PubMed (GeneRIF) for id: 26040

Year	Number of Results
2006	1
2009	1
2010	4
2011	2
2012	2
2013	11
2014	10
2015	7
2016	1
2017	7
2018	4
2019	2
2020	1
2021	4
2022	1
2023	6
2024	3

1

Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency.

Alesi V, Genovese S, Roberti MC, Sallicandro E, Di Tommaso S, Loddo S, Orlando V, Pompili D, Calacci C, Mei V, Pisaneschi E, Faggiano MV, Morgia A, Mammì C, Astrea G, Battini R, Priolo M, Dentici ML, Milone R, Novelli A. Alesi V, et al. Hum Genomics. 2024 Mar 22;18(1):29. doi: 10.1186/s40246-024-00600-0. Hum Genomics. 2024. PMID: 38520002 Free PMC article.

2

First-hit SETBP1 mutations cause a myeloproliferative disorder with bone marrow fibrosis.

Crespiatico I, Zaghi M, Mastini C, D'Aliberti D, Mauri M, Mercado CM, Fontana D, Spinelli S, Crippa V, Inzoli E, Manghisi B, Civettini I, Ramazzotti D, Sangiorgio V, Gengotti M, Brambilla V, Aroldi A, Banfi F, Barone C, Orsenigo R, Riera L, Riminucci M, Corsi A, Breccia M, Morotti A, Cilloni D, Roccaro A, Sacco A, Stagno F, Serafini M, Mottadelli F, Cazzaniga G, Pagni F, Chiarle R, Azzoni E, Sessa A, Gambacorti-Passerini C, Elli EM, Mologni L, Piazza R. Crespiatico I, et al. Blood. 2024 Apr 4;143(14):1399-1413. doi: 10.1182/blood.2023021349. Blood. 2024. PMID: 38194688

3

The landscape of SETBP1 gene expression and transcription factor activity across human tissues.

Whitlock JH, Wilk EJ, Howton TC, Clark AD, Lasseigne BN. Whitlock JH, et al. PLoS One. 2024 Jan 2;19(1):e0296328. doi: 10.1371/journal.pone.0296328. eCollection 2024. PLoS One. 2024. PMID: 38165902 Free PMC article.

4

Novel SETBP1 mutation in a chinese family with intellectual disability.

Wang L, Wang XD, Yang B, Wang XM, Peng YQ, Tan HJ, Xiao HM. Wang L, et al. BMC Med Genomics. 2023 Oct 5;16(1):233. doi: 10.1186/s12920-023-01649-x. BMC Med Genomics. 2023. PMID: 37798664 Free PMC article.

5

SETBP1 mutation determines sensitivity to immune checkpoint inhibitors in melanoma and NSCLC.

An F, Zhang W, Guo Y, Shi F, Kong Y, Tang L, Han C, Wang Q. An F, et al. Aging (Albany NY). 2023 Aug 2;15(15):7476-7495. doi: 10.18632/aging.204913. Epub 2023 Aug 2. Aging (Albany NY). 2023. PMID: 37535001 Free PMC article.

6

The impact of SETBP1 mutations in neurological diseases and cancer.

Kohyanagi N, Ohama T. Kohyanagi N, et al. Genes Cells. 2023 Sep;28(9):629-641. doi: 10.1111/gtc.13057. Epub 2023 Jul 25. Genes Cells. 2023. PMID: 37489294 Free article. Review.

7

Co-occurring mutations in ASXL1, SRSF2, and SETBP1 define a subset of myelodysplastic/ myeloproliferative neoplasm with neutrophilia.

Jain T, Ware AD, Dalton WB, Pasca S, Tsai HL, Gocke CD, Gondek LP, Xian RR, Borowitz MJ, Levis MJ. Jain T, et al. Leuk Res. 2023 Aug;131:107345. doi: 10.1016/j.leukres.2023.107345. Epub 2023 Jun 21. Leuk Res. 2023. PMID: 37354804

8

Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis.

Wang H, Gao Y, Qin L, Zhang M, Shi W, Feng Z, Guo L, Zhu B, Liao S. Wang H, et al. Orphanet J Rare Dis. 2023 May 7;18(1):107. doi: 10.1186/s13023-023-02705-6. Orphanet J Rare Dis. 2023. PMID: 37150818 Free PMC article.

9

Impaired neurogenesis and neural progenitor fate choice in a human stem cell model of SETBP1 disorder.

Cardo LF, de la Fuente DC, Li M. Cardo LF, et al. Mol Autism. 2023 Feb 20;14(1):8. doi: 10.1186/s13229-023-00540-x. Mol Autism. 2023. PMID: 36805818 Free PMC article.

10

Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1.

Zhou Y, Quan Y, Wu Y, Zhang Y. Zhou Y, et al. J Int Med Res. 2022 Sep;50(9):3000605221121955. doi: 10.1177/03000605221121955. J Int Med Res. 2022. PMID: 36113068 Free PMC article.

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