A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions - Concepedia

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A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions

DOI Full Paper Access

61

Citations

51

References

2020

Year

Paras Garg, Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain, Sofie Metsu, Hugh E. Olsen, Benedict Paten, Beate Ritz,

The American Journal of Human Genetics

Genome-wide Association StudyAllelic VariantRare Epigenetic VariationGeneticsCgg ExpansionsGenetic VariationGenomicsSystems BiologyMedicineEpigeneticsVariant Interpretation

References

	Year	Citations

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