M Tristani-Firouzi

Author PubWeight™ 18.20^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.	Cell	2001	4.25
2	Mutations in the hminK gene cause long QT syndrome and suppress IKs function.	Nat Genet	1997	3.90
3	The primary periodic paralyses: diagnosis, pathogenesis and treatment.	Brain	2005	2.17
4	The S4-S5 linker couples voltage sensing and activation of pacemaker channels.	Proc Natl Acad Sci U S A	2001	1.60
5	PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.	Neurology	2003	1.46
6	Functional effects of mutations in KvLQT1 that cause long QT syndrome.	J Cardiovasc Electrophysiol	1999	1.23
7	Andersen-Tawil syndrome: prospective cohort analysis and expansion of the phenotype.	Am J Med Genet A	2006	0.86
8	Evidence for early vessel involvement in the dysfunctional myocardium of Takayasu's arteritis.	Pediatr Cardiol	2001	0.85
9	Nebulized nitric oxide/nucleophile adduct reduces chronic pulmonary hypertension.	Cardiovasc Res	1996	0.81
10	Diversity of response in vascular smooth muscle cells to changes in oxygen tension.	Kidney Int	1997	0.79
11	Chronic infusion of nitric oxide in experimental pulmonary hypertension: pulmonary pressure-flow analysis.	Eur Respir J	1996	0.79