Manel Baena

Author PubWeight™ 5.50^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Mutations in the NKX2-5 gene in patients with stroke and patent foramen ovale.	Clin Neurol Neurosurg	2009	1.44
2	RNA analysis of eight BRCA1 and BRCA2 unclassified variants identified in breast/ovarian cancer families from Spain.	Hum Mutat	2003	0.91
3	Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser.	Thromb Haemost	2010	0.85
4	Rapid identification of female haemophilia A carriers with deletions in the factor VIII gene by quantitative real-time PCR analysis.	Thromb Haemost	2005	0.84
5	First report of two independent point factorVIII mutations in a family with haemophilia a: a word of caution for carrier diagnosis.	Thromb Haemost	2005	0.78
6	Identification of 31 novel mutations in the F8 gene in Spanish hemophilia A patients: structural analysis of 20 missense mutations suggests new intermolecular binding sites.	Blood	2008	0.75
7	Marker and real-time quantitative analyses to confirm hemophilia B carrier diagnosis of a complete deletion of the F9 gene.	Haematologica	2007	0.75