Kelly E. Jackson

1.5k total citations
15 papers, 375 citations indexed

About

Kelly E. Jackson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Kelly E. Jackson has authored 15 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in Kelly E. Jackson's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Metabolism and Genetic Disorders (3 papers). Kelly E. Jackson is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Metabolism and Genetic Disorders (3 papers). Kelly E. Jackson collaborates with scholars based in United States, Italy and Netherlands. Kelly E. Jackson's co-authors include Melanie Ehrlich, Corry M.R. Weemaes, Alexander Asamoah, Gordon C. Gowans, Bassem A. Bejjani, Lisa G. Shaffer, Pamela Brock, Rebecca R. Selzer, Suneeta Madan‐Khetarpal and Joel Geoghegan and has published in prestigious journals such as Nature Genetics, Pain and Ophthalmology.

In The Last Decade

Kelly E. Jackson

15 papers receiving 365 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kelly E. Jackson United States 8 211 204 50 40 33 15 375
Filomena Tiziana Papa Italy 14 257 1.2× 182 0.9× 41 0.8× 37 0.9× 30 0.9× 26 412
Eleni Katzaki Italy 11 231 1.1× 148 0.7× 31 0.6× 36 0.9× 19 0.6× 11 316
Teresa Neuhann Germany 14 189 0.9× 215 1.1× 62 1.2× 9 0.2× 40 1.2× 38 425
Chad Haldeman‐Englert United States 11 204 1.0× 184 0.9× 50 1.0× 42 1.1× 19 0.6× 21 359
Anand Saggar United Kingdom 8 231 1.1× 280 1.4× 32 0.6× 8 0.2× 26 0.8× 15 415
Hannah Verdin Belgium 14 268 1.3× 317 1.6× 29 0.6× 36 0.9× 9 0.3× 29 467
Siren Berland Norway 11 207 1.0× 360 1.8× 51 1.0× 9 0.2× 38 1.2× 28 478
V Der Kaloustian United States 9 149 0.7× 296 1.5× 38 0.8× 24 0.6× 177 5.4× 14 553
Marie‐Claire Vincent France 10 247 1.2× 279 1.4× 62 1.2× 32 0.8× 28 0.8× 13 406
Linda Meredith United Kingdom 10 198 0.9× 347 1.7× 36 0.7× 99 2.5× 55 1.7× 15 595

Countries citing papers authored by Kelly E. Jackson

Since Specialization
Citations

This map shows the geographic impact of Kelly 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 Kelly 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 Kelly E. Jackson more than expected).

Fields of papers citing papers by Kelly E. Jackson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

15 of 15 papers shown
1.
Jackson, Kelly E., et al.. (2022). Newborn screening for Pompe disease: Parental experiences and follow‐up care for a late‐onset diagnosis. Journal of Genetic Counseling. 31(6). 1404–1420. 13 indexed citations
2.
Huang, Yue, Rajesh Sharma, Annette Feigenbaum, et al.. (2021). Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia. Molecular Genetics and Metabolism Reports. 27. 100735–100735. 7 indexed citations
3.
Asamoah, Alexander, et al.. (2021). Diagnosis of Classic Homocystinuria in Two Boys Presenting with Acute Cerebral Venous Thrombosis and Neurologic Dysfunction after Normal Newborn Screening. International Journal of Neonatal Screening. 7(3). 48–48. 4 indexed citations
4.
Bellacchio, Emanuele, Kelly E. Jackson, Alexander Asamoah, et al.. (2019). Heme and sensory neuropathy: insights from novel mutations in the heme exporter feline leukemia virus subgroup C receptor 1. Pain. 160(12). 2766–2775. 14 indexed citations
5.
Vanderver, Adeline, Davide Tonduti, Sarah Auerbach, et al.. (2012). Neurotransmitter abnormalities and response to supplementation in SPG11. Molecular Genetics and Metabolism. 107(1-2). 229–233. 11 indexed citations
6.
7.
McGoey, Robin, Kelly E. Jackson, & Michael Marble. (2008). 45,X/47,XX,+18 and ring (18) mosaicism with mild phenotypic features including normal stature: clinical report and review of the literature. Clinical Dysmorphology. 18(1). 59–61. 1 indexed citations
8.
Ballif, Blake C., Elizabeth S. Jenkins, Suneeta Madan‐Khetarpal, et al.. (2007). Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2. Nature Genetics. 39(9). 1071–1073. 140 indexed citations
9.
Ehrlich, Melanie, Kelly E. Jackson, & Corry M.R. Weemaes. (2006). Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF). Orphanet Journal of Rare Diseases. 1(1). 2–2. 94 indexed citations
10.
Morava, Éva, Kelly E. Jackson, Fern Tsien, & Michael Marble. (2004). Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies.. PubMed. 15(4). 449–53. 6 indexed citations
11.
Jackson, Kelly E., et al.. (2004). Focal skin defect, limb anomalies and microphthalmia. Clinical Dysmorphology. 13(2). 113–115. 1 indexed citations
12.
Krousel‐Wood, Marie, et al.. (2003). Physicians’ perceived usefulness of and satisfaction with test reports for cystic fibrosis (ΔF508) and factor V Leiden. Genetics in Medicine. 5(3). 166–171. 13 indexed citations
13.
Andersson, Hans C., Marie Krousel‐Wood, Kelly E. Jackson, Janet C. Rice, & Ira M. Lubin. (2002). Medical genetic test reporting for cystic fibrosis (ΔF508) and factor V Leiden in North American laboratories. Genetics in Medicine. 4(5). 324–327. 13 indexed citations
14.
Jackson, Kelly E., Fern Tsien, & Michael Marble. (2000). Phenotypic features in a boy with monosomy 18 mosaicism. American Journal of Medical Genetics. 95(3). 229–232. 3 indexed citations
15.
Gorin, Michael B., Kelly E. Jackson, Robert E. Ferrell, et al.. (1995). A Peripherin/Retinal Degeneration Slow Mutation (Pro-210-Arg) Associated with Macular and Peripheral Retinal Degeneration. Ophthalmology. 102(2). 246–255. 50 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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