Estrella Gomez-Tortosa

Author PubWeight™ 6.62^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.	Am J Hum Genet	2012	1.05
2	Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein.	Mov Disord	2002	0.87
3	Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset.	Hum Genet	2012	0.83
4	TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.	Biochem Biophys Res Commun	2012	0.81
5	Extended kindred with recessive late-onset Alzheimer disease maps to locus 8p22-p21.2: a genome-wide linkage analysis.	Alzheimer Dis Assoc Disord	2012	0.79
6	Amusia as an early manifestation of frontotemporal dementia caused by a novel progranulin mutation.	J Neurol	2010	0.79
7	A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes.	Brain	2005	0.78
8	Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.	Neurogenetics	2013	0.77