Ross, Justyne
https://orcid.org/0000-0002-7437-8060
Mayo Clinic
University of North Carolina at Chapel Hill
Citations 2
Clinical testing panels for ALS: global distribution, consistency, and challenges
Dilliott, Allison A. , Nasser, Ahmad Al , Elnagheeb, Marwa , Fifita, Jennifer A. , Henden, Lyndal , Keseler, Ingrid M. , Lenz, Steven, Marriott, Heather , McCann, Emily P. , Mesaros, Maysen , Owens, Emma, Palus, Brooke, Ross, Justyne , Wang, Zhanjun , Benatar, Michael , Blair, Ian P. , Cooper‐Knock, Johnathan , Harrington, Elizabeth A. , Moreno, Cristiane Araújo Martins , Rampersaud, Evadnie , Roggenbuck, Jennifer , Blitterswijk, Marka van , Weishaupt, Jochen H. , Drury, Luke, Harms, Matthew B. , Panel, On behalf of the Amyotrophic lateral sclerosis spectrum disorders Gene Curation Expert, Opie-Martin, Sarah , Al-Chalabi, Ammar , Benatar, Michael , Farhan, Sali M K , van Blitterswijk, Marka , White, Hannah, Al‐Chalabi, Ammar , Andersen, Peter Munch , Harrington, Elizabeth A., Heckmann, Jeannine M. , Landers, John E. , Nel, Melissa , Rouleau, Guy Armand , Traynor, Bryan J. , Rheenen, Wouter van , Veldink, Jan H. , Panel, On behalf of the Amyotrophic lateral sclerosis spectrum disorders Gene Curation Expert
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | March 10, 2023 | Volume: 24 | Issue: 5-6 | Pages: 420-435
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
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.