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

Year Number of Results
1891 1
1896 1
1897 2
1898 4
1899 3
1903 1
1918 1
1921 1
1922 1
1923 1
1924 2
1925 1
1926 1
1927 1
1944 1
1946 1
1948 2
1949 3
1950 1
1951 3
1952 4
1953 5
1954 2
1955 4
1956 6
1957 6
1958 3
1959 7
1960 7
1961 9
1962 7
1963 8
1964 5
1965 3
1966 6
1967 11
1968 15
1969 12
1970 9
1971 19
1972 9
1973 22
1974 16
1975 9
1976 16
1977 15
1978 16
1979 16
1980 25
1981 25
1982 24
1983 22
1984 20
1985 20
1986 31
1987 29
1988 21
1989 27
1990 44
1991 41
1992 52
1993 58
1994 37
1995 40
1996 37
1997 27
1998 48
1999 31
2000 48
2001 46
2002 38
2003 44
2004 58
2005 73
2006 63
2007 60
2008 74
2009 74
2010 89
2011 87
2012 89
2013 78
2014 89
2015 92
2016 101
2017 92
2018 107
2019 102
2020 129
2021 137
2022 141
2023 124
2024 127
2025 94

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2,951 results

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Page 1
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss.
Oza AM, DiStefano MT, Hemphill SE, Cushman BJ, Grant AR, Siegert RK, Shen J, Chapin A, Boczek NJ, Schimmenti LA, Murry JB, Hasadsri L, Nara K, Kenna M, Booth KT, Azaiez H, Griffith A, Avraham KB, Kremer H, Rehm HL, Amr SS, Abou Tayoun AN; ClinGen Hearing Loss Clinical Domain Working Group. Oza AM, et al. Among authors: grant ar. Hum Mutat. 2018 Nov;39(11):1593-1613. doi: 10.1002/humu.23630. Hum Mutat. 2018. PMID: 30311386 Free PMC article.
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel.
Shen J, Oza AM, Del Castillo I, Duzkale H, Matsunaga T, Pandya A, Kang HP, Mar-Heyming R, Guha S, Moyer K, Lo C, Kenna M, Alexander JJ, Zhang Y, Hirsch Y, Luo M, Cao Y, Wai Choy K, Cheng YF, Avraham KB, Hu X, Garrido G, Moreno-Pelayo MA, Greinwald J, Zhang K, Zeng Y, Brownstein Z, Basel-Salmon L, Davidov B, Frydman M, Weiden T, Nagan N, Willis A, Hemphill SE, Grant AR, Siegert RK, DiStefano MT, Amr SS, Rehm HL, Abou Tayoun AN; ClinGen Hearing Loss Working Group. Shen J, et al. Among authors: grant ar. Genet Med. 2019 Nov;21(11):2442-2452. doi: 10.1038/s41436-019-0535-9. Epub 2019 Jun 4. Genet Med. 2019. PMID: 31160754 Free PMC article.
A realist review of health passports for Autistic adults.
Ellis R, Williams K, Brown A, Healer E, Grant A. Ellis R, et al. Among authors: grant a. PLoS One. 2023 Sep 8;18(9):e0279214. doi: 10.1371/journal.pone.0279214. eCollection 2023. PLoS One. 2023. PMID: 37682898 Free PMC article. Review.
Leprosy as a genetic disease.
Alter A, Grant A, Abel L, Alcaïs A, Schurr E. Alter A, et al. Among authors: grant a. Mamm Genome. 2011 Feb;22(1-2):19-31. doi: 10.1007/s00335-010-9287-1. Epub 2010 Oct 9. Mamm Genome. 2011. PMID: 20936290 Review.
Mendelian randomization for nephrologists.
Dobrijevic E, van Zwieten A, Kiryluk K, Grant AJ, Wong G, Teixeira-Pinto A. Dobrijevic E, et al. Among authors: grant aj. Kidney Int. 2023 Dec;104(6):1113-1123. doi: 10.1016/j.kint.2023.09.016. Epub 2023 Sep 30. Kidney Int. 2023. PMID: 37783446 Review.
Cardiac ion channels.
Grant AO. Grant AO. Circ Arrhythm Electrophysiol. 2009 Apr;2(2):185-94. doi: 10.1161/CIRCEP.108.789081. Circ Arrhythm Electrophysiol. 2009. PMID: 19808464 Review. No abstract available.
2,951 results