Clare Puttick

4.5k total citations
7 papers, 151 citations indexed

About

Clare Puttick is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Clare Puttick has authored 7 papers receiving a total of 151 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Clare Puttick's work include Genomics and Rare Diseases (4 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). Clare Puttick is often cited by papers focused on Genomics and Rare Diseases (4 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). Clare Puttick collaborates with scholars based in Australia, United Kingdom and Netherlands. Clare Puttick's co-authors include Mark J. Cowley, John Christodoulou, David R. Thorburn, Lisa G. Riley, Rocío Rius, Carolyn M. Sue, André E. Minoche, Velimir Gayevskiy, Marcel E. Dinger and Kishore R. Kumar and has published in prestigious journals such as Nature Genetics, Neurology and Genetics in Medicine.

In The Last Decade

Clare Puttick

7 papers receiving 151 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Clare Puttick Australia	5	103	56	48	24	15	7	151
Juvid Aryaman United Kingdom	9	212 2.1×	67 1.2×	30 0.6×	19 0.8×	27 1.8×	11	267
Gaurav V. Harlalka United Kingdom	10	184 1.8×	25 0.4×	95 2.0×	41 1.7×	19 1.3×	17	272
Huifang Yan China	9	108 1.0×	23 0.4×	79 1.6×	9 0.4×	10 0.7×	23	201
Maria Kibæk Denmark	10	163 1.6×	41 0.7×	135 2.8×	19 0.8×	9 0.6×	14	277
Dmitriy Niyazov United States	7	140 1.4×	37 0.7×	99 2.1×	11 0.5×	4 0.3×	8	208
Tim M. Strom Germany	3	224 2.2×	89 1.6×	62 1.3×	33 1.4×	10 0.7×	3	293
Marta Spodenkiewicz France	5	79 0.8×	19 0.3×	17 0.4×	25 1.0×	16 1.1×	8	156
Pedro Louro Portugal	6	66 0.6×	11 0.2×	44 0.9×	17 0.7×	14 0.9×	11	112
Selina Reich Germany	5	96 0.9×	17 0.3×	24 0.5×	37 1.5×	10 0.7×	8	127
Kether Guerrero Canada	9	195 1.9×	10 0.2×	23 0.5×	14 0.6×	19 1.3×	15	221

Countries citing papers authored by Clare Puttick

Since Specialization

Citations

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

Fields of papers citing papers by Clare Puttick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clare Puttick

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

All Works

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7 of 7 papers shown

1.

Puttick, Clare, Michelle Leung, Felipe Gálvez‐Cancino, et al.. (2024). MHC Hammer reveals genetic and non-genetic HLA disruption in cancer evolution. Nature Genetics. 56(10). 2121–2131. 15 indexed citations

2.

Puttick, Clare, Ryan L. Davis, Kishore R. Kumar, et al.. (2024). mity: A Highly Sensitive Mitochondrial Variant Analysis Pipeline for Whole Genome Sequencing Data. 7(1). 3 indexed citations

3.

Usaite, Ieva, Dhruva Biswas, Krijn K. Dijkstra, et al.. (2023). Quantifying the impact of immunotherapy on RNA dynamics in cancer. Journal for ImmunoTherapy of Cancer. 11(11). e007870–e007870. 2 indexed citations

4.

Davis, Ryan L., Kishore R. Kumar, Clare Puttick, et al.. (2022). Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis. Neurology. 99(7). e730–e742. 32 indexed citations

5.

Riley, Lisa G., Mark J. Cowley, Velimir Gayevskiy, et al.. (2020). The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease. Genetics in Medicine. 22(7). 1254–1261. 45 indexed citations

6.

Rius, Rocío, Mark J. Cowley, Lisa G. Riley, et al.. (2019). Biparental inheritance of mitochondrial DNA in humans is not a common phenomenon. Genetics in Medicine. 21(12). 2823–2826. 32 indexed citations

7.

Kumar, Kishore R., Gautam Wali, Mahesh Kamate, et al.. (2016). Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing. Neurogenetics. 17(4). 265–270. 22 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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