Christopher Barnett

4.8k total citations
61 papers, 1.1k citations indexed

About

Christopher Barnett is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Christopher Barnett has authored 61 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 21 papers in Molecular Biology and 19 papers in Surgery. Recurrent topics in Christopher Barnett's work include Gastroesophageal reflux and treatments (15 papers), Connective tissue disorders research (7 papers) and Neonatal Respiratory Health Research (7 papers). Christopher Barnett is often cited by papers focused on Gastroesophageal reflux and treatments (15 papers), Connective tissue disorders research (7 papers) and Neonatal Respiratory Health Research (7 papers). Christopher Barnett collaborates with scholars based in Australia, United States and Canada. Christopher Barnett's co-authors include Ross Haslam, Taher Omari, John Dent, Marc A. Benninga, Geoff Davidson, Geoffrey P. Davidson, Louise Goodchild, Jillian Nicholl, M Bakewell and Aleksander Hinek and has published in prestigious journals such as Gastroenterology, PEDIATRICS and Gut.

In The Last Decade

Christopher Barnett

59 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher Barnett Australia 21 430 399 259 245 229 61 1.1k
Lee M. Bass United States 16 428 1.0× 81 0.2× 69 0.3× 48 0.2× 351 1.5× 39 1.0k
Elke Fröhlich‐Reiterer Austria 23 580 1.3× 331 0.8× 983 3.8× 57 0.2× 25 0.1× 80 1.6k
Liat de Vries Israel 25 352 0.8× 48 0.1× 634 2.4× 492 2.0× 49 0.2× 59 1.6k
Tommaso Aversa Italy 26 200 0.5× 39 0.1× 493 1.9× 306 1.2× 86 0.4× 111 1.8k
Leah Hoechstetter United States 6 181 0.4× 201 0.5× 148 0.6× 40 0.2× 85 0.4× 7 612
J. M. Hutson Australia 21 498 1.2× 124 0.3× 180 0.7× 298 1.2× 133 0.6× 68 1.4k
Gönül Öçal Türkiye 18 153 0.4× 28 0.1× 397 1.5× 468 1.9× 52 0.2× 102 1.2k
Christine Simpson United States 19 143 0.3× 51 0.1× 167 0.6× 239 1.0× 118 0.5× 49 1.3k
Eirini Nestoridi United States 16 492 1.1× 27 0.1× 56 0.2× 194 0.8× 68 0.3× 48 984
Dorothy I. Shulman United States 20 358 0.8× 20 0.1× 602 2.3× 472 1.9× 140 0.6× 69 1.9k

Countries citing papers authored by Christopher Barnett

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Barnett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Barnett

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Barnett. A scholar is included among the top collaborators of Christopher Barnett 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 Christopher Barnett. Christopher Barnett 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.
Fitzgerald, Lara, et al.. (2024). Medicare‐funded reproductive genetic carrier screening in Australia has arrived: are we ready?. The Medical Journal of Australia. 220(8). 394–397. 2 indexed citations
2.
Karolak, Justyna A., Przemysław Szafrański, Tomasz Gambin, et al.. (2022). Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant. European Journal of Human Genetics. 30(10). 1182–1186. 2 indexed citations
3.
Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations
4.
Byrne, Alicia B., Jinghua Feng, Thuong Ha, et al.. (2021). Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia. BMC Medical Genomics. 14(1). 64–64. 5 indexed citations
5.
Arts, Peer, Alicia B. Byrne, Tristan Hardy, et al.. (2020). Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome. American Journal of Medical Genetics Part A. 182(5). 1273–1277. 11 indexed citations
6.
Stark, Zornitza, Amy Nisselle, Belinda McClaren, et al.. (2019). Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care. European Journal of Human Genetics. 27(10). 1493–1501. 37 indexed citations
7.
Pérez‐Jurado, Luis A., et al.. (2019). Novel KIT mutation presenting as marked lentiginosis. Pediatric Dermatology. 36(6). 922–925. 2 indexed citations
8.
LeBlanc, Shannon, Dávid Dávid, Alison Colley, et al.. (2018). Atypical Skin Manifestations in <b><i>FGFR2</i></b>-Related Craniosynostosis Syndromes Broaden the Phenotypic Spectrum. Molecular Syndromology. 9(3). 149–153. 1 indexed citations
9.
Wilkinson, Dominic, Christopher Barnett, Julian Savulescu, & Ainsley J. Newson. (2015). Genomic intensive care: should we perform genome testing in critically ill newborns?. Archives of Disease in Childhood Fetal & Neonatal. 101(2). F94–F98. 23 indexed citations
10.
Barnett, Christopher & Bregje W.M. van Bon. (2015). Monogenic and chromosomal causes of isolated speech and language impairment. Journal of Medical Genetics. 52(11). 719–729. 15 indexed citations
11.
Patel, Sandeep, et al.. (2012). Novel Clinical Features in Pontine Tegmental Cap Dysplasia. Pediatric Neurology. 46(6). 393–396. 10 indexed citations
12.
Barnett, Christopher, David Chitayat, Timothy J. Bradley, Yanting Wang, & Aleksander Hinek. (2011). Dexamethasone normalizes aberrant elastic fiber production and collagen 1 secretion by Loeys–Dietz syndrome fibroblasts: a possible treatment?. European Journal of Human Genetics. 19(6). 624–633. 27 indexed citations
13.
Moore, Lynette, et al.. (2011). Novel TSEN54 Mutation Causing Pontocerebellar Hypoplasia Type 4. Pediatric Neurology. 45(3). 185–188. 3 indexed citations
14.
Barnett, Christopher, Gregory J. Wilson, David A. Chiasson, et al.. (2010). Central nervous system abnormalities in two cases with neonatal Marfan syndrome with novel mutations in the fibrillin‐1 gene. American Journal of Medical Genetics Part A. 152A(9). 2409–2412. 5 indexed citations
15.
Barnett, Christopher, Jacob C. Langer, Aleksander Hinek, Timothy J. Bradley, & David Chitayat. (2009). Looking past the lump: genetic aspects of inguinal hernia in children. Journal of Pediatric Surgery. 44(7). 1423–1431. 21 indexed citations
16.
Omari, Taher, Christopher Barnett, Marc A. Benninga, et al.. (2002). Mechanisms of gastro-oesophageal reflux in preterm and term infants with reflux disease. Gut. 51(4). 475–479. 166 indexed citations
17.
Harford, William V., et al.. (2000). Acute gastritis with hypochlorhydria: report of 35 cases with long term follow up. Gut. 47(4). 467–472. 48 indexed citations
18.
Omari, Taher, Christopher Barnett, G.P. Davidson, et al.. (1999). Mechanism of gastroesophageal reflux in premature infants with chronic lung disease. Journal of Pediatric Surgery. 34(12). 1795–1798. 25 indexed citations
19.
Barnett, Christopher, et al.. (1998). Characteristics of upper esophageal sphincter relaxation in healthy premature infants. Gastroenterology. 114. A814–A814. 1 indexed citations
20.
Omari, Taher, Christopher Barnett, Wendy Goldsworthy, et al.. (1998). Mechanisms of gastroesophageal reflux in healthy premature infants. The Journal of Pediatrics. 133(5). 650–654. 94 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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