E Blair

Identification of the familial cylindromatosis tumour-suppressor gene

Graham R. Bignell, William Warren, Sheila Seal et al. · Nature Genetics · 2000 · 672 citations

Medicine, Genetics, Oncology +10

From the Editor: Nonresponse and Generalizability in Academic Research

E Blair · Journal of the Academy of Marketing Science · 2005 · 226 citations

Public Health, Biostatistics, Research Ethics +8

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok, Justine Rousseau, Joanna Twist et al. · Nature Communications · 2018 · 121 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Phenotypic variability in 49 cases of <i>ESCO2</i> mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with <i>ESCO2</i> expression and establishes the clinical criteria for Roberts syndrome

Horacio Astudillo‐de la Vega, Alison Trainer, Miriam Gordillo et al. · Journal of Medical Genetics · 2009 · 108 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Sampling in the Twenty-First Century

Seymour Sudman, E Blair · Journal of the Academy of Marketing Science · 1999 · 90 citations

Natural Resources, Anthropology, Stochastic Processes +9