Adam Shaw

6.3k total citations · 1 hit paper
27 papers, 1.5k citations indexed

About

Adam Shaw is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Adam Shaw has authored 27 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 7 papers in Immunology. Recurrent topics in Adam Shaw's work include Protein Tyrosine Phosphatases (10 papers), RNA modifications and cancer (7 papers) and Galectins and Cancer Biology (7 papers). Adam Shaw is often cited by papers focused on Protein Tyrosine Phosphatases (10 papers), RNA modifications and cancer (7 papers) and Galectins and Cancer Biology (7 papers). Adam Shaw collaborates with scholars based in United Kingdom, Netherlands and United States. Adam Shaw's co-authors include Andrew H. Crosby, Kamini Kalidas, Michael A. Patton, Marco Tartaglia, Steve Jeffery, Ineke van der Burgt, Bruce D. Gelb, Raoul C. M. Hennekam, Xiaoling Song and Han G. Brunner and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and British Journal of Dermatology.

In The Last Decade

Adam Shaw

27 papers receiving 1.5k 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.

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

2002 522 citations Marco Tartaglia, Kamini Kalidas et al. The American Journal of Human Genetics profile →

Peers

Adam Shaw

IMMUN

GENET

ONCOL

NEURO

Guilherme Lopes Yamamoto Brazil

M A Patton United Kingdom

David J. Pennisi Australia

Daniel Kelberman United Kingdom

Shalini N. Jhangiani United States

William K. Rashbaum United States

Susanne Lorenz Norway

Phillip J. Dexheimer United States

Francesca Faravelli Italy

Olaf Wendler Germany

Guilherme Lopes Yamamoto Brazil

Adam Shaw

732 ×0.7

215 ×0.4

IMMUN

469 ×1.3

GENET

178 ×0.8

ONCOL

98 ×0.7

NEURO

Citations per year, relative to Adam Shaw Adam Shaw (= 1×) peers Guilherme Lopes Yamamoto

Countries citing papers authored by Adam Shaw

Since Specialization

Citations

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

Fields of papers citing papers by Adam Shaw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adam Shaw

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

McRonald, Fiona E., Joanna Pethick, Margreet Lüchtenborg, et al.. (2024). Identification of people with Lynch syndrome from those presenting with colorectal cancer in England: baseline analysis of the diagnostic pathway. European Journal of Human Genetics. 32(5). 529–538. 7 indexed citations

Monahan, Kevin, Adam Shaw, Laura Monje‐Garcia, et al.. (2023). P293 Finding the missing 95%: the English national lynch syndrome transformation project. Poster presentations. A204.2–A204. 3 indexed citations

Monahan, Kevin, Neil Ryan, Laura Monje‐Garcia, et al.. (2023). The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programme. SHILAP Revista de lepidopterología. 2(1). e000124–e000124. 9 indexed citations

Shaw, Adam, et al.. (2021). The importance of neurology and genetic testing in the patient with non-cleft velopharyngeal dysfunction. International Journal of Pediatric Otorhinolaryngology. 146. 110776–110776. 3 indexed citations

Bowers, Naomi L., Claire Hartley, Philip Smith, et al.. (2020). Sporadic vestibular schwannoma: a molecular testing summary. Journal of Medical Genetics. 58(4). 227–233. 13 indexed citations

Holt, Tanya, et al.. (2020). Noninvasive ventilation for pediatric interfacility transports: a retrospective study. World Journal of Pediatrics. 16(4). 422–425. 8 indexed citations

Jones, Adrian L., Harry Joe, Miriam J. Smith, et al.. (2015). Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients. Journal of Medical Genetics. 52(10). 699–705. 63 indexed citations

Frigiola, Alessandra, Leema Robert, Adam Shaw, et al.. (2015). Vascular manifestations of syndromic aortopathies: role of current and emerging imaging techniques. Clinical Radiology. 70(12). 1344–1354. 8 indexed citations

Ferner, Rosalie E., Adam Shaw, D. Gareth Evans, et al.. (2014). Longitudinal evaluation of quality of life in 288 patients with neurofibromatosis 2. Journal of Neurology. 261(5). 963–969. 36 indexed citations

10.

Kar, Annekatrien L. van de, Gunnar Houge, Adam Shaw, et al.. (2014). Keloids in Rubinstein–Taybi syndrome: a clinical study. British Journal of Dermatology. 171(3). 615–621. 23 indexed citations

11.

Shaw, Adam, Mislen Bauer, Trevor Cole, et al.. (2010). Phenotype and natural history in Marshall–Smith syndrome. American Journal of Medical Genetics Part A. 152A(11). 2714–2726. 29 indexed citations

12.

Malan, Valérie, Diana Rajan, Sophie Thomas, et al.. (2010). Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome. The American Journal of Human Genetics. 87(2). 189–198. 107 indexed citations

13.

Shaw, Adam & Raoul C. M. Hennekam. (2009). Interpreting humanity's genes. European Journal of Medical Genetics. 52(6). 379–380. 1 indexed citations

14.

Shaw, Adam, Kamini Kalidas, Andrew H. Crosby, Steven Jeffery, & M A Patton. (2006). The natural history of Noonan syndrome: a long-term follow-up study. Archives of Disease in Childhood. 92(2). 128–132. 184 indexed citations

15.

Hammond, Peter, Tim J. Hutton, Judith Allanson, et al.. (2005). Discriminating Power of Localized Three-Dimensional Facial Morphology. The American Journal of Human Genetics. 77(6). 999–1010. 118 indexed citations

16.

Kalidas, Kamini, Adam Shaw, Andrew H. Crosby, et al.. (2004). Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11. Journal of Human Genetics. 50(1). 21–25. 19 indexed citations

17.

Hammond, Peter, Tim J. Hutton, Judith Allanson, et al.. (2004). 3D analysis of facial morphology. American Journal of Medical Genetics Part A. 126A(4). 339–348. 181 indexed citations

18.

Hammond, Peter, et al.. (2002). 3D digital stereo photogrammetric analysis of face shape in Noonan syndrome. Journal of Medical Genetics. 39. 2 indexed citations

19.

Tartaglia, Marco, Kamini Kalidas, Adam Shaw, et al.. (2002). PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity. The American Journal of Human Genetics. 70(6). 1555–1563. 522 indexed citations breakdown →

20.

Tartaglia, Marco, Xiaoling Song, Kamini Kalidas, et al.. (2002). Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome. Human Genetics. 111(4-5). 421–427. 27 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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