Ben Lundie

437 total citations
6 papers, 152 citations indexed

About

Ben Lundie is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Ben Lundie has authored 6 papers receiving a total of 152 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Ben Lundie's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Ben Lundie is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Ben Lundie collaborates with scholars based in Australia and United States. Ben Lundie's co-authors include Mark J. Cowley, Marcel E. Dinger, André E. Minoche, Vicki Gibbs, James Harraway, Janice M. Fullerton, Benjamin Kamien, Anna Heath, Nicole Schönrock and Leslie Burnett and has published in prestigious journals such as The American Journal of Human Genetics, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Ben Lundie

6 papers receiving 152 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ben Lundie Australia	5	89	72	36	19	12	6	152
Michael Kennemer United States	4	92 1.0×	92 1.3×	11 0.3×	25 1.3×	17 1.4×	4	181
Samantha Penney United States	5	68 0.8×	76 1.1×	20 0.6×	27 1.4×	9 0.8×	5	157
Natalie B. Tan Australia	6	50 0.6×	69 1.0×	8 0.2×	22 1.2×	9 0.8×	8	131
Anne‐Marie Guerrot France	8	136 1.5×	84 1.2×	8 0.2×	8 0.4×	8 0.7×	17	204
Haktan Bağış Erdem Türkiye	9	68 0.8×	53 0.7×	9 0.3×	11 0.6×	17 1.4×	34	161
Cristina Skrypnyk Bahrain	8	95 1.1×	28 0.4×	7 0.2×	48 2.5×	6 0.5×	17	155
Sawitree Rattanasopha Thailand	4	227 2.6×	112 1.6×	9 0.3×	18 0.9×	10 0.8×	5	297
Julie Kaylor United States	9	103 1.2×	104 1.4×	6 0.2×	8 0.4×	15 1.3×	11	206
Dmitriy Niyazov United States	7	140 1.6×	99 1.4×	11 0.3×	8 0.4×	11 0.9×	8	208
Thibaud Jouan France	5	66 0.7×	57 0.8×	22 0.6×	11 0.6×	26 2.2×	7	111

Countries citing papers authored by Ben Lundie

Since Specialization

Citations

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

Fields of papers citing papers by Ben Lundie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ben Lundie

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

All Works

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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.

Vadlamudi, Lata, Ben Lundie, Hnin Hnin Aung, et al.. (2022). A Multi-Disciplinary Team Approach to Genomic Testing for Drug-Resistant Epilepsy Patients—The GENIE Study. Journal of Clinical Medicine. 11(14). 4238–4238. 5 indexed citations

3.

Mallawaarachchi, Amali, Ben Lundie, Yvonne Hort, et al.. (2021). Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing. European Journal of Human Genetics. 29(5). 760–770. 30 indexed citations

4.

Minoche, André E., Ben Lundie, Greg B. Peters, et al.. (2021). ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data. Genome Medicine. 13(1). 32–32. 38 indexed citations

5.

Minoche, André E., Renée Johnson, Velimir Gayevskiy, et al.. (2018). Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy. Genetics in Medicine. 21(3). 650–662. 43 indexed citations

6.

Kamien, Benjamin, James Harraway, Ben Lundie, et al.. (2013). Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy. American Journal of Medical Genetics Part A. 164(3). 782–788. 33 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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