Author

Melissa Hanson

Observed institutions: National Institutes of Health, Mayo Clinic, National Institute of Neurological Disorders and Stroke, National Institute on Aging, Mayo Clinic in Florida

OpenAlex ID: A5109852769

Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation

2003 · Stephen Hague, Ekaterina Rogaeva, et al. · Annals of Neurology · 237

Profile of families with parkinsonism‐predominant spinocerebellar ataxia type 2 (SCA2)

2004 · Sarah Furtado, Haydeh Payami, et al. · Movement Disorders · 127

Glucocerebrosidase mutations are also found in subjects with early‐onset parkinsonism from Venezuela

2005 · Michael J. Eblan, Joann Nguyen, et al. · Movement Disorders · 70

The Tau H1 Haplotype is associated with Parkinson's disease in the Norwegian population

2002 · Matt Farrer, Lisa Skipper, et al. · Neuroscience Letters · 69

A Rare Truncating Mutation in ADH1C (G78Stop) Shows Significant Association With Parkinson Disease in a Large International Sample

2005 · Silvia Buervenich, Andrea Carmine, et al. · Archives of Neurology · 51

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

2005 · Javier Simon-Sanchez, Melissa Hanson, et al. · Neuroscience Letters · 43

Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features

2004 · Melissa Hanson, Melissa Honour, et al. · Journal of Neurology · 39

Exercise‐induced dystonia as a preceding symptom of familial Parkinson's disease

2003 · Michiko K. Bruno, Bernard Ravina, et al. · Movement Disorders · 29

A consanguineous Turkish family with early‐onset Parkinson's disease and an exon 4 parkin deletion

2004 · Okan Dogu, Janel Johnson, et al. · Movement Disorders · 26

A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts

2024 · Laura Bravo, Joana FF Simões, et al. · The Lancet Digital Health · 22

Accurate Determination of Ataxin-2 Polyglutamine Expansion in Patients with Intermediate-Range Repeats

2002 · Jennifer Hussey, Paul J. Lockhart, et al. · Genetic Testing · 22

Mutation at the SCA17 locus is not a common cause of parkinsonism

2003 · Dena Hernandez, Melissa Hanson, et al. · Parkinsonism & Related Disorders · 14

Familial Variants of Parkinson’s Disease

2002 · Katrina Gwinn-Hardy, Melissa Hanson, et al. · Advances in behavioral biology

Works count: 13

Citation count: 749

H-index: 12

I10-index: 12