Natalie Thorne

6.8k citations

36 papers · 3.7k indexed · 2 hit papers · h-index 21

Impact in

Cancer Research top 1%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
- Cancer Genomics and Diagnostics
Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases

Papers in

Genetics 17
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 9
Cancer Research 9
- Cancer Genomics and Diagnostics 5

Co-authors: Simon Tavaré Mark Dunning Nuno L. Barbosa‐Morais Carlos Caldas Matthew E. Hurles Barbara E. Stranger Emmanouil T. Dermitzakis Richard Redon
Journals: European Journal of Human Genetics (3 papers)Genome biology (3 papers)Nucleic Acids Research (3 papers)PLoS ONE (3 papers)Cancer Research (2 papers)
Partner nations: Australia United Kingdom United States

In The Last Decade

Natalie Thorne

36 papers receiving 3.6k citations

Hit Papers

align trajectories log scale

MicroRNA expression profiling of human breast cancer identifies new markers of tumor subtype 2007 · 750 citations

Peers

Countries citing papers authored by Natalie Thorne

Since Specialization

Citations

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

Fields of papers citing papers by Natalie Thorne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Natalie Thorne, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Natalie Thorne Line = papers co-authored together Natalie Thorne links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Future-proofing genomic data and consent management: a comprehensive review of technology innovations GigaScience ·Carla Maria Flores, Anubhav Kaphle, 위형원, Samkit Jain, Natalie A. Twine, Yuwan Malakar, B. Blarer, Marcel Keller, Thilina Ranbaduge, Eva K.F. Chan, James Breen, Sam Buckberry, Boris Guennewig, Matilda Haas, Alex Brown, Mark J. Cowley, Natalie Thorne, G Pawlonka, Denis C. Bauer	2024	7
2	Moving Genomics into the Clinic: Platforms for Implementing Clinical Genomic Data-Sharing in Ways That Address Ethical, Legal and Social Implications. PubMed ·Dianne Nicol, Margaret Otlowski, Yazeed Taweel, Natalie Thorne, Clara Gaff	2024	1
3	A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis European Journal of Human Genetics ·Tiong Yang Tan, Sebastian Lunke, Belinda Chong, Dean Phelan, Miriam Fanjul‐Fernández, Justine E. Marum, Duo Huang, Zornitza Stark, Alison Yeung, Natasha J. Brown, Chloe Stutterd, Martin B. Delatycki, Simon Sadedin, Melissa Martyn, Ilias Goranitis, Natalie Thorne, Clara Gaff, Susan M. White	2019	35
4	Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders European Journal of Human Genetics ·(unknown), Christianti Arya Putri, Sebastian Lunke, Zornitza Stark, Alison Yeung, Natalie Thorne, Clara Gaff, Susan M. White, Tiong Yang Tan	2018	83
5	A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data European Journal of Human Genetics ·(unknown), Zornitza Stark, Harriet Dashnow, Sebastian Lunke, Tiong Yang Tan, Alison Yeung, Simon Sadedin, Natalie Thorne, Ivan Macciocca, Clara Gaff, Alicia Oshlack, Susan M. White, Paul A. James	2017	13
6	Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsy Epilepsy Research ·Piero Perucca, Ingrid E. Scheffer, A. Simon Harvey, Paul A. James, Sebastian Lunke, Natalie Thorne, Clara Gaff, Brigid M. Regan, John A. Damiano, Michael S. Hildebrand, Samuel F. Berkovic, Terence J. O’Brien, Patrick Kwan	2017	67
7	Cpipe: a shared variant detection pipeline designed for diagnostic settings Genome Medicine ·Simon Sadedin, Harriet Dashnow, Paul A. James, Melanie Bahlo, Denis C. Bauer, Andrew Lonie, Sebastian Lunke, Ivan Macciocca, Jason P. Ross, Kirby Siemering, Zornitza Stark, Susan M. White, (unknown), Graham R. Taylor, Clara Gaff, Alicia Oshlack, Natalie Thorne	2015	54
8	High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNA BMC Medical Genomics ·Dineika Chandrananda, Natalie Thorne, Melanie Bahlo	2015	92
9	Investigating and Correcting Plasma DNA Sequencing Coverage Bias to Enhance Aneuploidy Discovery PLoS ONE ·Dineika Chandrananda, Natalie Thorne, Devika Ganesamoorthy, Damien L. Bruno, Yuval Benjamini, Terence P. Speed, Howard R. Slater, Melanie Bahlo	2014	21
10	The cost of reducing starting RNA quantity for Illumina BeadArrays: A bead-level dilution experiment BMC Genomics ·Andy G. Lynch, James Hadfield, Mark Dunning, Michelle Osborne, Natalie Thorne, Simon Tavaré	2010	4
11	Pediatric Malignant Germ Cell Tumors Show Characteristic Transcriptome Profiles Cancer Research ·Roger D. Palmer, Nuno L. Barbosa‐Morais, Mamoun Mohammed AL-Azzam, Balaji Muralidhar, Claire Thornton, Mark R. Pett, Ian Roberts, Dominik T. Schneider, Natalie Thorne, Simon Tavaré, James C. Nicholson, Nicholas Coleman, (unknown)	2008	54
12	AURKA overexpression accompanies dysregulation of DNA-damage response genes in invasive urothelial cell carcinoma Cell Cycle ·Abhi Veerakumarasivam, Leonard D. Goldstein, Kasra Saeb‐Parsy, Helen E. Scott, Anne Y. Warren, Natalie Thorne, Ian G. Mills, Ashok R. Venkitaraman, David E. Neal, John D. Kelly	2008	13
13	Tissue-specific splicing factor gene expression signatures Nucleic Acids Research ·Ana Rita Grosso, Anita Quintal Gomes, Nuno L. Barbosa‐Morais, Sandra Caldeira, Natalie Thorne, Godfrey Grech, Marieke von Lindern, Maria Carmo‐Fonseca	2008	141
14	Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor PLoS ONE ·Caitlin B. Conboy, Christiana Spyrou, Natalie Thorne, J. Calvo-Otero, Nuno L. Barbosa‐Morais, Michael D. Wilson, Arindam Bhattacharjee, Richard A. Young, Simon Tavaré, Jacqueline A. Lees, Duncan T. Odom	2007	44
15	Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization Genome biology ·John C. Marioni, Natalie Thorne, Armand Valsesia, Tomas Fitzgerald, Richard Redon, Heike Fiegler, T. Daniel Andrews, Barbara E. Stranger, Andy G. Lynch, Emmanouil T. Dermitzakis, Nigel P. Carter, Simon Tavaré, Matthew E. Hurles	2007	101
16	Missing channels in two-colour microarray experiments: Combining single-channel and two-channel data BMC Bioinformatics ·Andy G. Lynch, David E. Neal, John D. Kelly, A. Ojajärvi, Natalie Thorne	2007	3
17	MicroRNA expression profiling of human breast cancer identifies new markers of tumor subtype Genome biology ·Cherie Blenkiron, Leonard D. Goldstein, Natalie Thorne, Inmaculada Spiteri, Suet‐Feung Chin, Mark Dunning, Nuno L. Barbosa‐Morais, Andrew E. Teschendorff, Andrew R. Green, Ian O. Ellis, Simon Tavaré, Carlos Caldas, Eric A. Miska Hit paper breakdown →	2007	750
18	Metabolic Consequences of p300 Gene Deletion in Human Colon Cancer Cells Cancer Research ·Jacob G. Bundy, N. Gopalakrishna Iyer, Michelle Gentile, De‐En Hu, Mikko I. Kettunen, Ana-Teresa Maia, Natalie Thorne, James D. Brenton, Carlos Caldas, Kevin M. Brindle	2006	23
19	Using array-comparative genomic hybridization to define molecular portraits of primary breast cancers Oncogene ·Suet‐Feung Chin, Yanzhong Wang, Natalie Thorne, Andrew E. Teschendorff, Sarah E. Pinder, Maria Vias, Ali Naderi, Ian Roberts, Nuno L. Barbosa‐Morais, María J. García, N. Gopalakrishna Iyer, Xiaojing Li, J.F.R. Robertson, Samuel Aparício, Simon Tavaré, Ian O. Ellis, James D. Brenton, Carlos Caldas	2006	89
20	MMASS: an optimized array-based method for assessing CpG island methylation Nucleic Acids Research ·Ashraf E.K. Ibrahim, Natalie Thorne, Katie Baird, Nuno L. Barbosa‐Morais, Simon Tavaré, V. Peter Collins, Andrew H. Wyllie, Mark J. Arends, James D. Brenton	2006	35

About Natalie Thorne

Natalie Thorne is a scholar working on Genetics, Cancer Research, Molecular Biology, Information Systems and Management and Pediatrics, Perinatology and Child Health, having authored 36 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (9 papers), Gene expression and cancer classification (6 papers), Molecular Biology Techniques and Applications (5 papers), Cancer Genomics and Diagnostics (5 papers), Prenatal Screening and Diagnostics (4 papers), RNA modifications and cancer (4 papers) and Genomics and Chromatin Dynamics (4 papers). The work is most often cited by research in Cancer Research (1.3k citations), Genetics (1.5k citations), Molecular Biology (2.6k citations), Pediatrics, Perinatology and Child Health (219 citations) and Oncology (261 citations). Natalie Thorne has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Simon Tavaré, Mark Dunning, Nuno L. Barbosa‐Morais, Carlos Caldas, Matthew E. Hurles, Barbara E. Stranger, Emmanouil T. Dermitzakis, Richard Redon, Andrew E. Teschendorff and Suet‐Feung Chin. Their work appears in journals such as European Journal of Human Genetics, Genome biology, Nucleic Acids Research, PLoS ONE and Cancer Research.

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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