Conrad Leonard

29.8k total citations
8 papers, 42 citations indexed

About

Conrad Leonard is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Conrad Leonard has authored 8 papers receiving a total of 42 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Conrad Leonard's work include Genomics and Rare Diseases (3 papers), Cancer Genomics and Diagnostics (3 papers) and High-Energy Particle Collisions Research (1 paper). Conrad Leonard is often cited by papers focused on Genomics and Rare Diseases (3 papers), Cancer Genomics and Diagnostics (3 papers) and High-Energy Particle Collisions Research (1 paper). Conrad Leonard collaborates with scholars based in Australia. Conrad Leonard's co-authors include John V. Pearson, Nicola Waddell, Kátia Nones, Oliver Holmes, Felicity Newell, Scott Wood, Qinying Xu, Olga Kondrashova, Lloyd C. L. Hollenberg and Lambros T. Koufariotis and has published in prestigious journals such as Bioinformatics, Annals of Oncology and Human Mutation.

In The Last Decade

Conrad Leonard

8 papers receiving 42 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Conrad Leonard Australia	5	24	14	14	8	5	8	42
Ai Okada Japan	4	60 2.5×	8 0.6×	15 1.1×	18 2.3×	3 0.6×	9	79
Nikolay Chekanov Russia	5	73 3.0×	5 0.4×	24 1.7×	6 0.8×	4 0.8×	9	106
M.‐M. Garcia‐Barceló Hong Kong	2	19 0.8×	7 0.5×	8 0.6×	6 0.8×	3 0.6×	2	30
Paul Hale United States	2	35 1.5×	6 0.4×	19 1.4×	6 0.8×	4 0.8×	2	55
Frédéric Reinier France	4	40 1.7×	8 0.6×	14 1.0×	5 0.6×	3 0.6×	4	59
Krista Smith United States	3	54 2.3×	9 0.6×	14 1.0×	13 1.6×	9 1.8×	5	78
Joanne Dixon United Kingdom	2	29 1.2×	13 0.9×	17 1.2×	11 1.4×	1 0.2×	3	48
Cecilia E Kim United States	2	25 1.0×	5 0.4×	32 2.3×	8 1.0×	5 1.0×	4	53
Piers Wilkinson United Kingdom	2	66 2.8×	9 0.6×	12 0.9×	9 1.1×	3 0.6×	3	75
Kimberly Ingalls United States	5	43 1.8×	19 1.4×	11 0.8×	15 1.9×	21 4.2×	7	81

Countries citing papers authored by Conrad Leonard

Since Specialization

Citations

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

Fields of papers citing papers by Conrad Leonard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Conrad Leonard

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

All Works

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8 of 8 papers shown

1.

Leonard, Conrad. (2023). streammd : fast low-memory duplicate marking using a Bloom filter. Bioinformatics. 39(4). 2 indexed citations

2.

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

3.

Holmes, Oliver, Kátia Nones, Yue Tang, et al.. (2022). qmotif: determination of telomere content from whole-genome sequence data. Bioinformatics Advances. 2(1). vbac005–vbac005. 6 indexed citations

4.

Leonard, Conrad, Lambros T. Koufariotis, Michael T. Parsons, et al.. (2021). Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a model. Human Mutation. 42(5). 530–536. 5 indexed citations

5.

Newell, Felicity, Stephen H. Kazakoff, Günter Härtel, et al.. (2020). Using whole-genome sequencing data to derive the homologous recombination deficiency scores. npj Breast Cancer. 6(1). 33–33. 17 indexed citations

6.

Leonard, Conrad, Scott Wood, Oliver Holmes, et al.. (2019). Running Genomic Analyses in the Cloud. Studies in health technology and informatics. 266. 149–155. 2 indexed citations

7.

Nones, Kátia, Felicity Newell, Olga Kondrashova, et al.. (2019). Detection of actionable variants in various cancer types reveals value of whole-genome sequencing over in-silico whole-exome and hotspot panel sequencing. Annals of Oncology. 30. vii33–vii33. 1 indexed citations

8.

McKellar, Bruce H. J., Conrad Leonard, & Lloyd C. L. Hollenberg. (2000). COUPLED CLUSTER METHODS FOR LATTICE GAUGE THEORIES. International Journal of Modern Physics B. 14(19n20). 2023–2037. 4 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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