David A. Stevenson

4.4k total citations · 1 hit paper
57 papers, 2.6k citations indexed

About

David A. Stevenson is a scholar working on Neurology, Rheumatology and Genetics. According to data from OpenAlex, David A. Stevenson has authored 57 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Neurology, 19 papers in Rheumatology and 15 papers in Genetics. Recurrent topics in David A. Stevenson's work include Neurofibromatosis and Schwannoma Cases (23 papers), Soft tissue tumor case studies (9 papers) and Sarcoma Diagnosis and Treatment (7 papers). David A. Stevenson is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (23 papers), Soft tissue tumor case studies (9 papers) and Sarcoma Diagnosis and Treatment (7 papers). David A. Stevenson collaborates with scholars based in United States, United Kingdom and Germany. David A. Stevenson's co-authors include John C. Carey, Pınar Bayrak‐Toydemir, Jamie McDonald, Whitney Wooderchak‐Donahue, David Viskochil, Kevin J. Whitehead, Jacques DʼAstous, Laurie J. Moyer‐Mileur, Jeffry S. Nyman and Koichiro Ono and has published in prestigious journals such as Nature Medicine, The Journal of Clinical Endocrinology & Metabolism and PEDIATRICS.

In The Last Decade

David A. Stevenson

57 papers receiving 2.5k citations

Hit Papers

Hereditary hemorrhagic telangiectasia: genetics and molec... 2015 2026 2018 2022 2015 100 200 300 400 500
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. Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era
    2015 523 citations Jamie McDonald, Whitney Wooderchak‐Donahue et al. Frontiers in Genetics profile →

Peers

David A. Stevenson
Corey Raffel United States
Thomy de Ravel Belgium
Ahmad S. Teebi Canada
I Pascual-Castroviejo Spain
Carol A. Wise United States
Valerie Newton United Kingdom
Jamie McDonald United States
Peter D. Turnpenny United Kingdom
Wladimir Wertelecki United States
Maria Anvret Sweden
Corey Raffel United States
David A. Stevenson
Citations per year, relative to David A. Stevenson David A. Stevenson (= 1×) peers Corey Raffel

Countries citing papers authored by David A. Stevenson

Since Specialization
Citations

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

Fields of papers citing papers by David A. Stevenson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David A. Stevenson. 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 David A. Stevenson. The network helps show where David A. Stevenson may publish in the future.

Co-authorship network of co-authors of David A. Stevenson

This figure shows the co-authorship network connecting the top 25 collaborators of David A. Stevenson. A scholar is included among the top collaborators of David A. Stevenson 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 David A. Stevenson. David A. Stevenson 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.
Bilder, Deborah A., Amanda V. Bakian, David A. Stevenson, et al.. (2016). Brief Report: The Prevalence of Neurofibromatosis Type 1 among Children with Autism Spectrum Disorder Identified by the Autism and Developmental Disabilities Monitoring Network. Journal of Autism and Developmental Disorders. 46(10). 3369–3376. 15 indexed citations
2.
McDonald, Jamie, et al.. (2015). Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era. Frontiers in Genetics. 6. 1–1. 523 indexed citations breakdown →
3.
Ndong, Jean De La Croix, Alexander J. Makowski, Sasidhar Uppuganti, et al.. (2014). Asfotase-α improves bone growth, mineralization and strength in mouse models of neurofibromatosis type-1. Nature Medicine. 20(8). 904–910. 50 indexed citations
4.
Wooderchak‐Donahue, Whitney, Jamie McDonald, Brendan O’Fallon, et al.. (2013). BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia. The American Journal of Human Genetics. 93(3). 530–537. 226 indexed citations
5.
Stevenson, David A., Rena Vanzo, Kristy Damjanovich, et al.. (2012). Mosaicism in Stickler syndrome. European Journal of Medical Genetics. 55(6-7). 418–422. 10 indexed citations
6.
Stevenson, David A., Kristen L. Carroll, Richard Pimentel, et al.. (2012). Total Hip Arthroplasty, Hip Osteoarthritis, Total Knee Arthroplasty, and Knee Osteoarthritis in Patients With Developmental Dysplasia of the Hip and Their Family Members. Journal of Pediatric Orthopaedics. 32(6). 609–612. 11 indexed citations
7.
Johnson, Barbara, Bruce A. MacWilliams, John C. Carey, et al.. (2011). Lower extremity strength and hopping and jumping ground reaction forces in children with neurofibromatosis type 1. Human Movement Science. 31(1). 247–254. 16 indexed citations
8.
Kossler, Nadine, Sigmar Stricker, Christian Rödelsperger, et al.. (2011). Neurofibromin (Nf1) is required for skeletal muscle development. Human Molecular Genetics. 20(14). 2697–2709. 47 indexed citations
9.
Wooderchak‐Donahue, Whitney, David A. Stevenson, Jamie McDonald, et al.. (2011). RASA1 analysis: Clinical and molecular findings in a series of consecutive cases. European Journal of Medical Genetics. 55(2). 91–95. 26 indexed citations
10.
Damjanovich, Kristy, Carmen Langa, Francisco J. Blanco, et al.. (2011). 5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia. Orphanet Journal of Rare Diseases. 6(1). 85–85. 28 indexed citations
11.
Kissil, Joseph L., Jaishri O. Blakeley, Rosalie E. Ferner, et al.. (2010). What's new in neurofibromatosis? Proceedings from the 2009 NF Conference: New Frontiers. American Journal of Medical Genetics Part A. 152A(2). 269–283. 22 indexed citations
12.
Viskochil, David, et al.. (2010). Speech–language characteristics of children with neurofibromatosis type 1. American Journal of Medical Genetics Part A. 152A(2). 284–290. 28 indexed citations
13.
Stevenson, David A., Elisabeth L. Schwarz, David Viskochil, et al.. (2008). Evidence of Increased Bone Resorption in Neurofibromatosis Type 1 Using Urinary Pyridinium Crosslink Analysis. Pediatric Research. 63(6). 697–701. 29 indexed citations
14.
Stevenson, David A., David Viskochil, John C. Carey, et al.. (2008). Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomography. Bone. 44(4). 585–589. 11 indexed citations
15.
Stevenson, David A., Janalee Heinemann, Moris Angulo, et al.. (2007). Gastric Rupture and Necrosis in Prader‐Willi Syndrome. Journal of Pediatric Gastroenterology and Nutrition. 45(2). 272–274. 79 indexed citations
16.
Stevenson, David A., Holly Zhou, Ludwine Messiaen, et al.. (2006). Double Inactivation of NF1 in Tibial Pseudarthrosis. The American Journal of Human Genetics. 79(1). 143–148. 107 indexed citations
17.
Waggoner, Darrel, et al.. (2005). Calibration of 6q subtelomere deletions to define genotype/phenotype correlations. Clinical Genetics. 67(5). 396–403. 60 indexed citations
18.
Stevenson, David A. & John C. Carey. (2003). Contribution of malformations and genetic disorders to mortality in a children's hospital. American Journal of Medical Genetics Part A. 126A(4). 393–397. 49 indexed citations
19.
Stevenson, David A., Patricia Birch, Jan M. Friedman, et al.. (1999). Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1. American Journal of Medical Genetics. 84(5). 413–419. 96 indexed citations
20.
Gale, Rena, et al.. (1988). Birth Out of Wedlock and the Risk of Intrauterine Growth Retardation. American Journal of Perinatology. 5(3). 278–282. 5 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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