Edward S. Stenroos

10.4k total citations · 2 hit papers
24 papers, 7.9k citations indexed

About

Edward S. Stenroos is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Edward S. Stenroos has authored 24 papers receiving a total of 7.9k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in Edward S. Stenroos's work include Parkinson's Disease Mechanisms and Treatments (6 papers), RNA regulation and disease (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Edward S. Stenroos is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (6 papers), RNA regulation and disease (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Edward S. Stenroos collaborates with scholars based in United States, Italy and Greece. Edward S. Stenroos's co-authors include William G. Johnson, Alice Lazzarini, Lawrence I. Golbe, Giuseppe Di Iorio, Susan Ide, Robert L. Nussbaum, Mihael H. Polymeropoulos, Roger C. Duvoisin, Aglaia Athanassiadou and Amalia Dutra and has published in prestigious journals such as Science, Molecular and Cellular Biology and American Journal of Clinical Nutrition.

In The Last Decade

Edward S. Stenroos

24 papers receiving 7.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

1997 6.3k citations Mihael H. Polymeropoulos, Christian Lavedan et al. Science profile →
Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

1996 548 citations Mihael H. Polymeropoulos, Joseph Higgins et al. Science profile →

Peers

Edward S. Stenroos

NEURO

CMN

PHYSI

NEURO

Christian Lavedan United States

Alice Lazzarini United States

Susan Ide United States

Giuseppe Di Iorio Italy

Anindya Dehejia United States

Aglaia Athanassiadou Greece

R Boyer United States

Lysia S. Forno United States

Yaping Chu United States

Hiroto Matsumine Japan

Christian Lavedan United States

Edward S. Stenroos

5.7k ×1.0

NEURO

3.6k ×1.1

CMN

2.4k ×1.1

2.1k ×1.0

PHYSI

1.4k ×0.9

NEURO

Citations per year, relative to Edward S. Stenroos Edward S. Stenroos (= 1×) peers Christian Lavedan

Countries citing papers authored by Edward S. Stenroos

Since Specialization

Citations

This map shows the geographic impact of Edward S. Stenroos's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Edward S. Stenroos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edward S. Stenroos more than expected).

Fields of papers citing papers by Edward S. Stenroos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward S. Stenroos. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Edward S. Stenroos. The network helps show where Edward S. Stenroos may publish in the future.

Co-authorship network of co-authors of Edward S. Stenroos

This figure shows the co-authorship network connecting the top 25 collaborators of Edward S. Stenroos. A scholar is included among the top collaborators of Edward S. Stenroos based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Edward S. Stenroos. Edward S. Stenroos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Johnson, William G., Steven Buyske, Audrey Mars, et al.. (2009). HLA-DR4 as a Risk Allele for Autism Acting in Mothers of Probands Possibly During Pregnancy. Archives of Pediatrics and Adolescent Medicine. 163(6). 542–542. 61 indexed citations

Ming, Xue, William G. Johnson, Edward S. Stenroos, et al.. (2009). Genetic variant of glutathione peroxidase 1 in autism. Brain and Development. 32(2). 105–109. 64 indexed citations

Golbe, Lawrence I., Giuseppe Di Iorio, Katerina Markopoulou, et al.. (2006). Glutathione S‐transferase polymorphisms and onset age in α‐synuclein A53T mutant Parkinson's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(2). 254–258. 12 indexed citations

Buyske, Steven, Audrey Mars, Edward S. Stenroos, et al.. (2006). Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism. BMC Genetics. 7(1). 8–8. 58 indexed citations

Johnson, William G., et al.. (2005). Common dihydrofolate reductase 19–base pair deletion allele: a novel risk factor for preterm delivery1–3. American Journal of Clinical Nutrition. 81(3). 664–668. 50 indexed citations

Johnson, William G., et al.. (2003). New 19 bp deletion polymorphism in intron‐1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?. American Journal of Medical Genetics Part A. 124A(4). 339–345. 118 indexed citations

Doss-Pepe, Ellen, Edward S. Stenroos, William G. Johnson, & Kiran Madura. (2003). 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. Molecular and Cellular Biology. 23(18). 6469–6483. 187 indexed citations

Golbe, Lawrence I., Alice Lazzarini, William G. Johnson, et al.. (2001). The tau A0 allele in Parkinson's disease. Movement Disorders. 16(3). 442–447. 47 indexed citations

Lazzarini, Alice, Arthur S. Walters, Kathleen T. Hickey, et al.. (1999). Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees. Movement Disorders. 14(1). 111–116. 79 indexed citations

10.

Kugler, Steven L., et al.. (1998). Hereditary febrile seizures: Phenotype and evidence for a chromosome 19p locus. American Journal of Medical Genetics. 79(5). 354–361. 51 indexed citations

11.

Wisniewski, K. E., Nanbert Zhong, Wojciech Kaczmarski, et al.. (1998). Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis. Annals of Neurology. 43(1). 106–110. 46 indexed citations

12.

Lazzarini, Alice, Kirsten Schwarz, Shan Jiang, et al.. (1997). Pelizaeus-Merzbacher-like disease: Exclusion of the proteolipid protein locus and documentation of a new locus on Xq. Neurology. 49(3). 824–832. 13 indexed citations

13.

Polymeropoulos, Mihael H., Christian Lavedan, Elisabeth Leroy, et al.. (1997). Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease. Science. 276(5321). 2045–2047. 6341 indexed citations breakdown →

14.

Johnson, William G., et al.. (1996). Pedigree analysis in families with febrile seizures. American Journal of Medical Genetics. 61(4). 345–352. 58 indexed citations

15.

Polymeropoulos, Mihael H., Joseph Higgins, Lawrence I. Golbe, et al.. (1996). Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23. Science. 274(5290). 1197–1199. 548 indexed citations breakdown →

16.

Lindblad, K, Haydeh Payami, William G. Johnson, et al.. (1995). No evidence for association of familial Parkinson's disease with CAG repeat expansion. Neurology. 45(9). 1760–1763. 22 indexed citations

17.

Lazzarini, Alice, Edward S. Stenroos, Thomas Lehner, et al.. (1995). Short tandem repeat polymorphism linkage studies in a new family with X‐linked mental retardation (MRX20). American Journal of Medical Genetics. 57(4). 552–557. 12 indexed citations

18.

Chatkupt, Sansnee, Marcy C. Speer, Marc A. Thomas, et al.. (1994). Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele. American Journal of Medical Genetics. 52(1). 1–4. 9 indexed citations

19.

Johnson, William G., Hiroaki Yoshidome, Edward S. Stenroos, & Mercy M. Davidson. (1991). Origin of the Neuron‐Like Cells in Tuberous Sclerosis Tissues^a. Annals of the New York Academy of Sciences. 615(1). 211–219. 13 indexed citations

20.

Davidson, Mercy M., Hiroaki Yoshidome, Edward S. Stenroos, & William G. Johnson. (1991). Neuron‐Like Cells in Culture of Tuberous Sclerosis Tissue. Annals of the New York Academy of Sciences. 615(1). 196–210. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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