C. Nolan

机构：OrthoD (United Kingdom)

发表论文 21 篇 · 总被引 214 次 · h-index 6

代表论文

• Human de novo mutation rates from a four-generation pedigree reference (2025 · Nature · 被引 90)
• Predictive testing for BRCA1 and 2 mutations: a male contribution (2003 · Annals of Oncology · 被引 39)
• Elevated G2 chromosomal radiosensitivity in Irish breast cancer patients: a comparison with other studies (2005 · International Journal of Radiation Biology · 被引 34)
• A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigree (2024 · bioRxiv (Cold Spring Harbor Laboratory) · 被引 22)
• The Platinum Pedigree: a long-read benchmark for genetic variants (2025 · Nature Methods · 被引 14)
• The Platinum Pedigree: A long-read benchmark for genetic variants (2024 · bioRxiv (Cold Spring Harbor Laboratory) · 被引 6)