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

Year Number of Results
1923 1
1924 1
1948 2
1949 2
1950 2
1951 1
1952 2
1955 1
1956 1
1962 2
1968 2
1971 2
1972 2
1979 1
1980 1
1981 1
1982 2
1983 1
1984 9
1985 1
1986 4
1987 3
1988 2
1989 2
1990 5
1991 7
1992 11
1993 13
1994 10
1995 9
1996 14
1997 16
1998 3
1999 11
2000 10
2001 11
2002 11
2003 10
2004 7
2005 14
2006 14
2007 14
2008 17
2009 16
2010 21
2011 21
2012 24
2013 25
2014 26
2015 25
2016 14
2017 18
2018 20
2019 25
2020 19
2021 23
2022 22
2023 15
2024 27
2025 3

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534 results

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Page 1
Cytogenetic Nomenclature and Reporting.
Stevens-Kroef M, Simons A, Rack K, Hastings RJ. Stevens-Kroef M, et al. Among authors: simons a. Methods Mol Biol. 2017;1541:303-309. doi: 10.1007/978-1-4939-6703-2_24. Methods Mol Biol. 2017. PMID: 27910032 Review.
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS.
van der Made CI, Potjewijd J, Hoogstins A, Willems HPJ, Kwakernaak AJ, de Sevaux RGL, van Daele PLA, Simons A, Heijstek M, Beck DB, Netea MG, van Paassen P, Elizabeth Hak A, van der Veken LT, van Gijn ME, Hoischen A, van de Veerdonk FL, Leavis HL, Rutgers A. van der Made CI, et al. Among authors: simons a. J Allergy Clin Immunol. 2022 Jan;149(1):432-439.e4. doi: 10.1016/j.jaci.2021.05.014. Epub 2021 May 25. J Allergy Clin Immunol. 2022. PMID: 34048852
Causes of maladaptation.
Brady SP, Bolnick DI, Angert AL, Gonzalez A, Barrett RDH, Crispo E, Derry AM, Eckert CG, Fraser DJ, Fussmann GF, Guichard F, Lamy T, McAdam AG, Newman AEM, Paccard A, Rolshausen G, Simons AM, Hendry AP. Brady SP, et al. Among authors: simons am. Evol Appl. 2019 Aug 13;12(7):1229-1242. doi: 10.1111/eva.12844. eCollection 2019 Aug. Evol Appl. 2019. PMID: 31417611 Free PMC article. Review.
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition.
Zerella JR, Homan CC, Arts P, Lin X, Spinelli SJ, Venugopal P, Babic M, Brautigan PJ, Truong L, Arriola-Martinez L, Moore S, Hollins R, Parker WT, Nguyen H, Kassahn KS, Branford S, Feurstein S, Larcher L, Sicre de Fontbrune F, Demirdas S, de Munnik S, Antoine-Poirel H, Brichard B, Mansour S, Gordon K, Wlodarski MW, Koppayi A, Dobbins S, Mutsaers PGNJ, Nichols KE, Oak N, DeMille D, Mao R, Crawford A, McCarrier J, Basel D, Flores-Daboub J, Drazer MW, Phillips K, Poplawski NK, Birdsey GM, Pirri D, Ostergaard P, Simons A, Godley LA, Ross DM, Hiwase DK, Soulier J, Brown AL, Carmichael CL, Scott HS, Hahn CN. Zerella JR, et al. Among authors: simons a. Blood. 2024 Oct 24;144(17):1765-1780. doi: 10.1182/blood.2024024607. Blood. 2024. PMID: 38991192 Free PMC article.
Unraveling facets of MECOM-associated syndrome: somatic genetic rescue, clonal hematopoiesis, and phenotype expansion.
Venugopal P, Arts P, Fox LC, Simons A, Hiwase DK, Bardy PG, Swift A, Ross DM, van Vulpen LFD, Buijs A, Bolton KL, Getta B, Furlong E, Carter T, Krapels I, Hoeks M, Al Kindy A, Al Kindy F, de Munnik S, Evans P, Frank MSB, Bournazos AM, Cooper ST, Ha TT, Jackson MR, Arriola-Martinez L, Phillips K, Brennan Y, Bakshi M, Ambler K, Gao S, Kassahn KS, Kenyon R, Hung K, Babic M, McGovern A, Rawlings L, Vakulin C, Dejong L, Fathi R, McRae S, Myles N, Ladon D, Jongmans M, Kuiper RP, Poplawski NK, Barbaro P, Blombery P, Brown AL, Hahn CN, Scott HS. Venugopal P, et al. Among authors: simons a. Blood Adv. 2024 Jul 9;8(13):3437-3443. doi: 10.1182/bloodadvances.2023012331. Blood Adv. 2024. PMID: 38662475 Free PMC article. No abstract available.
Management of Childhood Glaucoma Following Cataract Surgery.
Simons AS, Casteels I, Grigg J, Stalmans I, Vandewalle E, Lemmens S. Simons AS, et al. J Clin Med. 2022 Feb 17;11(4):1041. doi: 10.3390/jcm11041041. J Clin Med. 2022. PMID: 35207320 Free PMC article. Review.
The evolutionary maintenance of Lévy flight foraging.
Campeau W, Simons AM, Stevens B. Campeau W, et al. Among authors: simons am. PLoS Comput Biol. 2022 Jan 18;18(1):e1009490. doi: 10.1371/journal.pcbi.1009490. eCollection 2022 Jan. PLoS Comput Biol. 2022. PMID: 35041659 Free PMC article.
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndrome.
van der Made CI, Kersten S, Chorin O, Engelhardt KR, Ramakrishnan G, Griffin H, Schim van der Loeff I, Venselaar H, Rothschild AR, Segev M, Schuurs-Hoeijmakers JHM, Mantere T, Essers R, Esteki MZ, Avital AL, Loo PS, Simons A, Pfundt R, Warris A, Seyger MM, van de Veerdonk FL, Netea MG, Slatter MA, Flood T, Gennery AR, Simon AJ, Lev A, Frizinsky S, Barel O, van der Burg M, Somech R, Hambleton S, Henriet SSV, Hoischen A. van der Made CI, et al. Among authors: simons a. Am J Hum Genet. 2024 Apr 4;111(4):791-804. doi: 10.1016/j.ajhg.2024.02.013. Epub 2024 Mar 18. Am J Hum Genet. 2024. PMID: 38503300 Free PMC article.
534 results