Justin Price

Author PubWeight™ 8.01^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Advances in catheter ablation: atrial fibrillation ablation in patients with mitral mechanical prosthetic valve.	Curr Cardiol Rev	2012	1.44
2	Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12.	J Clin Invest	2012	1.32
3	A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.	Am J Hum Genet	2010	1.11
4	Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease.	J Neurol	2009	0.97
5	Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2.	J Neurol	2011	0.95
6	In vivo electroporation and non-protein based screening assays to identify antibodies against native protein conformations.	Hybridoma (Larchmt)	2011	0.82
7	Characterization of the mitofusin 2 R94W mutation in a knock-in mouse model.	J Peripher Nerv Syst	2014	0.78
8	Efficacy of catheter ablation in nonparoxysmal atrial fibrillation patients with severe enlarged left atrium and its impact on left atrial structural remodeling.	J Cardiovasc Electrophysiol	2013	0.75