Stephanie E. King

843 total citations
19 papers, 584 citations indexed

About

Stephanie E. King is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Stephanie E. King has authored 19 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Pediatrics, Perinatology and Child Health and 4 papers in Genetics. Recurrent topics in Stephanie E. King's work include Epigenetics and DNA Methylation (9 papers), Birth, Development, and Health (7 papers) and Stress Responses and Cortisol (3 papers). Stephanie E. King is often cited by papers focused on Epigenetics and DNA Methylation (9 papers), Birth, Development, and Health (7 papers) and Stress Responses and Cortisol (3 papers). Stephanie E. King collaborates with scholars based in United States, Canada and France. Stephanie E. King's co-authors include Michael K. Skinner, Daniel Beck, Eric Nilsson, Ingrid Sadler‐Riggleman, Margaux McBirney, Paul Winchester, Settara C. Chandrasekharappa, Millissia Ben Maamar, Francis S. Collins and Wendy L. Flejter and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Stephanie E. King

16 papers receiving 577 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stephanie E. King United States 11 298 146 137 89 83 19 584
Lucjusz Jakubowski Poland 14 129 0.4× 132 0.9× 207 1.5× 32 0.4× 97 1.2× 33 614
Edmundo Bonilla Mexico 15 159 0.5× 88 0.6× 238 1.7× 32 0.4× 81 1.0× 38 726
Cristián Sobarzo Argentina 14 126 0.4× 71 0.5× 112 0.8× 42 0.5× 71 0.9× 32 552
Aparna Mahakali Zama United States 9 188 0.6× 131 0.9× 318 2.3× 39 0.4× 32 0.4× 11 603
Leon J. S. Brokken Finland 17 217 0.7× 107 0.7× 492 3.6× 66 0.7× 21 0.3× 27 1.0k
Christine Kervarrec France 13 177 0.6× 43 0.3× 69 0.5× 100 1.1× 140 1.7× 14 499
Aurore Gély-Pernot France 13 356 1.2× 51 0.3× 81 0.6× 103 1.2× 106 1.3× 16 775
Luke Montrose United States 15 167 0.6× 106 0.7× 305 2.2× 68 0.8× 78 0.9× 25 565
Delphine Franssen Belgium 17 148 0.5× 149 1.0× 350 2.6× 35 0.4× 39 0.5× 30 791
Tanvi Doshi India 8 223 0.7× 113 0.8× 621 4.5× 118 1.3× 39 0.5× 9 830

Countries citing papers authored by Stephanie E. King

Since Specialization
Citations

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

Fields of papers citing papers by Stephanie E. King

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephanie E. King. 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 Stephanie E. King. The network helps show where Stephanie E. King may publish in the future.

Co-authorship network of co-authors of Stephanie E. King

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

All Works

19 of 19 papers shown
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King, Stephanie E., et al.. (2025). Prenatal maternal stress in rats alters the epigenetic and transcriptomic landscape of the maternal-fetal interface across four generations. Communications Biology. 8(1). 38–38. 4 indexed citations
4.
Nilsson, Eric, Margaux McBirney, Stephanie E. King, et al.. (2023). Multiple generation distinct toxicant exposures induce epigenetic transgenerational inheritance of enhanced pathology and obesity. Current Zoology. 9(1). dvad006–dvad006. 11 indexed citations
5.
King, Stephanie E., et al.. (2023). Environmental Enrichment Promotes Transgenerational Programming of Uterine Inflammatory and Stress Markers Comparable to Gestational Chronic Variable Stress. International Journal of Molecular Sciences. 24(4). 3734–3734. 9 indexed citations
6.
King, Stephanie E. & Michael K. Skinner. (2020). Epigenetic Transgenerational Inheritance of Obesity Susceptibility. Trends in Endocrinology and Metabolism. 31(7). 478–494. 94 indexed citations
7.
Nilsson, Eric, et al.. (2019). Assessment of Glyphosate Induced Epigenetic Transgenerational Inheritance of Pathologies and Sperm Epimutations: Generational Toxicology. Scientific Reports. 9(1). 6372–6372. 141 indexed citations
8.
Maamar, Millissia Ben, Stephanie E. King, Eric Nilsson, Daniel Beck, & Michael K. Skinner. (2019). Epigenetic transgenerational inheritance of parent-of-origin allelic transmission of outcross pathology and sperm epimutations. Developmental Biology. 458(1). 106–119. 33 indexed citations
9.
King, Stephanie E., Margaux McBirney, Daniel Beck, et al.. (2019). Sperm epimutation biomarkers of obesity and pathologies following DDT induced epigenetic transgenerational inheritance of disease. Current Zoology. 5(2). dvz008–dvz008. 41 indexed citations
10.
King, Stephanie E., Eric Nilsson, Daniel Beck, & Michael K. Skinner. (2019). Adipocyte epigenetic alterations and potential therapeutic targets in transgenerationally inherited lean and obese phenotypes following ancestral exposures. Adipocyte. 8(1). 362–378. 17 indexed citations
11.
Nilsson, Eric, Stephanie E. King, Margaux McBirney, et al.. (2018). Vinclozolin induced epigenetic transgenerational inheritance of pathologies and sperm epimutation biomarkers for specific diseases. PLoS ONE. 13(8). e0202662–e0202662. 63 indexed citations
12.
McBirney, Margaux, Stephanie E. King, Eric Nilsson, et al.. (2017). Atrazine induced epigenetic transgenerational inheritance of disease, lean phenotype and sperm epimutation pathology biomarkers. PLoS ONE. 12(9). e0184306–e0184306. 109 indexed citations
13.
Kim, Woo Kyun, et al.. (2016). A high-fat diet differentially regulates glutathione phenotypes in the obesity-prone mouse strains DBA/2J, C57BL/6J, and AKR/J. Nutrition Research. 36(12). 1316–1324. 16 indexed citations
14.
Bennett‐Baker, Pamela E., Settara C. Chandrasekharappa, Stephanie E. King, et al.. (1996). Isolation of Tetranucleotide Repeat Polymorphisms Flanking theBRCA1Gene. Genomics. 32(1). 163–167. 1 indexed citations
15.
Law, David, Stephanie E. King, Yoon Hee Lee, et al.. (1995). Localization of the Human Estrogen-Responsive Finger Protein (EFP) Gene (ZNF147) within a YAC Contig Containing the Myeloperoxidase (MPO) Gene. Genomics. 28(2). 361–363. 10 indexed citations
16.
Chandrasekharappa, Settara C., Lori S. Friedman, Stephanie E. King, et al.. (1994). The Gene for Pancreatic Polypeptide (PPY) and the Anonymous Marker D17S78 Are within 45 kb of Each Other on Chromosome 17q21. Genomics. 21(2). 458–460.
17.
Flejter, Wendy L., et al.. (1993). Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12–q22. Human Molecular Genetics. 2(7). 1080–1080. 10 indexed citations
18.
King, Stephanie E., et al.. (1993). The CA repeat marker D17S791 islocated within 40 kb of the WNT3 gene on chromosome 17q. Genomics. 18(3). 728–729. 2 indexed citations
19.
Chandrasekharappa, Settara C., et al.. (1993). The human NME2 gene lies within 18kb of NME1 in chromosome 17. Genes Chromosomes and Cancer. 6(4). 245–248. 23 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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