Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

V. Speare · SciRah

Researcher profile · Semantic Scholar

V. Speare

Share profile

V. Speare — researcher profile on SciRah

h-index: 15
Works: 41
Citations: 1,158

Most-cited papers

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients
H. LaDuca, A. Stuenkel, Jill S. Dolinsky, S. Keiles +10 more
2014Genetics in Medicine357 citations Open access
Semantic Scholar
Clinical features and cancer risk in families with pathogenic CDH1 variants irrespective of clinical criteria
R. Xicola, Shuwei Li, N. Rodriguez, P. Reinecke +5 more
2019Journal of Medical Genetics121 citations Open access
Semantic Scholar
Somatic TP53 variants frequently confound germline testing results
J. Weitzel, Elizabeth C. Chao, Bita Nehoray, Lily R. Van Tongeren +14 more
2017Genetics in Medicine112 citations Open access
Semantic Scholar
Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing
H. Rana, R. Gelman, H. LaDuca, R. McFarland +6 more
2018Journal of the National Cancer Institute84 citations Open access
Semantic Scholar
Prospective study of germline genetic testing in incident cases of pancreatic adenocarcinoma
R. Brand, E. Borazanci, V. Speare, Beth Dudley +23 more
2018Cancer83 citations Open access
Semantic Scholar
Exome sequencing in neonates: diagnostic rates, characteristics, and time to diagnosis
Z. Powis, K. D. Farwell Hagman, V. Speare, Taylor Cain +10 more
2018Genetics in Medicine65 citations Open access
Semantic Scholar
Real-World Integration of Genomic Data into the Electronic Health Record: The PennChart Genomics Initiative
K. S. Lau-Min, Stephanie B Asher, Jessica Chen, S. Domchek +9 more
2020Genetics in Medicine52 citations Open access
Semantic Scholar
Unexpected CDH1 Mutations Identified on Multigene Panels Pose Clinical Management Challenges.
K. Lowstuter, C. Espenschied, D. Sturgeon, C. Ricker +13 more
2017JCO Precision Oncology50 citations
Semantic Scholar
An amicronucleate mutant of Tetrahymena thermophila.
A. R. Kaney, V. Speare
1983Experimental Cell Research45 citations
Semantic Scholar
Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencing
Johanna L. Schmidt, A. Pizzino, J. Nicholl, Allison Foley +23 more
2020American Journal of Medical Genetics. Part A35 citations Open access
Semantic Scholar
Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype–phenotype correlation in congenital central hypoventilation syndrome (CCHS)
A. Zhou, C. Rand, S. Hockney, G. Niewijk +11 more
2021Genetics in Medicine31 citations Open access
Semantic Scholar
Genotype–phenotype associations among panel-based TP53+ subjects
H. Rana, J. Clifford, Lily Hoang, H. LaDuca +7 more
2019Genetics in Medicine25 citations Open access
Semantic Scholar
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
T. Hartman, E. Demidova, Randy Lesh, Lily Hoang +8 more
2020Scientific Reports23 citations Open access
Semantic Scholar
Prevalence of germline variants in inflammatory breast cancer
H. Rana, R. Sacca, C. Drogan, S. Gutierrez +7 more
2019Cancer17 citations Open access
Semantic Scholar
Family communication and patient distress after germline genetic testing in individuals with pancreatic ductal adenocarcinoma
M. L. Peters, Lindsey Stobie, Beth Dudley, E. Karloski +11 more
2019Cancer17 citations Open access
Semantic Scholar
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations
A. Safonov, Tomoki T. Nomakuchi, Elizabeth C. Chao, Carrie Horton +23 more
2025Nature Communications14 citations Open access
Semantic Scholar
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations
A. Safonov, Tomoki T. Nomakuchi, Elizabeth C. Chao, Carrie Horton +12 more
2023medRxiv5 citations Open access
Semantic Scholar
A randomized controlled trial of video-education or in-person genetic counseling for men with prostate cancer (ProGen).
H. Rana, J. Stopfer, N. Petrucelli, Diane R. Koeller +16 more
2020Journal of Clinical Oncology5 citations
Semantic Scholar
Germline mutations in cancer predisposition genes among patients with thyroid cancer.
J. Kamihara, H. LaDuca, Emily Dalton, V. Speare +2 more
20175 citations
Semantic Scholar
Germline testing in hereditary cancer genes subsequent to the identification of mutations in tumor specimens.
V. Speare, Jill S. Dolinsky, H. LaDuca, C. Horton +4 more
20153 citations
Semantic Scholar
Germline genetic testing in unselected pancreatic ductal adenocarcinoma (PDAC) patients.
M. L. Peters, R. Brand, E. Borazanci, Lindsey Stobie +16 more
20172 citations
Semantic Scholar
Risk of HER2-positive breast cancer among germline CHEK2 mutation carriers with breast cancer.
Chethan Ramamurthy, Raji Shameem, A. Forman, Jill S. Dolinsky +7 more
20162 citations
Semantic Scholar
Fragile X mutation screening among unselected pregnant women seen for genetic counseling: Findings of a pilot study
B. Finucane, V. Speare, B. Allitto, J. Adelberg +3 more
1999Genetics in Medicine2 citations Open access
Semantic Scholar
A genetic screen for vegetative gene expression in the micronucleus of Tetrahymena thermophila.
A. R. Kaney, V. Speare
1992The Journal of Protozoology2 citations
Semantic Scholar
Clinician-Reported Impact of Germline Multigene Panel Testing on Cancer Risk Management Recommendations
C. Horton, Kirsten Blanco, Min-Tzu Lo, V. Speare +3 more
2022JNCI Cancer Spectrum1 citations Open access
Semantic Scholar
Genetic counseling processes and outcomes among prostate cancer patients (ProGen).
D. Vatnick, S. Aktar, J. Stopfer, L. Kipnis +14 more
2019Journal of Clinical Oncology1 citations
Semantic Scholar
Concordance of germline multigene panel testing with prior microsatellite instability and immunohistochemistry analyses in endometrial cancer patients
K. Jasperson, C. Espenschied, H. Hampel, P. Reineke +4 more
2018Gynecologic Oncology1 citations
Semantic Scholar
Multi-gene panel testing results prompt frequent and guideline adherent changes to cancer risk management recommendations based on clinician report
C. Horton, H. LaDuca, Kirsten Blanco, Min-Tzu Lo +3 more
20210 citations
Semantic Scholar
Paired-Like Homeobox Gene PHOX2B Non-Polyalanine Repeat Expansion Mutations: Genotype-Phenotype Correlation in Congenital Central Hypoventilation Syndrome and Later Onset-CCHS
S. Hockney, A. Zhou, G. Niewijk, C. Rand +9 more
20200 citations
Semantic Scholar
Paired tumor sequencing and germline testing in breast cancer management: An experience of a single academic center
Elizabeth Elliott, V. Speare, James Coggan, C. Espenschied +10 more
2020Cancer Reports0 citations Open access
Semantic Scholar
Prevalence of pathogenic variants in DNA damage response genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer
T. Hartman, E. Demidova, Randy Lesh, Lily Hoang +8 more
2020bioRxiv0 citations Open access
Semantic Scholar
Mo1737 - Accuracy of Physician Elicited Family History in Predicting Genetic Susceptibility to Pancreatic Ductal Adenocarcinoma
K. Han, Beth Dudley, E. Karloski, V. Speare +1 more
20180 citations
Semantic Scholar
Exome sequencing in neonates: diagnostic rates, characteristics, and time to diagnosis
Z. Powis, K. D. Farwell Hagman, V. Speare, Taylor Cain +10 more
2018Genetics in Medicine0 citations Open access
Semantic Scholar
Increased detection of germline cancer susceptibility mutations subsequent to tumor profiling.
V. Speare, Alexandra Meyer, P. Reineke, H. LaDuca
20180 citations
Semantic Scholar
Clinical and molecular characteristics of NF1 mutations identified on hereditary cancer multi-gene panels.
A. Safonov, V. Speare, Jill S. Dolinsky, Amal Yussuf +2 more
20180 citations
Semantic Scholar
Expanding BRCA1/2 testing criteria to include other confirmed breast and ovarian cancer susceptibility genes.
F. Couch, H. Shimelis, Jill S. Dolinsky, E. Polley +8 more
20180 citations
Semantic Scholar
Prevalence of Germline Mutations in Consecutive, Unselected Patients with Newly Diagnosed Adenocarcinoma of the Pancreas
R. Brand, N. Tung, Beth Dudley, E. Karloski +19 more
20170 citations
Semantic Scholar
Inherited Susceptibility to Biliary Tract and Ampullary Cancers
H. LaDuca, M. Black, V. Speare, F. Couch
20170 citations
Semantic Scholar
Diagnosing Hereditary Cancer Susceptibility Through Multigene Panel Testing
H. LaDuca, Shuwei Li, A. Stuenkel, V. Speare +2 more
20170 citations
Semantic Scholar
PALB2 mutation carriers: Are clinicians acting on the molecular diagnosis?
V. Speare, Emily Dalton, H. LaDuca, C. Grosvenor +3 more
20160 citations
Semantic Scholar
The genetic variation observed in BRCA 1/2 + families.
Rachael T. Brandt, E. Delgiacco, C. Nixon, Elizabeth C. Chao +5 more
20150 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Jill S. Dolinsky×23
Invite
Jill S. Dolinsky — researcher profile on SciRah
H. LaDuca×20
Invite
H. LaDuca — researcher profile on SciRah
Elizabeth C. Chao×9
Invite
Elizabeth C. Chao — researcher profile on SciRah
M. Black×7
Invite
M. Black — researcher profile on SciRah

×7

Invite

Emily Dalton — researcher profile on SciRah

Invite

J. Garber — researcher profile on SciRah

Invite

Shuwei Li — researcher profile on SciRah

Invite

H. Rana — researcher profile on SciRah

Invite

R. Brand — researcher profile on SciRah

Invite

Beth Dudley — researcher profile on SciRah

Invite

E. Karloski — researcher profile on SciRah

Kirsten Blanco×5

Invite

Kirsten Blanco — researcher profile on SciRah