deb W, Besnard T, Simon MEH, Amsterdam KH, Verbeek NE, Matalon D, Dykzeul N, White S, Spiteri E, Devriendt K, Boogaerts A, Willemsen M, Brunner HG, Sinnema M, De Vries BBA, Gerkes EH, Pfundt R, Izumi K, Krantz ID, Xu ZL, Murrell JR, Valenzuela I, Cusco I, Rovira-Moreno E, Yang Y, Bizaoui V, Patat O, Faivre L, Tran-Mau-Them F, Vitobello A, Denommé-Pichon AS, Philippe C, Bezieau S, Cogné B. Cuinat S, et al. Among authors: white s. Genet Med. 2022 Aug;24(8):1774-1780. doi: 10.1016/j.gim.2022.04.011. Epub 2022 May 14. Genet Med. 2022. PMID: 35567594 Free article.
Orthogeriatric Anaesthesia.
White SM. White SM. 2020 Aug 21. In: Falaschi P, Marsh D, editors. Orthogeriatrics: The Management of Older Patients with Fragility Fractures [Internet]. 2nd edition. Cham (CH): Springer; 2021. Chapter 8. 2020 Aug 21. In: Falaschi P, Marsh D, editors. Orthogeriatrics: The Management of Older Patients with Fragility Fractures [Internet]. 2nd edition. Cham (CH): Springer; 2021. Chapter 8. PMID: 33347233 Free Books & Documents. Review.
ANZJOG in 2025.
White SW. White SW. Aust N Z J Obstet Gynaecol. 2025 Feb;65(1):3-5. doi: 10.1111/ajo.70017. Epub 2025 Mar 14. Aust N Z J Obstet Gynaecol. 2025. PMID: 40084626 No abstract available.
Research Needs.
Devinsky O, Palusci VJ, Shapiro-Mendoza CK, Ackerman MJ, Crandall LG, White SM, Burns KM. Devinsky O, et al. Among authors: white sm. In: The National Association of Medical Examiners’ Panel on Sudden Unexpected Death in Pediatrics; Bundock EA, Corey TS, Andrew TA, Crandall LG, Eason EA, Gunther WM, Moon RY, Palusci VJ, Schmidt CM, Sens MA, editors. Unexplained Pediatric Deaths: Investigation, Certification, and Family Needs [Internet]. San Diego (CA): Academic Forensic Pathology International; 2019. Chapter 15. In: The National Association of Medical Examiners’ Panel on Sudden Unexpected Death in Pediatrics; Bundock EA, Corey TS, Andrew TA, Crandall LG, Eason EA, Gunther WM, Moon RY, Palusci VJ, Schmidt CM, Sens MA, editors. Unexplained Pediatric Deaths: Investigation, Certification, and Family Needs [Internet]. San Diego (CA): Academic Forensic Pathology International; 2019. Chapter 15. PMID: 35107923 Free Books & Documents. Review. No abstract available.
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.
Chen Y, Dawes R, Kim HC, Stenton SL, Walker S, Ljungdahl A, Lord J, Ganesh VS, Ma J, Martin-Geary AC, Lemire G, D'Souza EN, Dong S, Ellingford JM, Adams DR, Allan K, Bakshi M, Baldwin EE, Berger SI, Bernstein JA, Brown NJ, Burrage LC, Chapman K, Compton AG, Cunningham CA, D'Souza P, Délot EC, Dias KR, Elias ER, Evans CA, Ewans L, Ezell K, Fraser JL, Gallacher L, Genetti CA, Grant CL, Haack T, Kuechler A, Lalani SR, Leitão E, Fevre AL, Leventer RJ, Liebelt JE, Lockhart PJ, Ma AS, Macnamara EF, Maurer TM, Mendez HR, Montgomery SB, Nassogne MC, Neumann S, O'Leary M, Palmer EE, Phillips J, Pitsava G, Pysar R, Rehm HL, Reuter CM, Revencu N, Riess A, Rius R, Rodan L, Roscioli T, Rosenfeld JA, Sachdev R, Simons C, Sisodiya SM, Snell P, Clair L, Stark Z, Tan TY, Tan NB, Temple SE, Thorburn DR, Tifft CJ, Uebergang E, VanNoy GE, Vilain E, Viskochil DH, Wedd L, Wheeler MT, White SM, Wojcik M, Wolfe LA, Wolfenson Z, Xiao C, Zocche D, Rubenstein JL, Markenscoff-Papadimitriou E, Fica SM, Baralle D, Depienne C, MacArthur DG, Howson JM, Sanders SJ, O'Donnell-Luria A, Whiffin N. Chen Y, et al. Among authors: white sm. medRxiv [Preprint]. 2024 Apr 9:2024.04.07.24305438. doi: 10.1101/2024.04.07.24305438. medRxiv. 2024. Update in: Nature. 2024 Aug;632(8026):832-840. doi: 10.1038/s41586-024-07773-7. PMID: 38645094 Free PMC article. Updated. Preprint.
6,339 results