Tracey Lewis

4.2k total citations · 1 hit paper
23 papers, 1.4k citations indexed

About

Tracey Lewis is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Tracey Lewis has authored 23 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Oncology. Recurrent topics in Tracey Lewis's work include Genomics and Rare Diseases (5 papers), Molecular Biology Techniques and Applications (4 papers) and Metabolism and Genetic Disorders (3 papers). Tracey Lewis is often cited by papers focused on Genomics and Rare Diseases (5 papers), Molecular Biology Techniques and Applications (4 papers) and Metabolism and Genetic Disorders (3 papers). Tracey Lewis collaborates with scholars based in United States, United Kingdom and Canada. Tracey Lewis's co-authors include Robin J. Leach, B.E. Reus, Mark Leppert, Stephen G. Ryan, Carole Charlier, Nanda A. Singh, Philip S. Bernard, Ken Ward, Cheryl M. Coffin and G. David Roodman and has published in prestigious journals such as Nature Genetics, Cancer and Genome Research.

In The Last Decade

Tracey Lewis

23 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1998 729 citations Carole Charlier, Nanda A. Singh et al. Nature Genetics profile →

Peers

Tracey Lewis

CMN

CCM

PMH

GENET

Ana Lía Taratuto Argentina

Matthew Brooks United States

Alda Sousa Portugal

Yvonne J. Vos Netherlands

Kumaraswamy Sivakumar United States

Isabelle Thiffault United States

Jing Qian China

Jonathan T. Lu United States

Rafaëlle Bernard France

Alice Goldenberg France

Ana Lía Taratuto Argentina

Tracey Lewis

402 ×0.4

189 ×0.3

CMN

155 ×0.4

CCM

127 ×0.4

PMH

73 ×0.2

GENET

Citations per year, relative to Tracey Lewis Tracey Lewis (= 1×) peers Ana Lía Taratuto

Countries citing papers authored by Tracey Lewis

Since Specialization

Citations

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

Fields of papers citing papers by Tracey Lewis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tracey Lewis

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

All Works

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20 of 20 papers shown

O’Fallon, Brendan, et al.. (2022). Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing data. BMC Bioinformatics. 23(1). 285–285. 5 indexed citations

Millson, Alison, Tracey Lewis, Tina Pesaran, et al.. (2015). Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4. Journal of Molecular Diagnostics. 17(5). 576–582. 14 indexed citations

Sumner, Kelli, Jeffrey Swensen, Melinda Procter, et al.. (2014). Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing. Journal of Molecular Diagnostics. 16(5). 477–480. 3 indexed citations

Siegel, Dawn H., Joseph T.C. Shieh, David A. Stevenson, et al.. (2012). Candidate locus analysis for PHACE syndrome. American Journal of Medical Genetics Part A. 158A(6). 1363–1367. 16 indexed citations

Wooderchak‐Donahue, Whitney, Cecily P. Vaughn, Lan‐Szu Chou, et al.. (2011). Verification of Multiplex Ligation-Dependent Probe Amplification Probes in the Absence of Positive Samples. Genetic Testing and Molecular Biomarkers. 15(11). 793–799. 1 indexed citations

Furtado, Larissa V., Whitney Wooderchak‐Donahue, Alan F. Rope, et al.. (2011). Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification. BMC Medical Genetics. 12(1). 119–119. 26 indexed citations

Gedge, Friederike, Merry‐Lynn McDonald, Patti Krautscheid, et al.. (2010). Hereditary hemorrhagic telangiectasia: two distinct ENG deletions in one family. Clinical Genetics. 78(5). 484–489. 7 indexed citations

Lewis, Tracey, et al.. (2008). How clinical champions can improve quality. Nursing Management. 14(10). 24–27. 13 indexed citations

Bastien, Roy R. L., Tracey Lewis, Jason E. Hawkes, et al.. (2008). High-throughput amplicon scanning of the TP53 gene in breast cancer using high-resolution fluorescent melting curve analyses and automatic mutation calling. Human Mutation. 29(5). 757–764. 38 indexed citations

10.

Lewis, Tracey, Cheryl M. Coffin, & Philip S. Bernard. (2007). Differentiating Ewing's sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues. Modern Pathology. 20(3). 397–404. 70 indexed citations

11.

Lewis, Tracey, John Elder Robison, Roy R. L. Bastien, et al.. (2005). Molecular classification of melanoma using real‐time quantitative reverse transcriptase‐polymerase chain reaction. Cancer. 104(8). 1678–1686. 49 indexed citations

12.

Charlier, Carole, Nanda A. Singh, Stephen G. Ryan, et al.. (1998). A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nature Genetics. 18(1). 53–55. 729 indexed citations breakdown →

13.

Cody, Jannine D., Frederick R. Singer, G. David Roodman, et al.. (1997). Genetic Linkage of Paget Disease of the Bone to Chromosome 18q. The American Journal of Human Genetics. 61(5). 1117–1122. 122 indexed citations

14.

Lewis, Tracey, Stephen Wood, Elias K. Michaelis, Barbara R. DuPont, & Robin J. Leach. (1996). Localization of a Gene for a Glutamate Binding Subunit of a NMDA Receptor (GRINA) to 8q24. Genomics. 32(1). 131–133. 16 indexed citations

15.

Lewis, Tracey, Michael Shevell, Eva Andermann, Stephen G. Ryan, & Robin J. Leach. (1996). Evidence of a Third Locus for Benign Familial Convulsions. Journal of Child Neurology. 11(3). 211–214. 8 indexed citations

16.

Lewis, Tracey, Lawrence M. Nelson, Ken Ward, & Robin J. Leach. (1995). A radiation hybrid map of 40 loci for the distal long arm of human chromosome 8.. Genome Research. 5(4). 334–341. 2 indexed citations

17.

Levedakou, Eleni N., Min He, William G. Cance, et al.. (1994). Two novel human serine/threonine kinases with homologies to the cell cycle regulating Xenopus MO15, and NIMA kinases: cloning and characterization of their expression pattern.. PubMed. 9(7). 1977–88. 59 indexed citations

18.

Bookstein, Robert, Alina Levy, Donal MacGrogan, et al.. (1994). Yeast Artificial Chromosome and Radiation Hybrid Map of Loci in Chromosome Band 8p22, a Common Region of Allelic Loss in Multiple Human Cancers. Genomics. 24(2). 317–323. 20 indexed citations

19.

Lewis, Tracey, et al.. (1994). Localization of Glucose-Dependent Insulinotropic Polypeptide (GIP) to a Gene Cluster on Chromosome 17q. Genomics. 19(3). 589–591. 4 indexed citations

20.

Leach, Robin J., B.E. Reus, Shirley J. Hayes, et al.. (1994). Regional Localization of 188 Sequence Tagged Sites on a Somatic Cell Hybrid Mapping Panel for Human Chromosome 3. Genomics. 24(3). 549–556. 15 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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