Peter G. Procopis

587 total citations
28 papers, 426 citations indexed

About

Peter G. Procopis is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Peter G. Procopis has authored 28 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Clinical Biochemistry. Recurrent topics in Peter G. Procopis's work include Metabolism and Genetic Disorders (4 papers), Mitochondrial Function and Pathology (3 papers) and RNA regulation and disease (3 papers). Peter G. Procopis is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Mitochondrial Function and Pathology (3 papers) and RNA regulation and disease (3 papers). Peter G. Procopis collaborates with scholars based in Australia, United States and Singapore. Peter G. Procopis's co-authors include Robert Ouvrier, Monique M. Ryan, Jayne Antony, Padraic J. Grattan‐Smith, Graeme Morgan, Brian Turner, B Turner, John Christodoulou, Claire Cooke‐Yarborough and Alison G. Compton and has published in prestigious journals such as New England Journal of Medicine, Neurology and The American Journal of Human Genetics.

In The Last Decade

Peter G. Procopis

28 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter G. Procopis Australia 11 156 90 85 73 71 28 426
Lokesh Lingappa India 10 132 0.8× 86 1.0× 65 0.8× 40 0.5× 26 0.4× 44 366
Christopher Troedson Australia 13 147 0.9× 83 0.9× 136 1.6× 73 1.0× 19 0.3× 29 524
Christine Reyes United States 13 165 1.1× 100 1.1× 22 0.3× 57 0.8× 18 0.3× 22 586
Keitaro Yamada Japan 11 189 1.2× 57 0.6× 20 0.2× 23 0.3× 85 1.2× 31 347
Özlem Hergüner Türkiye 11 52 0.3× 42 0.5× 71 0.8× 38 0.5× 39 0.5× 44 377
Yuval E. Landau Israel 12 112 0.7× 72 0.8× 41 0.5× 14 0.2× 129 1.8× 24 367
Satoko Nakahara Japan 10 102 0.7× 79 0.9× 17 0.2× 47 0.6× 15 0.2× 12 391
Carl J. Crosley United States 9 36 0.2× 42 0.5× 109 1.3× 22 0.3× 12 0.2× 17 346
D C Poskanzer United States 10 47 0.3× 22 0.2× 168 2.0× 66 0.9× 14 0.2× 14 640
Linda Gailīte Latvia 12 155 1.0× 142 1.6× 35 0.4× 39 0.5× 19 0.3× 67 437

Countries citing papers authored by Peter G. Procopis

Since Specialization
Citations

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

Fields of papers citing papers by Peter G. Procopis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter G. Procopis. 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 Peter G. Procopis. The network helps show where Peter G. Procopis may publish in the future.

Co-authorship network of co-authors of Peter G. Procopis

This figure shows the co-authorship network connecting the top 25 collaborators of Peter G. Procopis. A scholar is included among the top collaborators of Peter G. Procopis 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 Peter G. Procopis. Peter G. Procopis 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.
Lake, Nicole J., Luke E. Formosa, David A. Stroud, et al.. (2019). A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein‐truncating variant. Human Mutation. 40(7). 893–898. 7 indexed citations
2.
Kothur, Kavitha, Katherine Holman, Elizabeth Farnsworth, et al.. (2018). Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy. Seizure. 59. 132–140. 55 indexed citations
3.
Lim, Sze Chern, Katherine R. Smith, David A. Stroud, et al.. (2014). A Founder Mutation in PET100 Causes Isolated Complex IV Deficiency in Lebanese Individuals with Leigh Syndrome. The American Journal of Human Genetics. 94(2). 209–222. 54 indexed citations
4.
Compton, Alison G., Christopher Troedson, Meredith Wilson, et al.. (2010). Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome. Mitochondrion. 11(1). 104–107. 11 indexed citations
5.
Procopis, Peter G.. (2007). Examination Paediatrics; A Guide to Paediatric Training. Journal of Paediatrics and Child Health. 43(4). 322–322. 1 indexed citations
6.
Procopis, Peter G.. (2002). Evidence‐based medicine. Developmental Medicine & Child Neurology. 44(7). 435–435. 7 indexed citations
7.
Ryan, Monique M., Claire Cooke‐Yarborough, Peter G. Procopis, & Robert Ouvrier. (2000). Anterior horn cell disease and olivopontocerebellar hypoplasia. Pediatric Neurology. 23(2). 180–184. 22 indexed citations
8.
Ryan, Monique M., Padraic J. Grattan‐Smith, Peter G. Procopis, Graeme Morgan, & Robert Ouvrier. (2000). Childhood chronic inflammatory demyelinating polyneuropathy: clinical course and long-term outcome. Neuromuscular Disorders. 10(6). 398–406. 65 indexed citations
9.
Grattan‐Smith, Padraic J., Monique M. Ryan, & Peter G. Procopis. (2000). Persistent or severe back pain and stiffness are ominous symptoms requiring prompt attention. Journal of Paediatrics and Child Health. 36(3). 208–212. 11 indexed citations
10.
Ryan, Monique M., Peter G. Procopis, & Robert Ouvrier. (1999). Influenza a encephalitis with movement disorder. Pediatric Neurology. 21(3). 669–673. 28 indexed citations
11.
Ouvrier, Robert, et al.. (1992). ACTH treatment in intractable seizures of childhood. Brain and Development. 14(2). 102–106. 10 indexed citations
12.
Shaw, Peter J., Peter G. Procopis, Margaret A. Menser, et al.. (1991). Bulbar and pseudobulbar palsy complicating therapy with high‐dose cytosine arabinoside in children with leukemia. Medical and Pediatric Oncology. 19(2). 122–125. 5 indexed citations
13.
Bergin, Mary, Margaret A. Menser, Peter G. Procopis, et al.. (1987). Central Nervous System Toxoplasmosis and Hemolytic Uremic Syndrome. New England Journal of Medicine. 317(24). 1540–1541. 10 indexed citations
14.
Morgan, Michael K., Michael Besser, & Peter G. Procopis. (1987). Moyamoya disease: presentation and treatment of two cases by surgery. The Medical Journal of Australia. 146(7). 381–383. 1 indexed citations
15.
Procopis, Peter G., et al.. (1983). Amoebic meningitis also occurs in NSW.. PubMed. 19. 77–80. 1 indexed citations
16.
Smith, Arabella & Peter G. Procopis. (1975). CYSTINURIA AND ITS RELATIONSHIP TO MENTAL RETARDATION. The Medical Journal of Australia. 2(25-26). 932–933. 7 indexed citations
17.
McQuillen, Michael P., Peter G. Procopis, & Robert Luke. (1973). NERVE EXCITABILITY IN CHRONIC RENAL DISEASE. ASAIO Journal. 19(1). 337–339. 2 indexed citations
18.
Procopis, Peter G.. (1972). Mental Retardation, Abnormal Fingers, and Skeletal Anomalies: Coffin's Syndrome. Archives of Pediatrics and Adolescent Medicine. 124(2). 258–258. 37 indexed citations
19.
Procopis, Peter G. & Brian Turner. (1971). Iminoaciduria: A benign renal tubular defect. The Journal of Pediatrics. 79(3). 419–422. 14 indexed citations
20.
Lyon, I., Peter G. Procopis, & B Turner. (1971). CYSTATHIONINURIA IN A WELL BABY POPULATION. Acta Paediatrica. 60(3). 324–328. 9 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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