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The aggregation of pig articular chondrocyte and synthesis of extracellular matrix by a lactose-modified chitosan.
Donati I, Stredanska S, Silvestrini G, et al. The aggregation of pig articular chondrocyte and synthesis of extracellular matrix by a lactose-modified chitosan. Biomaterials. 2005;26(9):987-98. doi:10.1016/j.biomaterials.2004.04.015PubMedDOIGoogle Scholar
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Generation of a Motor Nerve Organoid with Human Stem Cell-Derived Neurons.
Kawada J, Kaneda S, Kirihara T, et al. Generation of a Motor Nerve Organoid with Human Stem Cell-Derived Neurons. Stem Cell Reports. 2017;9(5):1441-1449. doi:10.1016/j.stemcr.2017.09.021Google ScholarPubMedDOI
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Are We There Yet? How and When Specific Biotechnologies Will Improve Human Health.
O’Day E, Hosta-Rigau L, Oyarzún DA, et al. Are We There Yet? How and When Specific Biotechnologies Will Improve Human Health. Biotechnol J. 2019;14(1):e1800195. doi:10.1002/biot.201800195PubMedGoogle ScholarDOI
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Analysis of the effects of five factors relevant to in vitro chondrogenesis of human mesenchymal stem cells using factorial design and high throughput mRNA-profiling.
Jakobsen RB, Østrup E, Zhang X, Mikkelsen TS, Brinchmann JE. Analysis of the effects of five factors relevant to in vitro chondrogenesis of human mesenchymal stem cells using factorial design and high throughput mRNA-profiling. PLoS One. 2014;9(5):e96615. doi:10.1371/journal.pone.0096615Google ScholarPubMedDOI
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Predicting clinical response to anticancer drugs using an ex vivo platform that captures tumour heterogeneity.
Majumder B, Baraneedharan U, Thiyagarajan S, et al. Predicting clinical response to anticancer drugs using an ex vivo platform that captures tumour heterogeneity. Nat Commun. 2015;6:6169. doi:10.1038/ncomms7169Google ScholarPubMedDOI
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An engineered multicomponent bone marrow niche for the recapitulation of hematopoiesis at ectopic transplantation sites.
Ferreira MSV, Bergmann C, Bodensiek I, et al. An engineered multicomponent bone marrow niche for the recapitulation of hematopoiesis at ectopic transplantation sites. J Hematol Oncol. 2016;9:4. doi:10.1186/s13045-016-0234-9Google ScholarPubMedDOI
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In March of 2020, Broad Institute converted a clinical genetics processing lab into a large-scale COVID-19 testing facility in less than two weeks.

We've screened more than 1,275 cancer cell lines as part of the Cancer Dependency Map (DepMap).

Broad Genomics Platform sequences a whole human genome every four minutes.

More than 11,000 individuals living with cancer in the United States and Canada have partnered with Count Me In to share their experiences and help accelerate cancer research.

The Drug Repurposing Hub is one of the most comprehensive and up-to-date biologically annotated collections of FDA-approved compounds in the world. Researchers anywhere can explore more than 6,000 drugs in the hub and search for possible new uses for them to jump-start new drug discovery.

In 2021, our sustainability efforts sent more than 80 percent of waste from the Genomics Platform to either a recycling facility or to an incineration plant that generates electricity.

Through Broad's Scientists in the Classroom program, Broad researchers visit every 8th grade classroom in Cambridge each year to talk about genetics and evolution.

Every summer, 18 high school students spend six weeks at Broad working side-by-side with mentors on cutting-edge research.

In November 2022, Broad’s Genomics Platform sequenced its 500,000th whole human genome, a mere four years after sequencing its 100,000th.

By the end of 2022, Broad’s COVID-19 testing lab had processed more than 37 million tests.

Working with Addgene, Broad Institute has shared CRISPR genome-editing reagents with researchers at more than 3,200 institutions in 76 countries.

The NeuroGAP-Psychosis project, a collaboration between the Stanley Center for Psychiatric Research and Harvard T.H. Chan School of Public Health to study the genetics of severe mental illness, has recruited more than 42,000 participants in Ethiopia, Kenya, Uganda, and South Africa.

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