Kumaraswamy Sivakumar

Author PubWeight™ 12.51^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.	Am J Hum Genet	2003	3.55
2	Gentamicin-induced readthrough of stop codons in Duchenne muscular dystrophy.	Ann Neurol	2010	1.81
3	Arterial thrombosis induced by IVIg and its treatment with tPA.	Neurology	2003	1.24
4	Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations.	Neuromuscul Disord	2003	1.17
5	Deafness and CMT disease associated with a novel four amino acid deletion in the PMP22 gene.	Neurology	2003	0.92
6	Meningioma with pneumosinus dilatans.	Neurology	2003	0.86
7	Charcot-Marie-Tooth disease: extensive cranial nerve involvement on CT and MR imaging.	AJNR Am J Neuroradiol	2004	0.81
8	Childhood-onset spastic paraplegia with NIPAL gene mutation.	J Child Neurol	2006	0.78
9	Painful brachial plexopathies in SEPT9 mutations: adverse outcome related to comorbid states.	J Clin Neuromuscul Dis	2008	0.77
10	Lower extremity predominant stiff-person syndrome and limbic encephalitis with amphiphysin antibodies in breast cancer.	J Clin Neuromuscul Dis	2012	0.76
11	Histopathologic progression and a novel mutation in a child with nemaline myopathy.	J Child Neurol	2008	0.75
12	Autosomal recessive spastic ataxia of Charlevoix-Saguenay: compound heterozygotes for nonsense mutations of the SACS gene.	J Child Neurol	2011	0.75