Reed E. Pyeritz

37.0k total citations · 9 hit papers
267 papers, 20.1k citations indexed

About

Reed E. Pyeritz is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Reed E. Pyeritz has authored 267 papers receiving a total of 20.1k indexed citations (citations by other indexed papers that have themselves been cited), including 128 papers in Genetics, 125 papers in Pulmonary and Respiratory Medicine and 77 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Reed E. Pyeritz's work include Connective tissue disorders research (92 papers), Aortic Disease and Treatment Approaches (88 papers) and Cardiac Valve Diseases and Treatments (52 papers). Reed E. Pyeritz is often cited by papers focused on Connective tissue disorders research (92 papers), Aortic Disease and Treatment Approaches (88 papers) and Cardiac Valve Diseases and Treatments (52 papers). Reed E. Pyeritz collaborates with scholars based in United States, Italy and Canada. Reed E. Pyeritz's co-authors include Harry C. Dietz, Victor A. McKusick, Richard B. Devereux, Clair A. Francomano, Edmond A. Murphy, Lynn Y. Sakai, Raoul C. M. Hennekam, Anne De Paepe, Barbara A. Bernhardt and Paul D. Sponseller and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Reed E. Pyeritz

259 papers receiving 19.3k citations

Hit Papers

Marfan syndrome caused by a recurrent de novo missense mu... 1979 2026 1994 2010 1991 1999 2010 1996 1985 400 800 1.2k
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.

  1. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
    1991 1.5k citations Harry C. Dietz, Reed E. Pyeritz et al. profile →
  2. Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta
    1999 1.4k citations Reed E. Pyeritz et al. profile →
  3. The revised Ghent nosology for the Marfan syndrome: Table 1
    2010 1.4k citations Bart Loeys, Harry C. Dietz et al. Journal of Medical Genetics profile →
  4. Revised diagnostic criteria for the Marfan syndrome
    1996 1.1k citations Richard B. Devereux, Harry C. Dietz et al. profile →
  5. The natural history of homocystinuria due to cystathionine beta-synthase deficiency.
    1985 960 citations Reed E. Pyeritz et al. PubMed profile →
  6. Progression of Aortic Dilatation and the Benefit of Long-Term β-Adrenergic Blockade in Marfan's Syndrome
    1994 676 citations Edmond A. Murphy, Reed E. Pyeritz et al. profile →
  7. The Marfan Syndrome: Diagnosis and Management
    1979 634 citations Reed E. Pyeritz et al. profile →
  8. Marfan syndrome
    2021 134 citations Dianna M. Milewicz, Alan C. Braverman et al. Nature Reviews Disease Primers profile →
  9. Early Mortality in Type A Acute Aortic Dissection
    2022 118 citations Kevin M. Harris, Christoph Nienaber et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Reed E. Pyeritz United States 67 9.8k 8.7k 6.4k 4.4k 2.9k 267 20.1k
Harry C. Dietz United States 83 15.2k 1.6× 12.1k 1.4× 8.3k 1.3× 4.3k 1.0× 8.0k 2.7× 251 28.2k
Dianna M. Milewicz United States 73 7.6k 0.8× 12.2k 1.4× 6.9k 1.1× 3.9k 0.9× 2.9k 1.0× 273 19.6k
Bart Loeys Belgium 50 7.1k 0.7× 5.3k 0.6× 3.3k 0.5× 1.8k 0.4× 3.0k 1.0× 209 11.9k
Richard C. Trembath United Kingdom 69 2.7k 0.3× 5.8k 0.7× 2.1k 0.3× 1.4k 0.3× 6.3k 2.2× 210 17.3k
Daniel P. Judge United States 66 4.6k 0.5× 3.6k 0.4× 8.9k 1.4× 1.8k 0.4× 4.8k 1.6× 220 16.1k
Julie M. Gastier‐Foster United States 36 9.0k 0.9× 2.1k 0.2× 2.2k 0.3× 1.8k 0.4× 10.4k 3.6× 122 22.8k
Sherri J. Bale United States 52 12.9k 1.3× 1.9k 0.2× 2.4k 0.4× 1.9k 0.4× 14.7k 5.0× 142 29.9k
Sue Richards United Kingdom 33 8.7k 0.9× 1.6k 0.2× 2.1k 0.3× 1.6k 0.4× 9.6k 3.3× 85 22.4k
David Bick United States 31 10.3k 1.0× 1.5k 0.2× 2.1k 0.3× 1.7k 0.4× 10.4k 3.6× 83 22.0k
Madhuri Hegde United States 35 10.7k 1.1× 1.7k 0.2× 2.4k 0.4× 1.8k 0.4× 11.5k 3.9× 138 23.8k

Countries citing papers authored by Reed E. Pyeritz

Since Specialization
Citations

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

Fields of papers citing papers by Reed E. Pyeritz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Reed E. Pyeritz. 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 Reed E. Pyeritz. The network helps show where Reed E. Pyeritz may publish in the future.

Co-authorship network of co-authors of Reed E. Pyeritz

This figure shows the co-authorship network connecting the top 25 collaborators of Reed E. Pyeritz. A scholar is included among the top collaborators of Reed E. Pyeritz 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 Reed E. Pyeritz. Reed E. Pyeritz 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.
Bossone, Eduardo, Kim A. Eagle, Christoph Nienaber, et al.. (2024). Acute Aortic Dissection: Observational Lessons Learned From 11 000 Patients. Circulation Cardiovascular Quality and Outcomes. 17(9). 2 indexed citations
2.
Strong, Alanna, Cara Skraban, Kevin Meyers, et al.. (2021). Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes. American Journal of Medical Genetics Part A. 185(12). 3762–3769. 1 indexed citations
3.
Milewicz, Dianna M., Alan C. Braverman, Julie De Backer, et al.. (2021). Marfan syndrome. Nature Reviews Disease Primers. 7(1). 64–64. 134 indexed citations breakdown →
4.
Beslow, Lauren A., Daniel J. Licht, J. Deane Waldman, et al.. (2020). Cerebrovascular Malformations in a Pediatric Hereditary Hemorrhagic Telangiectasia Cohort. Pediatric Neurology. 110. 49–54. 7 indexed citations
5.
Harris, Kevin M., Reed E. Pyeritz, Derek R. Brinster, et al.. (2020). AORTIC DISSECTION RELATED TO PREGNANCY: THE INTERNATIONAL REGISTRY OF ACUTE AORTIC DISSECTION (IRAD). Journal of the American College of Cardiology. 75(11). 2213–2213. 3 indexed citations
6.
Birtwell, David, et al.. (2019). Carnival: A Graph-Based Data Integration and Query Tool to Support Patient Cohort Generation for Clinical Research. Studies in health technology and informatics. 264. 35–39. 4 indexed citations
7.
Pyeritz, Reed E.. (2018). Marfan syndrome: improved clinical history results in expanded natural history. Genetics in Medicine. 21(8). 1683–1690. 58 indexed citations
8.
Evangelista, Arturo, Daniel Montgomery, Alan C. Braverman, et al.. (2014). AORTIC SIZE INDICES: A MORE COMPREHENSIVE EVALUATION OF AORTIC RISK. Journal of the American College of Cardiology. 63(12). A1209–A1209. 1 indexed citations
9.
Rimoin, David L., Reed E. Pyeritz, & Bruce R. Korf. (2013). Emery and Rimoin's Essential Medical Genetics. Elsevier eBooks. 11 indexed citations
10.
11.
Braverman, Alan C., Kevin M. Harris, Reed E. Pyeritz, et al.. (2012). AORTIC DISSECTION DURING PREGNANCY: RESULTS FROM THE INTERNATIONAL REGISTRY OF ACUTE AORTIC DISSECTION (IRAD). Journal of the American College of Cardiology. 59(13). E1903–E1903. 8 indexed citations
12.
Reiff, Marian, et al.. (2012). “What does it mean?”: Uncertainties in understanding results of chromosomal microarray testing. Genetics in Medicine. 14(2). 250–258. 90 indexed citations
13.
Bernhardt, Barbara A. & Reed E. Pyeritz. (2011). When genetic screening is useful, but not used.. PubMed. 16(8). 1–4.
14.
Loeys, Bart, Harry C. Dietz, Alan C. Braverman, et al.. (2010). The revised Ghent nosology for the Marfan syndrome: Table 1. Journal of Medical Genetics. 47(7). 476–485. 1350 indexed citations breakdown →
15.
Riegert‐Johnson, Douglas L., Bruce R. Korf, Raye Lynn Alford, et al.. (2004). Outline of a medical genetics curriculum for internal medicine residency training programs. Genetics in Medicine. 6(6). 543–547. 40 indexed citations
16.
17.
Haddow, J E, Glenn E. Palomaki, Linda Bradley, et al.. (1998). Screening of csytic fibrosis [3] (multiple letters). JAMA. 279(14). 1068–1069. 7 indexed citations
18.
Pyeritz, Reed E. & Edmond A. Murphy. (1989). Genetics and congenital heart disease: Perspectives and prospects. Journal of the American College of Cardiology. 13(7). 1458–1468. 20 indexed citations
19.
Reid, Cheryl S., Reed E. Pyeritz, Steven E. Kopits, et al.. (1987). Cervicomedullary compression in young patients with achondroplasia: Value of comprehensive neurologic and respiratory evaluation. The Journal of Pediatrics. 110(4). 522–530. 108 indexed citations
20.
Pyeritz, Reed E. & Charles A. Thomas. (1973). Regional organization of eukaryotic DNA sequences as studied by the formation of folded rings. Journal of Molecular Biology. 77(1). 57–73. 19 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Harry C. Dietz Breakdown of academic impact, for papers by Dianna M. Milewicz Breakdown of academic impact, for papers by Bart Loeys Breakdown of academic impact, for papers by Richard C. Trembath Breakdown of academic impact, for papers by Daniel P. Judge Breakdown of academic impact, for papers by Julie M. Gastier‐Foster Breakdown of academic impact, for papers by Sherri J. Bale Breakdown of academic impact, for papers by Sue Richards Breakdown of academic impact, for papers by David Bick Breakdown of academic impact, for papers by Madhuri Hegde
Rankless by CCL
2026