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Mehta, Nikita

https://orcid.org/0000-0003-1465-2934

Mayo Clinic

Memorial Sloan Kettering Cancer Center

Citations 4

Further Characterization of Hb Bronovo [α103(G10)His→Leu; HBA2: c.311A>T] and First Report of the Homozygous State
Mehta, Nikita , Johnston, J. Martin , Hein, Molly S., Kipp, Benjamin R. , Coon, Lea M., Savedra, Michelle E., Hoyer, James D., He, Rong , Rangan, Aruna , Oliveira, Jennifer L. , Herrick, Jennifer L. , Hein, Molly, Coon, Lea, Shi, Min

Hemoglobin | June 18, 2020 | Volume: 44 | Issue: 3 | Pages: 174-178

10.1080/03630269.2020.1776322 Get It

Unconventional Diagnosis Based on Somatic Findings through Germ Line Whole-Exome Sequencing
Lopes, Jaime L. , Rasmussen, Kristen , Mehta, Nikita , Boczek, Nicole J. , Hasadsri, Linda , Rasmussen, Kristen J , Lopes, Jaime

Clinical Chemistry | January 6, 2020 | Volume: 66 | Issue: 1 | Pages: 48-51

10.1093/clinchem.2019.304451 Get It

ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants
Luo, Xi , Feurstein, Simone , Mohan, Shruthi , Jackson, Sarah A. , Keel, Sioḃán , Chicka, Michael C., Brown, Anna , Agarwal, Anupriya , Luo, Minjie , Li, Zejuan , Ross, Justyne , Pineda‐Alvarez, Daniel , Bertuch, Alison A. , Mehta, Nikita , Vulliamy, Tom, Wang, Ying , Nichols, Kim E. , Malcovati, Luca , Walsh, Michael F. , Rawlings, Lesley , Soulier, Jean , Raimbault, Anna , Zhang, Liying , Ryan, Gabriella, Speck, Nancy A. , Wu, David , Godley, Lucy A. , Malcovati, Luca , Godley, Lucy A , Brown, Anna L , Jackson, Sarah A , Nichols, Kim E , Porter, Christopher C. , Kesserwan, Chimene A. , Baliakas, Panagiotis , DiNardo, Courtney D. , McWeeney, Shannon K. , Routbort, Mark J. , Ryan, Gabriella, Plon, Sharon E.

Blood Advances | October 16, 2019 | Volume: 3 | Issue: 20 | Pages: 2962-2979

10.1182/bloodadvances.2019000644 Get It

Key Points The ClinGen MM-VCEP has specified RUNX1-specific curation rules to address gene function, gene-specific domains, and phenotypic criteria. RUNX1-specific criteria resulted in a reduction in CONF and VUS variants by 33%, emphasizing the need for expert variant curation.