PubMed (OMIM) for id: 2244

Year	Number of Results
1953	1
1954	2
1963	3
1965	1
1968	1
1971	2
1972	2
1974	1
1977	1
1980	1
1983	3
1984	1
1985	1
1987	1
1988	2
1989	1
1990	1
1991	1
1992	3
1995	1
1997	1
1999	1
2000	2
2001	4
2002	2
2003	2
2004	2
2005	3
2006	2
2009	1
2010	1
2011	1
2024	0

1

Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).

Wassel CL, Lange LA, Keating BJ, Taylor KC, Johnson AD, Palmer C, Ho LA, Smith NL, Lange EM, Li Y, Yang Q, Delaney JA, Tang W, Tofler G, Redline S, Taylor HA Jr, Wilson JG, Tracy RP, Jacobs DR Jr, Folsom AR, Green D, O'Donnell CJ, Reiner AP. Wassel CL, et al. Blood. 2011 Jan 6;117(1):268-75. doi: 10.1182/blood-2010-06-289546. Epub 2010 Oct 26. Blood. 2011. PMID: 20978265 Free PMC article.

2

Congenital fibrinogen disorders.

de Moerloose P, Neerman-Arbez M. de Moerloose P, et al. Semin Thromb Hemost. 2009 Jun;35(4):356-66. doi: 10.1055/s-0029-1225758. Epub 2009 Jul 13. Semin Thromb Hemost. 2009. PMID: 19598064 Review.

3

The molecular basis of quantitative fibrinogen disorders.

Asselta R, Duga S, Tenchini ML. Asselta R, et al. J Thromb Haemost. 2006 Oct;4(10):2115-29. doi: 10.1111/j.1538-7836.2006.02094.x. J Thromb Haemost. 2006. PMID: 16999847 Free article. Review.

4

The fibrinogen Aalpha R16C mutation results in fibrinolytic resistance.

Flood VH, Al-Mondhiry HA, Farrell DH. Flood VH, et al. Br J Haematol. 2006 Jul;134(2):220-6. doi: 10.1111/j.1365-2141.2006.06129.x. Br J Haematol. 2006. PMID: 16846481 Free article.

5

Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.

Vu D, Di Sanza C, Caille D, de Moerloose P, Scheib H, Meda P, Neerman-Arbez M. Vu D, et al. Hum Mol Genet. 2005 Nov 1;14(21):3271-80. doi: 10.1093/hmg/ddi360. Epub 2005 Sep 29. Hum Mol Genet. 2005. PMID: 16195396

6

The fibrin-derived peptide Bbeta15-42 protects the myocardium against ischemia-reperfusion injury.

Petzelbauer P, Zacharowski PA, Miyazaki Y, Friedl P, Wickenhauser G, Castellino FJ, Gröger M, Wolff K, Zacharowski K. Petzelbauer P, et al. Nat Med. 2005 Mar;11(3):298-304. doi: 10.1038/nm1198. Epub 2005 Feb 20. Nat Med. 2005. PMID: 15723073

7

Fibrinogen Philadelphia, a hypodysfibrinogenemia characterized by abnormal polymerization and fibrinogen hypercatabolism due to gamma S378P mutation.

Keller MA, Martinez J, Baradet TC, Nagaswami C, Chernysh IN, Borowski MK, Surrey S, Weisel JW. Keller MA, et al. Blood. 2005 Apr 15;105(8):3162-8. doi: 10.1182/blood-2004-04-1621. Epub 2005 Jan 4. Blood. 2005. PMID: 15632207 Free article.

8

Missense or splicing mutation? The case of a fibrinogen Bbeta-chain mutation causing severe hypofibrinogenemia.

Asselta R, Duga S, Spena S, Peyvandi F, Castaman G, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Blood. 2004 Apr 15;103(8):3051-4. doi: 10.1182/blood-2003-10-3725. Epub 2003 Dec 24. Blood. 2004. PMID: 15070683 Free article.

9

Severe hypodysfibrinogenemia in compound heterozygotes of the fibrinogen AalphaIVS4 + 1G>T mutation and an AalphaGln328 truncation (fibrinogen Keokuk).

Lefebvre P, Velasco PT, Dear A, Lounes KC, Lord ST, Brennan SO, Green D, Lorand L. Lefebvre P, et al. Blood. 2004 Apr 1;103(7):2571-6. doi: 10.1182/blood-2003-07-2316. Epub 2003 Nov 13. Blood. 2004. PMID: 14615374 Free article.

10

[CONGENITAL AFIBRINOGENEMIA].

WERDER E. WERDER E. Helv Paediatr Acta. 1963 Sep;18:208-29. Helv Paediatr Acta. 1963. PMID: 14061913 German. No abstract available.

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