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Edward S. Stenroos | Researchclopedia

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Edward S. Stenroos

32

Works

10,379

Citations

17

h-index

25

i10-index

Research Topics

Parkinson's Disease Mechanisms and Treatments Autism Spectrum Disorder Research Folate and B Vitamins Research

Affiliations

Rutgers, The State University of New Jersey1994–2009

University of Patras1997–1997

Williams (United States)2009–2009

Harvard University Press2009–2009

Johnson University1994–2009

Top Works

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

Mihael H. Polymeropoulos,Christian Lavedan,et al.

19978,183 citations

Epilepsy research and treatment

Genetic Neurodegenerative Diseases

Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

Mihael H. Polymeropoulos,Joseph Higgins,et al.

1996779 citations

Ataxin-3 Interactions with Rad23 and Valosin-Containing Protein and Its Associations with Ubiquitin Chains and the Proteasome Are Consistent with a Role in Ubiquitin-Mediated Proteolysis

Ellen Doss-Pepe,Edward S. Stenroos,et al.

2003238 citations

New 19 bp deletion polymorphism in intron‐1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?

William G. Johnson,Edward S. Stenroos,et al.

2003152 citations

Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees

Alice Lazzarini,Arthur S. Walters,et al.

1999107 citations

Genetic variant of glutathione peroxidase 1 in autism

Xue Ming,William G. Johnson,et al.

200981 citations

HLA-DR4 as a Risk Allele for Autism Acting in Mothers of Probands Possibly During Pregnancy

William G. Johnson,Steven Buyske,et al.

200980 citations

Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism

Steven Buyske,Tanishia A. Williams,et al.

200674 citations

Common dihydrofolate reductase 19–base pair deletion allele: a novel risk factor for preterm delivery1–3

William G. Johnson,Theresa O. Scholl,et al.

200572 citations