Elise Ruark

3.7k total citations
10 papers, 601 citations indexed

About

Elise Ruark is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Elise Ruark has authored 10 papers receiving a total of 601 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Elise Ruark's work include Cancer Genomics and Diagnostics (4 papers), BRCA gene mutations in cancer (3 papers) and Genetic factors in colorectal cancer (3 papers). Elise Ruark is often cited by papers focused on Cancer Genomics and Diagnostics (4 papers), BRCA gene mutations in cancer (3 papers) and Genetic factors in colorectal cancer (3 papers). Elise Ruark collaborates with scholars based in United Kingdom, Austria and South Africa. Elise Ruark's co-authors include Nazneen Rahman, Sheila Seal, Shazia Mahamdallie, Emma Ramsay, Anna Elliott, Matthew Clarke, Anna Zachariou, Ann Strydom, Chey Loveday and Katrina Tatton‐Brown and has published in prestigious journals such as Nature Communications, Nature Genetics and Scientific Reports.

In The Last Decade

Elise Ruark

10 papers receiving 598 citations

Peers

Countries citing papers authored by Elise Ruark

Since Specialization

Citations

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

Fields of papers citing papers by Elise Ruark

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elise Ruark

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Insights into BRCA Cancer Predisposition from Integrated Germline and Somatic Analyses in 7632 Cancers 2019 ·JNCI Cancer Spectrum ·Shawn Yost, Elise Ruark, Ludmil B. Alexandrov, Nazneen Rahman	4
2	Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability 2017 ·The American Journal of Human Genetics ·Katrina Tatton‐Brown, Chey Loveday, Shawn Yost, Matthew Clarke, Emma Ramsay, Anna Zachariou, Anna Elliott, Harriet Wylie, Anna Ardissone, Olaf Rittinger, Fiona Stewart, I. Karen Temple, Trevor Cole, Shazia Mahamdallie, Sheila Seal, Elise Ruark, Nazneen Rahman	128
3	Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients 2016 ·Scientific Reports ·Angela George, (unknown), Sheila Seal, Sabrina Talukdar, Shazia Mahamdallie, Elise Ruark, (unknown), Ingrid Slade, Zoe Kemp, Martin Gore, Ann Strydom, Susana Banerjee, Helen Hanson, Nazneen Rahman	157
4	OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis 2016 ·Scientific Reports ·Elise Ruark, Márton Münz, Matthew Clarke, Anthony Renwick, Emma Ramsay, Anna Elliott, Sheila Seal, Gerton Lunter, Nazneen Rahman	4
5	Mutations in the PP2A regulatory subunit B family genesPPP2R5B,PPP2R5CandPPP2R5Dcause human overgrowth 2015 ·Human Molecular Genetics ·Chey Loveday, Katrina Tatton‐Brown, Matthew Clarke, Isaac M. Westwood, Anthony Renwick, Emma Ramsay, Andrea H. Németh, Jennifer Campbell, Shelagh Joss, (unknown), Anna Zachariou, Anna Elliott, Elise Ruark, Rob van Montfort, Nazneen Rahman	62
6	CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting 2015 ·Genome Medicine ·Márton Münz, Elise Ruark, Anthony Renwick, Emma Ramsay, Matthew Clarke, Shazia Mahamdallie, (unknown), Sheila Seal, Ann Strydom, Gerton Lunter, Nazneen Rahman	29
7	The ICR1000 UK exome series: a resource of gene variation in an outbred population [version 1; referees: 2 approved] 2015 ·Elise Ruark, Márton Münz, Anthony Renwick, Matthew Clarke, Emma Ramsay, Sandra Hanks, Shazia Mahamdallie, Anna Elliott, Sheila Seal, Ann Strydom, (unknown), Nazneen Rahman	2
8	Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour 2014 ·Nature Communications ·Sandra Hanks, Elizabeth R Perdeaux, Sheila Seal, Elise Ruark, Shazia Mahamdallie, Anne R. Murray, Emma Ramsay, (unknown), Anna Zachariou, (unknown), Margaret Warren-Perry, Anna Elliott, Alan Davidson, Helen P. Price, Charles Stiller, Kathy Pritchard‐Jones, Nazneen Rahman	64
9	Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14 2013 ·Nature Genetics ·Elise Ruark, Sheila Seal, Heather McDonald, Feng Zhang, (unknown), (unknown), Elizabeth R Perdeaux, Elizabeth Rapley, Rosalind A. Eeles, Julian Peto, Zsofia Kote‐Jarai, Kenneth Muir, Jérémie Nsengimana, Janet Shipley, D. Timothy Bishop, Michael R. Stratton, Douglas F. Easton, Robert Huddart, Nazneen Rahman, Clare Turnbull	115
10	Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer 2012 ·Breast Cancer Research and Treatment ·Katie Snape, Elise Ruark, Patrick Tarpey, Anthony Renwick, Clare Turnbull, Sheila Seal, Anne R. Murray, Sandra Hanks, Jenny Douglas, Michael R. Stratton, Nazneen Rahman	36

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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