Lisanne Vervoort

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Publications (5)

• Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome
  Genome Research 2025 DOI: 10.1101/gr.279331.124
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• Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome
  2024 DOI: 10.1101/2024.03.14.585046
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• Low copy repeats in the genome: from neglected to respected
  Exploration of Medicine 2023 DOI: 10.37349/emed.2023.00131
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• Human-specific expansion of 22q11.2 low copy repeats
  2020 DOI: 10.1101/2020.11.04.367920
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• Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins
  Human Molecular Genetics 2019 DOI: 10.1093/hmg/ddz166
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