Fiona Norris

650 total citations
11 papers, 282 citations indexed

About

Fiona Norris is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Fiona Norris has authored 11 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pediatrics, Perinatology and Child Health, 5 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in Fiona Norris's work include Prenatal Screening and Diagnostics (6 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Fiona Norris is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Fiona Norris collaborates with scholars based in Australia, United Kingdom and Netherlands. Fiona Norris's co-authors include Paul G. Ekert, Thomas Kaufmann, Vishva M. Dixit, Andreas Strasser, David C.S. Huang, Ralph K. Lindemann, Lin Tai, Ricky W. Johnstone, David Francis and Mark D. Pertile and has published in prestigious journals such as Cell, Clinical Science and European Journal of Human Genetics.

In The Last Decade

Fiona Norris

11 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fiona Norris Australia 8 153 76 63 61 38 11 282
Manuela Langbein Germany 5 208 1.4× 150 2.0× 62 1.0× 88 1.4× 12 0.3× 5 414
Katharina Schoner Germany 10 113 0.7× 66 0.9× 127 2.0× 35 0.6× 14 0.4× 20 272
Maribel Forero‐Castro Colombia 8 87 0.6× 41 0.5× 43 0.7× 50 0.8× 19 0.5× 29 269
George Rebello South Africa 10 158 1.0× 106 1.4× 67 1.1× 16 0.3× 39 1.0× 25 316
Kyle Gettler United States 6 114 0.7× 31 0.4× 99 1.6× 203 3.3× 25 0.7× 12 362
Daiana Vota Argentina 13 113 0.7× 87 1.1× 17 0.3× 156 2.6× 42 1.1× 31 462
Tatsushi Miyazaki Japan 9 246 1.6× 37 0.5× 127 2.0× 63 1.0× 25 0.7× 15 382
J. Seidel Germany 7 168 1.1× 26 0.3× 90 1.4× 22 0.4× 47 1.2× 18 304
Osamu Miyoshi Japan 11 176 1.2× 74 1.0× 116 1.8× 20 0.3× 12 0.3× 22 278
Jiansheng Xie China 10 155 1.0× 65 0.9× 71 1.1× 33 0.5× 12 0.3× 31 318

Countries citing papers authored by Fiona Norris

Since Specialization
Citations

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

Fields of papers citing papers by Fiona Norris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fiona Norris

This figure shows the co-authorship network connecting the top 25 collaborators of Fiona Norris. A scholar is included among the top collaborators of Fiona Norris 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 Fiona Norris. Fiona Norris is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Norris, Fiona, et al.. (2023). Perinatal outcomes and genomic characteristics of fetal copy number variants: An individual record linkage study of 713 pregnancies. Prenatal Diagnosis. 43(4). 516–526. 2 indexed citations
2.
Hui, Lisa, Sharon Lewis, David J. Amor, et al.. (2021). Study protocol: childhood outcomes of fetal genomic variants: the PrenatAL Microarray (PALM) cohort study. BMC Pediatrics. 21(1). 447–447. 1 indexed citations
3.
Halliday, Jane, Fiona Norris, Sharon Lewis, et al.. (2018). Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study. European Journal of Human Genetics. 26(4). 485–494. 20 indexed citations
5.
Yap, Patrick, George McGillivray, Fiona Norris, et al.. (2015). Fetal phenotype of 17q12 microdeletion syndrome: renal echogenicity and congenital diaphragmatic hernia in 2 cases. Prenatal Diagnosis. 35(12). 1265–1267. 11 indexed citations
6.
James, Paul A., Katherine Rose, David Francis, & Fiona Norris. (2011). High‐level 46XX/46XY chimerism without clinical effect in a healthy multiparous female. American Journal of Medical Genetics Part A. 155(10). 2484–2488. 15 indexed citations
7.
Kaufmann, Thomas, Lin Tai, Paul G. Ekert, et al.. (2007). The BH3-Only Protein Bid Is Dispensable for DNA Damage- and Replicative Stress-Induced Apoptosis or Cell-Cycle Arrest. Cell. 129(2). 423–433. 159 indexed citations
8.
Kaufmann, Thomas, Lin Tai, Paul G. Ekert, et al.. (2007). Response: Does Bid Play a Role in the DNA Damage Response?. Cell. 130(1). 10–11. 7 indexed citations
9.
Bruno, Damien L., Trent Burgess, Hua Ren, et al.. (2006). High‐throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy. American Journal of Medical Genetics Part A. 140A(24). 2786–2793. 45 indexed citations
10.
Norris, Fiona, et al.. (1999). Total IgE and Specific IgG Levels to β-Lactoglobulin and Ovalbumin and Allergy Outcome in Small for Gestational Age Infants: A Pilot Study. Pediatric Asthma Allergy & Immunology. 13(4). 169–175. 2 indexed citations
11.
Gama, Rousseau, Fiona Norris, Linda Morgan, et al.. (1997). Elevated Post-Prandial Gastric Inhibitory Polypeptide Concentrations in Hypertriglyceridaemic Subjects. Clinical Science. 93(4). 343–347. 11 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

Rankless by CCL
2026