Charles E. Jackson

17.4k total citations · 4 hit papers
139 papers, 11.6k citations indexed

About

Charles E. Jackson is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Charles E. Jackson has authored 139 papers receiving a total of 11.6k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 27 papers in Oncology and 25 papers in Genetics. Recurrent topics in Charles E. Jackson's work include Neuroendocrine Tumor Research Advances (16 papers), Thyroid Cancer Diagnosis and Treatment (15 papers) and Parathyroid Disorders and Treatments (15 papers). Charles E. Jackson is often cited by papers focused on Neuroendocrine Tumor Research Advances (16 papers), Thyroid Cancer Diagnosis and Treatment (15 papers) and Parathyroid Disorders and Treatments (15 papers). Charles E. Jackson collaborates with scholars based in United States, Canada and United Kingdom. Charles E. Jackson's co-authors include Douglas A. Marchuk, Mary Porteous, Carol J. Gallione, David W. Johnson, Alan E. Guttmacher, M. A. Pericak‐Vance, Paul J. Goodfellow, Jonathan Berg, E.A. Helmbold and Dorene S. Markel and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Charles E. Jackson

135 papers receiving 11.0k 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.

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

1994 1.1k citations Kimberly A. McAllister, David W. Johnson et al. profile →
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

1996 846 citations David W. Johnson, Jonathan Berg et al. profile →
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

1995 774 citations Odile Broux, Nathalie Bourg et al. profile →
C-Cell Hyperplasia Preceding Medullary Thyroid Carcinoma

1973 348 citations Hubert J. Wolfe, Kenneth E. W. Melvin et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charles E. Jackson United States	51	4.8k	2.3k	2.2k	2.0k	2.0k	139	11.6k
Catharina Larsson Sweden	62	6.1k 1.3×	4.2k 1.8×	2.8k 1.3×	2.1k 1.0×	1.3k 0.6×	358	14.4k
Bruce G. Robinson Australia	56	3.4k 0.7×	2.2k 0.9×	1.6k 0.7×	3.0k 1.5×	1.3k 0.6×	227	11.3k
Robert M.W. Hofstra Netherlands	60	5.1k 1.1×	2.7k 1.2×	2.4k 1.1×	3.4k 1.7×	1.2k 0.6×	251	12.9k
Elaine Spector United States	26	10.1k 2.1×	1.2k 0.5×	9.0k 4.1×	1.7k 0.8×	1.5k 0.7×	71	20.6k
Sue Richards United Kingdom	33	9.6k 2.0×	1.7k 0.7×	8.7k 4.0×	1.6k 0.8×	1.6k 0.8×	85	22.4k
Lois M. Mulligan Canada	43	3.7k 0.8×	2.3k 1.0×	1.7k 0.8×	2.2k 1.1×	770 0.4×	125	8.3k
Virginia V. Michels United States	47	3.1k 0.7×	1.2k 0.5×	2.6k 1.2×	1.3k 0.6×	914 0.4×	148	9.1k
Richard C. Trembath United Kingdom	69	6.3k 1.3×	1.3k 0.6×	2.7k 1.2×	1.4k 0.7×	5.8k 2.8×	210	17.3k
Stephen J. Marx United States	70	3.9k 0.8×	5.7k 2.4×	2.9k 1.3×	2.1k 1.0×	1.5k 0.7×	272	15.1k
David Bick United States	31	10.4k 2.2×	1.2k 0.5×	10.3k 4.7×	1.7k 0.8×	1.5k 0.8×	83	22.0k

Countries citing papers authored by Charles E. Jackson

Since Specialization

Citations

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

Fields of papers citing papers by Charles E. Jackson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charles E. Jackson

This figure shows the co-authorship network connecting the top 25 collaborators of Charles E. Jackson. A scholar is included among the top collaborators of Charles E. Jackson 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 Charles E. Jackson. Charles E. Jackson 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

Nagaraj, Satish, et al.. (2008). Role of Nucleotide Binding in Septin-Septin Interactions and Septin Localization in Saccharomyces cerevisiae. Molecular and Cellular Biology. 28(16). 5120–5137. 40 indexed citations

Walt, Joelle M. van der, William K. Scott, Susan Slifer, et al.. (2005). Maternal lineages and Alzheimer disease risk in the Old Order Amish. Human Genetics. 118(1). 115–122. 24 indexed citations

Nakabayashi, Kazuhiko, Yan Ren, Ulpu Saarialho‐Kere, et al.. (2005). Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy. The American Journal of Human Genetics. 76(3). 510–516. 55 indexed citations

Lewis, Frank R., John D. Mellinger, Allen Hayashi, et al.. (2001). Prophylactic total gastrectomy for familial gastric cancer. Surgery. 130(4). 612–619. 100 indexed citations

Duclos, Franck, Odile Broux, Nathalie Bourg, et al.. (1998). β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. Neuromuscular Disorders. 8(1). 30–38. 43 indexed citations

Amato, Anthony A., et al.. (1997). Evaluation of Neuromuscular Symptoms in Veterans of the Persian Gulf War. Neurology. 48(1). 4–12. 78 indexed citations

Feldman, Gerald L., et al.. (1995). Relationship of Familial Prominent Corneal Nerves and Lesions of the Tongue Resembling Neuromas to Multiple Endocrine Neoplasia Type 2B. American Journal of Ophthalmology. 120(4). 456–461. 16 indexed citations

Johnson, David W., Jonathan Berg, Carol J. Gallione, et al.. (1995). A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.. Genome Research. 5(1). 21–28. 124 indexed citations

Kitamura, Yutaka, N J Scavarda, Samuel A. Wells, Charles E. Jackson, & Paul J. Goodfellow. (1995). Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B. Human Molecular Genetics. 4(10). 1987–1988. 33 indexed citations

10.

McAllister, Kimberly A., Felicia Lennon, Wendy McKinnon, et al.. (1994). Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.. Journal of Medical Genetics. 31(12). 927–932. 79 indexed citations

11.

Mulligan, Lois M., Charis Eng, Catherine S. Healey, et al.. (1994). A de novo mutation of the RET proto-oncogene in a patient with MEN 2A. Human Molecular Genetics. 3(6). 1007–1008. 23 indexed citations

12.

Gagel, Robert F., Charles E. Jackson, Bruce A.J. Ponder, et al.. (1989). Multiple Endocrine Neoplasia Type 2 Syndromes: Nomenclature Recommendations from the Workshop Organizing Committee. 37(3). 99. 4 indexed citations

13.

Gagel, Robert F., Charles E. Jackson, Melvin A. Block, et al.. (1982). Age-related probability of development of hereditary medullary thyroid carcinoma. The Journal of Pediatrics. 101(6). 941–946. 52 indexed citations

14.

Conneally, P.M., et al.. (1976). Linkage Relations of the Loci for Kell and Phenylthiocarbamide Taste Sensitivity. Human Heredity. 26(4). 267–271. 27 indexed citations

15.

Jackson, Charles E., et al.. (1976). Craniosynostosis, midfacial hypoplasia, and foot abnormalities: An autosomal dominant phenotype in a large Amish kindred. The Journal of Pediatrics. 88(6). 963–968. 67 indexed citations

16.

Wolfe, Hubert J., et al.. (1973). C-Cell Hyperplasia Preceding Medullary Thyroid Carcinoma. New England Journal of Medicine. 289(9). 437–441. 348 indexed citations breakdown →

17.

Jackson, Charles E., et al.. (1960). Inheritance of primary systemic amyloidosis.. PubMed. 12. 434–9. 12 indexed citations

18.

Jackson, Charles E., et al.. (1959). Inheritance of gall-bladder disease.. PubMed. 46. 853–7. 21 indexed citations

19.

Jackson, Charles E., et al.. (1958). Consanguinity in a midwestern United States isolate.. PubMed. 10(1). 61–3. 12 indexed citations

20.

Jackson, Charles E.. (1955). Nomogram for Simple Calculation of Cardiac Output. Circulation. 11(4). 635–636. 11 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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