PubMed for id: 10019

Year	Number of Results
1993	1
1996	1
1997	1
2000	2
2002	2
2005	1
2006	3
2007	2
2008	6
2009	14
2010	14
2011	14
2012	6
2013	8
2014	10
2015	6
2016	10
2017	3
2018	6
2019	10
2020	4
2021	3
2022	2
2023	3
2024	1

1

Rare SH2B3 coding variants in lupus patients impair B cell tolerance and predispose to autoimmunity.

Zhang Y, Morris R, Brown GJ, Lorenzo AMD, Meng X, Kershaw NJ, Kiridena P, Burgio G, Gross S, Cappello JY, Shen Q, Wang H, Turnbull C, Lea-Henry T, Stanley M, Yu Z, Ballard FD, Chuah A, Lee JC, Hatch AM, Enders A, Masters SL, Headley AP, Trnka P, Mallon D, Fletcher JT, Walters GD, Šestan M, Jelušić M, Cook MC, Athanasopoulos V, Fulcher DA, Babon JJ, Vinuesa CG, Ellyard JI. Zhang Y, et al. J Exp Med. 2024 Apr 1;221(4):e20221080. doi: 10.1084/jem.20221080. Epub 2024 Feb 28. J Exp Med. 2024. PMID: 38417019

2

Acquired uniparental isodisomies involving chromosome 12 in paediatric B-cell precursor acute lymphoblastic leukaemia: Associations with chromosome 21 gains and SH2B3 mutations.

Lundin-Ström KB, Biloglav A, Castor A, Olsson-Arvidsson L, Johansson B. Lundin-Ström KB, et al. Br J Haematol. 2023 May;201(3):585-588. doi: 10.1111/bjh.18742. Epub 2023 Mar 10. Br J Haematol. 2023. PMID: 36899493 No abstract available.

3

Phosphorylation-related SNPs influence lipid levels and rheumatoid arthritis risk by altering gene expression and plasma protein levels.

Mo X, Guo Y, Qian Q, Fu M, Zhang H. Mo X, et al. Rheumatology (Oxford). 2020 Apr 1;59(4):889-898. doi: 10.1093/rheumatology/kez466. Rheumatology (Oxford). 2020. PMID: 31624844

4

The Longevity-Associated SH2B3 (LNK) Genetic Variant: Selected Aging Phenotypes in 379,758 Subjects.

Kuo CL, Joaquim M, Kuchel GA, Ferrucci L, Harries LW, Pilling LC, Melzer D. Kuo CL, et al. J Gerontol A Biol Sci Med Sci. 2020 Sep 16;75(9):1656-1662. doi: 10.1093/gerona/glz191. J Gerontol A Biol Sci Med Sci. 2020. PMID: 31428775 Free PMC article.

5

Germline SH2B3 pathogenic variant associated with myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis.

Coltro G, Lasho TL, Finke CM, Gangat N, Pardanani A, Tefferi A, Jevremovic D, Altman JK, Patnaik MM. Coltro G, et al. Am J Hematol. 2019 Sep;94(9):E231-E234. doi: 10.1002/ajh.25552. Epub 2019 Jun 14. Am J Hematol. 2019. PMID: 31173385 Free article. No abstract available.

6

SH2B3 inactivation through CN-LOH 12q is uniquely associated with B-cell precursor ALL with iAMP21 or other chromosome 21 gain.

Sinclair PB, Ryan S, Bashton M, Hollern S, Hanna R, Case M, Schwalbe EC, Schwab CJ, Cranston RE, Young BD, Irving JAE, Vora AJ, Moorman AV, Harrison CJ. Sinclair PB, et al. Leukemia. 2019 Aug;33(8):1881-1894. doi: 10.1038/s41375-019-0412-1. Epub 2019 Feb 28. Leukemia. 2019. PMID: 30816328 Free PMC article.

7

Role of SH2B3 R262W gene polymorphism and risk of coronary heart disease: A PRISMA-compliant meta-analysis.

Hong L, Jiang YF, Chen M, Zhang NN, Yang HJ, Rui Q, Zhou YF. Hong L, et al. Medicine (Baltimore). 2018 Nov;97(48):e13436. doi: 10.1097/MD.0000000000013436. Medicine (Baltimore). 2018. PMID: 30508957 Free PMC article.

8

Clinical significance of novel SH2B3 mutations in adult Chinese acute lymphoblastic leukemia patients.

Gu Y, Han Q, McGrath M, Song C, Ge Z. Gu Y, et al. Leuk Res. 2018 Sep;72:67-70. doi: 10.1016/j.leukres.2018.07.006. Epub 2018 Jul 10. Leuk Res. 2018. PMID: 30103202 Clinical Trial. No abstract available.

9

SH2B3 aberrations enriched in iAMP21 B lymphoblastic leukemia.

Baughn LB, Meredith MM, Oseth L, Smolarek TA, Hirsch B. Baughn LB, et al. Cancer Genet. 2018 Oct;226-227:30-35. doi: 10.1016/j.cancergen.2018.05.004. Epub 2018 Jun 8. Cancer Genet. 2018. PMID: 30005852

10

T784C LNK gene polymorphism and the risk of myeloproliferative disorders.

Olkhovskiy IA, Gorbenko AS, Stolyar MA, Vasiliev EV, Mikhalev MA, Tabakova KA. Olkhovskiy IA, et al. Leuk Lymphoma. 2019 Jan;60(1):277-278. doi: 10.1080/10428194.2018.1459604. Epub 2018 May 11. Leuk Lymphoma. 2019. PMID: 29749755 No abstract available.

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