Barry Lewis

1.1k total citations
22 papers, 385 citations indexed

About

Barry Lewis is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Barry Lewis has authored 22 papers receiving a total of 385 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Barry Lewis's work include Metabolism and Genetic Disorders (8 papers), Neonatal Health and Biochemistry (4 papers) and Mitochondrial Function and Pathology (3 papers). Barry Lewis is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Neonatal Health and Biochemistry (4 papers) and Mitochondrial Function and Pathology (3 papers). Barry Lewis collaborates with scholars based in Australia, Netherlands and Canada. Barry Lewis's co-authors include E. F. Robertson, Enzo Ranieri, C. Phillip Morris, Peter O’Leary, Elizabeth Geelhoed, W.F. Carey, Richard Ryall, Edwin P. Kirk, Carolyn Ellaway and Pamela Joy and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Clinical Chemistry.

In The Last Decade

Barry Lewis

21 papers receiving 372 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barry Lewis Australia 10 187 141 123 78 66 22 385
J H Walter United Kingdom 14 277 1.5× 125 0.9× 116 0.9× 52 0.7× 97 1.5× 29 457
A. Kimberly Iafolla United States 9 367 2.0× 298 2.1× 139 1.1× 76 1.0× 47 0.7× 13 517
Ayesha Ahmad United States 13 120 0.6× 151 1.1× 66 0.5× 108 1.4× 62 0.9× 37 392
Rulai Yang China 12 141 0.8× 128 0.9× 99 0.8× 70 0.9× 50 0.8× 31 336
Yolanda Lillquist Canada 10 146 0.8× 121 0.9× 40 0.3× 39 0.5× 52 0.8× 17 250
Dennis Bartholomew United States 11 151 0.8× 164 1.2× 61 0.5× 85 1.1× 15 0.2× 20 379
Serap Sivri Türkiye 11 182 1.0× 120 0.9× 52 0.4× 43 0.6× 62 0.9× 53 342
A. Briddon United Kingdom 10 220 1.2× 169 1.2× 61 0.5× 51 0.7× 108 1.6× 25 465
Gaetano Sabetta Italy 10 402 2.1× 340 2.4× 174 1.4× 62 0.8× 78 1.2× 11 631
Marta Camilot Italy 12 66 0.4× 157 1.1× 60 0.5× 80 1.0× 42 0.6× 29 385

Countries citing papers authored by Barry Lewis

Since Specialization
Citations

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

Fields of papers citing papers by Barry Lewis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barry Lewis

This figure shows the co-authorship network connecting the top 25 collaborators of Barry Lewis. A scholar is included among the top collaborators of Barry Lewis 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 Barry Lewis. Barry Lewis 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.
Shah, Snehal, et al.. (2020). Biotinidase deficiency presenting as Neuromyelitis Optica Spectrum Disorder. Brain and Development. 42(10). 762–766. 7 indexed citations
3.
Lewis, Barry, et al.. (2018). Project Management Capability Assessment. Auerbach Publications eBooks. 1 indexed citations
4.
Kava, Maina, Peter Walsh, Ravisha Srinivasjois, et al.. (2017). Clinical and Electrophysiological Characteristics of Vincristine Induced Peripheral Neuropathy in Children. SHILAP Revista de lepidopterología. 4 indexed citations
5.
Lewis, Barry, et al.. (2017). Documenting family history in children with hypercholesterolaemia: A lost opportunity. Journal of Paediatrics and Child Health. 53(5). 470–473. 6 indexed citations
7.
Lewis, Barry, et al.. (2016). Clinical Approach to a Neonate with Seizures. UWA Profiles and Research Repository (University of Western Australia). 114–127.
8.
Lewis, Barry, et al.. (2013). Serum ferritin and nutritional status: insights from an eating disorders clinic population. Archives of Disease in Childhood. 99(3). 221–224. 6 indexed citations
9.
Bower, Carol, et al.. (2012). Ethnic and gender differences in rates of congenital adrenal hyperplasia in Western Australia over a 21 year period. Journal of Paediatrics and Child Health. 48(11). 1029–1032. 12 indexed citations
10.
Bates, Timothy R., Barry Lewis, John R. Burnett, et al.. (2011). Late-Onset Carbamoyl Phosphate Synthetase 1 Deficiency in an Adult Cured by Liver Transplantation. Liver Transplantation. 17(12). 1481–1484. 12 indexed citations
11.
O’Çonnell, Susan, Stephanie Johnson, Barry Lewis, et al.. (2011). Structural chromosome disruption of the NR3C2 gene causing pseudohypoaldosteronism type 1 presenting in infancy. Journal of Pediatric Endocrinology and Metabolism. 24(7-8). 555–9. 7 indexed citations
12.
Wilcken, Bridget, Marion Haas, Pamela Joy, et al.. (2009). Expanded Newborn Screening: Outcome in Screened and Unscreened Patients at Age 6 Years. PEDIATRICS. 124(2). e241–e248. 127 indexed citations
13.
Geelhoed, Elizabeth, et al.. (2005). Economic evaluation of neonatal screening for phenylketonuria and congenital hypothyroidism. Journal of Paediatrics and Child Health. 41(11). 575–579. 46 indexed citations
14.
Sellner, Loryn N., Edward Edkins, Lawrence Greed, & Barry Lewis. (2004). Detection of mutations in the glycine decarboxylase gene in patients with nonketotic hyperglycinaemia. Molecular Genetics and Metabolism. 84(2). 167–171. 10 indexed citations
15.
Badcock, N R, et al.. (1995). Fecal coproporphyrin isomers in sporadic and familial porphyria cutanea tarda. Clinical Chemistry. 41(9). 1315–1317. 3 indexed citations
16.
Lewis, Barry, Paul V. Nelson, E. F. Robertson, & C. Phillip Morris. (1994). Mutation analysis of 28 Gaucher disease patients: The Australasian experience. American Journal of Medical Genetics. 49(2). 218–223. 27 indexed citations
17.
Ranieri, Enzo, Barry Lewis, Richard Ryall, et al.. (1994). Neonatal screening for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis: four years' experience. BMJ. 308(6942). 1469–1472. 62 indexed citations
18.
Lewis, Barry, et al.. (1994). Isolated Glycerol Kinase Deficiency in a Neonate. Journal of Child Neurology. 9(1). 70–73. 7 indexed citations
19.
Lewis, Barry, et al.. (1968). A study of thyroid disease in the Chikwaka region of Rhodesia.. PubMed. 14(4). 67–72. 1 indexed citations
20.
Boura, A.L.A., et al.. (1965). Automatic apparatus for recording duration of narcosis in mice. Journal of Pharmacy and Pharmacology. 17(1). 42–47. 3 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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