Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2002 1
2004 1
2007 11
2008 2
2009 4
2010 1
2011 1
2012 1
2013 1
2015 4
2016 2
2017 2
2019 1
2020 2
2021 4
2022 1
2023 4
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

42 results

Results by year

Filters applied: . Clear all
Page 1
Disease activity drives transcriptomic heterogeneity in early untreated rheumatoid synovitis.
Triaille C, Tilman G, Sokolova T, Loriot A, Marchandise J, De Montjoye S, Nzeusseu-Toukap A, Méric de Bellefon L, Bouzin C, Galant C, Durez P, Lauwerys BR, Limaye N. Triaille C, et al. Among authors: limaye n. Ann Rheum Dis. 2023 Dec;82(12):1538-1546. doi: 10.1136/ard-2023-224068. Epub 2023 Jul 28. Ann Rheum Dis. 2023. PMID: 37507201 Free PMC article.
Tumour-agnostic plasma assay for circulating tumour DNA predicts outcome in recurrent and/or metastatic squamous cell carcinoma of the head and neck treated with a PD-1 inhibitor.
Honoré N, van der Elst A, Dietz A, van Marcke C, Helaers R, Mendola A, Dahou H, Marbaix E, Poncin R, Seront E, Schmitz S, Limaye N, Galot R, Machiels JP. Honoré N, et al. Among authors: limaye n. Eur J Cancer. 2023 Dec;195:113372. doi: 10.1016/j.ejca.2023.113372. Epub 2023 Oct 9. Eur J Cancer. 2023. PMID: 37913682
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis.
Arts FA, Sciot R, Brichard B, Renard M, de Rocca Serra A, Dachy G, Noël LA, Velghe AI, Galant C, Debiec-Rychter M, Van Damme A, Vikkula M, Helaers R, Limaye N, Poirel HA, Demoulin JB. Arts FA, et al. Among authors: limaye n. Hum Mol Genet. 2017 May 15;26(10):1801-1810. doi: 10.1093/hmg/ddx081. Hum Mol Genet. 2017. PMID: 28334876
Somatic Activating PIK3CA Mutations Cause Venous Malformation.
Limaye N, Kangas J, Mendola A, Godfraind C, Schlögel MJ, Helaers R, Eklund L, Boon LM, Vikkula M. Limaye N, et al. Am J Hum Genet. 2015 Dec 3;97(6):914-21. doi: 10.1016/j.ajhg.2015.11.011. Am J Hum Genet. 2015. PMID: 26637981 Free PMC article.
Susceptibility genes in the pathogenesis of murine lupus.
Nguyen C, Limaye N, Wakeland EK. Nguyen C, et al. Among authors: limaye n. Arthritis Res. 2002;4 Suppl 3(Suppl 3):S255-63. doi: 10.1186/ar583. Epub 2002 May 9. Arthritis Res. 2002. PMID: 12110145 Free PMC article. Review.
Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis.
Dachy G, de Krijger RR, Fraitag S, Théate I, Brichard B, Hoffman SB, Libbrecht L, Arts FA, Brouillard P, Vikkula M, Limaye N, Demoulin JB. Dachy G, et al. Among authors: limaye n. JAMA Dermatol. 2019 Aug 1;155(8):946-950. doi: 10.1001/jamadermatol.2019.0114. JAMA Dermatol. 2019. PMID: 31017643 Free PMC article.
42 results