M Baena

Author PubWeight™ 3.76^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	The R71G BRCA1 is a founder Spanish mutation and leads to aberrant splicing of the transcript.	Hum Mutat	2001	1.36
2	Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8 gene.	Haemophilia	2008	0.86
3	BRCA2 mutation analysis of 87 Spanish breast/ovarian cancer families.	Ann Oncol	2001	0.84
4	F8 gene dosage defects in atypical patients with severe haemophilia A.	Haemophilia	2012	0.77
5	Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis.	Haemophilia	2005	0.75
6	[Clinical and pathological characteristics and clinical course of patients with breast cancer and BRCA1/BRCA2 mutations].	Med Clin (Barc)	2001	0.75
7	[Socioeconomic factors: do they influence the demand for care and the degree of satisfaction in primary care?].	Aten Primaria	1990	0.75
8	[Erythrocytosis and renal hydatid cyst].	Med Clin (Barc)	1983	0.75
9	Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A.	Haemophilia	2008	0.75