Elliot Stolerman

565 total citations
6 papers, 137 citations indexed

About

Elliot Stolerman is a scholar working on Surgery, Rheumatology and Genetics. According to data from OpenAlex, Elliot Stolerman has authored 6 papers receiving a total of 137 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Surgery, 2 papers in Rheumatology and 2 papers in Genetics. Recurrent topics in Elliot Stolerman's work include Cell Adhesion Molecules Research (2 papers), Osteoarthritis Treatment and Mechanisms (2 papers) and Pancreatic function and diabetes (1 paper). Elliot Stolerman is often cited by papers focused on Cell Adhesion Molecules Research (2 papers), Osteoarthritis Treatment and Mechanisms (2 papers) and Pancreatic function and diabetes (1 paper). Elliot Stolerman collaborates with scholars based in United States, Italy and Germany. Elliot Stolerman's co-authors include Cathy S. Carlson, Paul E. Di Cesare, Hermina Tulli, Mats Paulsson, Nik Hauser, Michael Leslie, Roberto Perris, Carrie Fang, Brooke Smith and Alka Chaubey and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Orthopaedic Research® and Molecular Genetics and Metabolism.

In The Last Decade

Elliot Stolerman

5 papers receiving 133 citations

Peers

Elliot Stolerman

RHEUM

MB

IA

GENET

CR

Renata Pellegrino da Silva United States

Maria Gnoli Italy

Nicole P. Safina United States

T. Seo United States

Sergey Malchenko United States

Xiumao Li China

Arne Olav Melleby Norway

Anatália Labilloy United States

Manaswini Sivaramakrishnan Australia

Vijayalakshmi Shridhar United States

Renata Pellegrino da Silva United States

Elliot Stolerman

98 ×1.2

RHEUM

134 ×2.9

MB

20 ×0.6

IA

91 ×3.3

GENET

56 ×2.2

CR

Citations per year, relative to Elliot Stolerman Elliot Stolerman (= 1×) peers Renata Pellegrino da Silva

Countries citing papers authored by Elliot Stolerman

Since Specialization

Citations

This map shows the geographic impact of Elliot Stolerman'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 Elliot Stolerman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elliot Stolerman more than expected).

Fields of papers citing papers by Elliot Stolerman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elliot Stolerman. 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 Elliot Stolerman. The network helps show where Elliot Stolerman may publish in the future.

Co-authorship network of co-authors of Elliot Stolerman

This figure shows the co-authorship network connecting the top 25 collaborators of Elliot Stolerman. A scholar is included among the top collaborators of Elliot Stolerman 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 Elliot Stolerman. Elliot Stolerman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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6 of 6 papers shown

1.

Poplawski, Andrzej, D. Le, Kameryn M. Butler, et al.. (2025). Expansion of genotype/phenotype correlation in an individual with compound heterozygous variants in CYP51A1 and congenital cataract. Molecular Genetics and Metabolism. 146(1-2). 109230–109230.

2.

Stolerman, Elliot, et al.. (2023). RNA analysis of intronic variants in the LAMA2 gene detected by whole genome sequencing confirms a rare dual diagnosis of incontinentia pigmenti with limb‐girdle muscular dystrophy. SHILAP Revista de lepidopterología. 11(4). e7165–e7165. 1 indexed citations

3.

Fang, Xiaolan, et al.. (2023). Clinical case report: mosaicANK3pathogenic variant in a patient with autism spectrum disorder and neurodevelopmental delay. Molecular Case Studies. 9(3). a006233–a006233. 3 indexed citations

4.

Stolerman, Elliot, Brooke Smith, Alka Chaubey, & Julie R. Jones. (2016). CHD8 intragenic deletion associated with autism spectrum disorder. European Journal of Medical Genetics. 59(4). 189–194. 20 indexed citations

5.

Fang, Carrie, Cathy S. Carlson, Michael Leslie, et al.. (2000). Molecular cloning, sequencing, and tissue and developmental expression of mouse cartilage oligomeric matrix protein (COMP). Journal of Orthopaedic Research®. 18(4). 593–603. 46 indexed citations

6.

Cesare, Paul E. Di, Cathy S. Carlson, Elliot Stolerman, et al.. (1996). Increased degradation and alteered tissue distribution of cartilage oligomeric matrix protein in human rheumatoid and osteoarthritic cartilage. Journal of Orthopaedic Research®. 14(6). 946–955. 67 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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