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

Year Number of Results
1953 1
1954 2
1955 1
1957 2
1960 5
1961 5
1962 3
1963 2
1965 1
1966 2
1967 4
1968 4
1970 5
1971 4
1972 10
1973 7
1975 3
1976 1
1977 1
1978 4
1979 5
1980 2
1981 3
1982 4
1983 2
1984 5
1985 4
1986 4
1987 10
1988 9
1989 8
1990 13
1991 3
1992 9
1993 7
1994 5
1995 8
1996 6
1997 16
1998 13
1999 14
2000 16
2001 14
2002 14
2003 28
2004 22
2005 29
2006 32
2007 23
2008 30
2009 47
2010 43
2011 47
2012 46
2013 41
2014 76
2015 52
2016 64
2017 123
2018 128
2019 182
2020 184
2021 208
2022 179
2023 216
2024 65

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1,984 results

Results by year

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Page 1
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Kaur M, Blair J, Devkota B, Fortunato S, Clark D, Lawrence A, Kim J, Do W, Semeo B, Katz O, Mehta D, Yamamoto N, Schindler E, Al Rawi Z, Wallace N, Wilde JJ, McCallum J, Liu J, Xu D, Jackson M, Rentas S, Tayoun AA, Zhe Z, Abdul-Rahman O, Allen B, Angula MA, Anyane-Yeboa K, Argente J, Arn PH, Armstrong L, Basel-Salmon L, Baynam G, Bird LM, Bruegger D, Ch'ng GS, Chitayat D, Clark R, Cox GF, Dave U, DeBaere E, Field M, Graham JM Jr, Gripp KW, Greenstein R, Gupta N, Heidenreich R, Hoffman J, Hopkin RJ, Jones KL, Jones MC, Kariminejad A, Kogan J, Lace B, Leroy J, Lynch SA, McDonald M, Meagher K, Mendelsohn N, Micule I, Moeschler J, Nampoothiri S, Ohashi K, Powell CM, Ramanathan S, Raskin S, Roeder E, Rio M, Rope AF, Sangha K, Scheuerle AE, Schneider A, Shalev S, Siu V, Smith R, Stevens C, Tkemaladze T, Toimie J, Toriello H, Turner A, Wheeler PG, White SM, Young T, Loomes KM, Pipan M, Harrington AT, Zackai E, Rajagopalan R, Conlin L, Deardorff MA, McEldrew D, Pie J, Ramos F, Musio A, Kline AD, Izumi K, Raible SE, Krantz ID. Kaur M, et al. Among authors: ramos f. Am J Med Genet A. 2023 Aug;191(8):2113-2131. doi: 10.1002/ajmg.a.63247. Epub 2023 Jun 28. Am J Med Genet A. 2023. PMID: 37377026
The role of endocrine disruptors in female infertility.
Silva ABP, Carreiró F, Ramos F, Sanches-Silva A. Silva ABP, et al. Among authors: ramos f. Mol Biol Rep. 2023 Aug;50(8):7069-7088. doi: 10.1007/s11033-023-08583-2. Epub 2023 Jul 4. Mol Biol Rep. 2023. PMID: 37402067 Free PMC article. Review.
The authors reply.
Santos SMCD, Ramos FP, Medeiros MAT, Mata MMD, Vasconcelos FAG. Santos SMCD, et al. Among authors: ramos fp. Cad Saude Publica. 2021 Oct 29;37Suppl 1(Suppl 1):e00176521. doi: 10.1590/0102-311X00176521. eCollection 2021. Cad Saude Publica. 2021. PMID: 34730733 Free article. English, Portuguese. No abstract available.
Thermochemical Study of 1-Methylhydantoin.
Ledo JM, Flores H, Ramos F, Camarillo EA. Ledo JM, et al. Among authors: ramos f. Molecules. 2022 Jan 16;27(2):556. doi: 10.3390/molecules27020556. Molecules. 2022. PMID: 35056871 Free PMC article.
Robot Learning From Randomized Simulations: A Review.
Muratore F, Ramos F, Turk G, Yu W, Gienger M, Peters J. Muratore F, et al. Among authors: ramos f. Front Robot AI. 2022 Apr 11;9:799893. doi: 10.3389/frobt.2022.799893. eCollection 2022. Front Robot AI. 2022. PMID: 35494543 Free PMC article. Review.
Analytical methods for amatoxins: A comprehensive review.
Barbosa I, Domingues C, Ramos F, Barbosa RM. Barbosa I, et al. Among authors: ramos f. J Pharm Biomed Anal. 2023 Aug 5;232:115421. doi: 10.1016/j.jpba.2023.115421. Epub 2023 Apr 28. J Pharm Biomed Anal. 2023. PMID: 37146495 Free article. Review.
Transcriptional and genomic characterization of measurable residual disease in acute myeloid leukaemia.
Simoes C, Villar S, Ariceta B, Garcés JJ, Burgos L, Alignani D, Sarvide S, Martínez-Cuadrón D, Bergua JM, Vives S, Algarra L, Tormo M, Martinez P, Serrano J, Herrera P, Ramos F, Salamero O, Lavilla E, Gil C, Lopez-Lorenzo JL, Vidriales MB, Chillon C, Labrador J, Falantes JF, Sayas MJ, Ayala R, Martinez-Lopez J, Pierola AA, Calasanz MJ, Prosper F, San-Miguel JF, Sanz MÁ, Paiva B, Montesinos P; PETHEMA cooperative study group. Simoes C, et al. Among authors: ramos f. Br J Haematol. 2023 Jun;201(6):1239-1244. doi: 10.1111/bjh.18815. Epub 2023 Apr 14. Br J Haematol. 2023. PMID: 37057357 No abstract available.
Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and Literature Review.
Pascual P, Tenorio-Castano J, Mignot C, Afenjar A, Arias P, Gallego-Zazo N, Parra A, Miranda L, Cazalla M, Silván C, Heron D, Keren B, Popa I, Palomares M, Rikeros E, Ramos FJ, Almoguera B, Ayuso C, Swafiri ST, Barbero AIS, Srinivasan VM, Gowda VK, Morleo M, Nigro V, D'Arrigo S, Ciaccio C, Martin Mesa C, Paumard B, Guillen G, Anton ATS, Jimenez MD, Seidel V, Suárez J, Cormier-Daire V, Consortium TS, Nevado J, Lapunzina P. Pascual P, et al. Among authors: ramos fj. Genes (Basel). 2023 Aug 23;14(9):1664. doi: 10.3390/genes14091664. Genes (Basel). 2023. PMID: 37761804 Free PMC article. Review.
Molecular Basis of the Schuurs-Hoeijmakers Syndrome: What We Know about the Gene and the PACS-1 Protein and Novel Therapeutic Approaches.
Arnedo M, Ascaso Á, Latorre-Pellicer A, Lucia-Campos C, Gil-Salvador M, Ayerza-Casas A, Pablo MJ, Gómez-Puertas P, Ramos FJ, Bueno-Lozano G, Pié J, Puisac B. Arnedo M, et al. Among authors: ramos fj. Int J Mol Sci. 2022 Aug 25;23(17):9649. doi: 10.3390/ijms23179649. Int J Mol Sci. 2022. PMID: 36077045 Free PMC article. Review.
1,984 results