Tracey Lewis

4.2k citations

23 papers · 1.4k indexed · 1 hit paper · h-index 14

Molecular Biology top 10%
Cellular and Molecular Neuroscience top 5%
Cardiology and Cardiovascular Medicine top 5%
Psychiatry and Mental health top 5%
Genetics top 10%

Co-authors: Robin J. Leach B.E. Reus Mark Leppert Stephen G. Ryan Carole Charlier Nanda A. Singh Philip S. Bernard Ken Ward
Topics: Genomics and Rare Diseases (5 papers)Molecular Biology Techniques and Applications (4 papers)Metabolism and Genetic Disorders (3 papers)
Cited by: Cellular and Molecular Neuroscience Psychiatry and Mental health Cardiology and Cardiovascular Medicine
Journals: Nature Genetics Cancer Genome Research
Partner nations: United States United Kingdom Canada

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

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

#	Work	Indexed citations
1	Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing data 2022 ·BMC Bioinformatics ·Brendan O’Fallon,Jacob Durtschi,(unknown),Tracey Lewis,Devin Close,Hunter Best	5
2	Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4 2015 ·Journal of Molecular Diagnostics ·Alison Millson,Tracey Lewis,Tina Pesaran,David Salvador,(unknown),Chia‐Ling Gau,Geneviève Pont-Kingdon,Elaine Lyon,Pınar Bayrak‐Toydemir	14
3	Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing 2014 ·Journal of Molecular Diagnostics ·Kelli Sumner,Jeffrey Swensen,Melinda Procter,Mohamed Jama,Whitney Wooderchak‐Donahue,Tracey Lewis,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Elaine Lyon,Pınar Bayrak‐Toydemir,Rong Mao,Geneviève Pont-Kingdon,D. Hunter Best	3
4	Candidate locus analysis for PHACE syndrome 2012 ·American Journal of Medical Genetics Part A ·(unknown),Dawn H. Siegel,Joseph T.C. Shieh,David A. Stevenson,J. Fredrik Grimmer,Tracey Lewis,Denise W. Metry,Ilona J. Frieden,Francine Blei,Hülya Kayserili,Beth A. Drolet,Pinar Bayrak‐Toydemir	16
5	Verification of Multiplex Ligation-Dependent Probe Amplification Probes in the Absence of Positive Samples 2011 ·Genetic Testing and Molecular Biomarkers ·Whitney Wooderchak‐Donahue,Cecily P. Vaughn,Lan‐Szu Chou,Tracey Lewis,Kelli Sumner,Melinda Procter,Friederike Gedge,Pınar Bayrak‐Toydemir,Elaine Lyon,Geneviève Pont-Kingdon	1
6	Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification 2011 ·BMC Medical Genetics ·Larissa V. Furtado,Whitney Wooderchak‐Donahue,Alan F. Rope,Angela Yetman,Tracey Lewis,(unknown),Pınar Bayrak‐Toydemir	26
7	Hereditary hemorrhagic telangiectasia: two distinct ENG deletions in one family 2010 ·Clinical Genetics ·(unknown),Friederike Gedge,Merry‐Lynn McDonald,Patti Krautscheid,Xia Wang,(unknown),(unknown),Tracey Lewis,Pınar Bayrak‐Toydemir	7
8	How clinical champions can improve quality 2008 ·Nursing Management ·Tracey Lewis,(unknown)	13
9	High-throughput amplicon scanning of the TP53 gene in breast cancer using high-resolution fluorescent melting curve analyses and automatic mutation calling 2008 ·Human Mutation ·Roy R. L. Bastien,Tracey Lewis,Jason E. Hawkes,John F. Quackenbush,(unknown),Juan Palazzo,Charles M. Perou,Philip S. Bernard	38
10	Differentiating Ewing's sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues 2007 ·Modern Pathology ·Tracey Lewis,Cheryl M. Coffin,Philip S. Bernard	70
11	Molecular classification of melanoma using real‐time quantitative reverse transcriptase‐polymerase chain reaction 2005 ·Cancer ·Tracey Lewis,John Elder Robison,Roy R. L. Bastien,Brett Milash,Kenneth M. Boucher,Wolfram E. Samlowski,Sancy A. Leachman,R. Dirk Noyes,Carl T. Wittwer,Laurent Perreard,Philip S. Bernard	49
12	A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy familybreakdown → 1998 ·Nature Genetics ·Carole Charlier,Nanda A. Singh,Stephen G. Ryan,Tracey Lewis,B.E. Reus,Robin J. Leach,Mark Leppert	729
13	Genetic Linkage of Paget Disease of the Bone to Chromosome 18q 1997 ·The American Journal of Human Genetics ·Jannine D. Cody,Frederick R. Singer,G. David Roodman,(unknown),Tracey Lewis,M. Leppert,Robin J. Leach	122
14	Localization of a Gene for a Glutamate Binding Subunit of a NMDA Receptor (GRINA) to 8q24 1996 ·Genomics ·Tracey Lewis,Stephen Wood,Elias K. Michaelis,Barbara R. DuPont,Robin J. Leach	16
15	Evidence of a Third Locus for Benign Familial Convulsions 1996 ·Journal of Child Neurology ·Tracey Lewis,Michael Shevell,Eva Andermann,Stephen G. Ryan,Robin J. Leach	8
16	A radiation hybrid map of 40 loci for the distal long arm of human chromosome 8. 1995 ·Genome Research ·Tracey Lewis,Lawrence M. Nelson,Ken Ward,Robin J. Leach	2
17	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. 1994 ·PubMed ·Eleni N. Levedakou,Min He,(unknown),(unknown),William G. Cance,Piri Welcsh,Andrew Simmons,Susan L. Naylor,Robin J. Leach,Tracey Lewis	59
18	Yeast Artificial Chromosome and Radiation Hybrid Map of Loci in Chromosome Band 8p22, a Common Region of Allelic Loss in Multiple Human Cancers 1994 ·Genomics ·Robert Bookstein,Alina Levy,Donal MacGrogan,Tracey Lewis,Jean Weissenbach,P. O’Connell,Robin J. Leach	20
19	Localization of Glucose-Dependent Insulinotropic Polypeptide (GIP) to a Gene Cluster on Chromosome 17q 1994 ·Genomics ·Tracey Lewis,(unknown),P. O’Connell,Robin J. Leach	4
20	Regional Localization of 188 Sequence Tagged Sites on a Somatic Cell Hybrid Mapping Panel for Human Chromosome 3 1994 ·Genomics ·Robin J. Leach,(unknown),B.E. Reus,Shirley J. Hayes,(unknown),(unknown),Joan Overhauser,Andrea Ballabio,HA Drabkin,Tracey Lewis,(unknown),Susan L. Naylor	15

About Tracey Lewis

Tracey Lewis is a scholar working on Clinical Biochemistry, Genetics and Genetics, having authored 23 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Molecular Biology Techniques and Applications (4 papers) and Metabolism and Genetic Disorders (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (549 citations), Psychiatry and Mental health (327 citations) and Cardiology and Cardiovascular Medicine (359 citations). Tracey Lewis has collaborated with scholars based in United States, United Kingdom and Canada. Frequent 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. Their work appears in journals such as Nature Genetics, Cancer and Genome 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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