Michael J. Kern

2.1k total citations
36 papers, 1.6k citations indexed

About

Michael J. Kern is a scholar working on Molecular Biology, Rheumatology and Genetics. According to data from OpenAlex, Michael J. Kern has authored 36 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 8 papers in Rheumatology and 8 papers in Genetics. Recurrent topics in Michael J. Kern's work include Developmental Biology and Gene Regulation (11 papers), Congenital heart defects research (5 papers) and Osteoarthritis Treatment and Mechanisms (5 papers). Michael J. Kern is often cited by papers focused on Developmental Biology and Gene Regulation (11 papers), Congenital heart defects research (5 papers) and Osteoarthritis Treatment and Mechanisms (5 papers). Michael J. Kern collaborates with scholars based in United States, Australia and Japan. Michael J. Kern's co-authors include Russell A. Norris, DP Turner, Ricardo A. Moreno‐Rodriguez, Corey H. Mjaatvedt, Takashi Nakaoka, Roger R. Markwald, Carol A. Eisenberg, S. Steven Potter, James F. Martin and Eric A. Argào and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and The Journal of Cell Biology.

In The Last Decade

Michael J. Kern

36 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael J. Kern United States 22 1.2k 279 234 194 149 36 1.6k
Mark J. Solloway United States 20 2.0k 1.7× 566 2.0× 252 1.1× 285 1.5× 105 0.7× 23 2.4k
Sonia Bartunkova Belgium 13 949 0.8× 212 0.8× 142 0.6× 93 0.5× 75 0.5× 15 1.2k
Kristine S. Vogel United States 16 845 0.7× 142 0.5× 183 0.8× 183 0.9× 285 1.9× 26 1.9k
Alessandra Maugeri Netherlands 20 1.2k 1.0× 674 2.4× 108 0.5× 172 0.9× 247 1.7× 43 1.9k
Emil M. Hansson Sweden 21 1.6k 1.4× 144 0.5× 105 0.4× 252 1.3× 126 0.8× 30 2.5k
Marko Uutela Finland 11 998 0.8× 227 0.8× 76 0.3× 118 0.6× 173 1.2× 13 1.8k
Kyungmin Hahm United States 20 1.6k 1.3× 270 1.0× 113 0.5× 210 1.1× 286 1.9× 24 3.0k
Nina Schumacher Germany 15 866 0.7× 148 0.5× 85 0.4× 165 0.9× 80 0.5× 24 1.2k
Liesbeth van Iperen Netherlands 22 813 0.7× 151 0.5× 128 0.5× 80 0.4× 111 0.7× 29 1.3k
Hosung Min United States 9 1.5k 1.3× 211 0.8× 65 0.3× 169 0.9× 277 1.9× 12 2.1k

Countries citing papers authored by Michael J. Kern

Since Specialization
Citations

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

Fields of papers citing papers by Michael J. Kern

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael J. Kern

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

All Works

20 of 20 papers shown
1.
Wu, Yongren, Matthew C. Coombs, Feng Wei, et al.. (2019). Effect of Sustained Joint Loading on TMJ Disc Nutrient Environment. Journal of Dental Research. 98(8). 888–895. 18 indexed citations
2.
Patel, Yogin, Alexander Awgulewitsch, Michael J. Kern, et al.. (2018). Overexpression of miR-489 derails mammary hierarchy structure and inhibits HER2/neu-induced tumorigenesis. Oncogene. 38(3). 445–453. 17 indexed citations
3.
Wright, Gregory J., Matthew C. Coombs, Yongren Wu, et al.. (2017). Electrical Conductivity Method to Determine Sexual Dimorphisms in Human Temporomandibular Disc Fixed Charge Density. Annals of Biomedical Engineering. 46(2). 310–317. 9 indexed citations
4.
Zhang, Lixin, et al.. (2015). The effects of oxygen level and glucose concentration on the metabolism of porcine TMJ disc cells. Osteoarthritis and Cartilage. 23(10). 1790–1796. 24 indexed citations
5.
Potter, Christopher J., Michael J. Kern, Nathanael Pruett, et al.. (2015). Dysregulated expression of sterol O-acyltransferase 1 (Soat1) in the hair shaft of Hoxc13 null mice. Experimental and Molecular Pathology. 99(3). 441–444. 5 indexed citations
6.
Potter, Christopher J., Nathanael Pruett, Michael J. Kern, et al.. (2010). The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation. Journal of Investigative Dermatology. 131(4). 828–837. 57 indexed citations
7.
Alderson, Nathan L., Eduardo N. Maldonado, Michael J. Kern, Narayan R. Bhat, & Hiroko Hama. (2006). FA2H-dependent fatty acid 2-hydroxylation in postnatal mouse brain. Journal of Lipid Research. 47(12). 2772–2780. 46 indexed citations
8.
Potter, Christopher J., Ron Peterson, Jeremy L. Barth, et al.. (2006). Evidence That the Satin Hair Mutant Gene Foxq1 Is among Multiple and Functionally Diverse Regulatory Targets for Hoxc13 during Hair Follicle Differentiation. Journal of Biological Chemistry. 281(39). 29245–29255. 59 indexed citations
9.
Peterson, Richard E., Stanley Hoffman, & Michael J. Kern. (2005). Opposing roles of two isoforms of the Prx1 homeobox gene in chondrogenesis. Developmental Dynamics. 233(3). 811–821. 22 indexed citations
10.
Norris, Russell A., et al.. (2003). GeneChip Microarrays Facilitate Identification of Protease Nexin-1 as a Target Gene of the Prx2 (S8) Homeoprotein. DNA and Cell Biology. 22(2). 95–105. 6 indexed citations
11.
Norris, Russell A. & Michael J. Kern. (2001). Identification of Domains Mediating Transcription Activation, Repression, and Inhibition in the Paired-Related Homeobox Protein, Prx2 (S8). DNA and Cell Biology. 20(2). 89–99. 38 indexed citations
12.
Norris, Russell A. & Michael J. Kern. (2001). The Identification of Prx1 Transcription Regulatory Domains Provides a Mechanism for Unequal Compensation by thePrx1 and Prx2 Loci. Journal of Biological Chemistry. 276(29). 26829–26837. 48 indexed citations
13.
Peterson, Richard E., et al.. (2001). Investigation of Prx1 protein expression provides evidence for conservation of cardiac‐specific posttranscriptional regulation in vertebrates. Developmental Dynamics. 222(3). 459–470. 16 indexed citations
14.
Kern, Michael J., et al.. (2001). Comparative analysis of Prx1 and Prx2 expression in mice provides evidence for incomplete compensation. The Anatomical Record. 266(1). 1–4. 15 indexed citations
15.
Mjaatvedt, Corey H., Takashi Nakaoka, Ricardo A. Moreno‐Rodriguez, et al.. (2001). The Outflow Tract of the Heart Is Recruited from a Novel Heart-Forming Field. Developmental Biology. 238(1). 97–109. 421 indexed citations
16.
Norris, Russell A., Clara S. Moore, Gail Stetten, et al.. (2000). Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome. Mammalian Genome. 11(11). 1000–1005. 40 indexed citations
17.
Bergwerff, Maarten, Adriana C. Gittenberger–de Groot, Lambertus J. Wisse, et al.. (2000). Loss of function of the Prx1 and Prx2 homeobox genes alters architecture of the great elastic arteries and ductus arteriosus. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 436(1). 12–19. 68 indexed citations
18.
Argào, Eric A., Michael J. Kern, William W. Branford, William J. Scott, & S. Steven Potter. (1995). Malformations of the heart, kidney, palate, and skeleton in α-MHC-Hoxb-7 transgenic mice. Mechanisms of Development. 52(2-3). 291–303. 23 indexed citations
19.
Kern, Michael J., Eric A. Argào, & S. Steven Potter. (1995). Homeobox genes and heart development. Trends in Cardiovascular Medicine. 5(2). 47–54. 25 indexed citations
20.
Kern, Michael J. & Jerold G. Woodward. (1991). The Same CCAAT Box-Binding Factor Binds to the Promoter of Two Coordinately Regulated Major Histocompatibility Complex Class II Genes. Molecular and Cellular Biology. 11(1). 578–581. 5 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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