PubMed for id: 4784

Year	Number of Results
1993	1
1994	1
1995	1
1996	1
1997	3
2000	3
2002	2
2003	1
2004	2
2005	1
2006	2
2008	1
2009	5
2010	4
2011	3
2012	3
2013	2
2014	5
2015	3
2016	3
2017	8
2018	9
2019	6
2020	4
2021	5
2022	5
2023	6
2024	0

1

A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndrome.

Uzman CY, Gürsoy S, Hazan F. Uzman CY, et al. Int J Dev Neurosci. 2023 Aug;83(5):479-485. doi: 10.1002/jdn.10280. Epub 2023 Jun 19. Int J Dev Neurosci. 2023. PMID: 37336770

2

NFIXing Cancer: The Role of NFIX in Oxidative Stress Response and Cell Fate.

Ribeiro V, Martins SG, Lopes AS, Thorsteinsdóttir S, Zilhão R, Carlos AR. Ribeiro V, et al. Int J Mol Sci. 2023 Feb 21;24(5):4293. doi: 10.3390/ijms24054293. Int J Mol Sci. 2023. PMID: 36901722 Free PMC article. Review.

3

CircNFIX stimulates the proliferation, invasion, and stemness properties of ovarian cancer cells by enhancing SH3RF3 mRNA stability via binding LIN28B.

Yu XZ, Yang BW, Ao MY, Wu YK, Ye H, Wang RY, Xi MR, Hou MM. Yu XZ, et al. Kaohsiung J Med Sci. 2023 Mar;39(3):234-243. doi: 10.1002/kjm2.12632. Epub 2022 Dec 10. Kaohsiung J Med Sci. 2023. PMID: 36495291 Free article.

4

Pathogenic variant in NFIX gene affecting three sisters due to paternal mosaicism.

Sihombing NRB, Winarni TI, van Bokhoven H, van der Burgt I, de Leeuw N, Faradz SMH. Sihombing NRB, et al. Am J Med Genet A. 2020 Nov;182(11):2731-2736. doi: 10.1002/ajmg.a.61835. Epub 2020 Sep 18. Am J Med Genet A. 2020. PMID: 32945093

5

A de-novo NFIX mutation causes a case of neonatal lethal Marshall-Smith syndrome.

Bupp C, Junewick J, Hess JL. Bupp C, et al. Clin Dysmorphol. 2020 Oct;29(4):214-216. doi: 10.1097/MCD.0000000000000339. Clin Dysmorphol. 2020. PMID: 32701632 No abstract available.

6

Parental gonadal but not somatic mosaicism leading to de novo NFIX variants shared by two brothers with Malan syndrome.

Hancarova M, Havlovicova M, Putzova M, Vseticka J, Prchalova D, Stranecky V, Sedlacek Z. Hancarova M, et al. Am J Med Genet A. 2019 Oct;179(10):2119-2123. doi: 10.1002/ajmg.a.61302. Epub 2019 Aug 1. Am J Med Genet A. 2019. PMID: 31369202

7

NFIX downregulation independently predicts poor prognosis in lung adenocarcinoma, but not in squamous cell carcinoma.

Ge J, Dong H, Yang Y, Liu B, Zheng M, Cheng Q, Peng L, Li J. Ge J, et al. Future Oncol. 2018 Dec;14(30):3135-3144. doi: 10.2217/fon-2018-0164. Epub 2018 Nov 12. Future Oncol. 2018. PMID: 30418046

8

Nuclear Factor One X in Development and Disease.

Piper M, Gronostajski R, Messina G. Piper M, et al. Trends Cell Biol. 2019 Jan;29(1):20-30. doi: 10.1016/j.tcb.2018.09.003. Epub 2018 Oct 1. Trends Cell Biol. 2019. PMID: 30287093 Review.

9

Nuclear factor I X is a recurrent target for HPV16 insertions in anal carcinomas.

Jeannot E, Harlé A, Holmes A, Sastre-Garau X. Jeannot E, et al. Genes Chromosomes Cancer. 2018 Dec;57(12):638-644. doi: 10.1002/gcc.22675. Epub 2018 Sep 27. Genes Chromosomes Cancer. 2018. PMID: 30264502

10

Further delineation of Malan syndrome.

Priolo M, Schanze D, Tatton-Brown K, Mulder PA, Tenorio J, Kooblall K, Acero IH, Alkuraya FS, Arias P, Bernardini L, Bijlsma EK, Cole T, Coubes C, Dapia I, Davies S, Di Donato N, Elcioglu NH, Fahrner JA, Foster A, González NG, Huber I, Iascone M, Kaiser AS, Kamath A, Liebelt J, Lynch SA, Maas SM, Mammì C, Mathijssen IB, McKee S, Menke LA, Mirzaa GM, Montgomery T, Neubauer D, Neumann TE, Pintomalli L, Pisanti MA, Plomp AS, Price S, Salter C, Santos-Simarro F, Sarda P, Segovia M, Shaw-Smith C, Smithson S, Suri M, Valdez RM, Van Haeringen A, Van Hagen JM, Zollino M, Lapunzina P, Thakker RV, Zenker M, Hennekam RC. Priolo M, et al. Hum Mutat. 2018 Sep;39(9):1226-1237. doi: 10.1002/humu.23563. Epub 2018 Jun 25. Hum Mutat. 2018. PMID: 29897170 Free PMC article.

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