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

Year Number of Results
1947 1
1950 2
1951 1
1952 1
1953 1
1955 1
1963 3
1964 5
1970 1
1972 1
1974 1
1975 2
1976 1
1977 2
1979 1
1981 1
1982 3
1983 9
1984 9
1985 6
1986 5
1987 8
1988 11
1989 6
1990 11
1991 7
1992 4
1993 9
1994 9
1995 13
1996 8
1997 13
1998 12
1999 18
2000 9
2001 23
2002 22
2003 19
2004 20
2005 19
2006 20
2007 31
2008 35
2009 25
2010 17
2011 29
2012 33
2013 31
2014 19
2015 26
2016 22
2017 27
2018 38
2019 40
2020 50
2021 70
2022 61
2023 50
2024 50
2025 2

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875 results

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Page 1
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios.
Byrska-Bishop M, Evani US, Zhao X, Basile AO, Abel HJ, Regier AA, Corvelo A, Clarke WE, Musunuri R, Nagulapalli K, Fairley S, Runnels A, Winterkorn L, Lowy E; Human Genome Structural Variation Consortium; Paul Flicek, Germer S, Brand H, Hall IM, Talkowski ME, Narzisi G, Zody MC. Byrska-Bishop M, et al. Among authors: basile ao. Cell. 2022 Sep 1;185(18):3426-3440.e19. doi: 10.1016/j.cell.2022.08.004. Cell. 2022. PMID: 36055201 Free PMC article.
Pelvic Congestion Syndrome.
Basile A, Failla G, Gozzo C. Basile A, et al. Semin Ultrasound CT MR. 2021 Feb;42(1):3-12. doi: 10.1053/j.sult.2020.07.001. Epub 2020 Jul 9. Semin Ultrasound CT MR. 2021. PMID: 33541587 Review.
The Symptoms-Varices-Pathophysiology classification of pelvic venous disorders: A report of the American Vein & Lymphatic Society International Working Group on Pelvic Venous Disorders.
Meissner MH, Khilnani NM, Labropoulos N, Gasparis AP, Gibson K, Greiner M, Learman LA, Atashroo D, Lurie F, Passman MA, Basile A, Lazarshvilli Z, Lohr J, Kim MD, Nicolini PH, Pabon-Ramos WM, Rosenblatt M. Meissner MH, et al. Among authors: basile a. J Vasc Surg Venous Lymphat Disord. 2021 May;9(3):568-584. doi: 10.1016/j.jvsv.2020.12.084. Epub 2021 Jan 30. J Vasc Surg Venous Lymphat Disord. 2021. PMID: 33529720 Free article.
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation.
Gustafson JA, Gibson SB, Damaraju N, Zalusky MP, Hoekzema K, Twesigomwe D, Yang L, Snead AA, Richmond PA, De Coster W, Olson ND, Guarracino A, Li Q, Miller AL, Goffena J, Anderson Z, Storz SH, Ward SA, Sinha M, Gonzaga-Jauregui C, Clarke WE, Basile AO, Corvelo A, Reeves C, Helland A, Musunuri RL, Revsine M, Patterson KE, Paschal CR, Zakarian C, Goodwin S, Jensen TD, Robb E; 1000 Genomes ONT Sequencing Consortium; University of Washington Center for Rare Disease Research (UW-CRDR); Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; McCombie WR, Sedlazeck FJ, Zook JM, Montgomery SB, Garrison E, Kolmogorov M, Schatz MC, McLaughlin RN Jr, Dashnow H, Zody MC, Loose M, Jain M, Eichler EE, Miller DE. Gustafson JA, et al. Among authors: basile ao. medRxiv [Preprint]. 2024 Mar 7:2024.03.05.24303792. doi: 10.1101/2024.03.05.24303792. medRxiv. 2024. Update in: Genome Res. 2024 Nov 20;34(11):2061-2073. doi: 10.1101/gr.279273.124 PMID: 38496498 Free PMC article. Updated. Preprint.
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation.
Gustafson JA, Gibson SB, Damaraju N, Zalusky MPG, Hoekzema K, Twesigomwe D, Yang L, Snead AA, Richmond PA, De Coster W, Olson ND, Guarracino A, Li Q, Miller AL, Goffena J, Anderson ZB, Storz SHR, Ward SA, Sinha M, Gonzaga-Jauregui C, Clarke WE, Basile AO, Corvelo A, Reeves C, Helland A, Musunuri RL, Revsine M, Patterson KE, Paschal CR, Zakarian C, Goodwin S, Jensen TD, Robb E; 1000 Genomes ONT Sequencing Consortium; University of Washington Center for Rare Disease Research (UW-CRDR); Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; McCombie WR, Sedlazeck FJ, Zook JM, Montgomery SB, Garrison E, Kolmogorov M, Schatz MC, McLaughlin RN Jr, Dashnow H, Zody MC, Loose M, Jain M, Eichler EE, Miller DE. Gustafson JA, et al. Among authors: basile ao. Genome Res. 2024 Nov 20;34(11):2061-2073. doi: 10.1101/gr.279273.124. Genome Res. 2024. PMID: 39358015 Free PMC article.
Multi-omic analysis of Huntington's disease reveals a compensatory astrocyte state.
Paryani F, Kwon JS, Ng CW, Jakubiak K, Madden N, Ofori K, Tang A, Lu H, Xia S, Li J, Mahajan A, Davidson SM, Basile AO, McHugh C, Vonsattel JP, Hickman R, Zody MC, Housman DE, Goldman JE, Yoo AS, Menon V, Al-Dalahmah O. Paryani F, et al. Among authors: basile ao. Nat Commun. 2024 Aug 8;15(1):6742. doi: 10.1038/s41467-024-50626-0. Nat Commun. 2024. PMID: 39112488 Free PMC article.
Neuroimaging features of WOREE syndrome: a mini-review of the literature.
Battaglia L, Scorrano G, Spiaggia R, Basile A, Palmucci S, Foti PV, Spatola C, Iacomino M, Marinangeli F, Francia E, Comisi F, Corsello A, Salpietro V, Vittori A, David E. Battaglia L, et al. Among authors: basile a. Front Pediatr. 2023 Dec 15;11:1301166. doi: 10.3389/fped.2023.1301166. eCollection 2023. Front Pediatr. 2023. PMID: 38161429 Free PMC article. Review.
The snowflake sign.
Castiglione D, Tiralongo F, Farina R, David E, Basile A. Castiglione D, et al. Among authors: basile a. Abdom Radiol (NY). 2024 Nov 18. doi: 10.1007/s00261-024-04700-2. Online ahead of print. Abdom Radiol (NY). 2024. PMID: 39551839
The "claw" sign.
Castiglione D, Delfa G, Tiralongo F, Inì C, Basile A. Castiglione D, et al. Among authors: basile a. Abdom Radiol (NY). 2024 Jul;49(7):2554-2558. doi: 10.1007/s00261-024-04478-3. Epub 2024 Jul 11. Abdom Radiol (NY). 2024. PMID: 38990303 Review. No abstract available.
875 results