Eamonn G. Sheridan

机构：University of Leeds · ORCID：0000-0002-7237-6280

发表论文 163 篇 · 总被引 10461 次 · h-index 57

代表论文

Evidence for 28 genetic disorders discovered by combining healthcare and research data (2020 · Nature · 被引 699)
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018 · Nature Communications · 被引 125)
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy (2019 · The American Journal of Human Genetics · 被引 102)
PEDIA: prioritization of exome data by image analysis (2019 · Genetics in Medicine · 被引 90)
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2018 · Nature Communications · 被引 89)
Germline TET2 loss of function causes childhood immunodeficiency and lymphoma (2020 · Blood · 被引 88)