Amanda Gerard

504 total citations
8 papers, 49 citations indexed

About

Amanda Gerard is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Amanda Gerard has authored 8 papers receiving a total of 49 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Amanda Gerard's work include BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (1 paper). Amanda Gerard is often cited by papers focused on BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (1 paper). Amanda Gerard collaborates with scholars based in United States, Hong Kong and Canada. Amanda Gerard's co-authors include Rebecca O. Littlejohn, Hadley Stevens Smith, Haley Streff, Andrea M. Lewis, S. Shahrukh Hashmi, Blair Stevens, Kimberly Nugent, Sarah Noblin, Katie Bergstrom and William Mattox and has published in prestigious journals such as Genetics in Medicine, American Journal of Medical Genetics Part A and Journal of Genetic Counseling.

In The Last Decade

Amanda Gerard

5 papers receiving 48 citations

Peers

Amanda Gerard

GENET

MB

PPCH

CN

GS

Lyndon Gallacher Australia

Julie McCarrier United States

Frederico Monfardini Brazil

Lauren K. Walsh United States

Emily Glanton United States

Alyssa Blesson United States

Caroline McGowan United States

Mattia Cordioli Finland

Cassandra Runke United States

Uma Mallya United Kingdom

Lyndon Gallacher Australia

Amanda Gerard

52 ×1.4

GENET

15 ×1.2

MB

19 ×1.9

PPCH

5 ×0.6

CN

0 ×0.0

GS

Citations per year, relative to Amanda Gerard Amanda Gerard (= 1×) peers Lyndon Gallacher

Countries citing papers authored by Amanda Gerard

Since Specialization

Citations

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

Fields of papers citing papers by Amanda Gerard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Gerard

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

All Works

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8 of 8 papers shown

1.

Gerard, Amanda, Carrie Mohila, Jill V. Hunter, et al.. (2024). Intracranial calcifications simulating Aicardi‐Goutières syndrome in PARS2‐related mitochondrial disease. American Journal of Medical Genetics Part A. 194(7). e63589–e63589. 1 indexed citations

2.

Morrow, Michelle, Erin Torti, Kirsty McWalter, et al.. (2024). MGA-related syndrome: A proposed novel disorder. Human Genetics and Genomics Advances. 6(1). 100387–100387.

3.

Streff, Haley, et al.. (2022). Access to clinically indicated genetic tests for pediatric patients with Medicaid: Evidence from outpatient genetics clinics in Texas. Genetics in Medicine. 25(3). 100350–100350. 4 indexed citations

4.

Streff, Haley, et al.. (2022). eP517: Differences in genetic testing uptake in a large metropolitan pediatric outpatient genetics clinic over time. Genetics in Medicine. 24(3). S330–S330.

5.

Zhao, Xiaonan, Amanda Gerard, Fernando Scaglia, et al.. (2022). Evidence for an association between Coffin‐Siris syndrome and congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 188(9). 2718–2723.

6.

Rosenfeld, Jill A., Lauren Westerfield, Amanda Gerard, et al.. (2021). Clinical characterization of individuals with the distal 1q21.1 microdeletion. American Journal of Medical Genetics Part A. 185(5). 1388–1398. 13 indexed citations

7.

Smith, Hadley Stevens, Andrea M. Lewis, Amanda Gerard, et al.. (2021). Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics. Genetics in Medicine. 23(5). 950–955. 19 indexed citations

8.

Gerard, Amanda, Sarah Noblin, S. Shahrukh Hashmi, et al.. (2018). Undergraduate Student Perceptions and Awareness of Genetic Counseling. Journal of Genetic Counseling. 28(1). 27–39. 12 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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