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Results by year

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

Year Number of Results
1874 2
1876 2
1877 1
1878 1
1880 2
1881 1
1882 2
1883 1
1885 3
1887 2
1892 3
1893 1
1895 2
1898 5
1899 1
1903 1
1908 2
1910 1
1911 1
1912 2
1928 1
1929 1
1930 1
1933 1
1945 2
1946 9
1947 8
1948 8
1949 2
1950 7
1951 13
1952 4
1953 10
1954 5
1955 9
1956 9
1957 5
1958 5
1959 8
1960 6
1961 17
1962 7
1963 19
1964 11
1965 14
1966 13
1967 12
1968 20
1969 28
1970 35
1971 37
1972 34
1973 32
1974 49
1975 35
1976 46
1977 40
1978 29
1979 37
1980 38
1981 44
1982 17
1983 24
1984 21
1985 36
1986 39
1987 35
1988 31
1989 30
1990 28
1991 27
1992 30
1993 30
1994 38
1995 29
1996 35
1997 48
1998 34
1999 41
2000 53
2001 41
2002 34
2003 24
2004 34
2005 38
2006 39
2007 46
2008 39
2009 34
2010 45
2011 41
2012 36
2013 41
2014 40
2015 77
2016 62
2017 50
2018 45
2019 52
2020 73
2021 83
2022 65
2023 64
2024 26

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Article type

Publication date

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2,353 results

Results by year

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Page 1
Genome sequence analyses identify novel risk loci for multiple system atrophy.
Chia R, Ray A, Shah Z, Ding J, Ruffo P, Fujita M, Menon V, Saez-Atienzar S, Reho P, Kaivola K, Walton RL, Reynolds RH, Karra R, Sait S, Akcimen F, Diez-Fairen M, Alvarez I, Fanciulli A, Stefanova N, Seppi K, Duerr S, Leys F, Krismer F, Sidoroff V, Zimprich A, Pirker W, Rascol O, Foubert-Samier A, Meissner WG, Tison F, Pavy-Le Traon A, Pellecchia MT, Barone P, Russillo MC, Marín-Lahoz J, Kulisevsky J, Torres S, Mir P, Periñán MT, Proukakis C, Chelban V, Wu L, Goh YY, Parkkinen L, Hu MT, Kobylecki C, Saxon JA, Rollinson S, Garland E, Biaggioni I, Litvan I, Rubio I, Alcalay RN, Kwei KT, Lubbe SJ, Mao Q, Flanagan ME, Castellani RJ, Khurana V, Ndayisaba A, Calvo A, Mora G, Canosa A, Floris G, Bohannan RC, Moore A, Norcliffe-Kaufmann L, Palma JA, Kaufmann H, Kim C, Iba M, Masliah E, Dawson TM, Rosenthal LS, Pantelyat A, Albert MS, Pletnikova O, Troncoso JC, Infante J, Lage C, Sánchez-Juan P, Serrano GE, Beach TG, Pastor P, Morris HR, Albani D, Clarimon J, Wenning GK, Hardy JA, Ryten M, Topol E, Torkamani A, Chiò A, Bennett DA, De Jager PL, Low PA, Singer W, Cheshire WP, Wszolek ZK, Dickson DW, Traynor BJ, Gibbs JR, Dalgard CL, Ross OA, Houlden H, Scholz SW. Chia R, et al. Among authors: morris hr. Neuron. 2024 Apr 24:S0896-6273(24)00240-X. doi: 10.1016/j.neuron.2024.04.002. Online ahead of print. Neuron. 2024. PMID: 38701790
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study.
Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, Christopher EA, DeTure M, Seeley WW, Lee EB, Frosch MP, Molina-Porcel L, Gefen T, Redding-Ochoa J, Ghetti B, Robinson AC, Kobylecki C, Rowe JB, Beach TG, Teich AF, Keith JL, Bodi I, Halliday GM, Gearing M, Arzberger T, Morris CM, White CL 3rd, Mechawar N, Boluda S, MacKenzie IR, McLean C, Cykowski MD, Wang SJ, Graff C, Nagra RM, Kovacs GG, Giaccone G, Neumann M, Ang LC, Carvalho A, Morris HR, Rademakers R, Hardy JA, Dickson DW, Rohrer JD, Ross OA; Pick's disease International Consortium. Valentino RR, et al. Among authors: morris hr. Lancet Neurol. 2024 May;23(5):487-499. doi: 10.1016/S1474-4422(24)00083-8. Lancet Neurol. 2024. PMID: 38631765 Free article.
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.
Gustavsson EK, Follett J, Trinh J, Barodia SK, Real R, Liu Z, Grant-Peters M, Fox JD, Appel-Cresswell S, Stoessl AJ, Rajput A, Rajput AH, Auer R, Tilney R, Sturm M, Haack TB, Lesage S, Tesson C, Brice A, Vilariño-Güell C, Ryten M, Goldberg MS, West AB, Hu MT, Morris HR, Sharma M, Gan-Or Z, Samanci B, Lis P, Periñan MT, Amouri R, Ben Sassi S, Hentati F; Global Parkinson's Genetics Program (GP2); Tonelli F, Alessi DR, Farrer MJ. Gustavsson EK, et al. Among authors: morris hr. Lancet Neurol. 2024 Apr 10:S1474-4422(24)00121-2. doi: 10.1016/S1474-4422(24)00121-2. Online ahead of print. Lancet Neurol. 2024. PMID: 38614108 Free article.
High concordance between nonalcoholic fatty liver disease and metabolic dysfunction associated steatotic liver disease in the TARGET-NASH real world cohort.
Barritt AS 4th, Yu F, Mospan AR, Newsome P, Roden M, Morris HL, Loomba R, Neuschwander-Tetri BA; TARGET-NASH investigators. Barritt AS 4th, et al. Among authors: morris hl. Am J Gastroenterol. 2024 Apr 8. doi: 10.14309/ajg.0000000000002796. Online ahead of print. Am J Gastroenterol. 2024. PMID: 38587293
Characterizing Cancer Burden in the American Indian Population in North Carolina.
Spees LP, Jackson BE, Raveendran Y, Morris HN, Emerson MA, Baggett CD, Bell RA, Salas AI, Meernik C, Akinyemiju TF, Wheeler SB. Spees LP, et al. Among authors: morris hn. Cancer Epidemiol Biomarkers Prev. 2024 Apr 5. doi: 10.1158/1055-9965.EPI-24-0030. Online ahead of print. Cancer Epidemiol Biomarkers Prev. 2024. PMID: 38578081
Handling 'carbon footprint' in orthopaedics.
Shah S, Morris H, Thiagarajah S, Gordon A, Sharma S, Haslam P, Garcia J, Ali F. Shah S, et al. Among authors: morris h. Ann R Coll Surg Engl. 2024 Apr 2. doi: 10.1308/rcsann.2023.0052. Online ahead of print. Ann R Coll Surg Engl. 2024. PMID: 38563077 Free article.
Distinct spatiotemporal atrophy patterns in corticobasal syndrome are associated with different underlying pathologies.
Scotton WJ, Shand C, Todd EG, Bocchetta M, Cash DM, VandeVrede L, Heuer HW, Young AL, Oxtoby N, Alexander DC, Rowe JB, Morris HR; PROSPECT Consortium; Boxer AL; 4RTNI Consortium; Rohrer JD, Wijeratne PA. Scotton WJ, et al. Among authors: morris hr. medRxiv [Preprint]. 2024 Mar 18:2024.03.14.24304298. doi: 10.1101/2024.03.14.24304298. medRxiv. 2024. PMID: 38562801 Free PMC article. Preprint.
2,353 results