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Results by year

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

Year Number of Results
1832 1
1884 1
1885 2
1886 3
1897 1
1898 1
1900 1
1908 1
1921 1
1922 1
1923 1
1931 1
1937 3
1938 4
1939 4
1943 1
1945 1
1946 14
1947 12
1948 5
1949 4
1950 7
1951 11
1952 14
1953 14
1954 11
1955 18
1956 9
1957 16
1958 10
1959 16
1960 17
1961 9
1962 15
1963 14
1964 15
1965 8
1966 14
1967 20
1968 24
1969 18
1970 21
1971 26
1972 26
1973 29
1974 22
1975 32
1976 20
1977 33
1978 28
1979 35
1980 36
1981 33
1982 42
1983 40
1984 51
1985 45
1986 40
1987 33
1988 54
1989 56
1990 41
1991 40
1992 48
1993 43
1994 43
1995 46
1996 46
1997 55
1998 60
1999 46
2000 66
2001 61
2002 52
2003 57
2004 53
2005 61
2006 70
2007 73
2008 60
2009 71
2010 92
2011 115
2012 94
2013 103
2014 96
2015 133
2016 96
2017 98
2018 115
2019 120
2020 130
2021 136
2022 134
2023 135
2024 127
2025 13

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Search Results

3,617 results

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Page 1
Digenic Alport Syndrome.
Savige J, Renieri A, Ars E, Daga S, Pinto AM, Rothe H, Gale DP, Aksenova M, Cerkauskaite A, Bielska O, Lipska-Zietkiewicz B, Gibson JT. Savige J, et al. Among authors: gibson jt. Clin J Am Soc Nephrol. 2022 Nov;17(11):1697-1706. doi: 10.2215/CJN.03120322. Epub 2022 Jun 8. Clin J Am Soc Nephrol. 2022. PMID: 35675912 Free PMC article. Review.
Aspiration Pneumonia.
Sanivarapu RR, Vaqar S, Gibson J. Sanivarapu RR, et al. Among authors: gibson j. 2024 Mar 20. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2024 Mar 20. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 29261921 Free Books & Documents.
Editorial.
Shahane SA, Gibson J. Shahane SA, et al. Among authors: gibson j. Shoulder Elbow. 2014 Apr;6(2):71. doi: 10.1177/1758573214524936. Epub 2014 Apr 4. Shoulder Elbow. 2014. PMID: 27582916 Free PMC article. No abstract available.
Defining response to anti-VEGF therapies in neovascular AMD.
Amoaku WM, Chakravarthy U, Gale R, Gavin M, Ghanchi F, Gibson J, Harding S, Johnston RL, Kelly SP, Lotery A, Mahmood S, Menon G, Sivaprasad S, Talks J, Tufail A, Yang Y. Amoaku WM, et al. Among authors: gibson j. Eye (Lond). 2015 Jun;29(6):721-31. doi: 10.1038/eye.2015.48. Epub 2015 Apr 17. Eye (Lond). 2015. PMID: 25882328 Free PMC article. Review.
Prevalence Estimates of Predicted Pathogenic COL4A3-COL4A5 Variants in a Population Sequencing Database and Their Implications for Alport Syndrome.
Gibson J, Fieldhouse R, Chan MMY, Sadeghi-Alavijeh O, Burnett L, Izzi V, Persikov AV, Gale DP, Storey H, Savige J; Genomics England Research Consortium. Gibson J, et al. J Am Soc Nephrol. 2021 Sep;32(9):2273-2290. doi: 10.1681/ASN.2020071065. Epub 2021 Jun 18. J Am Soc Nephrol. 2021. PMID: 34400539 Free PMC article.
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.
Howard DM, Adams MJ, Shirali M, Clarke TK, Marioni RE, Davies G, Coleman JRI, Alloza C, Shen X, Barbu MC, Wigmore EM, Gibson J; 23andMe Research Team; Hagenaars SP, Lewis CM, Ward J, Smith DJ, Sullivan PF, Haley CS, Breen G, Deary IJ, McIntosh AM. Howard DM, et al. Among authors: gibson j. Nat Commun. 2018 Apr 16;9(1):1470. doi: 10.1038/s41467-018-03819-3. Nat Commun. 2018. PMID: 29662059 Free PMC article.
Aspiration Pneumonia (Nursing).
Sanivarapu RR, Vaqar S, Gibson J, Overmeyer KA. Sanivarapu RR, et al. Among authors: gibson j. 2024 Mar 20. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2024 Mar 20. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 33760529 Free Books & Documents.
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.
Miller MJ, Burrage LC, Gibson JB, Strenk ME, Lose EJ, Bick DP, Elsea SH, Sutton VR, Sun Q, Graham BH, Craigen WJ, Zhang VW, Wong LJ. Miller MJ, et al. Among authors: gibson jb. Mol Genet Metab. 2015 Nov;116(3):139-45. doi: 10.1016/j.ymgme.2015.08.011. Epub 2015 Sep 2. Mol Genet Metab. 2015. PMID: 26385305 Free PMC article.
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, McBride KL, Komara M, Al-Gazali L, Al Shamsi A, Fanning EA, Wierenga KJ, Scott DA, Ben-Neriah Z, Meiner V, Cassuto H, Elpeleg O, Holder JL Jr, Burrage LC, Seaver LH, Van Maldergem L, Mahida S, Soul JS, Marlatt M, Matyakhina L, Vogt J, Gold JA, Park SM, Varghese V, Lampe AK, Kumar A, Lees M, Holder-Espinasse M, McConnell V, Bernhard B, Blair E, Harrison V; DDD study; Muzny DM, Gibbs RA, Elsea SH, Posey JE, Bi W, Lalani S, Xia F, Yang Y, Eng CM, Lupski JR, Liu P. Vetrini F, et al. Among authors: gibson jb. Genome Med. 2019 Feb 28;11(1):12. doi: 10.1186/s13073-019-0623-0. Genome Med. 2019. PMID: 30819258 Free PMC article.
3,617 results