Laura Tooke

755 total citations
8 papers, 534 citations indexed

About

Laura Tooke is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laura Tooke has authored 8 papers receiving a total of 534 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laura Tooke's work include Cancer Mechanisms and Therapy (3 papers), Prenatal Screening and Diagnostics (3 papers) and Chromatin Remodeling and Cancer (3 papers). Laura Tooke is often cited by papers focused on Cancer Mechanisms and Therapy (3 papers), Prenatal Screening and Diagnostics (3 papers) and Chromatin Remodeling and Cancer (3 papers). Laura Tooke collaborates with scholars based in United States. Laura Tooke's co-authors include Jaclyn A. Biegel, Alexander R. Judkins, Luanne Wainwright, Håkon Håkonarson, Xiaowu Gai, Tamim H. Shaikh, Eric M. Jackson, Juan C. Perín, Angela J. Sievert and Hongbo Xie and has published in prestigious journals such as Clinical Cancer Research, Brain Pathology and Genes Chromosomes and Cancer.

In The Last Decade

Laura Tooke

8 papers receiving 525 citations

Peers

Countries citing papers authored by Laura Tooke

Since Specialization

Citations

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

Fields of papers citing papers by Laura Tooke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Tooke

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

#	Work	Indexed citations
1	Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients 2017 ·Genes Chromosomes and Cancer ·Tracy Busse, Jacquelyn J. Roth, (unknown), Luanne Wainwright, Laura Tooke, Jaclyn A. Biegel	19
2	Malignant rhabdoid tumor of the bladder and ganglioglioma in a 14 year-old male with a germline 22q11.2 deletion 2014 ·Cancer Genetics ·Kristopher R. Bosse, Aseem R. Shukla, Bruce Pawel, Kudakwashe Chikwava, Mariarita Santi, Laura Tooke, (unknown), Jaclyn A. Biegel, Rochelle Bagatell	12
3	Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors 2014 ·Cancer Genetics ·Jacquelyn J. Roth, Mariarita Santi, Lucy B. Rorke‐Adams, Brian Harding, Tracy Busse, Laura Tooke, Jaclyn A. Biegel	34
4	Chromosome Band 7q34 Deletions Resulting in KIAA1549‐BRAF and FAM131B‐BRAF Fusions in Pediatric Low‐Grade Gliomas 2014 ·Brain Pathology ·Jacquelyn J. Roth, Mariarita Santi, Avrum N. Pollock, Brian Harding, Lucy B. Rorke‐Adams, Laura Tooke, Jaclyn A. Biegel	40
5	Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors 2012 ·Cancer Genetics ·Margaret Dougherty, Laura Tooke, Lisa Sullivan, Håkon Håkonarson, Luanne Wainwright, Jaclyn A. Biegel	15
6	Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies 2011 ·Cancer Genetics ·Margaret Dougherty, (unknown), Laura Tooke, Tamim H. Shaikh, Xiaowu Gai, Håkon Håkonarson, Jaclyn A. Biegel	26
7	Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors 2010 ·Pediatric Blood & Cancer ·(unknown), Laura Tooke, Luanne Wainwright, Alexander R. Judkins, Jaclyn A. Biegel	246
8	Genomic Analysis Using High-Density Single Nucleotide Polymorphism-Based Oligonucleotide Arrays and Multiplex Ligation-Dependent Probe Amplification Provides a Comprehensive Analysis of INI1/SMARCB1 in Malignant Rhabdoid Tumors 2009 ·Clinical Cancer Research ·Eric M. Jackson, Angela J. Sievert, Xiaowu Gai, Håkon Håkonarson, Alexander R. Judkins, Laura Tooke, Juan C. Perín, Hongbo Xie, Tamim H. Shaikh, Jaclyn A. Biegel	142

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.

Explore authors with similar magnitude of impact