Lisa Mahanta

1.3k total citations
15 papers, 552 citations indexed

About

Lisa Mahanta is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Lisa Mahanta has authored 15 papers receiving a total of 552 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Lisa Mahanta's work include Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Lisa Mahanta is often cited by papers focused on Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Lisa Mahanta collaborates with scholars based in United States and Canada. Lisa Mahanta's co-authors include Heidi L. Rehm, Matthew S. Lebo, Mark Bowser, Birgit Funke, Elizabeth Hynes, Trevor J. Pugh, Sivakumar Gowrisankar, Bryan D. Harrison, Sami S. Amr and Samantha Baxter and has published in prestigious journals such as The American Journal of Human Genetics, Human Mutation and Genetics in Medicine.

In The Last Decade

Lisa Mahanta

15 papers receiving 544 citations

Peers

Countries citing papers authored by Lisa Mahanta

Since Specialization

Citations

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

Fields of papers citing papers by Lisa Mahanta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa Mahanta

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	P736: An assessment of a novel capillary blood collection system for research sample collection in adults 2025 ·Genetics in Medicine Open ·Emily S. Miller, (unknown), (unknown), Lisa Mahanta, Matthew S. Lebo, (unknown)	1
2	The Evolution of a Large Biobank at Mass General Brigham 2022 ·Journal of Personalized Medicine ·Natalie Boutin, (unknown), Emma Perez, (unknown), (unknown), Vivian S. Gainer, Matthew S. Lebo, Lisa Mahanta, Elizabeth W. Karlson, Jordan W. Smoller	26
3	Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test 2021 ·Genetics in Medicine ·Deanna Brockman, Christina Austin‐Tse, (unknown), (unknown), Candace Patterson, (unknown), (unknown), Kimberly O’Brien, Lisa Mahanta, Matthew S. Lebo, Christine Y. Lu, Pradeep Natarajan, Amit V. Khera, Krishna G. Aragam, Sekar Kathiresan, Heidi L. Rehm, Miriam S. Udler	11
4	Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates 2021 ·Genetics in Medicine ·Hana Zouk, Wanfeng Yu, Andrea M. Oza, Megan Hawley, (unknown), Christopher Koch, Lisa Mahanta, John B. Harley, Gail P. Jarvik, Elizabeth W. Karlson, Kathleen A. Leppig, Melanie F. Myers, Cynthia A. Prows, Marc S. Williams, Scott T. Weiss, Matthew S. Lebo, Heidi L. Rehm	7
5	Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization 2021 ·The American Journal of Human Genetics ·Carrie L. Blout Zawatsky, Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D. Christensen, Hana Zouk, Marcie Steeves, Christopher Koch, Melissa Kurtz Uveges, (unknown), Nina B. Gold, Joel B. Krier, Natalie Boutin, Lisa Mahanta, Heidi L. Rehm, Scott T. Weiss, Elizabeth W. Karlson, Jordan W. Smoller, Matthew S. Lebo, Robert C. Green	32
6	Remote Fingerstick Blood Collection for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Antibody Testing 2020 ·Archives of Pathology & Laboratory Medicine ·Wilfredo F. García-Beltrán, Tyler E. Miller, (unknown), (unknown), Michael G. Astudillo, Diane Yang, Lisa Mahanta, Mandakolathur R. Murali, Anand S. Dighe, Jochen K. Lennerz, Julia Thierauf, Vivek Naranbhai, A. John Iafrate	10
7	Analyzing and Reanalyzing the Genome: Findings from the MedSeq Project 2019 ·The American Journal of Human Genetics ·Kalotina Machini, Ozge Ceyhan‐Birsoy, Danielle R. Azzariti, Himanshu Sharma, (unknown), Lisa Mahanta, Laura Hutchinson, Heather M. McLaughlin, Robert C. Green, Matthew S. Lebo, Heidi L. Rehm	26
8	Information Technology Support for Clinical Genetic Testing within an Academic Medical Center 2016 ·Journal of Personalized Medicine ·Samuel Aronson, Lisa Mahanta, (unknown), Eugene Clark, Lawrence Babb, (unknown), Heidi L. Rehm, Matthew S. Lebo	10
9	The Translational Genomics Core at Partners Personalized Medicine: Facilitating the Transition of Research towards Personalized Medicine 2016 ·Journal of Personalized Medicine ·(unknown), Alison Brown, Lisa Mahanta, Sami S. Amr	5
10	The Information Technology Infrastructure for the Translational Genomics Core and the Partners Biobank at Partners Personalized Medicine 2016 ·Journal of Personalized Medicine ·Natalie Boutin, (unknown), Lisa Mahanta, (unknown), (unknown), (unknown), Irene León, (unknown), (unknown)	17
11	VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data 2015 ·Genetics in Medicine ·Trevor J. Pugh, Sami S. Amr, Mark Bowser, Sivakumar Gowrisankar, Elizabeth Hynes, Lisa Mahanta, Heidi L. Rehm, Birgit Funke, Matthew S. Lebo	55
12	Next generation sequencing‐based copy number analysis reveals low prevalence of deletions and duplications in 46 genes associated with genetic cardiomyopathies 2015 ·Molecular Genetics & Genomic Medicine ·Ozge Ceyhan‐Birsoy, Trevor J. Pugh, Mark Bowser, Elizabeth Hynes, (unknown), Lisa Mahanta, Matthew S. Lebo, Sami S. Amr, Birgit Funke	28
13	Targeted Droplet-Digital PCR as a Tool for Novel Deletion Discovery at the DFNB1 Locus 2015 ·Human Mutation ·Ahmad Abou Tayoun, Heather Mason‐Suares, (unknown), Mark Bowser, Elizabeth Hynes, Lisa Mahanta, Birgit Funke, Heidi L. Rehm, Sami S. Amr	33
14	Comprehensive Diagnostic Testing for Stereocilin 2014 ·Journal of Molecular Diagnostics ·Diana Mandelker, Sami S. Amr, Trevor J. Pugh, Sivakumar Gowrisankar, (unknown), Elizabeth Hynes, Mark Bowser, Bryan D. Harrison, (unknown), Lisa Mahanta, Heidi L. Rehm, Birgit Funke	46
15	The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing 2014 ·Genetics in Medicine ·Trevor J. Pugh, Melissa Kelly, Sivakumar Gowrisankar, Elizabeth Hynes, Michael A. Seidman, Samantha Baxter, Mark Bowser, Bryan D. Harrison, Daniel Aaron, Lisa Mahanta, Neal K. Lakdawala, Gregory C McDermott, Emily White, Heidi L. Rehm, Matthew S. Lebo, Birgit Funke	245

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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