Susan Rojahn

617 total citations · 1 hit paper
13 papers, 263 citations indexed

About

Susan Rojahn is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Cancer Research. According to data from OpenAlex, Susan Rojahn has authored 13 papers receiving a total of 263 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Cardiology and Cardiovascular Medicine and 3 papers in Cancer Research. Recurrent topics in Susan Rojahn's work include Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Susan Rojahn is often cited by papers focused on Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Susan Rojahn collaborates with scholars based in United States, Chile and Japan. Susan Rojahn's co-authors include Robert L. Nussbaum, Kathryn E. Hatchell, Karen Ouyang, Swaroop Aradhya, Britt Johnson, Rebecca Truty, Ana Morales, Sulagna C. Saitta, Edward D. Esplin and Shivani Nazareth and has published in prestigious journals such as Circulation, The American Journal of Human Genetics and Obstetrics and Gynecology.

In The Last Decade

Susan Rojahn

12 papers receiving 262 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing

2023 78 citations Elaine Chen, Flavia M. Facio et al. JAMA Network Open profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Susan Rojahn United States	8	137	79	49	33	21	13	263
Daniela Siváková Slovakia	11	170 1.2×	57 0.7×	53 1.1×	11 0.3×	34 1.6×	51	342
Giuseppina Casu Italy	8	192 1.4×	96 1.2×	21 0.4×	12 0.4×	16 0.8×	13	325
Kathryn E. Hatchell United States	10	207 1.5×	124 1.6×	37 0.8×	82 2.5×	25 1.2×	40	402
Diptavo Dutta United States	8	153 1.1×	111 1.4×	19 0.4×	13 0.4×	21 1.0×	17	291
Xianghong Hu China	7	136 1.0×	86 1.1×	17 0.3×	27 0.8×	30 1.4×	7	263
Sophie Eichenbaum‐Voline France	7	50 0.4×	53 0.7×	72 1.5×	24 0.7×	74 3.5×	11	231
Paul Brennan United Kingdom	10	76 0.6×	124 1.6×	118 2.4×	7 0.2×	24 1.1×	22	331
Amitabh Sharma United Kingdom	2	223 1.6×	75 0.9×	139 2.8×	17 0.5×	104 5.0×	4	390
Bastian Salewsky Germany	11	49 0.4×	148 1.9×	31 0.6×	25 0.8×	57 2.7×	15	298
Amanda Dobbyn United States	7	81 0.6×	128 1.6×	37 0.8×	22 0.7×	25 1.2×	11	262

Countries citing papers authored by Susan Rojahn

Since Specialization

Citations

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

Fields of papers citing papers by Susan Rojahn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Rojahn

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

All Works

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13 of 13 papers shown

Brimble, Elise, et al.. (2024). Validation and clinical discovery demonstration of breast cancer data from a real-world data extraction platform. JAMIA Open. 7(2).

Truty, Rebecca, Susan Rojahn, Karen Ouyang, et al.. (2023). Patterns of mosaicism for sequence and copy-number variants discovered through clinical deep sequencing of disease-related genes in one million individuals. The American Journal of Human Genetics. 110(4). 551–564. 8 indexed citations

Morales, Ana, Ren Sheng, Thomas E. Callis, et al.. (2023). Real-World Genetic Testing Utilization Among Patients With Cardiomyopathy. Circulation Genomic and Precision Medicine. 17(1). e004028–e004028. 2 indexed citations

Chen, Elaine, Flavia M. Facio, Susan Rojahn, et al.. (2023). Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing. JAMA Network Open. 6(10). e2339571–e2339571. 78 indexed citations breakdown →

Heald, Brandie, Sarah M. Nielsen, Susan Rojahn, et al.. (2022). Unexpected actionable genetic variants revealed by multigene panel testing of patients with uterine cancer. Gynecologic Oncology. 166(2). 344–350. 7 indexed citations

Johnson, Britt, Karen Ouyang, Lauren B. Frank, et al.. (2022). Systematic use of phenotype evidence in clinical genetic testing reduces the frequency of variants of uncertain significance. American Journal of Medical Genetics Part A. 188(9). 2642–2651. 14 indexed citations

Dellefave‐Castillo, Lisa, Allison L. Cirino, Thomas E. Callis, et al.. (2022). Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing. JAMA Cardiology. 7(9). 966–966. 36 indexed citations

Morales, Ana, Susan Rojahn, John Garcia, et al.. (2021). Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic Conditions. Pediatric Cardiology. 43(3). 616–623. 6 indexed citations

Nazareth, Shivani, et al.. (2021). Hereditary Cancer Risk Using a Genetic Chatbot Before Routine Care Visits. Obstetrics and Gynecology. 138(6). 860–870. 47 indexed citations

10.

Ashcraft, Kristine, et al.. (2021). Unmanaged Pharmacogenomic and Drug Interaction Risk Associations with Hospital Length of Stay among Medicare Advantage Members with COVID-19: A Retrospective Cohort Study. Journal of Personalized Medicine. 11(11). 1192–1192. 6 indexed citations

11.

Sheng, Ren, Joline Dalton, Taryn O. Hall, et al.. (2021). Abstract 10555: Genetic Testing Underutilization in Patients with Cardiomyopathy: A Real-World Data Analysis. Circulation. 144(Suppl_1). 3 indexed citations

12.

Sturm, Amy C., Rebecca Truty, Thomas E. Callis, et al.. (2021). Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis. JAMA Cardiology. 6(8). 902–902. 18 indexed citations

13.

Truty, Rebecca, Karen Ouyang, Susan Rojahn, et al.. (2021). Spectrum of splicing variants in disease genes and the ability of RNA analysis to reduce uncertainty in clinical interpretation. The American Journal of Human Genetics. 108(4). 696–708. 38 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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