Virginia Speare

1.2k total citations
23 papers, 595 citations indexed

About

Virginia Speare is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Virginia Speare has authored 23 papers receiving a total of 595 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Virginia Speare's work include BRCA gene mutations in cancer (11 papers), Genetic factors in colorectal cancer (6 papers) and Cancer Genomics and Diagnostics (6 papers). Virginia Speare is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Genetic factors in colorectal cancer (6 papers) and Cancer Genomics and Diagnostics (6 papers). Virginia Speare collaborates with scholars based in United States, United Kingdom and Russia. Virginia Speare's co-authors include Holly LaDuca, Jill S. Dolinsky, Elizabeth Chao, Chia‐Ling Gau, Steven Keiles, Elaine Chen, Erika Palmaer, Tina Pesaran, Stephanie Gandomi and Divya Shah and has published in prestigious journals such as Journal of Clinical Oncology, JNCI Journal of the National Cancer Institute and Cancer.

In The Last Decade

Virginia Speare

22 papers receiving 585 citations

Peers

Countries citing papers authored by Virginia Speare

Since Specialization

Citations

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

Fields of papers citing papers by Virginia Speare

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Virginia Speare

This figure shows the co-authorship network connecting the top 25 collaborators of Virginia Speare. A scholar is included among the top collaborators of Virginia Speare 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 Virginia Speare. Virginia Speare 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	Clinician-Reported Impact of Germline Multigene Panel Testing on Cancer Risk Management Recommendations 2022 ·JNCI Cancer Spectrum ·Carolyn Horton, Kirsten Blanco, Min‐Tzu Lo, Virginia Speare, Holly LaDuca, Jill S. Dolinsky, Allison W. Kurian	3
2	Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype–phenotype correlation in congenital central hypoventilation syndrome (CCHS) 2021 ·Genetics in Medicine ·Amy Zhou, Casey M. Rand, (unknown), (unknown), Patrick Reineke, Virginia Speare, Elizabeth Berry‐Kravis, Lili Zhou, Lawrence J. Jennings, Min Yu, Isabella Ceccherini, Tiziana Bachetti, (unknown), Kai Lee Yap, Debra E. Weese‐Mayer	16
3	Prevalence of pathogenic variants in DNA damage response and repair genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer 2020 ·Scientific Reports ·Tiffiney R. Hartman, (unknown), (unknown), Lily Hoang, Marcy E. Richardson, Andrea Forman, Lisa Kessler, Virginia Speare, Erica A. Golemis, Michael J. Hall, Mary B. Daly, Sanjeevani Arora	15
4	Real-world integration of genomic data into the electronic health record: the PennChart Genomics Initiative 2020 ·Genetics in Medicine ·Kelsey S. Lau‐Min, (unknown), Jessica Chen, Susan M. Domchek, Michael D. Feldman, Steven Joffe, (unknown), Virginia Speare, (unknown), Sony Tuteja, (unknown), Marylyn D. Ritchie, Katherine L. Nathanson	31
5	A randomized controlled trial of video-education or in-person genetic counseling for men with prostate cancer (ProGen). 2020 ·Journal of Clinical Oncology ·Huma Q. Rana, Jill E. Stopfer, Nancie Petrucelli, (unknown), Sara Pirzadeh‐Miller, (unknown), (unknown), (unknown), (unknown), Rebecca Silver, (unknown), Rebecca Gelman, (unknown), Virginia Speare, Jill S. Dolinsky, Elisabeth I. Heath, Theodora S. Ross, Kevin D. Courtney, Judy E. Garber, Mary‐Ellen Taplin, (unknown)	6
6	Paired tumor sequencing and germline testing in breast cancer management: An experience of a single academic center 2020 ·Cancer Reports ·(unknown), Virginia Speare, (unknown), Carin R. Espenschied, Holly LaDuca, Amal Yussuf, (unknown), Phillip Gray, Melody Cobleigh, Ruta Rao, (unknown), Timothy M. Kuzel, Lela Buckingham, Lydia Usha	0
7	Clinical features and cancer risk in families with pathogenic CDH1 variants irrespective of clinical criteria 2019 ·Journal of Medical Genetics ·Rosa M. Xicola, Shuwei Li, (unknown), (unknown), Rachid Karam, Virginia Speare, Mary Helen Black, Holly LaDuca, Xavier Llor	75
8	Genotype–phenotype associations among panel-based TP53+ subjects 2019 ·Genetics in Medicine ·Huma Q. Rana, (unknown), Lily Hoang, Holly LaDuca, Mary Helen Black, Shuwei Li, Kelly McGoldrick, Virginia Speare, Jill S. Dolinsky, Chia‐Ling Gau, Judy E. Garber	18
9	Genetic counseling processes and outcomes among prostate cancer patients (ProGen). 2019 ·Journal of Clinical Oncology ·(unknown), (unknown), Jill E. Stopfer, (unknown), (unknown), (unknown), (unknown), (unknown), Kerry L. Kilbridge, Bradley A. McGregor, Christopher J. Sweeney, Virginia Speare, Brigette Tippin Davis, Jill S. Dolinsky, Judy E. Garber, Huma Q. Rana, Mary‐Ellen Taplin, Mark M. Pomerantz	1
10	Prevalence of germline variants in inflammatory breast cancer 2019 ·Cancer ·Huma Q. Rana, Rosalba Sacca, (unknown), Stephanie Gutierrez, (unknown), Meredith M. Regan, Virginia Speare, Holly LaDuca, Jill S. Dolinsky, Judy E. Garber, Beth Overmoyer	13
11	Exome sequencing in neonates: diagnostic rates, characteristics, and time to diagnosis 2018 ·Genetics in Medicine ·Zöe Powis, Kelly D. Farwell Hagman, Virginia Speare, (unknown), Kirsten Blanco, (unknown), (unknown), David Tilstra, (unknown), Jesse M. Hunter, (unknown), Lina Ghaloul‐Gonzalez, Jerry Vockley, Sha Tang	24
12	Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing 2018 ·JNCI Journal of the National Cancer Institute ·Huma Q. Rana, Rebecca Gelman, Holly LaDuca, Rachel McFarland, Emily Dalton, Jennifer Thompson, Virginia Speare, Jill S. Dolinsky, Elizabeth Chao, Judy E. Garber	62
13	Concordance of germline multigene panel testing with prior microsatellite instability and immunohistochemistry analyses in endometrial cancer patients 2018 ·Gynecologic Oncology ·Kory Jasperson, (unknown), Heather Hampel, Patrick Reineke, Tina Pesaran, Virginia Speare, Jessica Profato, Ian M. Frayling	1
14	Germline mutations in cancer predisposition genes among patients with thyroid cancer. 2017 ·Journal of Clinical Oncology ·Junne Kamihara, Holly LaDuca, Emily Dalton, Virginia Speare, Judy E. Garber, Mary Helen Black	5
15	Germline genetic testing in unselected pancreatic ductal adenocarcinoma (PDAC) patients. 2017 ·Journal of Clinical Oncology ·Mary Linton B. Peters, Randall E. Brand, Erkut Borazanci, (unknown), Beth Dudley, (unknown), A. James Moser, (unknown), Cynthia Lim, Nathan Bahary, Weijing Sun, John C. Rhee, Barry C. Lembersky, Ronald G. Stoller, Holly LaDuca, Jill S. Dolinsky, Emily Dalton, Virginia Speare, Mary Helen Black, Nadine Tung	1
16	Germline testing in hereditary cancer genes subsequent to the identification of mutations in tumor specimens. 2015 ·Journal of Clinical Oncology ·Virginia Speare, Jill S. Dolinsky, Holly LaDuca, Carolyn Horton, (unknown), (unknown), Emily Dalton, Elizabeth Chao	1
17	Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients 2014 ·Genetics in Medicine ·Holly LaDuca, Aaron J. Stuenkel, Jill S. Dolinsky, Steven Keiles, (unknown), Tina Pesaran, Elaine Chen, Chia‐Ling Gau, Erika Palmaer, (unknown), Divya Shah, Virginia Speare, Stephanie Gandomi, Elizabeth Chao	237
18	Fragile X mutation screening among unselected pregnant women seen for genetic counseling: Findings of a pilot study 1999 ·Genetics in Medicine ·Brenda Finucane, Virginia Speare, Bernice A. Allitto, (unknown), (unknown), (unknown), Natalie Blagowidow	1
19	A Genetic Screen for Vegetative Gene Expression in the Micronucleus of Tetrahymena thermophila 1992 ·The Journal of Protozoology ·(unknown), Virginia Speare	2
20	An amicronucleate mutant of Tetrahymena thermophila 1983 ·Experimental Cell Research ·(unknown), Virginia Speare	38

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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