Anne C. Madeo

1.4k total citations
20 papers, 549 citations indexed

About

Anne C. Madeo is a scholar working on Sensory Systems, Pediatrics, Perinatology and Child Health and Neurology. According to data from OpenAlex, Anne C. Madeo has authored 20 papers receiving a total of 549 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Sensory Systems, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Neurology. Recurrent topics in Anne C. Madeo's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Vestibular and auditory disorders (6 papers) and Ethics and Legal Issues in Pediatric Healthcare (5 papers). Anne C. Madeo is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), Vestibular and auditory disorders (6 papers) and Ethics and Legal Issues in Pediatric Healthcare (5 papers). Anne C. Madeo collaborates with scholars based in United States, France and Italy. Anne C. Madeo's co-authors include Andrew J. Griffith, Barbara B. Biesecker, Yandan Yang, Barbara A. Bernhardt, Robert J. Morell, Adelaida G. Filoteo, Alan R. Penheiter, Carmen C. Brewer, Ariel J. Caride and John T. Penniston and has published in prestigious journals such as New England Journal of Medicine, Applied and Environmental Microbiology and The Laryngoscope.

In The Last Decade

Anne C. Madeo

19 papers receiving 544 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne C. Madeo United States 12 277 232 131 92 86 20 549
Raye Lynn Alford United States 11 301 1.1× 318 1.4× 116 0.9× 104 1.1× 157 1.8× 29 675
Shannon Pryor United States 11 229 0.8× 110 0.5× 105 0.8× 82 0.9× 29 0.3× 23 402
Haya Levi Israel 12 393 1.4× 191 0.8× 97 0.7× 123 1.3× 14 0.2× 20 587
Caroline Fischer Germany 12 116 0.4× 96 0.4× 26 0.2× 40 0.4× 24 0.3× 19 517
Samuel Mawuli Adadey Ghana 11 133 0.5× 122 0.5× 46 0.4× 18 0.2× 31 0.4× 43 428
Ayesha Imtiaz Pakistan 8 145 0.5× 128 0.6× 55 0.4× 36 0.4× 18 0.2× 33 271
Mehdi Sadeghi Sweden 12 254 0.9× 194 0.8× 97 0.7× 58 0.6× 24 0.3× 28 503
Norio Kasai Japan 11 189 0.7× 106 0.5× 36 0.3× 48 0.5× 18 0.2× 25 353
С.А. Федорова Russia 12 119 0.4× 171 0.7× 67 0.5× 17 0.2× 308 3.6× 65 576
Karen A. Abrashkin United States 9 627 2.3× 191 0.8× 159 1.2× 140 1.5× 14 0.2× 13 914

Countries citing papers authored by Anne C. Madeo

Since Specialization
Citations

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

Fields of papers citing papers by Anne C. Madeo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne C. Madeo. 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 Anne C. Madeo. The network helps show where Anne C. Madeo may publish in the future.

Co-authorship network of co-authors of Anne C. Madeo

This figure shows the co-authorship network connecting the top 25 collaborators of Anne C. Madeo. A scholar is included among the top collaborators of Anne C. Madeo 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 Anne C. Madeo. Anne C. Madeo 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.
Madeo, Anne C., et al.. (2025). How women respond to uncertainty in the context of genetic screening: A qualitative analysis framed by the uncertainty tolerance model. Journal of Genetic Counseling. 34(5). e70110–e70110. 1 indexed citations
2.
Madeo, Anne C., et al.. (2024). Women’s preferences for genetic screening in routine care: A qualitative study. Patient Education and Counseling. 130. 108439–108439.
3.
Umstead, Kendall L., Sarah S. Kalia, Anne C. Madeo, et al.. (2018). Social comparisons and quality of life following a prostate cancer diagnosis. Journal of Psychosocial Oncology. 36(3). 350–363. 5 indexed citations
4.
Senter, Leigha, Robin L. Bennett, Anne C. Madeo, et al.. (2017). National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions. Journal of Genetic Counseling. 27(1). 9–15. 4 indexed citations
5.
Madeo, Anne C., Kenneth P. Tercyak, Beth A. Tarini, & Colleen M. McBride. (2013). Effects of Undergoing Multiplex Genetic Susceptibility Testing on Parent Attitudes towards Testing Their Children. Annals of Behavioral Medicine. 47(3). 388–394. 5 indexed citations
6.
Madeo, Anne C., et al.. (2013). Presented Abstracts from the Thirty Second Annual Education Conference of the National Society of Genetic Counselors (Anaheim, CA, October 2013). Journal of Genetic Counseling. 22(6). 925–1021. 1 indexed citations
7.
Chattaraj, Parna, Julie Muskett, Boris E. Shmukler, et al.. (2013). Use ofSLC26A4Mutation Testing for Unilateral Enlargement of the Vestibular Aqueduct. JAMA Otolaryngology–Head & Neck Surgery. 139(9). 907–907. 19 indexed citations
8.
Madeo, Anne C., et al.. (2012). Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions. American Journal of Medical Genetics Part A. 158A(8). 1877–1884. 57 indexed citations
9.
Heald, Brandie, et al.. (2012). Presented Abstracts from the Thirty First Annual Education Conference of the National Society of Genetic Counselors (Boston, MA, October 2012). Journal of Genetic Counseling. 21(6). 884–984. 1 indexed citations
10.
Madeo, Anne C., Barbara B. Biesecker, Campbell K. Brasington, Lori H. Erby, & Kathryn F. Peters. (2011). The relationship between the genetic counseling profession and the disability community: A commentary. American Journal of Medical Genetics Part A. 155(8). 1777–1785. 41 indexed citations
11.
Madeo, Anne C., Ani Manichaikul, James C. Reynolds, et al.. (2009). Evaluation of the Thyroid in Patients With Hearing Loss and Enlarged Vestibular Aqueducts. Archives of Otolaryngology - Head and Neck Surgery. 135(7). 670–670. 21 indexed citations
12.
King, Kelly, Byung Yoon Choi, Christopher Zalewski, et al.. (2009). SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct. The Laryngoscope. 120(2). 384–389. 64 indexed citations
13.
Peters, Linda, et al.. (2008). A locus for autosomal dominant progressive non‐syndromic hearing loss, DFNA27, is on chromosome 4q12‐13.1. Clinical Genetics. 73(4). 367–372. 14 indexed citations
14.
Makishima, Tomoko, Anne C. Madeo, Carmen C. Brewer, et al.. (2007). Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain. American Journal of Medical Genetics Part A. 143A(14). 1592–1598. 34 indexed citations
15.
Labay, Valentina, Gema Garrido, Anne C. Madeo, et al.. (2007). Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNASer(UCN) in sensorineural hearing loss. Clinical Genetics. 73(1). 50–54. 11 indexed citations
16.
Madeo, Anne C., Shannon Pryor, Carmen C. Brewer, et al.. (2006). Pendred Syndrome. Seminars in Hearing. 27(3). 160–170. 4 indexed citations
17.
Schultz, Julie M., Yandan Yang, Ariel J. Caride, et al.. (2005). Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2. New England Journal of Medicine. 352(15). 1557–1564. 138 indexed citations
18.
Pryor, Shannon, Gail J. Demmler, Anne C. Madeo, et al.. (2005). Investigation of the Role of Congenital Cytomegalovirus Infection in the Etiology of Enlarged Vestibular Aqueducts. Archives of Otolaryngology - Head and Neck Surgery. 131(5). 388–388. 15 indexed citations
19.
Ben‐Yosef, Tamar, Seth Ness, Anne C. Madeo, et al.. (2003). A Mutation ofPCDH15among Ashkenazi Jews with the Type 1 Usher Syndrome. New England Journal of Medicine. 348(17). 1664–1670. 71 indexed citations
20.

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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