Annual Review of Genomics and Human Genetics
- SEQUENCE
VARIATION IN GENES
AND GENOMIC DNA: Methods for
Large-Scale Analysis
- Erratum: Transcriptional Control of Skeletogenesis
- CREATIONISM AND INTELLIGENT DESIGN
- Positive Selection in the Human Genome: From Genome Scans to Biological Significance
- Phenotypic Outcomes of Imprinted Gene Models in Mice: Elucidation of Pre- and Postnatal Functions of Imprinted Genes
- The Genetics of Innocence: Analysis of 194 U.S. DNA Exonerations
- Newborn Sequencing: The Promise and Perils
- Breast Cancer: Genetic Risk Assessment, Diagnostics, and Therapeutics in African Populations
- Indigenous Data Sovereignty in Genomics and Human Genetics: Genomic Equity and Justice for Indigenous Peoples
- Social and Behavioral Genomics: On the Ethics of the Research and Its Downstream Applications
- Pharmacogenomics in Africa: A Potential Catalyst for Precision Medicine in Genetically Diverse Populations
- Copy Number Variants: Deletion and Duplication Syndromes
- Disability, Genetic Counseling, and Medical Education: From Eugenics to Anti-Ableism
- Inequalities and Inclusion in Genomics Applied to Healthcare: A Latin American Perspective
- Pediatric Cancer Genetics and Genomics
- Brain Organoids: Tools for Understanding the Uniqueness and Individual Variability of the Human Brain
- Memories of the Human Genome Project at the Sanger Centre
- How a Medical Student Found Himself in a Human Genome Free for All
- Workforce Development in Genomic Data Science for Health: A Worldview
- Rethinking the Genomic Diversity Problem: Rejecting Inclusion in Defense of Indigenous Sovereignty
- Functional Neurogenomics to Dissect Disease Mechanisms Across Models
- The Genomics of Aging at the Single-Cell Scale
- Human Synthetic Biology and Programmable Gene Regulation Control
- Mechanisms of Enhancer-Mediated Gene Activation in the Context of the 3D Genome
- The Hallmarks of Aneuploidy in Cancer and Congenital Syndromes
- From Tiny Exons to Big Insights: The Expanding Field of Microexons
- Emerging Functions of the Repeat Genome in Nuclear Structure: A View from the Human Karyotype
- Beyond the Human Genome Project: The Age of Complete Human Genome Sequences and Pangenome References
- Population Diversity at the Single-Cell Level
- Genome-Wide Screening Approaches for Biochemical Reactions Independent of Cell Growth
- Causes and Consequences of Varying Transposable Element Activity: An Evolutionary Perspective
- The prevalence and linkage disequilibrium of 21 genetic variations related to thrombophilia, folate cycle, and hypertension in reproductive age women of Rostov region (Russia)
- Issue Information
- An indel introduced by Neanderthal introgression, rs3835124:ATTTATT > ATT, might contribute to prostate cancer risk by regulating PDK1 expression
- Clinical application of prospective whole‐exome sequencing in the diagnosis of genetic disease: Experience of a regional disease center in South Korea
- A comprehensive meta‐analysis to identify susceptibility genetic variants for precocious puberty
- The effect of TRIM5 variants on the susceptibility to HIV‐1 infection and disease progression in the Polish population
- Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting
- Association of blood lipid profiles and asthma: A bidirectional two‐sample Mendelian randomization study
- Nonsense suppression induces read‐through of a novel BMPR1A variant in a Chinese family with hereditary colorectal cancer
- ABCA1 variant rs9282541 is associated with metabolic syndrome in Maya children
- Investigation of the association between the Toll‐like receptor 1 rs4833095 variation and gastric adenocarcinoma recurrence
- Exploring the clinical significance of miR‐148 expression variations in distinct subtypes of irritable bowel syndrome
- A comprehensive review of HVS‐I mitochondrial DNA variation of 19 Iranian populations
- Using the Bayesian variational spike and slab model in a genome‐wide association study for finding associated loci with bipolar disorder
- Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low‐GGT intrahepatic cholestasis: Genetic diagnosis and genotype–phenotype correlation assessment
- Expression analysis of NF1‐mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR
- Open Data in the Era of the GDPR: Lessons from the Human Cell Atlas
