James McGill

2.1k total citations
37 papers, 768 citations indexed

About

James McGill is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, James McGill has authored 37 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Molecular Biology and 12 papers in Clinical Biochemistry. Recurrent topics in James McGill's work include Metabolism and Genetic Disorders (12 papers), Connective tissue disorders research (8 papers) and Neonatal Health and Biochemistry (4 papers). James McGill is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Connective tissue disorders research (8 papers) and Neonatal Health and Biochemistry (4 papers). James McGill collaborates with scholars based in Australia, United States and Canada. James McGill's co-authors include Vazken M. Der Kaloustian, Robert S. Ware, Sharron Townshend, Verity Pacey, Andreas Zankl, David Sillence, Leanne M. Johnston, Ravi Savarirayan, J. Ault and Hinda Kopelman and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Applied Ecology and Developmental Medicine & Child Neurology.

In The Last Decade

James McGill

36 papers receiving 729 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James McGill Australia 17 385 366 176 138 86 37 768
Felicity Collins Australia 16 326 0.8× 406 1.1× 140 0.8× 133 1.0× 155 1.8× 22 760
Thaddeus W. Kurczynski United States 18 366 1.0× 230 0.6× 116 0.7× 119 0.9× 40 0.5× 47 842
Christiane Theda Australia 16 520 1.4× 774 2.1× 158 0.9× 181 1.3× 172 2.0× 24 1.3k
Melissa Maisenbacher United States 17 401 1.0× 511 1.4× 86 0.5× 331 2.4× 82 1.0× 33 1.0k
Tanya N. Nelson Canada 21 450 1.2× 308 0.8× 51 0.3× 276 2.0× 68 0.8× 51 1.0k
Karen L. David United States 12 491 1.3× 263 0.7× 57 0.3× 226 1.6× 44 0.5× 14 899
Alessandro De Grandi Italy 14 301 0.8× 316 0.9× 115 0.7× 28 0.2× 37 0.4× 32 819
Shaoke Chen China 17 238 0.6× 326 0.9× 47 0.3× 171 1.2× 49 0.6× 69 778
Sofia Helena Valente de Lemos‐Marini Brazil 16 440 1.1× 526 1.4× 66 0.4× 66 0.5× 18 0.2× 99 880
E A Werder Switzerland 20 675 1.8× 767 2.1× 47 0.3× 299 2.2× 45 0.5× 46 1.3k

Countries citing papers authored by James McGill

Since Specialization
Citations

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

Fields of papers citing papers by James McGill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James McGill

This figure shows the co-authorship network connecting the top 25 collaborators of James McGill. A scholar is included among the top collaborators of James 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 James McGill. James 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.
Coman, David, Adam D. Ewing, Sally Smith, et al.. (2024). Molecular genetic analysis of candidate genes for glutaric aciduria type II in a cohort of patients from Queensland, Australia. Molecular Genetics and Metabolism. 142(4). 108516–108516. 6 indexed citations
2.
Coman, David, Lisenka E.L.M. Vissers, Lisa G. Riley, et al.. (2018). Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis. The American Journal of Human Genetics. 103(1). 125–130. 23 indexed citations
3.
McGill, James, Andreas Zankl, Robert S. Ware, et al.. (2012). Development in children with achondroplasia: a prospective clinical cohort study. Developmental Medicine & Child Neurology. 54(6). 532–537. 49 indexed citations
4.
McGill, James, Andreas Zankl, Robert S. Ware, et al.. (2011). Functional performance in young Australian children with achondroplasia. Developmental Medicine & Child Neurology. 53(10). 944–950. 52 indexed citations
5.
Johnson, Sarah E., Leanne M. Johnston, Robert S. Ware, et al.. (2011). Medical management of children with achondroplasia: Evaluation of an Australasian cohort aged 0–5 years. Journal of Paediatrics and Child Health. 48(5). 443–449. 19 indexed citations
6.
Mazzeu, Juliana F., Ana Cristina Victorino Krepischi, Astrid Oudakker, et al.. (2010). Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clinical Genetics. 77(4). 404–407. 9 indexed citations
7.
Johnson, Sarah E., Leanne M. Johnston, James McGill, et al.. (2010). Developmental Milestones in Infants and Young Australasian Children With Achondroplasia. Journal of Developmental & Behavioral Pediatrics. 31(1). 41–47. 33 indexed citations
8.
Ong, Beng Beng, et al.. (2009). Retinal hemorrhages associated with meningitis in a child with a congenital disorder of glycosylation. Forensic Science Medicine and Pathology. 5(4). 307–312. 6 indexed citations
9.
Sharman, Rachael, Karen A. Sullivan, Ross McD. Young, & James McGill. (2009). Biochemical markers associated with executive function in adolescents with early and continuously treated phenylketonuria. Clinical Genetics. 75(2). 169–174. 22 indexed citations
10.
Coman, David, James McGill, R. MacDonald, et al.. (2007). Congenital disorder of glycosylation type 1a: Three siblings with a mild neurological phenotype. Journal of Clinical Neuroscience. 14(7). 668–672. 28 indexed citations
11.
Coman, David, Jianping Huang, Steven McTaggart, et al.. (2005). Renal transplantation in a 14-year-old girl with vitamin B12-responsive cblA-type methylmalonic acidaemia. Pediatric Nephrology. 21(2). 270–273. 15 indexed citations
12.
Bowling, Francis, et al.. (1999). Maternal gonadal mosaicism causing ornithine transcarbamylase deficiency. American Journal of Medical Genetics. 85(5). 452–454. 9 indexed citations
13.
White, S. L., Sara Shanske, James McGill, et al.. (1999). Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue‐ or age‐related variation. Journal of Inherited Metabolic Disease. 22(8). 899–914. 78 indexed citations
14.
Callen, David F., Helen J. Eyre, Yuqiang Fang, et al.. (1999). Origins of accessory small ring marker chromosomes derived from chromosome 1. Journal of Medical Genetics. 36(11). 847–853. 14 indexed citations
15.
Healey, Sue, et al.. (1994). Distinct phenotype in maternal uniparental disomy of chromosome 14. American Journal of Medical Genetics. 51(2). 147–149. 56 indexed citations
16.
Logan, J. S. & James McGill. (1992). Study of particle emission in vacuum from film deposits. Journal of Vacuum Science & Technology A Vacuum Surfaces and Films. 10(4). 1875–1878. 18 indexed citations
17.
Schwartz, Charles E., Angela Brown, Vazken M. Der Kaloustian, James McGill, & Robert A. Saul. (1991). DNA Fingerprinting: The Utilization of Minisatellite Probes to Detect a Somatic Mutation in the Proteus Syndrome. Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions. 58. 95–105. 16 indexed citations
18.
Kaloustian, Vazken M. Der, James McGill, Michel Vekemans, & Hinda Kopelman. (1990). Clonal lines of aneuploid cells in Rothmund‐Thomson syndrome. American Journal of Medical Genetics. 37(3). 336–339. 51 indexed citations
19.
McGill, James, Gabrielle Mettler, David S. Rosenblatt, & Charles R. Scriver. (1990). Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: Paradigm of Pitfalls in phenotypes. American Journal of Medical Genetics. 36(1). 45–52. 26 indexed citations
20.
McGill, James, et al.. (1981). ENVENOMATION BY SEA SNAKE IN QUEENSLAND. The Medical Journal of Australia. 1(3). 130–132. 10 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 Felicity Collins Breakdown of academic impact, for papers by Thaddeus W. Kurczynski Breakdown of academic impact, for papers by Christiane Theda Breakdown of academic impact, for papers by Melissa Maisenbacher Breakdown of academic impact, for papers by Tanya N. Nelson Breakdown of academic impact, for papers by Karen L. David Breakdown of academic impact, for papers by Alessandro De Grandi Breakdown of academic impact, for papers by Shaoke Chen Breakdown of academic impact, for papers by Sofia Helena Valente de Lemos‐Marini Breakdown of academic impact, for papers by E A Werder
Rankless by CCL
2026