Jim McGill

1.6k total citations
34 papers, 829 citations indexed

About

Jim McGill is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Jim McGill has authored 34 papers receiving a total of 829 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Clinical Biochemistry, 11 papers in Physiology and 7 papers in Molecular Biology. Recurrent topics in Jim McGill's work include Metabolism and Genetic Disorders (13 papers), Lysosomal Storage Disorders Research (9 papers) and Trypanosoma species research and implications (4 papers). Jim McGill is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Lysosomal Storage Disorders Research (9 papers) and Trypanosoma species research and implications (4 papers). Jim McGill collaborates with scholars based in Australia, United States and Malaysia. Jim McGill's co-authors include Janice M. Fletcher, Bridget Wilcken, Marion Haas, Veronica Wiley, Pamela Joy, Avihu Boneh, Rachael Sharman, Carlina Black, Michael Lynch and Amanda Clacy and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and PEDIATRICS.

In The Last Decade

Jim McGill

33 papers receiving 813 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jim McGill Australia 15 376 306 243 198 182 34 829
David Coman Australia 20 302 0.8× 583 1.9× 302 1.2× 149 0.8× 227 1.2× 79 1.2k
Ali Dursun Türkiye 17 438 1.2× 434 1.4× 215 0.9× 165 0.8× 145 0.8× 97 995
Carolina Fischinger Moura de Souza Brazil 19 362 1.0× 507 1.7× 427 1.8× 279 1.4× 183 1.0× 110 1.2k
François Eyskens Belgium 17 331 0.9× 462 1.5× 158 0.7× 80 0.4× 94 0.5× 38 779
Dimitar Gavrilov United States 15 437 1.2× 403 1.3× 345 1.4× 152 0.8× 121 0.7× 35 901
Mohammed Almannai Saudi Arabia 17 381 1.0× 597 2.0× 125 0.5× 60 0.3× 137 0.8× 43 935
Joyce A. Kobori United States 11 234 0.6× 277 0.9× 329 1.4× 178 0.9× 93 0.5× 14 686
Zuhair N. Al‐Hassnan Saudi Arabia 18 291 0.8× 549 1.8× 166 0.7× 114 0.6× 248 1.4× 78 1.0k
Brendan C. Lanpher United States 17 259 0.7× 581 1.9× 109 0.4× 175 0.9× 465 2.6× 41 1.2k
Ayşegül Tokatlı Türkiye 17 575 1.5× 610 2.0× 249 1.0× 184 0.9× 116 0.6× 101 1.3k

Countries citing papers authored by Jim McGill

Since Specialization
Citations

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

Fields of papers citing papers by Jim McGill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jim McGill

This figure shows the co-authorship network connecting the top 25 collaborators of Jim McGill. A scholar is included among the top collaborators of Jim McGill 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 Jim McGill. Jim McGill 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.
Pretorius, Carel, Paulette Barahona, Jim McGill, et al.. (2023). Feasibility of Targeted Next-Generation DNA Sequencing for Expanding Population Newborn Screening. Clinical Chemistry. 69(8). 890–900. 5 indexed citations
2.
Williams, Clare, et al.. (2019). Nutrition process improvements for adult inpatients with inborn errors of metabolism using the i‐PARIHS framework. Nutrition & Dietetics. 76(2). 141–149. 5 indexed citations
3.
Sharman, Rachael, Karen A. Sullivan, Ross McD. Young, & Jim McGill. (2015). Executive function in adolescents with PKU and their siblings: Associations with biochemistry. SHILAP Revista de lepidopterología. 4. 87–88. 10 indexed citations
4.
Zankl, Andreas, Emma L. Duncan, Paul Leo, et al.. (2014). Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB. The American Journal of Human Genetics. 94(4). 643–643. 3 indexed citations
5.
Leadley, Regina, Shona Lang, Kate Misso, et al.. (2014). A systematic review of the prevalence of Morquio A syndrome: challenges for study reporting in rare diseases. Orphanet Journal of Rare Diseases. 9(1). 173–173. 66 indexed citations
6.
Clacy, Amanda, Rachael Sharman, & Jim McGill. (2014). Depression, Anxiety, and Stress in Young Adults with Phenylketonuria. Journal of Developmental & Behavioral Pediatrics. 35(6). 388–391. 31 indexed citations
7.
Hwu, Wuh‐Liang, Torayuki Okuyama, Xuefan Gu, et al.. (2012). Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region. Molecular Genetics and Metabolism. 107(1-2). 136–144. 5 indexed citations
8.
Zankl, Andreas, Emma L. Duncan, Paul Leo, et al.. (2012). Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB. The American Journal of Human Genetics. 90(3). 494–501. 78 indexed citations
9.
Briody, Julie, J. Ault, Michael Fietz, et al.. (2010). The natural history and osteodystrophy of mucolipidosis types II and III. Journal of Paediatrics and Child Health. 46(6). 316–322. 34 indexed citations
10.
Goldblatt, Jack, Janice M. Fletcher, Jim McGill, Jeff Szer, & Meredith Wilson. (2010). Enzyme replacement therapy “drug holiday”: Results from an unexpected shortage of an orphan drug supply in Australia. Blood Cells Molecules and Diseases. 46(1). 107–110. 37 indexed citations
11.
Sharman, Rachael, Karen A. Sullivan, Ross McD. Young, & Jim McGill. (2009). A Preliminary Investigation of the Role of the Phenylalynine:Tyrosine Ratio in Children With Early and Continuously Treated Phenylketonuria: Toward Identification of “Safe” Levels. Developmental Neuropsychology. 35(1). 57–65. 22 indexed citations
12.
McGill, Jim, et al.. (2008). Fourier Transform Infrared Reflectance Spectra of Latent Fingerprints: A Biometric Gauge for the Age of an Individual*. Journal of Forensic Sciences. 53(2). 369–376. 42 indexed citations
13.
Tran, Khoa D., et al.. (2008). Acute hyperammonemic encephalopathy in adult onset ornithine transcarbamylase deficiency. Intensive Care Medicine. 34(10). 1922–1924. 29 indexed citations
14.
Wilcken, Bridget, Marion Haas, Pamela Joy, et al.. (2007). Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study. The Lancet. 369(9555). 37–42. 127 indexed citations
15.
Coman, David, et al.. (2006). Carbamyl phosphate synthase deficiency: Diagnosed during pregnancy in a 41-year-old. Journal of Clinical Neuroscience. 13(6). 702–706. 18 indexed citations
16.
Schoffer, Kerrie, John D. O’Sullivan, & Jim McGill. (2006). Congenital disorder of glycosylation type Ia presenting as early‐onset cerebellar ataxia in an adult. Movement Disorders. 21(6). 869–872. 5 indexed citations
17.
Goldblatt, Jack, Jeff Szer, Janice M. Fletcher, et al.. (2005). Enzyme replacement therapy for Gaucher disease in Australia. Internal Medicine Journal. 35(3). 156–161. 9 indexed citations
18.
Gaustadnes, Mette, Bridget Wilcken, Jana Oliveriusová, et al.. (2002). The molecular basis of cystathionine ?-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment. Human Mutation. 20(2). 117–126. 45 indexed citations
19.
McGill, Jim, et al.. (2001). Silver Toxicity in an Infant of Strict Vegan Parents. Journal of Pediatric Gastroenterology and Nutrition. 33(4). 501–502. 6 indexed citations
20.
McGill, Jim, et al.. (2001). Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families. Human Mutation. 17(4). 351–351. 52 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by David Coman Breakdown of academic impact, for papers by Ali Dursun Breakdown of academic impact, for papers by Carolina Fischinger Moura de Souza Breakdown of academic impact, for papers by François Eyskens Breakdown of academic impact, for papers by Dimitar Gavrilov Breakdown of academic impact, for papers by Mohammed Almannai Breakdown of academic impact, for papers by Joyce A. Kobori Breakdown of academic impact, for papers by Zuhair N. Al‐Hassnan Breakdown of academic impact, for papers by Brendan C. Lanpher Breakdown of academic impact, for papers by Ayşegül Tokatlı
Rankless by CCL
2026