Sharon Sand

2.0k total citations
26 papers, 583 citations indexed

About

Sharon Sand is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Sharon Sand has authored 26 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 8 papers in Molecular Biology and 8 papers in Cancer Research. Recurrent topics in Sharon Sand's work include BRCA gene mutations in cancer (23 papers), Cancer Genomics and Diagnostics (8 papers) and DNA Repair Mechanisms (5 papers). Sharon Sand is often cited by papers focused on BRCA gene mutations in cancer (23 papers), Cancer Genomics and Diagnostics (8 papers) and DNA Repair Mechanisms (5 papers). Sharon Sand collaborates with scholars based in United States, Mexico and Peru. Sharon Sand's co-authors include Jeffrey N. Weitzel, Deborah J. MacDonald, Jessica Clague, Kathleen R. Blazer, Kai Yang, Charité Ricker, Julie O. Culver, Susan L. Neuhausen, Marcia Grant and Gwen Uman and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and JNCI Journal of the National Cancer Institute.

In The Last Decade

Sharon Sand

26 papers receiving 569 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Sharon Sand United States	12	409	164	138	112	78	26	583
Gord Glendon Canada	12	435 1.1×	118 0.7×	131 0.9×	203 1.8×	100 1.3×	20	608
Elaine Hiller United States	6	393 1.0×	93 0.6×	140 1.0×	145 1.3×	88 1.1×	9	526
Jean‐Pierre Fricker France	11	303 0.7×	252 1.5×	126 0.9×	145 1.3×	99 1.3×	15	576
Kristen J. Vogel United States	13	231 0.6×	100 0.6×	100 0.7×	125 1.1×	80 1.0×	19	430
Nancy Feldman United States	11	249 0.6×	114 0.7×	75 0.5×	174 1.6×	40 0.5×	24	563
S Gershman Canada	4	409 1.0×	84 0.5×	230 1.7×	107 1.0×	66 0.8×	5	481
Devon Bonner United States	7	376 0.9×	74 0.5×	142 1.0×	147 1.3×	51 0.7×	15	451
Veronica I. Lagos United States	8	420 1.0×	148 0.9×	125 0.9×	91 0.8×	78 1.0×	9	493
Cecelia Bellcross United States	12	496 1.2×	99 0.6×	141 1.0×	195 1.7×	203 2.6×	41	692
Belinda Rahman Australia	13	434 1.1×	101 0.6×	82 0.6×	158 1.4×	44 0.6×	27	633

Countries citing papers authored by Sharon Sand

Since Specialization

Citations

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

Fields of papers citing papers by Sharon Sand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sharon Sand

This figure shows the co-authorship network connecting the top 25 collaborators of Sharon Sand. A scholar is included among the top collaborators of Sharon Sand 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 Sharon Sand. Sharon Sand 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

Castillo, Danielle, Bita Nehoray, Kai Yang, et al.. (2022). Clonal Hematopoiesis and Mosaicism Revealed by a Multi-Tissue Analysis of Constitutional TP53 Status. Cancer Epidemiology Biomarkers & Prevention. 31(8). 1621–1629. 7 indexed citations

Reckamp, Karen L., Carolyn E. Behrendt, Thomas P. Slavin, et al.. (2021). Germline mutations and age at onset of lung adenocarcinoma. Cancer. 127(15). 2801–2806. 18 indexed citations

Chávarri-Guerra, Yanin, Carolyn B. Hendricks, Terrence P. Cescon, et al.. (2020). Breast cancer associated pathogenic variants among women 61 years and older with triple negative breast cancer. Journal of Geriatric Oncology. 12(5). 749–751. 8 indexed citations

Weitzel, Jeffrey N., Susan L. Neuhausen, Aaron W. Adamson, et al.. (2019). Pathogenic and likely pathogenic variants in PALB2 , CHEK2 , and other known breast cancer susceptibility genes among 1054 BRCA ‐negative Hispanics with breast cancer. Cancer. 125(16). 2829–2836. 36 indexed citations

Chávarri-Guerra, Yanin, Carolyn B. Hendricks, Sandra M. Brown, et al.. (2019). The Burden of Breast Cancer Predisposition Variants Across The Age Spectrum Among 10 000 Patients. Journal of the American Geriatrics Society. 67(5). 884–888. 10 indexed citations

Weitzel, Jeffrey N., Kathleen R. Blazer, Thomas P. Slavin, et al.. (2019). Germline mutation profile among Hispanic women with epithelial ovarian cancer (EOC).. Journal of Clinical Oncology. 37(15_suppl). 1584–1584. 1 indexed citations

Slavin, Thomas P., Carolyn E. Behrendt, Ilana Solomon, et al.. (2018). Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry. JNCI Journal of the National Cancer Institute. 110(10). 1059–1066. 42 indexed citations

Chávarri-Guerra, Yanin, Kai Yang, Ian K. Komenaka, et al.. (2018). Abstract P6-09-05: Factors associated with the uptake of risk-reducing surgeries among Hispanic women at high risk of breast and ovarian cancer. Cancer Research. 78(4_Supplement). P6–9. 1 indexed citations

Clague, Jessica, et al.. (2013). Variants of uncertain significance in BRCA testing: evaluation of surgical decisions, risk perception, and cancer distress. Clinical Genetics. 84(5). 464–472. 76 indexed citations

10.

Liu, Joyce F., Mihaela Cristea, Paul Frankel, et al.. (2012). Clinical characteristics and outcomes of BRCA-associated ovarian cancer: genotype and survival. Cancer Genetics. 205(1-2). 34–41. 36 indexed citations

11.

Pilarski, Robert, Divya A. Patel, Jeffrey N. Weitzel, et al.. (2012). The KRAS-Variant Is Associated with Risk of Developing Double Primary Breast and Ovarian Cancer. PLoS ONE. 7(5). e37891–e37891. 27 indexed citations

12.

Espenschied, Carin R., Deborah J. MacDonald, Julie O. Culver, et al.. (2012). Closing the Loop: Action Research in a Multimodal Hereditary Cancer Patient Conference is an Effective Tool to Assess and Address Patient Needs. Journal of Cancer Education. 27(3). 467–477. 5 indexed citations

13.

Weitzel, Jeffrey N., Jessica Clague, Arelis Martir-Negron, et al.. (2012). Prevalence and Type ofBRCAMutations in Hispanics Undergoing Genetic Cancer Risk Assessment in the Southwestern United States: A Report From the Clinical Cancer Genetics Community Research Network. Journal of Clinical Oncology. 31(2). 210–216. 115 indexed citations

14.

Weitzel, Jeffrey N., Arelis Martir-Negron, Josef Herzog, et al.. (2011). Prevalence and ancestral origin of BRCA mutations in the Hispanic population: Insights for ancestry-informed genetic cancer risk assessment.. Journal of Clinical Oncology. 29(15_suppl). 1514–1514. 1 indexed citations

15.

Cristea, Mihaela, Judy E. Garber, Susan L. Neuhausen, et al.. (2010). Clinical characteristics and outcomes of BRCA-associated ovarian cancer (OC): Genotype and survival.. Journal of Clinical Oncology. 28(15_suppl). 5017–5017. 1 indexed citations

16.

Brown, Sandra M., Julie O. Culver, Kathryn Osann, et al.. (2010). Health literacy, numeracy, and interpretation of graphical breast cancer risk estimates. Patient Education and Counseling. 83(1). 92–98. 66 indexed citations

17.

Lowstuter, Katrina, Sharon Sand, Kathleen R. Blazer, et al.. (2008). Influence of genetic discrimination perceptions and knowledge on cancer genetics referral practice among clinicians. Genetics in Medicine. 10(9). 691–698. 48 indexed citations

18.

MacDonald, Deborah J., Sharon Sand, F Kass, et al.. (2006). The Power of Partnership: Extending Comprehensive Cancer Center Expertise in Clinical Cancer Genetics to Community Breast Care Centers. 9(1). 39–47. 4 indexed citations

19.

Blazer, Kathleen R., Deborah J. MacDonald, Charité Ricker, et al.. (2005). Outcomes from intensive training in genetic cancer risk counseling for clinicians. Genetics in Medicine. 7(1). 40–47. 32 indexed citations

20.

Sand, Sharon, et al.. (2005). Linkage of a Pedigree Drawing Program and Database to a Program for Determining BRCA Mutation Carrier Probability. Familial Cancer. 4(4). 313–316. 4 indexed citations

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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