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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
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Mark
Rare germline copy number variants (CNVs) and breast cancer risk
(
- Contribution to journal › Article
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Mark
Somatic copy number variant load in neurons of healthy controls and Alzheimer’s disease patients
(
- Contribution to journal › Article
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Mark
Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis
(
- Contribution to journal › Article
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Mark
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
(
- 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
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Mark
Blood parasites shape extreme major histocompatibility complex diversity in a migratory passerine
(
- Contribution to journal › Article
- 2017
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Mark
Dietary starch intake modifies the relation between copy number variation in the salivary amylase gene and BMI
(
- Contribution to journal › Article