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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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Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity.
Furth N, Cohen N, Spitzer A, et al. Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(1):e2403862122. doi:10.1073/pnas.2403862122
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Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity.
Furth N, Cohen N, Spitzer A, et al. Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(1):e2403862122. doi:10.1073/pnas.2403862122
Read more
Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity.
Furth N, Cohen N, Spitzer A, et al. Oncogenic IDH1 drives robust loss of histone acetylation and increases chromatin heterogeneity. Proceedings of the National Academy of Sciences of the United States of America. 2025;122(1):e2403862122. doi:10.1073/pnas.2403862122
Read more
Increased nuclear factor I-mediated chromatin access drives transition to androgen receptor splice variant dependence in prostate cancer.
Poluben L, Nouri M, Liang J, et al. Increased nuclear factor I-mediated chromatin access drives transition to androgen receptor splice variant dependence in prostate cancer. Cell reports. 2024;44(1):115089. doi:10.1016/j.celrep.2024.115089
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Technical variability across the 450K, EPICv1, and EPICv2 DNA methylation arrays: lessons learned for clinical and longitudinal studies.
Lussier AA, Schuurmans IK, Großbach A, et al. Technical variability across the 450K, EPICv1, and EPICv2 DNA methylation arrays: lessons learned for clinical and longitudinal studies. Clinical epigenetics. 2024;16(1):166. doi:10.1186/s13148-024-01761-4
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Manipulating cell fate through reprogramming: approaches and applications.
Yagi M, Horng JE, Hochedlinger K. Manipulating cell fate through reprogramming: approaches and applications. Development (Cambridge, England). 2024;151(19). doi:10.1242/dev.203090
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A Genotype/Phenotype Study of -Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense Variants.
Borroto MC, Michaud C, Hudon C, et al. A Genotype/Phenotype Study of -Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense Variants. Genes. 2024;15(8). doi:10.3390/genes15081033
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Phosphorothioate DNA modification by BREX Type 4 systems in the human gut microbiome.
Yuan Y, DeMott MS, Byrne SR, et al. Phosphorothioate DNA modification by BREX Type 4 systems in the human gut microbiome. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.03.597175
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Nucleotide depletion promotes cell fate transitions by inducing DNA replication stress.
Do BT, Hsu PP, Vermeulen SY, et al. Nucleotide depletion promotes cell fate transitions by inducing DNA replication stress. Developmental cell. 2024. doi:10.1016/j.devcel.2024.05.010
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Challenges in IBD Research 2024: Preclinical Human IBD Mechanisms.
Ciorba MA, Konnikova L, Hirota SA, et al. Challenges in IBD Research 2024: Preclinical Human IBD Mechanisms. Inflammatory bowel diseases. 2024;30(Supplement_2):S5-S18. doi:10.1093/ibd/izae081
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Ó³»­´«Ã½'s gene-editing technologies—CRISPR-Cas9, base editing, and prime editing—are being tested in more than 25 clinical trials to treat or cure leukemias, rare genetic diseases, high cholesterol, and other conditions.

NIH-funded discoveries from the Ó³»­´«Ã½ are powering nearly 20 clinical trials from companies testing new treatments for diseases like cancer and heart disease.

Ó³»­´«Ã½ developed a technology — partly supported by NIH funding —  that can detect trace amounts of cancer DNA from blood tests and help cancer patients find out their risk of disease recurrence earlier.

Using NIH funding, the Ó³»­´«Ã½â€™s Rare Genomes Project has worked with more than 1,300 families from all 50 U.S. states to diagnose rare genetic diseases.

Ó³»­´«Ã½ Clinical Labs has directly partnered with tens of thousands of cancer patients to analyze their DNA and accelerate research.

During the COVID-19 pandemic, Ó³»­´«Ã½ launched a large-scale diagnostic testing lab that processed over 37 million tests and saved state and federal programs nearly $2 billion.

The Ó³»­´«Ã½'s Cancer Dependency Map helps cancer researchers and drug developers discover therapeutic targets for new cancer treatments.

gnomAD, a large human genetic variant reference database developed by the Ó³»­´«Ã½ with NIH funding, has contributed to over 13 million genetic disease diagnoses since its launch in 2014.

Datasets generated at the Ó³»­´«Ã½ were used to train AlphaGenome, a cutting-edge AI model from Google DeepMind that predicts how genetic variants affect gene regulation.

the FDA granted accelerated approval for a lung cancer drug that was developed with Ó³»­´«Ã½ science and is for patients who otherwise had few treatment options.

David Liu and his team used NIH funding to invent precise gene-editing technologies, including one that may vastly improve access to genetic therapies for patients with rare disease.

NIH-funded Ó³»­´«Ã½ research is shedding new light on the biological roots of many diseases, including Alzheimer’s, Parkinson’s, and Huntington’s disease.

Scientists with Ó³»­´«Ã½â€™s Stanley Center for Psychiatric Research have found key genetic factors for schizophrenia and bipolar disorder.

Ó³»­´«Ã½ scientists are using AI to design new antibiotics and other drugs, predict drug toxicity, and pinpoint genes, molecules, and cells that might be causing disease.

Ó³»­´«Ã½ Clinical Labs has sequenced nearly 900,000 whole human genomes, producing, on average, one human genome sequence every three minutes.

Ó³»­´«Ã½ Clinical Labs developed a new method for genome sequencing that costs 75 percent less than existing methods.

 Ó³»­´«Ã½ Clinical Labs is the largest genome sequencing center of its kind in the world.

Ó³»­´«Ã½ Clinical Labs has partnered with MyOme and Southern Research Institute in Birmingham, Alabama to provide free genetic tests to people in Alabama.

Ó³»­´«Ã½ Clinical Labs has partnered with Mass General Brigham and Everygene to provide no-cost genetic testing to people throughout the US with cardiomyopathy, a disorder that can cause sudden cardiac death.

Ó³»­´«Ã½ Clinical labs and Mass General Brigham used data from NIH’s All of Us program to develop a genetic test that predicts risk of eight different heart conditions. This test is now available to patients.

Thanks to NIH funding, Ó³»­´«Ã½ Clinical Labs is collaborating with scientists across the U.S. to sequence DNA from tens of thousands of children with cancer and birth defects to study common biological pathways.

Ó³»­´«Ã½ Clinical Labs holds the world record for fastest DNA sequencing, completing whole genome sequencing and analysis in less than four hours at their facility in Burlington, Massachusetts.

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