Hetal S. Vig

437 total citations
9 papers, 267 citations indexed

About

Hetal S. Vig is a scholar working on Genetics, Pathology and Forensic Medicine and Cancer Research. According to data from OpenAlex, Hetal S. Vig has authored 9 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Pathology and Forensic Medicine and 3 papers in Cancer Research. Recurrent topics in Hetal S. Vig's work include BRCA gene mutations in cancer (8 papers), Genetic factors in colorectal cancer (4 papers) and Cancer Genomics and Diagnostics (3 papers). Hetal S. Vig is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Genetic factors in colorectal cancer (4 papers) and Cancer Genomics and Diagnostics (3 papers). Hetal S. Vig collaborates with scholars based in United States, Netherlands and India. Hetal S. Vig's co-authors include Neal J. Meropol, Stephanie A. Cohen, Bronson D. Riley, Julie Rousseau, Shanna Gustafson, Monica Marvin, Sharon L. Manne, Mary B. Daly, Angela R. Bradbury and Daniel C. Chung and has published in prestigious journals such as Journal of Clinical Oncology, Cancer Research and Cancer Epidemiology Biomarkers & Prevention.

In The Last Decade

Hetal S. Vig

9 papers receiving 261 citations

Peers

Hetal S. Vig

GENET

PHEOH

PFM

PPCH

CR

Margaret M. McGovern United States

Robin Lee United States

Amanda Brandt United States

Sherry Grumet United States

Erica M. Bednar United States

Marian J. Gilmore United States

Elana Levinson United States

Wendy Kohlmann United States

Kimberly Childers United States

Beth Ford United States

Margaret M. McGovern United States

Hetal S. Vig

257 ×1.2

GENET

88 ×1.5

PHEOH

72 ×1.2

PFM

39 ×0.7

PPCH

55 ×1.1

CR

Citations per year, relative to Hetal S. Vig Hetal S. Vig (= 1×) peers Margaret M. McGovern

Countries citing papers authored by Hetal S. Vig

Since Specialization

Citations

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

Fields of papers citing papers by Hetal S. Vig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hetal S. Vig. 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 Hetal S. Vig. The network helps show where Hetal S. Vig may publish in the future.

Co-authorship network of co-authors of Hetal S. Vig

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

All Works

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9 of 9 papers shown

1.

Yang, Sherry X., Karen Ouyang, Karl F. Erhard, et al.. (2018). Abstract P4-06-02: Germline analysis of breast cancer patients with abnormal somatic results: Ancillary assessment or critical co-diagnostic?. Cancer Research. 78(4_Supplement). P4–6. 1 indexed citations

2.

Khiabanian, Hossein, Kim M. Hirshfield, Mendel Goldfinger, et al.. (2018). Inference of Germline Mutational Status and Evaluation of Loss of Heterozygosity in High-Depth, Tumor-Only Sequencing Data. JCO Precision Oncology. 2018(2). 1–15. 19 indexed citations

3.

Cohen, Stephanie A., Monica Marvin, Bronson D. Riley, et al.. (2013). Identification of Genetic Counseling Service Delivery Models in Practice: A Report from the NSGC Service Delivery Model Task Force. Journal of Genetic Counseling. 22(4). 411–421. 90 indexed citations

4.

Vig, Hetal S., et al.. (2013). Age at Diagnosis May Trump Family History in DrivingBRCATesting in a Population of Breast Cancer Patients. Cancer Epidemiology Biomarkers & Prevention. 22(10). 1778–1785. 6 indexed citations

5.

Meropol, Neal J., et al.. (2011). Delivery of Internet-based cancer genetic counselling services to patients' homes: a feasibility study. Journal of Telemedicine and Telecare. 17(1). 36–40. 39 indexed citations

6.

Manne, Sharon L., Neal J. Meropol, David S. Weinberg, et al.. (2010). Facilitating Informed Decisions Regarding Microsatellite Instability Testing Among High-Risk Individuals Diagnosed With Colorectal Cancer. Journal of Clinical Oncology. 28(8). 1366–1372. 34 indexed citations

7.

Vig, Hetal S., Joanne Armstrong, Brian L. Egleston, et al.. (2009). Cancer Genetic Risk Assessment and Referral Patterns in Primary Care. Genetic Testing and Molecular Biomarkers. 13(6). 735–741. 55 indexed citations

8.

Vig, Hetal S., et al.. (2007). Hereditary colorectal cancer syndromes. Start risk assessment in primary care.. PubMed. 15(7). 49–52. 1 indexed citations

9.

Manne, Sharon L., Daniel C. Chung, David S. Weinberg, et al.. (2007). Knowledge and Attitudes about Microsatellite Instability Testing among High-Risk Individuals Diagnosed with Colorectal Cancer. Cancer Epidemiology Biomarkers & Prevention. 16(10). 2110–2117. 22 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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