David A. Stevenson

8.0k citations

149 papers · 2.9k indexed · 1 hit paper · h-index 30

Impact in

Neurology top 2%
- Neurofibromatosis and Schwannoma Cases
- Vascular Malformations Diagnosis and Treatment
Genetics top 5%

Papers in

Neurology 30
- Neurofibromatosis and Schwannoma Cases 23
- Vascular Malformations Diagnosis and Treatment 10
Chemical Health and Safety 1

Co-authors: H. Paul Maruska P. M. Borsenberger Patrick H. Rooney J. I. Pánkové N E Haites Feng‐Chun Yang Pinar Bayrak‐Toydemir Nancy Jiang
Journals: Genetics in Medicine (7 papers)Journal of Physics and Chemistry of Solids (5 papers)Journal of The Electrochemical Society (4 papers)Journal of Pediatric Orthopaedics (4 papers)Applied Physics Letters (4 papers)
Partner nations: United States United Kingdom Italy

In The Last Decade

David A. Stevenson

142 papers receiving 2.8k citations

Hit Papers

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Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia 2015 · 216 citations

Peers

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-authors

The 25 scholars most cited alongside David A. Stevenson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David A. Stevenson Line = papers co-authored together David A. Stevenson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Influences of RASopathies on Neuroanatomical Variation in Children Biological Psychiatry Cognitive Neuroscience and Neuroimaging ·Samarappuli Mudiyanselage Sav Gunarathne, Lih Wei Yeow, Wójcik Magdalena, 静子嶋本, P.K. Singh, David A. Stevenson, Jennifer L. Bruno, Mira M. Raman, Tamar Green	2024	3
2	Immunological and hematological findings as major features in a patient with a new germline pathogenic CBL variant American Journal of Medical Genetics Part A ·Emilia Stellacci, P.F. Sahr, Luca Pannone, David A. Stevenson, Wallace S. Hay, Serenella Venanzi, (unknown), Jonathan A. Bernstein, Marco Tartaglia, Simone Martinelli	2024	0
3	7519 Withdrawal of DCCR (Diazoxide Choline) Extended-Release Tablets Worsens Hyperphagia and Increases Weight and BMI in a 16-week Double-blind, Placebo-controlled, Randomized Withdrawal Period in Patients with Prader Willi Syndrome Journal of the Endocrine Society ·Evelien Gevers, Jennifer Miller, Nicola Bridges, Eric I. Felner, Parisa Salehi, David A. Stevenson, Jack A. Yanovski, Lynne M. Bird, Virginia Kimonis, Ashley H. Shoemaker, Kathryn Obrynba, Sarah Backer, Elizabeth Littlejohn, Julie Laclau, Julie Laclau, A. Evelien Doornbos-Burema, Shaila Ballal, Lîsîi Aliona, Michael Huang, Anish Bhatnagar	2024	1
4	Two epilepsy‐associated variants in KCNA2 (K_V1.2) at position H310 oppositely affect channel functional expression The Journal of Physiology ·Min Gi Cho, Emilia Porter, Yiqiao Jin, S. Lindström, Torsti Hyyrylänen, Stuart A. Scott, Elizabeth Spiteri, David A. Stevenson, Euan A. Ashley, Cecilia Gunnarsson, Antonios Pantazis	2023	6
5	Frequency of epistaxis and telangiectasia in patients with hereditary hemorrhagic telangiectasia (HHT) in comparison with the general population: Curaçao diagnostic criteria revisited Genetics in Medicine ·Jamie McDonald, Dal-Yob Lee, David A. Stevenson, Andrea Hanson‐Kahn, А Н Дмитриева, John James, Hetanshi Naik, Kevin J. Whitehead	2023	10
6	Single Versus Multigene Testing for Hereditary Hearing Loss: Use and Costs in a Commercially Insured Cohort Otolaryngology ·Peter K. Moon, Z. Jason Qian, David A. Stevenson, Kay W. Chang	2023	3
7	Bone health in RASopathies American Journal of Medical Genetics Part C Seminars in Medical Genetics ·David A. Stevenson, Christian Benno Stabernack, Chiara Leoni	2022	7
8	Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome SHILAP Revista de lepidopterología ·Emma Wakeling, Meriel McEntagart, E. De Clercq, Charles Shaw‐Smith, Karen Stals, Matthew N. Wakeling, Angela Barnicoat, Clare Beesley, Andrea Hanson‐Kahn, Mary K. Kukolich, David A. Stevenson, Philippe M. Campeau, Sian Ellard, Sarah H. Elsea, Xiang-Jiao Yang, Richard Caswell	2020	11
9	Costello syndrome: Clinical phenotype, genotype, and management guidelines American Journal of Medical Genetics Part A ·Karen W. Gripp, 刘晓平, Marni E. Axelrad, Kathryn C. Chatfield, Aaron Chidekel, William B. Dobyns, Daniel Doyle, Bronwyn Kerr, Angela E. Lin, David D. Schwartz, Barbara Sibbles, Dawn H. Siegel, Suma P. Shankar, David A. Stevenson, Mihir M. Thacker, K. Nicole Weaver, Sue M. White, Katherine A. Rauen	2019	72
10	Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review American Journal of Medical Genetics Part A ·Akash Kumar, Diane B. Zastrow, Elijah Kravets, Daniah Beleford, Maura Ruzhnikov, Megan E. Grove, Annika M. Dries, Jennefer N. Kohler, Daryl Waggott, Yaping Yang, Yong Huang, (unknown), Katherine M. Mackenzie, Christine M. Eng, Paul G. Fisher, Euan A. Ashley, Joyce Teng, David A. Stevenson, Joseph T.C. Shieh, Matthew T. Wheeler, Jonathan A. Bernstein	2019	16
11	Contributing factors of mortality in Prader–Willi syndrome American Journal of Medical Genetics Part A ·Shinomi Yagi, Kathryn Osann, J. B. Drewes, Virginia Kimonis, Janalee Heinemann, Merlin G. Butler, David A. Stevenson, June‐Anne Gold	2018	45
12	Dietary intervention rescues myopathy associated with neurofibromatosis type 1 Human Molecular Genetics ·Matthew A. Summers, Thusitha Rupasinghe, C. Wolfe-Christensen, Frances J. Evesson, Kathy Mikulec, Lauren Peacock, Kate Quinlan, Sandra T. Cooper, Ute Roessner, David A. Stevenson, David G. Little, Aaron Schindeler	2017	19
13	RASA1 somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome American Journal of Medical Genetics Part A ·Colleen Macmurdo, Whitney Wooderchak‐Donahue, Pinar Bayrak‐Toydemir, Г.Ш. Магомедов, Matthew B. Wallenstein, Carlos Milla, Joyce Teng, Jonathan A. Bernstein, David A. Stevenson	2016	72
14	Function and disability in children with Costello syndrome and Cardiofaciocutaneous syndrome American Journal of Medical Genetics Part A ·Barbara Johnson, G. Lee-Glauser, Karen W. Gripp, Mihir M. Thacker, Chiara Leoni, David A. Stevenson	2014	18
15	Approaches to Treating NF1 Tibial Pseudarthrosis Journal of Pediatric Orthopaedics ·David A. Stevenson, David G. Little, Linlea Armstrong, Alvin H. Crawford, Deborah M. Eastwood, Jan M. Friedman, Tiziana Greggi, Gloria E. Gutierrez, Kim Hunter‐Schaedle, David L. Kendler, Mateusz Kolanczyk, Fergal Monsell, Matthew E. Oetgen, B. Stephens Richards, Aaron Schindeler, Elizabeth K. Schorry, David Wilkes, David Viskochil, Feng‐Chun Yang, Florent Elefteriou	2013	44
16	RASA1-Related Disorders Pınar Bayrak‐Toydemir, David A. Stevenson	2013	9
17	The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case–control study American Journal of Medical Genetics Part A ·Linlea Armstrong, Kimberly Jett, Patricia Birch, David L. Kendler, Heather McKay, Erica S. Tsang, David A. Stevenson, David A. Hanley, C. H. Duan, Melonie Burrows, Jan M. Friedman	2013	22
18	Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome American Journal of Medical Genetics Part A ·Karen W. Gripp, Deborah L. Stabley, Marie-Véronique Henry-Wittmann, Elizabeth Hopkins, David A. Stevenson, John C. Carey, Katia Sol‐Church	2011	13
19	Detection of a common amplification of 7q in docetaxel resistant breast cancer cell lines by comparative hybridisation European Journal of Cancer ·Sarah McDonald, HELEN M. DeMARCO, David A. Stevenson, Steven D. Heys, Andrew Craig Schofield	2003	0
20	Core storage as a slave memory for disk storage devices. IFIP Congress ·David A. Stevenson, コウヘイコマツ	1968	2

About David A. Stevenson

David A. Stevenson is a scholar working on Neurology, Chemical Health and Safety, Genetics, Rheumatology and Pathology and Forensic Medicine, having authored 149 papers that have together received 2.9k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (23 papers), Protein Tyrosine Phosphatases (19 papers), Vascular Malformations and Hemangiomas (12 papers), Advanced Semiconductor Detectors and Materials (11 papers), Vascular Malformations Diagnosis and Treatment (10 papers), Genomic variations and chromosomal abnormalities (8 papers), Sarcoma Diagnosis and Treatment (8 papers) and Advancements in Solid Oxide Fuel Cells (8 papers). The work is most often cited by research in Neurology (478 citations), Genetics (193 citations), Condensed Matter Physics (202 citations), Genetics (400 citations) and Rheumatology (205 citations). David A. Stevenson has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include H. Paul Maruska, P. M. Borsenberger, Patrick H. Rooney, J. I. Pánkové, N E Haites, Feng‐Chun Yang, Pinar Bayrak‐Toydemir, Nancy Jiang, A. F. Marshall and Graeme I. Murray. Their work appears in journals such as Genetics in Medicine, Journal of Physics and Chemistry of Solids, Journal of The Electrochemical Society, Journal of Pediatric Orthopaedics and Applied Physics Letters.

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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