Benjamin M. Helm

729 total citations
49 papers, 445 citations indexed

About

Benjamin M. Helm is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Benjamin M. Helm has authored 49 papers receiving a total of 445 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 19 papers in Molecular Biology and 14 papers in Epidemiology. Recurrent topics in Benjamin M. Helm's work include Congenital heart defects research (16 papers), Congenital Heart Disease Studies (14 papers) and Genomics and Rare Diseases (12 papers). Benjamin M. Helm is often cited by papers focused on Congenital heart defects research (16 papers), Congenital Heart Disease Studies (14 papers) and Genomics and Rare Diseases (12 papers). Benjamin M. Helm collaborates with scholars based in United States, United Kingdom and Australia. Benjamin M. Helm's co-authors include Stephanie M. Ware, Benjamin J. Landis, Samantha A. Schrier Vergano, Adam C. Kean, Andrew P. Landstrom, Prince J. Kannankeril, Christopher Semsarian, Bruce D. Gelb, Amy C. Sturm and Martin Tristani‐Firouzi and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and PEDIATRICS.

In The Last Decade

Benjamin M. Helm

44 papers receiving 427 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benjamin M. Helm United States 13 207 176 127 110 87 49 445
Siv Fokstuen Switzerland 15 238 1.1× 250 1.4× 105 0.8× 177 1.6× 106 1.2× 33 573
Anna Baroncini Italy 13 256 1.2× 149 0.8× 64 0.5× 45 0.4× 128 1.5× 29 458
Benedicte Paus Norway 13 320 1.5× 67 0.4× 56 0.4× 139 1.3× 22 0.3× 28 531
Jason Cowan United States 12 79 0.4× 299 1.7× 138 1.1× 378 3.4× 30 0.3× 16 625
B Krag-Olsen Denmark 8 208 1.0× 135 0.8× 38 0.3× 40 0.4× 79 0.9× 17 373
Birsen Karaman Türkiye 12 157 0.8× 180 1.0× 44 0.3× 24 0.2× 57 0.7× 58 345
Tara Wenger United States 11 196 0.9× 144 0.8× 46 0.4× 13 0.1× 50 0.6× 42 377
Alba Pilotta Italy 15 268 1.3× 229 1.3× 15 0.1× 27 0.2× 86 1.0× 26 586
Jae Ho Lee United States 10 73 0.4× 197 1.1× 53 0.4× 54 0.5× 35 0.4× 14 433
Isabella Lopes Monlleó Brazil 14 343 1.7× 196 1.1× 81 0.6× 10 0.1× 36 0.4× 47 499

Countries citing papers authored by Benjamin M. Helm

Since Specialization
Citations

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

Fields of papers citing papers by Benjamin M. Helm

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benjamin M. Helm. 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 Benjamin M. Helm. The network helps show where Benjamin M. Helm may publish in the future.

Co-authorship network of co-authors of Benjamin M. Helm

This figure shows the co-authorship network connecting the top 25 collaborators of Benjamin M. Helm. A scholar is included among the top collaborators of Benjamin M. Helm 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 Benjamin M. Helm. Benjamin M. Helm 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.
Wetherill, Leah, et al.. (2025). Factors influencing retention of patient‐facing genetic counselors: Role of generational age and work environment. Journal of Genetic Counseling. 34(4). e70076–e70076. 1 indexed citations
2.
Helm, Benjamin M., Leah Wetherill, Benjamin J. Landis, & Stephanie M. Ware. (2025). Dysmorphology-Based Prediction Model for Genetic Disorders in Infants With Congenital Heart Disease. Circulation Genomic and Precision Medicine. 18(2). e004895–e004895. 1 indexed citations
3.
Fitzgerald‐Butt, Sara, et al.. (2025). Experiences of people with elevated lipoprotein(a) and the impact on family and child screening. Journal of clinical lipidology. 19(6). 1598–1609. 1 indexed citations
4.
Helm, Benjamin M., Matthew Hays, Kayleigh A. Swaggart, et al.. (2025). Standardized Criteria for Genomic Testing in the NICU. PEDIATRICS. 156(1).
5.
Landis, Benjamin J., Benjamin M. Helm, Jeremy L. Herrmann, et al.. (2024). Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery. Journal of Clinical Investigation. 134(18). 1 indexed citations
6.
Fitzgerald‐Butt, Sara, et al.. (2023). Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility. Journal of Genetic Counseling. 33(5). 1004–1014.
7.
Geddes, Gabrielle C., et al.. (2023). Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects. The Journal of Pediatrics. 260. 113495–113495. 8 indexed citations
8.
Helm, Benjamin M., et al.. (2023). Effects of hypermobile Ehlers‐Danlos syndrome patients on the workflow and professional satisfaction of genetic counselors. Journal of Genetic Counseling. 33(6). 1215–1225. 4 indexed citations
9.
Li, Ming, William L. Border, Sara Fitzgerald‐Butt, et al.. (2023). A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices. SHILAP Revista de lepidopterología. 1(1). 100814–100814. 9 indexed citations
10.
Helm, Benjamin M., et al.. (2023). Disruption of FBN1 by an Alu element insertion: A novel genetic cause of Marfan syndrome. European Journal of Medical Genetics. 66(7). 104775–104775.
11.
Landis, Benjamin J., Benjamin M. Helm, Jeremy L. Herrmann, et al.. (2022). Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease. Journal of the American Heart Association. 11(19). e026369–e026369. 12 indexed citations
12.
13.
Prucka, Sandra K., et al.. (2022). Comparison of willingness and preference for genetic counseling via telemedicine: before vs. during the COVID-19 pandemic. Journal of Community Genetics. 13(4). 449–458. 5 indexed citations
14.
Landstrom, Andrew P., Jeffrey J. Kim, Bruce D. Gelb, et al.. (2021). Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association. Circulation Genomic and Precision Medicine. 14(5). e000086–e000086. 56 indexed citations
15.
Helm, Benjamin M., et al.. (2019). How Can Stoic Philosophy Inspire Psychosocial Genetic Counseling Practice? An Introduction and Exploration. Journal of Rational-Emotive & Cognitive-Behavior Therapy. 38(2). 155–172. 2 indexed citations
16.
Parent, John J., et al.. (2019). An adult female with 5q34-q35.2 deletion: A rare syndromic presentation of left ventricular non-compaction and congenital heart disease. European Journal of Medical Genetics. 63(4). 103797–103797. 6 indexed citations
17.
Helm, Benjamin M., Jason R. Willer, Azita Sadeghpour, et al.. (2017). Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome. Human Genomics. 11(1). 16–16. 18 indexed citations
18.
Landis, Benjamin J., et al.. (2016). Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling. PMC. 1 indexed citations
19.
Helm, Benjamin M., et al.. (2015). Mosaic trisomy 15 in a liveborn infant. American Journal of Medical Genetics Part A. 167(4). 821–825. 17 indexed citations
20.
Russell, Bianca, Jennifer J. Johnston, Leslie G. Biesecker, et al.. (2015). Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance. American Journal of Medical Genetics Part A. 167(9). 2122–2131. 47 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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