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- 2023
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A novel scatterplot-based method to detect copy number variation (CNV)
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- Contribution to journal › Article
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Systematic errors in annotations of truncations, loss-of-function and synonymous variants
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- Contribution to journal › Article
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Identification of a candidate dwarfing gene in Pallas, the first commercial barley cultivar generated through mutational breeding
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- Contribution to journal › Article
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Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci
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- Contribution to journal › Article
- 2022
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Mark
Editorial : Extracellular matrix in homeostasis and cancer
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- Contribution to journal › Debate/Note/Editorial
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Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model
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- Contribution to journal › Article
- 2021
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Mark
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations
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- Contribution to journal › Article
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Novel Reclassification of Adult Diabetes Is Useful to Distinguish Stages of β-Cell Function Linked to the Risk of Vascular Complications : The DOLCE Study From Northern Ukraine
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- Contribution to journal › Article
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A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study
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- Contribution to journal › Article
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Mark
In vivo Cross-Linking MS of the Complement System MAC Assembled on Live Gram-Positive Bacteria
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- Contribution to journal › Article
- 2020
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Mark
Pronounced Plastic and Evolutionary Responses to Unpredictable Thermal Fluctuations in Drosophila simulans
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- Contribution to journal › Article
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Incomplete Sterility of Chromosomal Hybrids : Implications for Karyotype Evolution and Homoploid Hybrid Speciation
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- Contribution to journal › Article
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Designing Regulatory Frameworks for Access to Genetic Resources: A Multi-Stakeholder Multi-Criteria Approach
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- Contribution to journal › Article
- 2019
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Mark
Comprehensive Assessment of BARD1 Messenger Ribonucleic Acid Splicing With Implications for Variant Classification
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- Contribution to journal › Article
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Mark
Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186
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- Contribution to journal › Article