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

Year Number of Results
2006 1
2007 1
2008 7
2009 1
2010 1
2011 3
2012 3
2013 3
2014 5
2015 8
2016 4
2017 6
2018 3
2019 2
2020 2
2021 2
2022 3
2024 2

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46 results

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Page 1
A global reference for human genetic variation.
1000 Genomes Project Consortium; Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR. 1000 Genomes Project Consortium, et al. Nature. 2015 Oct 1;526(7571):68-74. doi: 10.1038/nature15393. Nature. 2015. PMID: 26432245 Free PMC article.
Tertiary lymphoid structures and B cells determine clinically relevant T cell phenotypes in ovarian cancer.
Kasikova L, Rakova J, Hensler M, Lanickova T, Tomankova J, Pasulka J, Drozenova J, Mojzisova K, Fialova A, Vosahlikova S, Laco J, Ryska A, Dundr P, Kocian R, Brtnicky T, Skapa P, Capkova L, Kovar M, Prochazka J, Praznovec I, Koblizek V, Taskova A, Tanaka H, Lischke R, Mendez FC, Vachtenheim J Jr, Heinzelmann-Schwarz V, Jacob F, McNeish IA, Halaska MJ, Rob L, Cibula D, Orsulic S, Galluzzi L, Spisek R, Fucikova J. Kasikova L, et al. Among authors: mendez fc. Nat Commun. 2024 Mar 21;15(1):2528. doi: 10.1038/s41467-024-46873-w. Nat Commun. 2024. PMID: 38514660 Free PMC article.
Blind testing of shoreline evolution models.
Montaño J, Coco G, Antolínez JAA, Beuzen T, Bryan KR, Cagigal L, Castelle B, Davidson MA, Goldstein EB, Ibaceta R, Idier D, Ludka BC, Masoud-Ansari S, Méndez FJ, Murray AB, Plant NG, Ratliff KM, Robinet A, Rueda A, Sénéchal N, Simmons JA, Splinter KD, Stephens S, Townend I, Vitousek S, Vos K. Montaño J, et al. Among authors: mendez fj. Sci Rep. 2020 Feb 7;10(1):2137. doi: 10.1038/s41598-020-59018-y. Sci Rep. 2020. PMID: 32034246 Free PMC article.
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.
Poznik GD, Xue Y, Mendez FL, Willems TF, Massaia A, Wilson Sayres MA, Ayub Q, McCarthy SA, Narechania A, Kashin S, Chen Y, Banerjee R, Rodriguez-Flores JL, Cerezo M, Shao H, Gymrek M, Malhotra A, Louzada S, Desalle R, Ritchie GR, Cerveira E, Fitzgerald TW, Garrison E, Marcketta A, Mittelman D, Romanovitch M, Zhang C, Zheng-Bradley X, Abecasis GR, McCarroll SA, Flicek P, Underhill PA, Coin L, Zerbino DR, Yang F, Lee C, Clarke L, Auton A, Erlich Y, Handsaker RE; 1000 Genomes Project Consortium; Bustamante CD, Tyler-Smith C. Poznik GD, et al. Among authors: mendez fl. Nat Genet. 2016 Jun;48(6):593-9. doi: 10.1038/ng.3559. Epub 2016 Apr 25. Nat Genet. 2016. PMID: 27111036 Free PMC article. Review.
Scalable detection of technically challenging variants through modified next-generation sequencing.
Rojahn S, Hambuch T, Adrian J, Gafni E, Gileta A, Hatchell H, Johnson B, Kallman B, Karfilis K, Kautzer C, Kennemer M, Kirk L, Kvitek D, Lettes J, Macrae F, Mendez F, Paul J, Pellegrino M, Preciado R, Risinger J, Schultz M, Spurka L, Swamy S, Truty R, Usem N, Velenich A, Aradhya S. Rojahn S, et al. Among authors: mendez f. Mol Genet Genomic Med. 2022 Dec;10(12):e2072. doi: 10.1002/mgg3.2072. Epub 2022 Oct 17. Mol Genet Genomic Med. 2022. PMID: 36251442 Free PMC article.
Genetic evidence for archaic admixture in Africa.
Hammer MF, Woerner AE, Mendez FL, Watkins JC, Wall JD. Hammer MF, et al. Among authors: mendez fl. Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15123-8. doi: 10.1073/pnas.1109300108. Epub 2011 Sep 6. Proc Natl Acad Sci U S A. 2011. PMID: 21896735 Free PMC article.
Ultra-sensitive molecular residual disease detection through whole genome sequencing with single-read error correction.
Li X, Liu T, Bacchiocchi A, Li M, Cheng W, Wittkop T, Mendez F, Wang Y, Tang P, Yao Q, Bosenberg MW, Sznol M, Yan Q, Faham M, Weng L, Halaban R, Jin H, Hu Z. Li X, et al. Among authors: mendez f. medRxiv [Preprint]. 2024 Jan 22:2024.01.13.24301070. doi: 10.1101/2024.01.13.24301070. medRxiv. 2024. PMID: 38260271 Free PMC article. Preprint.
46 results