C Seidman

Author PubWeight™ 24.92^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.	N Engl J Med	1999	5.61
2	The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms.	Cell	2001	5.35
3	Biochemistry and genetics of Klebsiella pneumoniae mutant strains unable to fix N2.	J Bacteriol	1975	2.89
4	Sudden death due to troponin T mutations.	J Am Coll Cardiol	1997	2.07
5	Human fatty acid synthesis is stimulated by a eucaloric low fat, high carbohydrate diet.	J Clin Invest	1996	2.05
6	Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.	J Med Genet	2005	2.04
7	Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay.	Am J Physiol Heart Circ Physiol	2007	1.82
8	Altered crossbridge kinetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy.	Circ Res	1999	1.28
9	The metabolic and immunologic effects of short-term thalidomide treatment of patients infected with the human immunodeficiency virus.	AIDS Res Hum Retroviruses	1997	0.86
10	Synaptogenesis in mouse cerebellum: a comparative in vivo and tissue culture study.	Neuroscience	1981	0.79
11	Mutations in COCH (formerly Coch5b2) cause DFNA9.	Adv Otorhinolaryngol	2000	0.78
12	In memorium.	J Mol Cell Cardiol	2001	0.75
13	Clinical and genetic linkage analysis of a large Venezuelan kindred with Usher syndrome.	Int J Pediatr Otorhinolaryngol	2004	0.75