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      5. Novo Nordisk Foundation Center for Genomic Mechanisms of Disease This center is developing new paradigms and technologies to scale the discovery of biological mechanisms of common, complex diseases, by facilitating close collaborations between the Ó³»­´«Ã½ and the Danish research community.
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Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminates their genetic architectures.
Jee YH, Wang Y, Jung KJ, et al. Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminates their genetic architectures. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.05.17.24307550
Read more
Identifying drug targets for schizophrenia through gene prioritization.
Kraft J, Braun A, Awasthi S, et al. Identifying drug targets for schizophrenia through gene prioritization. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.05.15.24307423
Read more
Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminates their genetic architectures.
Jee YH, Wang Y, Jung KJ, et al. Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminates their genetic architectures. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.05.17.24307550
Read more
Identifying drug targets for schizophrenia through gene prioritization.
Kraft J, Braun A, Awasthi S, et al. Identifying drug targets for schizophrenia through gene prioritization. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.05.15.24307423
Read more
Identifying drug targets for schizophrenia through gene prioritization.
Kraft J, Braun A, Awasthi S, et al. Identifying drug targets for schizophrenia through gene prioritization. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.05.15.24307423
Read more
Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminates their genetic architectures.
Jee YH, Wang Y, Jung KJ, et al. Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminates their genetic architectures. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.05.17.24307550
Read more
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias.
Weng LC, Khurshid S, Hall AW, et al. Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias. Circulation. Genomic and precision medicine. 2024:e004320. doi:10.1161/CIRCGEN.123.004320
Read more
An integrative framework to prioritize genes in more than 500 loci associated with body mass index.
Hemerich D, Svenstrup V, Obrero VD, et al. An integrative framework to prioritize genes in more than 500 loci associated with body mass index. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.04.016
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Genome sequence analyses identify novel risk loci for multiple system atrophy.
Chia R, Ray A, Shah Z, et al. Genome sequence analyses identify novel risk loci for multiple system atrophy. Neuron. 2024. doi:10.1016/j.neuron.2024.04.002
Read more
Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects.
Broberg M, Ampuja M, Jones S, et al. Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects. BMC genomics. 2024;25(1):256. doi:10.1186/s12864-024-10172-x
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In March of 2020, Ó³»­´«Ã½ 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).

Ó³»­´«Ã½ 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 Ó³»­´«Ã½'s Scientists in the Classroom program, Ó³»­´«Ã½ 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 Ó³»­´«Ã½ working side-by-side with mentors on cutting-edge research.

In November 2022, Ó³»­´«Ã½â€™s Genomics Platform sequenced its 500,000th whole human genome, a mere four years after sequencing its 100,000th.

By the end of 2022, Ó³»­´«Ã½â€™s COVID-19 testing lab had processed more than 37 million tests.

Working with Addgene, Ó³»­´«Ã½ 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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