Steven J. Steinberg

4.0k total citations
74 papers, 2.9k citations indexed

About

Steven J. Steinberg is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Steven J. Steinberg has authored 74 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 24 papers in Clinical Biochemistry and 19 papers in Physiology. Recurrent topics in Steven J. Steinberg's work include Peroxisome Proliferator-Activated Receptors (39 papers), Metabolism and Genetic Disorders (24 papers) and Adipose Tissue and Metabolism (16 papers). Steven J. Steinberg is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (39 papers), Metabolism and Genetic Disorders (24 papers) and Adipose Tissue and Metabolism (16 papers). Steven J. Steinberg collaborates with scholars based in United States, Canada and United Kingdom. Steven J. Steinberg's co-authors include Ann B. Moser, Paul A. Watkins, Nancy Braverman, Gerald V. Raymond, Hugo W. Moser, Kirby D. Smith, Gabriele Dodt, Joseph G. Hacia, Stephanie J. Mihalik and A. H. Fensom and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Immunology.

In The Last Decade

Steven J. Steinberg

72 papers receiving 2.8k citations

Peers

Steven J. Steinberg

PHYSI

BIOCH

ONCOL

Matthew McKenzie Australia

Laura Vilarinho Portugal

Andreas Werner United Kingdom

Chris Ottolenghi France

Hans Geir Eiken Norway

Takeshi Yasuda Japan

Yvonne H. Edwards United Kingdom

D. Sasse Germany

Rafael Garesse Spain

Edward Owusu-Ansah United States

Matthew McKenzie Australia

Steven J. Steinberg

3.6k ×1.8

1.3k ×1.9

416 ×0.6

PHYSI

116 ×0.4

BIOCH

91 ×0.4

ONCOL

Citations per year, relative to Steven J. Steinberg Steven J. Steinberg (= 1×) peers Matthew McKenzie

Countries citing papers authored by Steven J. Steinberg

Since Specialization

Citations

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

Fields of papers citing papers by Steven J. Steinberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven J. Steinberg. 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 Steven J. Steinberg. The network helps show where Steven J. Steinberg may publish in the future.

Co-authorship network of co-authors of Steven J. Steinberg

This figure shows the co-authorship network connecting the top 25 collaborators of Steven J. Steinberg. A scholar is included among the top collaborators of Steven J. Steinberg 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 Steven J. Steinberg. Steven J. Steinberg 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

Biase, Irene De, Silvia Tortorelli, Lisa E. Kratz, et al.. (2019). Laboratory diagnosis of disorders of peroxisomal biogenesis and function: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 22(4). 686–697. 14 indexed citations

Arnold, Benjamin F., Kenneth Schiff, Ayşe Ercümen, et al.. (2017). Acute Illness Among Surfers After Exposure to Seawater in Dry- and Wet-Weather Conditions. American Journal of Epidemiology. 186(7). 866–875. 53 indexed citations

Falkenberg, Kim D., Nancy Braverman, Ann B. Moser, et al.. (2017). Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder. The American Journal of Human Genetics. 101(6). 965–976. 34 indexed citations

Wang, Xiao Ming, Peilin Zhang, Wange Lu, et al.. (2015). Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities. Stem Cell Research & Therapy. 6(1). 158–158. 11 indexed citations

Tran, Christel, Stacy Hewson, Steven J. Steinberg, & Saadet Mercimek‐Mahmutoglu. (2014). Late-Onset Zellweger Spectrum Disorder Caused by PEX6 Mutations Mimicking X-Linked Adrenoleukodystrophy. Pediatric Neurology. 51(2). 262–265. 17 indexed citations

Nielsen, Dahlia M., Andrew Singleton, Noriko Tonomura, et al.. (2014). Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24. PLoS Genetics. 10(2). e1003991–e1003991. 35 indexed citations

Lévesque, Sébastien, Charles Morin, Simon‐Pierre Guay, et al.. (2012). A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population. BMC Medical Genetics. 13(1). 72–72. 31 indexed citations

Moser, Ann B., Steven J. Steinberg, Paul A. Watkins, et al.. (2011). Human and great ape red blood cells differ in plasmalogen levels and composition. Lipids in Health and Disease. 10(1). 101–101. 27 indexed citations

Wang, Ying, Catherine Reeves, Lena Bezman, et al.. (2011). X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism. Molecular Genetics and Metabolism. 104(1-2). 160–166. 32 indexed citations

10.

Newman, Jennifer, et al.. (2009). A framework using service oriented architecture in a community information and referral system. Journal of computing sciences in colleges. 24(4). 252–258. 3 indexed citations

11.

Braverman, Nancy, Rui Zhang, Li Chen, et al.. (2009). A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton. Molecular Genetics and Metabolism. 99(4). 408–416. 51 indexed citations

12.

Cost, Nicholas G., Aaron T. Ludwig, Duncan T. Wilcox, et al.. (2009). A novel SOX9 mutation, 972delC, causes 46,XY sex-reversed campomelic dysplasia with nephrocalcinosis, urolithiasis, and dysgerminoma. Journal of Pediatric Surgery. 44(2). 451–454. 7 indexed citations

13.

Steinberg, Steven J., et al.. (2008). Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders. Human Mutation. 30(3). E467–E480. 56 indexed citations

14.

Boyle, Sarah A., Malini Seth, Hewang Li, et al.. (2006). Bap31 Enhances the Endoplasmic Reticulum Export and Quality Control of Human Class I MHC Molecules. The Journal of Immunology. 177(9). 6172–6181. 56 indexed citations

15.

Bryan, Jeffrey N., Carolyn J. Henry, Susan E. Turnquist, et al.. (2006). Primary Renal Neoplasia of Dogs. Journal of Veterinary Internal Medicine. 20(5). 1155–1155. 55 indexed citations

16.

Steinberg, Steven J., Gabriele Dodt, Gerald V. Raymond, et al.. (2006). Peroxisome biogenesis disorders. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1763(12). 1733–1748. 379 indexed citations

17.

Steinberg, Steven J., Li Chen, Ann B. Moser, et al.. (2004). The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum. Molecular Genetics and Metabolism. 83(3). 252–263. 91 indexed citations

18.

Corzo, Deyanira, William T. Gibson, Grant A. Mitchell, et al.. (2002). Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders. The American Journal of Human Genetics. 70(6). 1520–1531. 50 indexed citations

19.

Steinberg, Steven J., et al.. (1999). Human Very-Long-Chain Acyl-CoA Synthetase: Cloning, Topography, and Relevance to Branched-Chain Fatty Acid Metabolism. Biochemical and Biophysical Research Communications. 257(2). 615–621. 123 indexed citations

20.

Steinberg, Steven J., Stephan Kemp, Lelita T. Braiterman, & Paul A. Watkins. (1999). Role of very-long-chain acyl-coenzyme A synthetase in X-linked adrenoleukodystrophy. Annals of Neurology. 46(3). 409–412. 33 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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