Lisa M. Vincent

2.2k total citations
19 papers, 659 citations indexed

About

Lisa M. Vincent is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Lisa M. Vincent has authored 19 papers receiving a total of 659 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Lisa M. Vincent's work include Genomics and Rare Diseases (5 papers), Protein Tyrosine Phosphatases (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Lisa M. Vincent is often cited by papers focused on Genomics and Rare Diseases (5 papers), Protein Tyrosine Phosphatases (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Lisa M. Vincent collaborates with scholars based in United States, Germany and France. Lisa M. Vincent's co-authors include Heidi L. Rehm, Soma Das, Elizabeth Chao, Sherri J. Bale, Lora Jh Bean, Dianna M. Milewicz, Sinh Tran, Tracy A Bensend, Björn Dahlbäck and Tina Pesaran and has published in prestigious journals such as Journal of Clinical Investigation, Blood and The American Journal of Human Genetics.

In The Last Decade

Lisa M. Vincent

18 papers receiving 651 citations

Peers

Countries citing papers authored by Lisa M. Vincent

Since Specialization

Citations

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

Fields of papers citing papers by Lisa M. Vincent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lisa M. Vincent. 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 Lisa M. Vincent. The network helps show where Lisa M. Vincent may publish in the future.

Co-authorship network of co-authors of Lisa M. Vincent

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Updated ACMG/AMP specifications for variant interpretation and gene curations from the ClinGen RASopathy expert panels 2025 ·Genetics in Medicine Open ·(unknown), (unknown), (unknown), (unknown), Hélène Cavé, Marina T. DiStefano, (unknown), (unknown), Bruce D. Gelb, Karen W. Gripp, Shoji Ichikawa, Jennifer A. Lee, (unknown), Marco Tartaglia, Bradley A. Williams, Martin Zenker, Lisa M. Vincent, Heather Mason‐Suares, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2
2	Prevalence of Mendelian Kidney Disease Among Patients With High-Risk APOL1 Genotypes Undergoing Commercial Genetic Testing in the United States 2024 ·Kidney International Reports ·Ronaldo da Silva Francisco, Sumit Punj, Lisa M. Vincent, (unknown), Vivek Bhalla, Glenn M. Chertow, (unknown), Vivek Charu	1
3	Heterozygous loss of function variants in IFT140 are associated with polycystic kidney disease 2024 ·American Journal of Medical Genetics Part A ·Dinah Clark, Robert Burns, Michelle S. Bloom, Karen Phaik Har Lim, (unknown), Lisa M. Vincent, Jing Xie, Yuan Chao Xue, Sumit Punj	0
4	Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG) 2021 ·Genetics in Medicine ·Catherine Rehder, Lora Jh Bean, David Bick, Elizabeth Chao, Wendy K. Chung, Soma Das, Julianne O’Daniel, Heidi L. Rehm, Vandana Shashi, Lisa M. Vincent	75
5	Effect of a Neoprene Knee Sleeve on Performance and Muscle Activity in Men and Women During High-Intensity, High-Volume Resistance Training 2021 ·The Journal of Strength and Conditioning Research ·Disa L. Hatfield, Andrew Stranieri, Lisa M. Vincent, Jacob E. Earp	2
6	Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants 2019 ·Genetics in Medicine ·Tracy Brandt, Laura M. Sack, Dolores Arjona, (unknown), Hui Mei, Hong Cui, Hua Gao, Lora Jh Bean, Arunkanth Ankala, Daniela del Gaudio, Amy Knight Johnson, Lisa M. Vincent, (unknown), (unknown), Gabriele Richard, Jeanne Meck	88
7	Reclassification of the BRAF p.Ile208Val variant by case-level data sharing 2018 ·Molecular Case Studies ·Andrew R. Grant, Sarah E. Hemphill, Lisa M. Vincent, Heidi L. Rehm	3
8	National Scouting Combine Scores as Performance Predictors in the National Football League 2018 ·The Journal of Strength and Conditioning Research ·Lisa M. Vincent, Bryan Blissmer, Disa L. Hatfield	16
9	ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation 2018 ·Genetics in Medicine ·Bruce D. Gelb, Hélène Cavé, Mitchell W. Dillon, Karen W. Gripp, Jennifer A. Lee, Heather Mason‐Suares, Katherine A. Rauen, Bradley A. Williams, Martin Zenker, Lisa M. Vincent	90
10	Assessing the gene–disease association of 19 genes with the RASopathies using the ClinGen gene curation framework 2018 ·Human Mutation ·Andrew R. Grant, Brandon J. Cushman, Hélène Cavé, Mitchell W. Dillon, Bruce D. Gelb, Karen W. Gripp, Jennifer A. Lee, Heather Mason‐Suares, Katherine A. Rauen, Marco Tartaglia, Lisa M. Vincent, Martin Zenker	61
11	78: Multi-gene NGS panel yields high diagnostic rate of skeletal dysplasias detected by fetal ultrasound 2018 ·American Journal of Obstetrics and Gynecology ·Lisa M. Vincent, (unknown), Tara Funari, Gabriele Richard, Jeanne Meck	1
12	Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar 2017 ·Genetics in Medicine ·Steven M. Harrison, Jill S. Dolinsky, Amy E. Knight Johnson, Tina Pesaran, Danielle R. Azzariti, Sherri J. Bale, Elizabeth Chao, Soma Das, Lisa M. Vincent, Heidi L. Rehm	145
13	Reassessment of Genomic Sequence Variation to Harmonize Interpretation for Personalized Medicine 2016 ·The American Journal of Human Genetics ·Kathryn B. Garber, Lisa M. Vincent, John Alexander, Lora Jh Bean, Sherri J. Bale, Madhuri Hegde	35
14	Coagulation factor VA2440G causes east Texas bleeding disorder via TFPIα 2013 ·Journal of Clinical Investigation ·Lisa M. Vincent, Sinh Tran, (unknown), Tracy A Bensend, Dianna M. Milewicz, Björn Dahlbäck	103
15	148: Increased nuchal translucency and normal karyotype: value of additional testing 2013 ·American Journal of Obstetrics and Gynecology ·(unknown), (unknown), Vimla S. Aggarwal, Sherri J. Bale, (unknown), (unknown), Vaidehi Jobanputra, (unknown), Lisa M. Vincent, Bradley R. Williams, Jeanne Meck, Ronald J. Wapner, Brynn Levy	1
16	Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2 2010 ·Molecular Genetics and Metabolism ·Lisa M. Vincent, Fiona J. Gilbert, Jennifer DiPace, Carla Ciccone, Thomas C. Markello, (unknown), Heidi Dorward, Wendy Westbroek, William A. Gahl, James B. Bussel, Marjan Huizing	11
17	Hermansky–Pudlak syndrome type 1 in patients of Indian descent 2009 ·Molecular Genetics and Metabolism ·Lisa M. Vincent, David R. Adams, Richard A. Hess, Shira G. Ziegler, Ekaterini Tsilou, (unknown), Kevin O’Brien, James G. White, Marjan Huizing, William A. Gahl	15
18	Hermansky–Pudlak syndrome in two African‐American brothers 2009 ·American Journal of Medical Genetics Part A ·Melissa A. Merideth, Lisa M. Vincent, Susan Sparks, Richard A. Hess, Irini Manoli, Kevin O’Brien, Ekaterina Tsilou, James G. White, Marjan Huizing, William A. Gahl	9
19	Dysregulation of Alternative Splicing of Coagulation Factor V Results in Bleeding Disorder, East Texas Type. 2006 ·Blood ·Lisa M. Vincent, Sinh Tran, Van Tran‐Fadulu, William P. Dubinsky, Björn Dahlbäck, Dianna M. Milewicz	1

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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