Base by Base
Total duration:
12 h 23 min
128: LINE‑1 Promoters Orchestrate Early Human Brain Development
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15:26
127: In silico generation of synthetic cancer genomes using generative AI
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17:36
126: Molecular and developmental deficits in Smith-Magenis syndrome human stem cell-derived cortical neural models
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20:59
125: Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: A new generation of opportunities
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22:46
124: Exploring the Omnigenic Architecture of Selected Complex Traits
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23:47
123: Dominant‑Negative ATP5F1A Variants Uncouple Complex V and Drive Neurological Disease
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18:12
122: Patient Stratification Reveals the Molecular Basis of Disease Co-Occurrences
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19:57
121: G-quadruplexes as a Source of Vulnerability in BRCA2-deficient Granule Cell Progenitors and Medulloblastoma
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19:02
120: Rare BMAL1 Variants Link the Circadian Clock to Neurodevelopment
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22:30
119: G‑Quadruplex Stabilization Triggers Pericentromeric DNA Breaks in B Cells
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18:35
118: Cancer cells subvert the primate-specific KRAB zinc finger protein ZNF93 to control APOBEC3B
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19:11
117: Pol III–linked polyadenylation fuels SINE RNA accumulation during infection
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16:00
116: Cell Type–Specific Purifying Selection of Synonymous mtDNA Variation
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15:53
115: A Transcriptomic, Proteomic, and Functional Genetic Atlas Dissects Neurofibromin Function in the Peripheral Nervous System
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15:24
114: One-hour extraction-free loop-mediated isothermal amplification HPV DNA assay for point-of-care testing in Maputo, Mozambique
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16:31
113: Joint, Multifaceted Genomic Analysis Enables Diagnosis of Ultra-Rare Monogenic Presentations
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22:08
112: Local Genetic Sex Differences in Quantitative Traits
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21:16
111: A Multimodal Dataset for Precision Oncology in Head and Neck Cancer
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17:06
110: Whole-exome sequencing identifies new schizophrenia risk genes
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20:31
109: Autocrine Interferon Poisoning: ADAR1–BRCA Synthetic Lethality
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18:10
108: Epigenome Editing Reverses HBG Silencing
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20:53
107: Genome-wide Association Study Reveals Genetic Links to Pulpal and Apical Diseases
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19:07
106: Decoding Brain Maps for Pharmacotranscriptomics
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19:25
105: Genome-level Selection as a Universal Marker of Cancer Therapy Resistance
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18:28
104: Cross-population GWAS and proteomics improve risk prediction and reveal mechanisms in atrial fibrillation
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16:56
103: Genome Sequencing Forecasts Outcomes After Congenital Cardiac Surgery
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17:56
102: Clinical Impact of Pharmacogenetic Risk Variants in a Large Chinese Cohort
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14:38
101: JAK2 Inhibition Selects RAS-Mutant Clones in Myelofibrosis
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18:25
️ 100: Epigenomic Diagnosis and Prognosis of Acute Myeloid Leukemia
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14:44
️ 99: NXT2: A Testis-Specific RNA Export Factor Essential for Spermatogenesis
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14:36
️ 98: Cell Marker Accordion: Interpretable Single-Cell and Spatial Omics Annotation in Health and Disease
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19:20
️ 97: Pancreatic Cancer Genomics: Insights from the COMPASS Trial
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21:43
️ 96: Early Cerebrospinal Fluid Proteomic Changes in Down Syndrome and Alzheimer’s Disease
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16:39
️ 95: Mitochondria on the Move: Biotechnological Strategies for Transfer and Transplantation
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19:10
️ 94: Intraindividual Epigenetic Heterogeneity in Advanced Prostate Cancer
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20:29
️ 93: Neuroinvasive and Pulmonary Virulence of H5N1 Clade 2.3.4.4b Genotype B3.13
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19:01
️ 92: Genetic Loss of CFHR5 Function Protects Against Age-Related Macular Degeneration
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16:49
️ 91: Genome-wide Association of Plasma N-Glycome Reveals Links to Liver Disease and Anti-Inflammatory Proteins
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17:42
️ 90: Variable and Interactive Effects of Sex, APOE ε4 and TREM2 on Tau Deposition
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15:57
️ 89: Decoding the Genetics of Smell: Sex-Specific Variants in Olfactory Identification
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20:28