Carol E. Anderson

1.9k total citations
45 papers, 1.2k citations indexed

About

Carol E. Anderson is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Carol E. Anderson has authored 45 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 13 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Carol E. Anderson's work include Diabetes and associated disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Pancreatic function and diabetes (4 papers). Carol E. Anderson is often cited by papers focused on Diabetes and associated disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Pancreatic function and diabetes (4 papers). Carol E. Anderson collaborates with scholars based in United States, France and Australia. Carol E. Anderson's co-authors include Michael Clare‐Salzler, Jerome I. Rotter, Katja Van Herle, Andrea Chai, Susan E. Hodge, David L. Rimoin, R.S. Sparkes, Katherine Neiswanger, D L Rimoin and Paul I. Terasaki and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Investigation and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Carol E. Anderson

45 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carol E. Anderson United States 20 563 364 270 248 180 45 1.2k
Boleslaw Goldman Israel 22 575 1.0× 746 2.0× 49 0.2× 161 0.6× 65 0.4× 74 1.7k
Géraldine Viot France 21 647 1.1× 674 1.9× 60 0.2× 144 0.6× 68 0.4× 56 1.4k
Sergio Aguilera Chile 24 175 0.3× 548 1.5× 311 1.2× 271 1.1× 93 0.5× 100 1.6k
P. Saccucci Italy 14 231 0.4× 271 0.7× 169 0.6× 58 0.2× 49 0.3× 65 670
Marie van Dijk Netherlands 21 129 0.2× 436 1.2× 290 1.1× 156 0.6× 124 0.7× 48 1.4k
Mei Baker United States 20 620 1.1× 418 1.1× 290 1.1× 84 0.3× 71 0.4× 58 1.4k
M Gautier France 16 498 0.9× 396 1.1× 61 0.2× 637 2.6× 51 0.3× 60 1.7k
Marte K. Viken Norway 20 343 0.6× 339 0.9× 498 1.8× 96 0.4× 56 0.3× 50 1.3k
Stephen R. Braddock United States 25 538 1.0× 525 1.4× 238 0.9× 240 1.0× 25 0.1× 71 1.7k
Henry T. Lau United States 15 253 0.4× 273 0.8× 262 1.0× 656 2.6× 81 0.5× 32 1.3k

Countries citing papers authored by Carol E. Anderson

Since Specialization
Citations

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

Fields of papers citing papers by Carol E. Anderson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carol E. Anderson

This figure shows the co-authorship network connecting the top 25 collaborators of Carol E. Anderson. A scholar is included among the top collaborators of Carol E. Anderson 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 Carol E. Anderson. Carol E. Anderson 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.
Imitola, Jaime, Carol E. Anderson, Reena Jethva, et al.. (2014). Fraternal Twins With Autism, Severe Cognitive Deficit, and Epilepsy: Diagnostic Role of Chromosomal Microarray Analysis. Seminars in Pediatric Neurology. 21(2). 167–171. 14 indexed citations
2.
Katsetos, Christos D., et al.. (2014). Brainstem Tegmental Necrosis and Olivary Hypoplasia: Raising Awareness of a Rare Neuropathologic Correlate of Congenital Apnea. Seminars in Pediatric Neurology. 21(2). 177–183. 1 indexed citations
3.
Anderson, Carol E., et al.. (2014). Co‐occurrence of non‐mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: Case report and review of the literature. American Journal of Medical Genetics Part A. 164(12). 3187–3193. 7 indexed citations
4.
Anderson, Carol E., et al.. (2010). Microarray Analysis in Children With Developmental Disorder or Epilepsy. Pediatric Neurology. 43(6). 391–394. 16 indexed citations
5.
Cushman, Lisa J., Wilfredo Torres‐Martinez, Athena M. Cherry, et al.. (2005). A report of three patients with an interstitial deletion of chromosome 15q24. American Journal of Medical Genetics Part A. 137A(1). 65–71. 27 indexed citations
6.
Anderson, Carol E., Hope H. Punnett, Vicki Huff, & Jean‐Pierre de Chadarévian. (2003). Characterization of a Wilms tumor in a 9‐year‐old girl with trisomy 18. American Journal of Medical Genetics Part A. 121A(1). 52–55. 19 indexed citations
7.
Newschaffer, Craig J., James Cocroft, Carol E. Anderson, Walter W. Hauck, & Barbara J. Turner. (2000). Prenatal Zidovudine Use and Congenital Anomalies in a Medicaid Population. JAIDS Journal of Acquired Immune Deficiency Syndromes. 24(3). 249–256. 28 indexed citations
8.
Wallerstein, Robert S., Jennifer Kacmar, Carol E. Anderson, & Laird Jackson. (1997). Dubowitz syndrome in a boy without developmental delay: Further evidence for phenotypic variability. American Journal of Medical Genetics. 68(2). 216–218. 1 indexed citations
9.
Anderson, Carol E., et al.. (1997). Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome. American Journal of Medical Genetics. 72(3). 281–285. 1 indexed citations
10.
Rabinowitz, Linda G., et al.. (1995). Painful keratoderma and photophobia: Hallmarks of tyrosinemia type II. The Journal of Pediatrics. 126(2). 266–269. 30 indexed citations
11.
Vabres, P., Didier Lacombe, Linda G. Rabinowitz, et al.. (1995). The Gene for Bazex-Dupré-Christol Syndrome Maps to Chromosome Xq. Journal of Investigative Dermatology. 105(1). 87–91. 41 indexed citations
12.
Anderson, Carol E., et al.. (1994). The natural history of euploid pregnancies with first-trimester cystic hygromas. American Journal of Obstetrics and Gynecology. 170(5). 1279–1284. 48 indexed citations
13.
Clare‐Salzler, Michael, et al.. (1992). Prevention of diabetes in nonobese diabetic mice by dendritic cell transfer.. Journal of Clinical Investigation. 90(3). 741–748. 179 indexed citations
14.
Spence, A. Michael, Mary L. Marazita, Maryellen C. Sparkes, et al.. (1984). Estimating the Recombination Frequency for the MN and the Ss Loci. Human Heredity. 34(6). 343–347. 2 indexed citations
15.
Anderson, Carol E., Jerry Z. Finklestein, Eliezer Nussbaum, et al.. (1984). Association of hemolytic anemia and early-onset pulmonary emphysema in three siblings. The Journal of Pediatrics. 105(2). 247–251. 6 indexed citations
16.
Sparkes, R S, Maryellen C. Sparkes, Michol Crist, & Carol E. Anderson. (1983). Glyoxalase I ?null? allele in a new family: Identification by abnormal segregation pattern and quantitative assay. Human Genetics. 64(2). 146–147. 5 indexed citations
17.
Grodsky, Gerold M., Carol E. Anderson, Douglas L. Coleman, et al.. (1982). Metabolic and Underlying Causes of Diabetes Mellitus. Diabetes. 31(Supplement_1). 45–53. 35 indexed citations
18.
Pang, Songya, L S Levine, Lars L. Cederqvist, et al.. (1980). Amniotic Fluid Concentrations of Δ5 and Δ4 Steroids in Fetuses with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Deficiency and in Anencephalic Fetuses*. The Journal of Clinical Endocrinology & Metabolism. 51(2). 223–229. 88 indexed citations
19.
Anderson, Carol E., Jerome I. Rotter, & Jonathan Zonana. (1978). Hereditary Considerations in Common Disorders. Pediatric Clinics of North America. 25(3). 539–556. 2 indexed citations
20.
Anderson, Carol E., Paul M. Fernhoff, & Linda Quan. (1977). Dominant polysyndactyly: A report of two families. The Journal of Pediatrics. 90(6). 961–962. 2 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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