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

Year Number of Results
1873 1
1877 1
1879 1
1899 1
1935 2
1936 1
1939 1
1943 1
1945 1
1946 3
1947 3
1948 2
1949 10
1950 6
1951 4
1952 10
1953 5
1954 6
1955 11
1956 8
1957 7
1958 4
1959 8
1960 10
1961 11
1962 19
1963 13
1964 15
1965 15
1966 11
1967 19
1968 13
1969 15
1970 18
1971 24
1972 21
1973 20
1974 19
1975 33
1976 50
1977 28
1978 28
1979 37
1980 34
1981 44
1982 41
1983 36
1984 56
1985 53
1986 62
1987 61
1988 51
1989 56
1990 63
1991 61
1992 67
1993 76
1994 52
1995 76
1996 88
1997 77
1998 86
1999 87
2000 105
2001 89
2002 105
2003 142
2004 143
2005 138
2006 163
2007 166
2008 195
2009 194
2010 251
2011 270
2012 275
2013 261
2014 294
2015 306
2016 299
2017 293
2018 278
2019 285
2020 316
2021 343
2022 333
2023 300
2024 286
2025 2

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6,936 results

Results by year

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Page 1
Genomic diagnosis for children with intellectual disability and/or developmental delay.
Bowling KM, Thompson ML, Amaral MD, Finnila CR, Hiatt SM, Engel KL, Cochran JN, Brothers KB, East KM, Gray DE, Kelley WV, Lamb NE, Lose EJ, Rich CA, Simmons S, Whittle JS, Weaver BT, Nesmith AS, Myers RM, Barsh GS, Bebin EM, Cooper GM. Bowling KM, et al. Among authors: thompson ml. Genome Med. 2017 May 30;9(1):43. doi: 10.1186/s13073-017-0433-1. Genome Med. 2017. PMID: 28554332 Free PMC article.
Issues in Nutrition: Carbohydrates.
Thompson ME, Noel MB. Thompson ME, et al. FP Essent. 2017 Jan;452:26-30. FP Essent. 2017. PMID: 28092151 Review.
Pirtobrutinib monotherapy in Bruton tyrosine kinase inhibitor-intolerant patients with B-cell malignancies: results of the phase I/II BRUIN trial.
Shah NN, Wang M, Roeker LE, Patel K, Woyach JA, Wierda WG, Ujjani CS, Eyre TA, Zinzani PL, Alencar AJ, Ghia P, Lamanna N, Hoffmann MS, Patel MR, Flinn I, Gerson JN, Ma S, Coombs CC, Cheah CY, Lech-Maranda E, Fakhri B, Kim WS, Barve MA, Cohen JB, Jurczak W, Munir T, Thompson MC, Tsai DE, Bao K, Cangemi NA, Kherani JF, Walgren RA, Han H, Ruppert AS, Brown JR. Shah NN, et al. Among authors: thompson mc. Haematologica. 2024 Oct 3. doi: 10.3324/haematol.2024.285754. Online ahead of print. Haematologica. 2024. PMID: 39363864 Free article.
ARF1-related disorder: phenotypic and molecular spectrum.
de Sainte Agathe JM, Pode-Shakked B, Naudion S, Michaud V, Arveiler B, Fergelot P, Delmas J, Keren B, Poirsier C, Alkuraya FS, Tabarki B, Bend E, Davis K, Bebin M, Thompson ML, Bryant EM, Wagner M, Hannibal I, Lenberg J, Krenn M, Wigby KM, Friedman JR, Iascone M, Cereda A, Miao T, LeGuern E, Argilli E, Sherr E, Caluseriu O, Tidwell T, Bayrak-Toydemir P, Hagedorn C, Brugger M, Vill K, Morneau-Jacob FD, Chung W, Weaver KN, Owens JW, Husami A, Chaudhari BP, Stone BS, Burns K, Li R, de Lange IM, Biehler M, Ginglinger E, Gérard B, Stottmann RW, Trimouille A. de Sainte Agathe JM, et al. Among authors: thompson ml. J Med Genet. 2023 Oct;60(10):999-1005. doi: 10.1136/jmg-2022-108803. Epub 2023 Apr 25. J Med Genet. 2023. PMID: 37185208 Free PMC article.
Author Correction: Universal DNA methylation age across mammalian tissues.
Lu AT, Fei Z, Haghani A, Robeck TR, Zoller JA, Li CZ, Lowe R, Yan Q, Zhang J, Vu H, Ablaeva J, Acosta-Rodriguez VA, Adams DM, Almunia J, Aloysius A, Ardehali R, Arneson A, Baker CS, Banks G, Belov K, Bennett NC, Black P, Blumstein DT, Bors EK, Breeze CE, Brooke RT, Brown JL, Carter GG, Caulton A, Cavin JM, Chakrabarti L, Chatzistamou I, Chen H, Cheng K, Chiavellini P, Choi OW, Clarke SM, Cooper LN, Cossette ML, Day J, DeYoung J, DiRocco S, Dold C, Ehmke EE, Emmons CK, Emmrich S, Erbay E, Erlacher-Reid C, Faulkes CG, Ferguson SH, Finno CJ, Flower JE, Gaillard JM, Garde E, Gerber L, Gladyshev VN, Gorbunova V, Goya RG, Grant MJ, Green CB, Hales EN, Hanson MB, Hart DW, Haulena M, Herrick K, Hogan AN, Hogg CJ, Hore TA, Huang T, Izpisua Belmonte JC, Jasinska AJ, Jones G, Jourdain E, Kashpur O, Katcher H, Katsumata E, Kaza V, Kiaris H, Kobor MS, Kordowitzki P, Koski WR, Krützen M, Kwon SB, Larison B, Lee SG, Lehmann M, Lemaitre JF, Levine AJ, Li C, Li X, Lim AR, Lin DTS, Lindemann DM, Little TJ, Macoretta N, Maddox D, Matkin CO, Mattison JA, McClure M, Mergl J, Meudt JJ, Montano GA, Mozhui K, Munshi-South J, Naderi A, Nagy M, Narayan P, Nathanielsz PW, Nguyen NB, Niehrs C, O'Brien JK, O'… See abstract for full author list ➔ Lu AT, et al. Among authors: thompson mj. Nat Aging. 2023 Nov;3(11):1462. doi: 10.1038/s43587-023-00499-7. Nat Aging. 2023. PMID: 37674040 Free PMC article. No abstract available.
Supergenes and their role in evolution.
Thompson MJ, Jiggins CD. Thompson MJ, et al. Heredity (Edinb). 2014 Jul;113(1):1-8. doi: 10.1038/hdy.2014.20. Epub 2014 Mar 19. Heredity (Edinb). 2014. PMID: 24642887 Free PMC article. Review.
Mitochondria in lung diseases.
Aravamudan B, Thompson MA, Pabelick CM, Prakash YS. Aravamudan B, et al. Among authors: thompson ma. Expert Rev Respir Med. 2013 Dec;7(6):631-46. doi: 10.1586/17476348.2013.834252. Epub 2013 Aug 27. Expert Rev Respir Med. 2013. PMID: 23978003 Free PMC article. Review.
Man with forehead swelling.
Williams Chen MC, Passons SM, Gullett JP, Thompson MA, Pigott DC, Burleson SL. Williams Chen MC, et al. Among authors: thompson ma. J Am Coll Emerg Physicians Open. 2024 Sep 10;5(5):e13256. doi: 10.1002/emp2.13256. eCollection 2024 Oct. J Am Coll Emerg Physicians Open. 2024. PMID: 39257838 Free PMC article. No abstract available.
6,936 results