Heather Zimmermann

580 total citations
5 papers, 21 citations indexed

About

Heather Zimmermann is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Heather Zimmermann has authored 5 papers receiving a total of 21 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Surgery. Recurrent topics in Heather Zimmermann's work include Dermatological and Skeletal Disorders (1 paper), Genomics and Rare Diseases (1 paper) and Cancer Genomics and Diagnostics (1 paper). Heather Zimmermann is often cited by papers focused on Dermatological and Skeletal Disorders (1 paper), Genomics and Rare Diseases (1 paper) and Cancer Genomics and Diagnostics (1 paper). Heather Zimmermann collaborates with scholars based in United States. Heather Zimmermann's co-authors include Huy Gia Vuong, Ashley Cass, Lily Hoang, J. Patel, Andrew M. Rosen, Arvind Narayana, Adam Chamberlin, Steven M. Harrison, Holly LaDuca and Rachid Karam and has published in prestigious journals such as SHILAP Revista de lepidopterología, JAMA Oncology and Genetics in Medicine.

In The Last Decade

Heather Zimmermann

2 papers receiving 21 citations

Peers

Heather Zimmermann

MB

GENET

PFM

CR

ONCOL

Davide Bondavalli Italy

Shanaka R. Gunawardena United States

AA Roger Thompson United Kingdom

Deirdre Donnelly United Kingdom

Mette Rasmussen Denmark

Milena Jakimovska North Macedonia

Erh‐Chan Yeh Taiwan

Ikhlas Ben Ayed Tunisia

Sarah K. Macklin‐Mantia United States

Davide Bondavalli Italy

Heather Zimmermann

15 ×1.1

MB

11 ×1.6

GENET

12 ×2.0

PFM

5 ×1.0

CR

4 ×1.3

ONCOL

Citations per year, relative to Heather Zimmermann Heather Zimmermann (= 1×) peers Davide Bondavalli

Countries citing papers authored by Heather Zimmermann

Since Specialization

Citations

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

Fields of papers citing papers by Heather Zimmermann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heather Zimmermann

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

All Works

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5 of 5 papers shown

1.

Towne, Meghan C., et al.. (2024). P644: Unlocking the code: When SpliceAI falls short in variant assessment. SHILAP Revista de lepidopterología. 2. 101550–101550.

2.

Horton, Carolyn, Lily Hoang, Heather Zimmermann, et al.. (2023). Diagnostic Outcomes of Concurrent DNA and RNA Sequencing in Individuals Undergoing Hereditary Cancer Testing. JAMA Oncology. 10(2). 212–212. 14 indexed citations

3.

Patel, J., et al.. (2022). Three Newly Recognized Likely Pathogenic Gene Variants Associated with Hereditary Transthyretin Amyloidosis. Neurology and Therapy. 11(4). 1595–1607. 7 indexed citations

4.

Horton, Carolyn, Lily Hoang, Min‐Tzu Lo, et al.. (2022). OP036: Application of RNA sequencing evidence improves equity in variant interpretation. Genetics in Medicine. 24(3). S363–S363.

5.

Zimmermann, Heather, et al.. (2022). RNA Studies Demonstrate that the LDLR c.2389+4A>G Intronic Variant Causes Familial Hypercholesterolemia through an RNA Splicing Impact. Journal of clinical lipidology. 16(1). e10–e10.

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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