Giles D J Watts

Author PubWeight™ 11.54^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations.	J Neuropathol Exp Neurol	2006	2.43
2	Mutant valosin-containing protein causes a novel type of frontotemporal dementia.	Ann Neurol	2005	1.94
3	Mutations in SEPT9 cause hereditary neuralgic amyotrophy.	Nat Genet	2005	1.68
4	Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.	Am J Med Genet A	2008	1.57
5	APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD).	Genet Med	2007	0.99
6	Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.	Alzheimer Dis Assoc Disord	2005	0.97
7	Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.	Bone	2005	0.77
8	Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy.	Am J Med Genet A	2006	0.76
9	A case of late-onset proximal and distal muscle weakness.	Neurology	2009	0.75