PubMed (GeneRIF) for id: 2243

Year	Number of Results
1983	1
2000	1
2001	4
2002	7
2003	4
2004	4
2005	14
2006	13
2007	24
2008	16
2009	23
2010	19
2011	14
2012	17
2013	16
2014	9
2015	15
2016	11
2017	22
2018	7
2019	13
2020	12
2021	7
2022	1
2023	5
2024	0

1

[Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene].

Shao X, Ma J, Wang Z, Sun M, Huang Z, Jiang Z, Liu X, Li S, Liu Y. Shao X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Nov 10;40(11):1324-1329. doi: 10.3760/cma.j.cn511374-20220112-00027. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37906135 Chinese.

2

Fibrinogen Aα gene genotyping in patients with inherited afibrinogenemia deficiency; a novel mutation in Iranian afibrinogenemia patients.

Moazzeni A, Naderi M, Dorgalaleh A, Alizadeh S. Moazzeni A, et al. Blood Coagul Fibrinolysis. 2023 Dec 1;34(8):517-522. doi: 10.1097/MBC.0000000000001260. Epub 2023 Oct 10. Blood Coagul Fibrinolysis. 2023. PMID: 37823427

3

Interaction Between Platelet and Fibrinogen on Clot Strength in Healthy Patients.

Maslow A, Cheves T, Joyce MF, Apruzzese P, Sweeney J. Maslow A, et al. J Cardiothorac Vasc Anesth. 2023 Jun;37(6):942-947. doi: 10.1053/j.jvca.2023.02.022. Epub 2023 Feb 20. J Cardiothorac Vasc Anesth. 2023. PMID: 36933991

4

Fibrinogen-Aα THR312ALA Polymorphism is Associated to Chronic Thromboembolic Pulmonary Hypertension in Turkey.

Çörtük M, Yıldızeli B, Kurar E, Kayış SA, Tanrıverdi E, Çetinkaya E. Çörtük M, et al. Anatol J Cardiol. 2023 Mar;27(3):153-159. doi: 10.14744/AnatolJCardiol.2022.2392. Anatol J Cardiol. 2023. PMID: 36856592 Free PMC article.

5

Two Novel Heterozygous Mutations (p.γPhe230Val and p.AαAsn839Thr) Cause Hereditary Hypodysfibrinogenemia in Two Chinese Independent Families.

Ge S, Luo Y, Dong R, Guo X, Wang M, Chen Y. Ge S, et al. Acta Haematol. 2023;146(3):252-258. doi: 10.1159/000527952. Epub 2023 Jan 4. Acta Haematol. 2023. PMID: 36599322

6

FGA Controls VEGFA Secretion to Promote Angiogenesis by Activating the VEGFR2-FAK Signalling Pathway.

Li H, Cai E, Cheng H, Ye X, Ma R, Zhu H, Chang X. Li H, et al. Front Endocrinol (Lausanne). 2022 Apr 13;13:791860. doi: 10.3389/fendo.2022.791860. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35498401 Free PMC article.

7

Fibrinogen and Antifibrinolytic Proteins: Interactions and Future Therapeutics.

Pechlivani N, Kearney KJ, Ajjan RA. Pechlivani N, et al. Int J Mol Sci. 2021 Nov 21;22(22):12537. doi: 10.3390/ijms222212537. Int J Mol Sci. 2021. PMID: 34830419 Free PMC article. Review.

8

Protein Misfolding and Aggregation: The Relatedness between Parkinson's Disease and Hepatic Endoplasmic Reticulum Storage Disorders.

Padilla-Godínez FJ, Ramos-Acevedo R, Martínez-Becerril HA, Bernal-Conde LD, Garrido-Figueroa JF, Hiriart M, Hernández-López A, Argüero-Sánchez R, Callea F, Guerra-Crespo M. Padilla-Godínez FJ, et al. Int J Mol Sci. 2021 Nov 18;22(22):12467. doi: 10.3390/ijms222212467. Int J Mol Sci. 2021. PMID: 34830348 Free PMC article. Review.

9

Afibrinogenemia with two compound heterozygous mutations in FGA gene.

Feugray G, Billoir P, Casini A, Neerman-Arbez M, Barbay V, Chamouni P, Schneider P, Le Cam Duchez V. Feugray G, et al. Haemophilia. 2021 Sep;27(5):e641-e644. doi: 10.1111/hae.14377. Epub 2021 Jul 13. Haemophilia. 2021. PMID: 34255402 No abstract available.

10

An association between fibrinogen gene polymorphisms and diabetic peripheral neuropathy in young patients with type 1 diabetes.

Vojtková J, Kolková Z, Motyková K, Kostková M, Suroviaková S, Grendár M, Bánovčin P. Vojtková J, et al. Mol Biol Rep. 2021 May;48(5):4397-4404. doi: 10.1007/s11033-021-06455-1. Epub 2021 Jun 1. Mol Biol Rep. 2021. PMID: 34061326

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