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- 2023
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Mark
Improved haplotype resolution of highly duplicated MHC genes in a long-read genome assembly using MiSeq amplicons
- Contribution to journal › Article
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Mark
Frequent use of IGHV3-30-3 in SARS-CoV-2 neutralizing antibody responses
- Contribution to journal › Article
- 2022
-
Mark
Somatic copy number variant load in neurons of healthy controls and Alzheimer’s disease patients
- Contribution to journal › Article
-
Mark
Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis
- Contribution to journal › Article
-
Mark
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
- Contribution to journal › Article
-
Mark
Rare germline copy number variants (CNVs) and breast cancer risk
- Contribution to journal › Article
- 2021
-
Mark
Gene-environment interactions and metal toxicity
(2021) p.349-368
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2018
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Mark
Enrichment of rare copy number variation in children with developmental language disorder
- Contribution to journal › Article
-
Mark
Blood parasites shape extreme major histocompatibility complex diversity in a migratory passerine
- Contribution to journal › Article
- 2017
-
Mark
Testing genotyping strategies for ultra-deep sequencing of a co-amplifying gene family : MHC class I in a passerine bird
- Contribution to journal › Article
