Emma Tudini

646 total citations
6 papers, 21 citations indexed

About

Emma Tudini is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Emma Tudini has authored 6 papers receiving a total of 21 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Emma Tudini's work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers) and Ethics in Clinical Research (1 paper). Emma Tudini is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers) and Ethics in Clinical Research (1 paper). Emma Tudini collaborates with scholars based in Australia, United States and Netherlands. Emma Tudini's co-authors include Amanda B. Spurdle, Michael T. Parsons, Olga Kondrashova, John V. Pearson, Matilda Haas, Lizet van der Kolk, Nicola Waddell, Barbara Wappenschmidt, Conxi Lázaro and Georgina E. Hollway and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Breast Cancer Research and Treatment.

In The Last Decade

Emma Tudini

6 papers receiving 21 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emma Tudini Australia	3	17	11	3	2	2	6	21
Diane Masser‐Frye United States	2	12 0.7×	8 0.7×	3 1.0×	2 1.0×	2 1.0×	3	18
Kendra Engleman United States	4	12 0.7×	16 1.5×	2 0.7×	4 2.0×	2 1.0×	6	26
Timothy Poterba United States	3	12 0.7×	7 0.6×	5 1.7×	2 1.0×		4	19
Marc Hanauer France	3	20 1.2×	21 1.9×	4 1.3×	2 1.0×		5	27
Kimberley Gamet New Zealand	2	8 0.5×	7 0.6×	3 1.0×		2 1.0×	5	14
Ken Wiley United States	2	19 1.1×	12 1.1×	3 1.0×	1 0.5×		6	23
Lisa Salz United States	4	15 0.9×	8 0.7×	4 1.3×	1 0.5×		4	25
Dilbar Dalimova Uzbekistan	3	24 1.4×	9 0.8×	2 0.7×	4 2.0×	1 0.5×	4	33
Thomas Defay United States	3	18 1.1×	10 0.9×	2 0.7×	1 0.5×	1 0.5×	4	22

Countries citing papers authored by Emma Tudini

Since Specialization

Citations

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

Fields of papers citing papers by Emma Tudini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Tudini

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Villani, Rehan M., Bronwyn Terrill, Emma Tudini, et al.. (2025). Consultation informs strategies for improving the use of functional evidence in variant classification. The American Journal of Human Genetics. 112(6). 1489–1495. 3 indexed citations

2.

Best, Stephanie, C. Richards, Michael C. Quinn, et al.. (2024). Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services. European Journal of Human Genetics. 32(11). 1428–1435. 2 indexed citations

3.

Tudini, Emma, et al.. (2023). Reporting clinically relevant genetic variants unrelated to genomic test requests: a survey of Australian clinical laboratory policies and practices. Journal of Medical Genetics. 60(6). 609–614. 2 indexed citations

4.

Kondrashova, Olga, Conrad Leonard, Scott Wood, et al.. (2022). Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions. Human Mutation. 43(12). 2054–2062. 5 indexed citations

5.

Ip, Emilia, Catriona M. McNeil, Peter Grimison, et al.. (2021). Catastrophic chemotherapy toxicity leading to diagnosis of Fanconi anaemia due to FANCD1/BRCA2 during adulthood: description of an emerging phenotype. Journal of Medical Genetics. 59(9). 912–915. 2 indexed citations

6.

Tudini, Emma, Setareh Moghadasi, Michael T. Parsons, et al.. (2018). Substantial evidence for the clinical significance of missense variant BRCA1 c.5309G>T p.(Gly1770Val). Breast Cancer Research and Treatment. 172(2). 497–503. 7 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