Do COVID-19 Policies Affect Mobility Behaviour? Evidence from 75 Canadian and American Cities

por Armstrong, David A., Lebo, Matthew J., Lucas, Jack
Publicado 2020

Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations

por Lerner-Ellis, Jordan, Wang, Marina, White, Shana, Lebo, Matthew S
Publicado 2015

Somatic, germline and sex hierarchy regulated gene expression during Drosophila metamorphosis

por Lebo, Matthew S, Sanders, Laura E, Sun, Fengzhu, Arbeitman, Michelle N
Publicado 2009

Expanding the Noonan spectrum/RASopathy NGS panel: Benefits of adding NF1 and SPRED1

por Witkowski, Leora, Dillon, Mitchell W., Murphy, Elissa, S Lebo, Matthew, Mason‐Suares, Heather
Publicado 2020

Information Technology Support for Clinical Genetic Testing within an Academic Medical Center

por Aronson, Samuel, Mahanta, Lisa, Ros, Lei Lei, Clark, Eugene, Babb, Lawrence, Oates, Michael, Rehm, Heidi, Lebo, Matthew
Publicado 2016

Bioinformatics Workflow for Clinical Whole Genome Sequencing at Partners HealthCare Personalized Medicine

por Tsai, Ellen A., Shakbatyan, Rimma, Evans, Jason, Rossetti, Peter, Graham, Chet, Sharma, Himanshu, Lin, Chiao-Feng, Lebo, Matthew S.
Publicado 2016

Genetic variant pathogenicity prediction trained using disease-specific clinical sequencing data sets

por Evans, Perry, Wu, Chao, Lindy, Amanda, McKnight, Dianalee A., Lebo, Matthew, Sarmady, Mahdi, Abou Tayoun, Ahmad N.
Publicado 2019

VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data

por Pugh, Trevor J., Amr, Sami S., Bowser, Mark J., Gowrisankar, Sivakumar, Hynes, Elizabeth, Mahanta, Lisa M., Rehm, Heidi L., Funke, Birgit, Lebo, Matthew S.
Publicado 2016

Dynamic, mating-induced gene expression changes in female head and brain tissues of Drosophila melanogaster

por Dalton, Justin E, Kacheria, Tanvi S, Knott, Simon RV, Lebo, Matthew S, Nishitani, Allison, Sanders, Laura E, Stirling, Emma J, Winbush, Ari, Arbeitman, Michelle N
Publicado 2010

A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing–Detected Variants with an Orthogonal Method in Clinical Genetic Testing

por Lincoln, Stephen E., Truty, Rebecca, Lin, Chiao-Feng, Zook, Justin M., Paul, Joshua, Ramey, Vincent H., Salit, Marc, Rehm, Heidi L., Nussbaum, Robert L., Lebo, Matthew S.
Publicado 2019

The Evolution of a Large Biobank at Mass General Brigham

por Boutin, Natalie T., Schecter, Samantha B., Perez, Emma F., Tchamitchian, Natasha S., Cerretani, Xander R., Gainer, Vivian S., Lebo, Matthew S., Mahanta, Lisa M., Karlson, Elizabeth W., Smoller, Jordan W.
Publicado 2022

A comprehensive genome report for COVID-19 patients: GENCOV Study Canada

por Frangione, Erika, Casalino, Selina, Chowdhary, Sunakshi, Mighton, Chloe, Faghfoury, Hanna, Bombard, Yvonne, Strug, Lisa, Pugh, Trevor, Simpson, Jared, Lebo, Matthew, Hao, Limin, Lane, William, Taher, Jennifer, Lerner-Ellis, Jordan
Publicado 2021

Harmonizing variant classification for return of results in the All of Us Research Program

por Harrison, Steven M., Austin‐Tse, Christina A., Kim, Serra, Lebo, Matthew, Leon, Annette, Murdock, David, Radhakrishnan, Aparna, Shirts, Brian H., Steeves, Marcie, Venner, Eric, Gibbs, Richard A., Jarvik, Gail P., Rehm, Heidi L.
Publicado 2021

Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease

por Chopra, Sameer S, Leshchiner, Ignaty, Duzkale, Hatice, McLaughlin, Heather, Giovanni, Monica, Zhang, Chengsheng, Stitziel, Nathan, Fingeroth, Joyce, Joyce, Robin M, Lebo, Matthew, Rehm, Heidi, Vuzman, Dana, Maas, Richard, Sunyaev, Shamil R, Murray, Michael, Cassa, Christopher A
Publicado 2015

Pathology informatics fellowship training: Focus on molecular pathology

por Mandelker, Diana, Lee, Roy E., Platt, Mia Y., Riedlinger, Gregory, Quinn, Andrew, Rao, Luigi K. F., Klepeis, Veronica E., Mahowald, Michael, Lane, William J., Beckwith, Bruce A., Baron, Jason M., McClintock, David S., Kuo, Frank C., Lebo, Matthew S., Gilbertson, John R.
Publicado 2014

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions

por Fahed, Akl C., Wang, Minxian, Homburger, Julian R., Patel, Aniruddh P., Bick, Alexander G., Neben, Cynthia L., Lai, Carmen, Brockman, Deanna, Philippakis, Anthony, Ellinor, Patrick T., Cassa, Christopher A., Lebo, Matthew, Ng, Kenney, Lander, Eric S., Zhou, Alicia Y., Kathiresan, Sekar, Khera, Amit V.
Publicado 2020

Decoding Genetics, Ancestry, and Geospatial Context for Precision Health

por Koyama, Satoshi, Wang, Ying, Paruchuri, Kaavya, Uddin, Md Mesbah, Cho, So Mi J., Urbut, Sarah M., Haidermota, Sara, Hornsby, Whitney E., Green, Robert C., Daly, Mark J., Neale, Benjamin M., Ellinor, Patrick T., Smoller, Jordan W., Lebo, Matthew S., Karlson, Elizabeth W., Martin, Alicia R., Natarajan, Pradeep
Publicado 2023

A systematic approach to the reporting of medically relevant findings from whole genome sequencing

por McLaughlin, Heather M, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Kohane, Isaac S, Krier, Joel, Lane, William J, Lautenbach, Denise, Lebo, Matthew S, Machini, Kalotina, MacRae, Calum A, Azzariti, Danielle R, Murray, Michael F, Seidman, Christine E, Vassy, Jason L, Green, Robert C, Rehm, Heidi L
Publicado 2014

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

por Blout Zawatsky, Carrie L., Shah, Nidhi, Machini, Kalotina, Perez, Emma, Christensen, Kurt D., Zouk, Hana, Steeves, Marcie, Koch, Christopher, Uveges, Melissa, Shea, Janelle, Gold, Nina, Krier, Joel, Boutin, Natalie, Mahanta, Lisa, Rehm, Heidi L., Weiss, Scott T., Karlson, Elizabeth W., Smoller, Jordan W., Lebo, Matthew S., Green, Robert C.
Publicado 2021

Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report

por Murry, Jaclyn B., Machini, Kalotina, Ceyhan-Birsoy, Ozge, Kritzer, Amy, Krier, Joel B., Lebo, Matthew S., Fayer, Shawn, Genetti, Casie A., VanNoy, Grace E., Yu, Timothy W., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Beggs, Alan H., Rehm, Heidi L.
Publicado 2018