Eleanor Feingold

12.3k total citations
185 papers, 5.6k citations indexed

About

Eleanor Feingold is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eleanor Feingold has authored 185 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 106 papers in Genetics, 76 papers in Molecular Biology and 26 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eleanor Feingold's work include Genetic Associations and Epidemiology (35 papers), Genetic Mapping and Diversity in Plants and Animals (30 papers) and Genomic variations and chromosomal abnormalities (26 papers). Eleanor Feingold is often cited by papers focused on Genetic Associations and Epidemiology (35 papers), Genetic Mapping and Diversity in Plants and Animals (30 papers) and Genomic variations and chromosomal abnormalities (26 papers). Eleanor Feingold collaborates with scholars based in United States, Taiwan and United Kingdom. Eleanor Feingold's co-authors include Stephanie L. Sherman, George C. Tseng, Debashis Ghosh, John R. Shaffer, Mary L. Marazita, David Siegmund, Patrick O. Brown, Daniel E. Weeks, M. Ilyas Kamboh and Robert E. Ferrell and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Circulation.

In The Last Decade

Eleanor Feingold

181 papers receiving 5.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eleanor Feingold United States 38 2.3k 2.2k 791 611 542 185 5.6k
Jeffrey M. Craig Australia 52 1.8k 0.8× 4.8k 2.2× 2.1k 2.7× 539 0.9× 845 1.6× 185 8.2k
Liborio Stuppia Italy 40 1.7k 0.7× 2.4k 1.1× 904 1.1× 447 0.7× 713 1.3× 325 6.0k
Apiwat Mutirangura Thailand 42 1.3k 0.6× 3.4k 1.6× 602 0.8× 367 0.6× 162 0.3× 211 5.7k
Yukinori Okada Japan 43 3.1k 1.4× 2.2k 1.0× 257 0.3× 509 0.8× 305 0.6× 171 7.5k
Jean‐Jacques Cassiman Belgium 37 990 0.4× 2.0k 0.9× 280 0.4× 450 0.7× 491 0.9× 185 4.9k
Holly K. Tabor United States 30 2.8k 1.2× 2.4k 1.1× 495 0.6× 390 0.6× 476 0.9× 62 6.0k
Jane Worthington United Kingdom 56 1.9k 0.9× 1.8k 0.8× 104 0.1× 499 0.8× 226 0.4× 215 9.7k
Hans Eiberg Denmark 48 2.0k 0.9× 3.9k 1.8× 410 0.5× 634 1.0× 172 0.3× 196 7.4k
Bryan Howie United States 15 4.5k 2.0× 2.6k 1.2× 245 0.3× 416 0.7× 284 0.5× 17 7.6k
Lisa F. Barcellos United States 49 1.3k 0.6× 2.2k 1.0× 400 0.5× 376 0.6× 479 0.9× 157 8.1k

Countries citing papers authored by Eleanor Feingold

Since Specialization
Citations

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

Fields of papers citing papers by Eleanor Feingold

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eleanor Feingold. 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 Eleanor Feingold. The network helps show where Eleanor Feingold may publish in the future.

Co-authorship network of co-authors of Eleanor Feingold

This figure shows the co-authorship network connecting the top 25 collaborators of Eleanor Feingold. A scholar is included among the top collaborators of Eleanor Feingold 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 Eleanor Feingold. Eleanor Feingold 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.
Snitz, Beth E., Mary Ganguli, Steven T. DeKosky, et al.. (2023). Meta‐analysis of age‐related cognitive decline reveals a novel locus for the attention domain and implicates a COVID‐19‐related gene for global cognitive function. Alzheimer s & Dementia. 19(11). 5010–5022. 5 indexed citations
2.
Gorijala, Priyanka, Muhammad Aslam, Laura Xicota, et al.. (2023). Alzheimer's polygenic risk scores are associated with cognitive phenotypes in Down syndrome. Alzheimer s & Dementia. 20(2). 1038–1049. 4 indexed citations
3.
Orlova, Ekaterina, Tom Dudding, Simon Haworth, et al.. (2022). Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study. Genes. 14(1). 59–59. 10 indexed citations
4.
Yan, Qi, Kwangsik Nho, Jorge L. Del‐Aguila, et al.. (2018). Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging. Digital Commons@Becker (Washington University School of Medicine). 1 indexed citations
5.
Carlson, Jenna C., Margaret A. Taub, Eleanor Feingold, et al.. (2017). Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. Birth Defects Research. 109(13). 1030–1038. 32 indexed citations
6.
Leslie, Elizabeth J., Jenna C. Carlson, John R. Shaffer, et al.. (2017). Association studies of low‐frequency coding variants in nonsyndromic cleft lip with or without cleft palate. American Journal of Medical Genetics Part A. 173(6). 1531–1538. 30 indexed citations
7.
Herazo‐Maya, Jose D., Imre Noth, Steven R. Duncan, et al.. (2013). Peripheral Blood Mononuclear Cell Gene Expression Profiles Predict Poor Outcome in Idiopathic Pulmonary Fibrosis. Science Translational Medicine. 5(205). 205ra136–205ra136. 194 indexed citations
8.
Wang, Quan, Peilin Jia, Karen T. Cuenco, et al.. (2013). Multi-Dimensional Prioritization of Dental Caries Candidate Genes and Its Enriched Dense Network Modules. PLoS ONE. 8(10). e76666–e76666. 23 indexed citations
9.
Finegold, David N., Catherine J. Baty, Sarah E. Noon, et al.. (2012). Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment. Clinical Cancer Research. 18(8). 2382–2390. 85 indexed citations
10.
Shaffer, John R., Eleanor Feingold, Xiaojing Wang, et al.. (2012). Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses. BMC Oral Health. 12(1). 7–7. 29 indexed citations
11.
D’Angelo, Gina, M. Ilyas Kamboh, & Eleanor Feingold. (2010). A Likelihood-Based Approach for Missing Genotype Data. Human Heredity. 69(3). 171–183. 2 indexed citations
12.
Mukhopadhyay, Indranil, Eleanor Feingold, Daniel E. Weeks, & Anbupalam Thalamuthu. (2009). Association tests using kernel‐based measures of multi‐locus genotype similarity between individuals. Genetic Epidemiology. 34(3). 213–221. 61 indexed citations
13.
Bhattacharjee, Samsiddhi, et al.. (2006). The elusive goal of pedigree weights. Genetic Epidemiology. 31(1). 51–65. 5 indexed citations
14.
Sundar, Purnima, Eleanor Feingold, Ryan L. Minster, Steven T. DeKosky, & M. Ilyas Kamboh. (2006). Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease. Neurobiology of Aging. 28(6). 856–862. 64 indexed citations
15.
Corcoran, David L., Eleanor Feingold, & Panayiotis V. Benos. (2005). FOOTER: a web tool for finding mammalian DNA regulatory regions using phylogenetic footprinting. Nucleic Acids Research. 33(Web Server). W442–W446. 22 indexed citations
16.
Szatkiewicz, Jin & Eleanor Feingold. (2004). A Powerful and Robust New Linkage Statistic for Discordant Sibling Pairs. The American Journal of Human Genetics. 75(5). 906–909. 6 indexed citations
17.
Cuenco, Karen T., Jin Szatkiewicz, & Eleanor Feingold. (2003). Recent Advances in Human Quantitative-Trait–Locus Mapping: Comparison of Methods for Selected Sibling Pairs. The American Journal of Human Genetics. 73(4). 863–873. 25 indexed citations
18.
Forrest, William F. & Eleanor Feingold. (2000). Composite Statistics for QTL Mapping with Moderately Discordant Sibling Pairs. The American Journal of Human Genetics. 66(5). 1642–1660. 37 indexed citations
19.
Lamb, Neil E., et al.. (1994). Increased disomic homozygosity in the telomeric region of chromosome 21 among Down Syndrome individuals with duodenal atresia. The American Journal of Human Genetics. 55. 1 indexed citations
20.
Feingold, Eleanor. (1993). Modeling a new genetic mapping method. UMI eBooks. 1 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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