Anna Morgan

5.2k total citations
84 papers, 801 citations indexed

About

Anna Morgan is a scholar working on Sensory Systems, Molecular Biology and General Health Professions. According to data from OpenAlex, Anna Morgan has authored 84 papers receiving a total of 801 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Sensory Systems, 22 papers in Molecular Biology and 13 papers in General Health Professions. Recurrent topics in Anna Morgan's work include Hearing, Cochlea, Tinnitus, Genetics (27 papers), Biochemical Analysis and Sensing Techniques (10 papers) and Connexins and lens biology (7 papers). Anna Morgan is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (27 papers), Biochemical Analysis and Sensing Techniques (10 papers) and Connexins and lens biology (7 papers). Anna Morgan collaborates with scholars based in Italy, United States and United Kingdom. Anna Morgan's co-authors include Paolo Gasparini, Giorgia Girotto, Diego Vozzi, Flavio Faletra, Gary E. Weissman, Joshua M. Liao, Krisda H. Chaiyachati, Angela D’Eustacchio, Pio D’Adamo and Eliza W. Kinsey and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Annals of Surgery.

In The Last Decade

Anna Morgan

73 papers receiving 776 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Morgan Italy 18 256 248 129 125 81 84 801
Hsiao‐Lin Hwa Taiwan 23 478 1.9× 98 0.4× 32 0.2× 294 2.4× 45 0.6× 106 1.6k
Min Jung Cho South Korea 17 100 0.4× 80 0.3× 100 0.8× 83 0.7× 104 1.3× 48 810
Rachel Fisher United States 14 367 1.4× 390 1.6× 46 0.4× 34 0.3× 130 1.6× 40 1.0k
P. Froggatt United Kingdom 19 424 1.7× 120 0.5× 84 0.7× 40 0.3× 30 0.4× 68 1.3k
Anne L. Matthews United States 13 42 0.2× 84 0.3× 59 0.5× 292 2.3× 14 0.2× 31 639
Ningdong Li China 10 187 0.7× 30 0.1× 54 0.4× 42 0.3× 64 0.8× 59 489
Ravikumar Balasubramanian United States 21 468 1.8× 56 0.2× 48 0.4× 423 3.4× 12 0.1× 58 1.5k
Alicia Wang United States 12 536 2.1× 40 0.2× 21 0.2× 12 0.1× 72 0.9× 28 904
Tara Rachakonda United States 8 89 0.3× 114 0.5× 19 0.1× 23 0.2× 37 0.5× 11 1.0k
Heather L. Burrows United States 15 217 0.8× 10 0.0× 47 0.4× 116 0.9× 7 0.1× 46 953

Countries citing papers authored by Anna Morgan

Since Specialization
Citations

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

Fields of papers citing papers by Anna Morgan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Morgan

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Morgan. A scholar is included among the top collaborators of Anna Morgan 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 Anna Morgan. Anna Morgan 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.
Kinsey, Eliza W., et al.. (2024). Patient-Portal Compared with Supplemental In-Office Tablet Screening for Health-Related Social Needs in Primary Care. Journal of General Internal Medicine. 39(13). 2425–2431. 2 indexed citations
2.
Lefebvre, Mathilde, Caterina Zanus, Irene Bruno, et al.. (2024). In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder. Biomolecules. 14(12). 1626–1626. 1 indexed citations
3.
Morgan, Anna, et al.. (2024). Cash Transfers and After-School Programs: A Randomized Controlled Trial for Young Men at Risk of Violence Exposure in Wilmington, Delaware. Journal of Urban Health. 101(3). 595–619. 1 indexed citations
4.
Spedicati, Beatrice, Anna Morgan, Stefania Lenarduzzi, et al.. (2023). Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort. Biomedicines. 11(8). 2122–2122. 7 indexed citations
5.
Stazio, Mariateresa Di, Caterina Zanus, Flavio Faletra, et al.. (2023). Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders. Genes. 14(2). 250–250. 3 indexed citations
6.
Tesolin, Paola, et al.. (2023). Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders. Audiology Research. 13(6). 989–995. 3 indexed citations
7.
Concas, Maria Pina, et al.. (2022). Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals. Foods. 11(5). 735–735. 3 indexed citations
8.
Spedicati, Beatrice, Anna Morgan, Giulia Pianigiani, et al.. (2022). Challenging Occam’s Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures. Genes. 13(11). 2023–2023. 9 indexed citations
9.
Tesolin, Paola, Francesca Bertinetto, Stefania Cappellani, et al.. (2022). High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of Personalized Medicine. 12(10). 1618–1618. 4 indexed citations
10.
Ciorba, Andrea, et al.. (2021). Non-Syndromic Sensorineural Prelingual and Postlingual Hearing Loss due to COL11A1 Gene Mutation. The Journal of International Advanced Otology. 17(1). 81–83.
11.
Concas, Maria Pina, Alessandra Minelli, Anna Morgan, et al.. (2021). Genetic Dissection of Temperament Personality Traits in Italian Isolates. Genes. 13(1). 4–4. 1 indexed citations
12.
Tesolin, Paola, Stefania Lenarduzzi, Eva Orzan, et al.. (2021). Pendred Syndrome, or Not Pendred Syndrome? That Is the Question. Genes. 12(10). 1569–1569. 6 indexed citations
13.
Spedicati, Beatrice, Massimiliano Cocca, Flavio Faletra, et al.. (2021). Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates. European Journal of Human Genetics. 29(8). 1272–1281. 3 indexed citations
14.
Concas, Maria Pina, Anna Morgan, A. Paul Nagtegaal, et al.. (2021). Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability. Genes. 12(8). 1228–1228. 4 indexed citations
15.
Tesolin, Paola, Anna Morgan, Michela Notarangelo, et al.. (2021). Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene. Genes. 12(7). 1043–1043. 4 indexed citations
16.
Morgan, Anna, Flavio Faletra, Martina La Bianca, et al.. (2021). There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss. Biomedicines. 10(1). 12–12. 2 indexed citations
17.
Cotner, Cody E., David Do, Suzanne McGettigan, et al.. (2021). Automated Text-Based Symptom Monitoring With Rapid Clinician Triage for Patients With Cancer and Suspected or Confirmed COVID-19. JCO Clinical Cancer Informatics. 5(5). 1134–1140. 1 indexed citations
18.
Morgan, Anna, Daniel C. Koboldt, Elizabeth S. Barrie, et al.. (2019). Mutations in PLS1 , encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss. Human Mutation. 40(12). 2286–2295. 15 indexed citations
19.
Stazio, Mariateresa Di, Chiara Collesi, Diego Vozzi, et al.. (2018). TBL1Y: a new gene involved in syndromic hearing loss. European Journal of Human Genetics. 27(3). 466–474. 15 indexed citations
20.
Morgan, Anna, Dragana Vuckovic, Navaneethakrishnan Krishnamoorthy, et al.. (2018). Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. European Journal of Human Genetics. 27(1). 70–79. 18 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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