Categoría: Annual Review of Genomics and Human Genetics
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Indigenous Data Sovereignty in Genomics and Human Genetics: Genomic Equity and Justice for Indigenous Peoples
As the field of genomics and human genetics continues to push our understanding of disease and biodiversity through an ever-increasing pool of genomic data, it is critical to consider the social, ethical, and legal implications of using such data. This…
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Social and Behavioral Genomics: On the Ethics of the Research and Its Downstream Applications
Social and behavioral scientists increasingly work with geneticists or adapt the methods of genetic research to investigate genomic variation in a wide variety of behavioral and social phenotypes. Using genome-wide association studies, these social and…
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Pharmacogenomics in Africa: A Potential Catalyst for Precision Medicine in Genetically Diverse Populations
Genetic variation is a major determinant of drug response across populations. Owing to advances in sequencing technologies over the last two decades, several clinically actionable variants or haplotypes have been characterized in genes that encode prot…
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Copy Number Variants: Deletion and Duplication Syndromes
Rare genetic variants have illuminated mechanisms of common diseases and have even led to novel treatment approaches. Some copy number variants (CNVs) have been associated with extraordinary risk for complex neuropsychiatric phenotypes and thus offer a…
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Disability, Genetic Counseling, and Medical Education: From Eugenics to Anti-Ableism
Genetic counselors have a complex relationship with disability communities due to both the legacy of eugenics and their ongoing role counseling families about prenatal testing. Drawing on a social model of disability and highlighting mistaken assumptio…
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Inequalities and Inclusion in Genomics Applied to Healthcare: A Latin American Perspective
Integrating genomics into healthcare within the precision medicine (PM) framework poses distinct challenges in resource-limited regions like Latin America and the Caribbean (LAC). These challenges arise partly from the lack of PM models tailored for lo…
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Pediatric Cancer Genetics and Genomics
Molecular profiling of DNA and RNA from pediatric cancers by next-generation sequencing has been demonstrated to improve diagnosis and prognosis and to identify somatic alterations indicating vulnerability to targeted therapies. Hence, much like in the…
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Brain Organoids: Tools for Understanding the Uniqueness and Individual Variability of the Human Brain
Understanding the drivers of human brain specialization, and how specialized properties are codified during development and evolution, seems to be within reach for the first time. Improved cell-based experimental models of the human brain have empowere…
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Memories of the Human Genome Project at the Sanger Centre
2025 marks the twenty-fifth anniversary of the completion of a working draft of the 3-Gb human genome sequence and its availability in public databases to promote research into human health and disease for the benefit of all. The sequence was produced …
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How a Medical Student Found Himself in a Human Genome Free for All
In this short memoir, I recount the series of improbable interactions and events that led me from medical school to a leadership role in the Human Genome Project.
