Elaine Lyon

38.5k total citations · 4 hit papers
102 papers, 23.2k citations indexed

About

Elaine Lyon is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Elaine Lyon has authored 102 papers receiving a total of 23.2k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Genetics, 38 papers in Molecular Biology and 20 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Elaine Lyon's work include Genomics and Rare Diseases (27 papers), Cystic Fibrosis Research Advances (14 papers) and BRCA gene mutations in cancer (13 papers). Elaine Lyon is often cited by papers focused on Genomics and Rare Diseases (27 papers), Cystic Fibrosis Research Advances (14 papers) and BRCA gene mutations in cancer (13 papers). Elaine Lyon collaborates with scholars based in United States, Palestinian Territory and Canada. Elaine Lyon's co-authors include Madhuri Hegde, Sherri J. Bale, Wayne W. Grody, Soma Das, Heidi L. Rehm, Elaine Spector, Karl V. Voelkerding, David Bick, Julie M. Gastier‐Foster and Sue Richards and has published in prestigious journals such as Blood, Gastroenterology and PLoS ONE.

In The Last Decade

Elaine Lyon

101 papers receiving 22.8k 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.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

2015 18.9k citations Sue Richards, Nazneen Aziz et al. Genetics in Medicine profile →
ACMG clinical laboratory standards for next-generation sequencing

2013 631 citations Heidi L. Rehm, Sherri J. Bale et al. Genetics in Medicine profile →
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

2008 569 citations C. Sue Richards, Sherri J. Bale et al. Genetics in Medicine profile →
Genotyping of Single-Nucleotide Polymorphisms by High-Resolution Melting of Small Amplicons

2004 525 citations Robert Palais, Cindy Meadows et al. profile →

Peers

Countries citing papers authored by Elaine Lyon

Since Specialization

Citations

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

Fields of papers citing papers by Elaine Lyon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elaine Lyon

This figure shows the co-authorship network connecting the top 25 collaborators of Elaine Lyon. A scholar is included among the top collaborators of Elaine Lyon 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 Elaine Lyon. Elaine Lyon 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	Reducing Sanger confirmation testing through false positive prediction algorithms 2021 ·Genetics in Medicine ·James Holt, Melissa Kelly, (unknown), Ghunwa Nakouzi, David Bick, Elaine Lyon	9
2	The Spectrum of Clinical Utilities in Molecular Pathology Testing Procedures for Inherited Conditions and Cancer 2016 ·Journal of Molecular Diagnostics ·Loren Joseph, Milena Cankovic, (unknown), Pranil Chandra, Rajyasree Emmadi, Jill Hagenkord, Stephanie Hallam, (unknown), Roger D. Klein, Victoria M. Pratt, Paul G. Rothberg, Robyn Temple‐Smolkin, Elaine Lyon	44
3	Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology breakdown → 2015 ·Genetics in Medicine ·Sue Richards, Nazneen Aziz, Sherri J. Bale, David Bick, Soma Das, Julie M. Gastier‐Foster, Wayne W. Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector, Karl V. Voelkerding, Heidi L. Rehm	18892
4	Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine 2015 ·PLoS ONE ·(unknown), Mohamed Jama, Nisreen Rumman, Hiyam Marzouqa, (unknown), Elaine Lyon, Musa Hindiyeh	13
5	Molecular genetic testing for cystic fibrosis: laboratory performance on the College of American Pathologists external proficiency surveys 2014 ·Genetics in Medicine ·Elaine Lyon, Iris Schrijver, Karen E. Weck, Andrea Ferreira‐Gonzalez, C. Sue Richards, Glenn E. Palomaki	9
6	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
7	Laboratory testing of CYP2D6 alleles in relation to tamoxifen therapy 2012 ·Genetics in Medicine ·Elaine Lyon, (unknown), Glenn E. Palomaki, Victoria M. Pratt, Kristen K. Reynolds, (unknown), Stuart A. Scott, Patrik Vitazka	34
8	Copy Number Variation and Incomplete Linkage Disequilibrium Interfere with the HCP5 Genotyping Assay for Abacavir Hypersensitivity 2012 ·Genetic Testing and Molecular Biomarkers ·Roberta Melis, Tracy R. Lewis, Alison Millson, Elaine Lyon, (unknown), Patricia Slev, Jeffrey Swensen	13
9	Validation of an Unlabeled Probe Melting Analysis Assay Combined with High-Throughput Extractions for Genotyping of the Most Common Variants in HFE -Associated Hereditary Hemochromatosis, C282Y, H63D, and S65C 2012 ·Genetic Testing and Molecular Biomarkers ·Kelli Sumner, (unknown), Geneviève Pont-Kingdon, (unknown), (unknown), Andrew Wilson, Cindy Meadows, Kojo S.J. Elenitoba‐Johnson, (unknown), Steven F. Dobrowolski, Hunter Best, Elaine Lyon	2
10	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
11	Implementation of a Cost-Effective Unlabeled Probe High-Resolution Melt Assay for Genotyping of Factor V Leiden 2011 ·Genetic Testing and Molecular Biomarkers ·Annika Svensson, Lan‐Szu Chou, Cindy Meadows, Christine E. Miller, Robert Palais, Kelli Sumner, (unknown), Rong Mao, Elaine Lyon	2
12	Detection of Large Rearrangements in the Cystic Fibrosis Transmembrane Conductance Regulator Gene by Multiplex Ligation-Dependent Probe Amplification Assay When Sequencing Fails to Detect Two Disease-Causing Mutations 2010 ·Genetic Testing and Molecular Biomarkers ·Annika Svensson, Lan-Szu Chou, Christine E. Miller, (unknown), Jeffrey Swensen, Karl V. Voelkerding, Rong Mao, Elaine Lyon	11
13	A Simple, High-Throughput Assay for Fragile X Expanded Alleles Using Triple Repeat Primed PCR and Capillary Electrophoresis 2010 ·Journal of Molecular Diagnostics ·Elaine Lyon, (unknown), (unknown), Mohamed Jama, Keith E. Young, (unknown), Natalia Marlowe	75
14	Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report 2009 ·Journal of Molecular Diagnostics ·Ira M. Lubin, Margaret M. McGovern, (unknown), Susan J. Gross, Elaine Lyon, Roberta A Pagon, Victoria M. Pratt, (unknown), Colleen Shaw, (unknown), Tracy L. Trotter, Marc S. Williams, Jean Amos Wilson, Kenneth A. Pass	41
15	Pharmacogenetic Testing for Warfarin Sensitivity 2008 ·Clinics in Laboratory Medicine ·Elaine Lyon, (unknown), Roberta Melis	3
16	Pharmacogenetic testing of CYP2C9 and VKORC1 alleles for warfarin 2008 ·Genetics in Medicine ·David A. Flockhart, Dennis J. O’Kane, Marc S. Williams, Michael S. Watson, Brian F. Gage, (unknown), Richard A. King, Elaine Lyon, Robert L. Nussbaum, Kevin A. Schulman, David L. Veenstra	157
17	Simultaneous Amplification, Detection, and Analysis of Common Mutations in the Galactose-1-Phosphate Uridyl Transferase Gene 2007 ·Journal of Molecular Diagnostics ·Mohamed Jama, Lesa Nelson, Rong Mao, Elaine Lyon	11
18	A Comparison of High-Resolution Melting Analysis With Denaturing High-Performance Liquid Chromatography for Mutation Scanning: Cystic Fibrosis Transmembrane Conductance Regulator Gene as a Model 2005 ·American Journal of Clinical Pathology ·Lan-Szu Chou, Elaine Lyon, Carl T. Wittwer	79
19	Long-Range (17.7 kb) Allele-Specific Polymerase Chain Reaction Method for Direct Haplotyping of R117H and IVS-8 Mutations of the Cystic Fibrosis Transmembrane Regulator Gene 2004 ·Journal of Molecular Diagnostics ·Geneviève Pont-Kingdon, Mohamed Jama, Christine Miller, Alison Millson, Elaine Lyon	15
20	Genetic testing for a BRCA1 mutation: Prophylactic surgery and screening behavior in women 2 years post testing 2003 ·American Journal of Medical Genetics Part A ·Jeffrey R. Botkin, Ken R. Smith, Robert T. Croyle, Bonnie Jeanne Baty, (unknown), (unknown), Anna Chan, Heidi Hamann, Caryn Lerman, Jamie McDonald, Vickie L. Venne, John H. Ward, Elaine Lyon	163

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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