Diptasri Mandal

4.8k total citations
24 papers, 406 citations indexed

About

Diptasri Mandal is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Diptasri Mandal has authored 24 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Diptasri Mandal's work include Genetic Associations and Epidemiology (7 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Prostate Cancer Treatment and Research (6 papers). Diptasri Mandal is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Prostate Cancer Treatment and Research (6 papers). Diptasri Mandal collaborates with scholars based in United States, Canada and Italy. Diptasri Mandal's co-authors include Joan E. Bailey‐Wilson, Ken R. Smith, Sara E. Simonsen, Bonnie Jeanne Baty, Anita Y. Kinney, Susan L. Neuhausen, Alexander F. Wilson, Elisa M. Ledet, Ann G. Schwartz and Elena Kupert and has published in prestigious journals such as Journal of Clinical Oncology, Cancer and Cancer Research.

In The Last Decade

Diptasri Mandal

24 papers receiving 398 citations

Peers

Diptasri Mandal

GENET

PRM

ONCOL

Wenndy Hernandez United States

Anne‐Bine Skytte Denmark

Yelena Kemel United States

Monica Emanuelsson Sweden

Rebecca Doherty United Kingdom

Elisabetta De Matteis Italy

Nicole Bürki Switzerland

Diane Logan Canada

Kristen J. Vogel United States

Jacquelyn Powers United States

Wenndy Hernandez United States

Diptasri Mandal

205 ×1.1

GENET

137 ×0.9

146 ×1.2

PRM

62 ×0.9

77 ×1.2

ONCOL

Citations per year, relative to Diptasri Mandal Diptasri Mandal (= 1×) peers Wenndy Hernandez

Countries citing papers authored by Diptasri Mandal

Since Specialization

Citations

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

Fields of papers citing papers by Diptasri Mandal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diptasri Mandal

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Zhang, Guanyi, Zemin Wang, Jasmin Bavarva, et al.. (2022). A Recurrent ADPRHL1 Germline Mutation Activates PARP1 and Confers Prostate Cancer Risk in African American Families. Molecular Cancer Research. 20(12). 1776–1784. 3 indexed citations

Musolf, Anthony M., Claire L. Simpson, Claudio W. Pikielny, et al.. (2021). Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. Cancer Research. 81(12). 3162–3173. 7 indexed citations

Musolf, Anthony M., Haiming Sun, Claudio W. Pikielny, et al.. (2019). Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q. Cancer Epidemiology Biomarkers & Prevention. 29(2). 434–442. 10 indexed citations

Musolf, Anthony M., Claire L. Simpson, Mariza de Andrade, et al.. (2016). Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer. Human Heredity. 82(1-2). 64–74. 10 indexed citations

Xiong, Donghai, Yian Wang, Elena Kupert, et al.. (2015). A Recurrent Mutation in PARK2 Is Associated with Familial Lung Cancer. The American Journal of Human Genetics. 96(2). 301–308. 57 indexed citations

Simpson, Claire L., Aaron J. Goldenberg, Denise Daley, et al.. (2014). Practical Barriers and Ethical Challenges in Genetic Data Sharing. International Journal of Environmental Research and Public Health. 11(8). 8383–8398. 16 indexed citations

Ledet, Elisa M., et al.. (2012). Characterization of germline copy number variation in high‐risk African American families with prostate cancer. The Prostate. 73(6). 614–623. 24 indexed citations

Ledet, Elisa M., Oliver Sartor, Walter Rayford, Joan E. Bailey‐Wilson, & Diptasri Mandal. (2011). Suggestive evidence of linkage identified at chromosomes 12q24 and 2p16 in African American prostate cancer families from louisiana. The Prostate. 72(9). 938–947. 17 indexed citations

Liu, Pengyuan, Haris G. Vikis, Yan Lü, et al.. (2010). Cumulative Effect of Multiple Loci on Genetic Susceptibility to Familial Lung Cancer. Cancer Epidemiology Biomarkers & Prevention. 19(2). 517–524. 26 indexed citations

10.

Amos, Christopher I., Susan M. Pinney, Yafang Li, et al.. (2010). A Susceptibility Locus on Chromosome 6q Greatly Increases Lung Cancer Risk among Light and Never Smokers. Cancer Research. 70(6). 2359–2367. 37 indexed citations

11.

Hu, Siyi, Tao Liu, Zhenzhen Liu, et al.. (2010). Identification of a novel germline missense mutation of the androgen receptor in African American men with familial prostate cancer. Asian Journal of Andrology. 12(3). 336–343. 12 indexed citations

12.

Mandal, Diptasri, et al.. (2008). Recruitment strategies and comparison of prostate cancer-specific clinical data on African-American and Caucasian males with and without family history. Prostate Cancer and Prostatic Diseases. 11(3). 274–279. 5 indexed citations

13.

Kinney, Anita Y., Sara E. Simonsen, Bonnie Jeanne Baty, et al.. (2006). Acceptance of genetic testing for hereditary breast ovarian cancer among study enrollees from an African American kindred. American Journal of Medical Genetics Part A. 140A(8). 813–826. 34 indexed citations

14.

Mandal, Diptasri, Alexa J.M. Sorant, Larry D. Atwood, Alexander F. Wilson, & Joan E. Bailey‐Wilson. (2006). Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment. BMC Genetics. 7(1). 21–21. 9 indexed citations

15.

Kinney, Anita Y., Sara E. Simonsen, Bonnie Jeanne Baty, et al.. (2006). Risk Reduction Behaviors and Provider Communication Following Genetic Counseling and BRCA1 Mutation Testing in an African American Kindred. Journal of Genetic Counseling. 15(4). 293–305. 38 indexed citations

16.

Kinney, Anita Y., Lindsey E. Bloor, Diptasri Mandal, et al.. (2005). The impact of receiving genetic test results on general and cancer‐specific psychologic distress among members of an African‐American kindred with a BRCA1 mutation. Cancer. 104(11). 2508–2516. 36 indexed citations

17.

Klein, Alison P., Alexa J.M. Sorant, Agnes Baffoe‐Bonnie, et al.. (2003). Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis. BMC Genetics. 4(Suppl 1). S73–S73. 7 indexed citations

18.

Mandal, Diptasri, Alexa J.M. Sorant, Elizabeth Pugh, et al.. (1999). Environmental covariates: Effects on the power of sib‐pair linkage methods. Genetic Epidemiology. 17(S1). S643–8. 9 indexed citations

19.

Mandal, Diptasri, Alexander F. Wilson, Robert C. Elston, et al.. (1999). Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis. Human Heredity. 50(2). 126–132. 14 indexed citations

20.

Pugh, Elizabeth, Diptasri Mandal, & Alexander F. Wilson. (1995). A graphical approach for presenting linkage results from a genomic screen. Genetic Epidemiology. 12(6). 807–812. 10 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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