Robert S. Sparkes

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

Satoshi Tsukada, Douglas C. Saffran, David J. Rawlings et al. · Cell · 1993 · 1.3K citations

Autoimmune Disease, Receptor Tyrosine Kinase, Malignant Blood Disorder +8

Localization of an ataxia-telangiectasia gene to chromosome 11q22–23

Richard A. Gatti, İzzet Berkel, Elena Boder et al. · Nature · 1988 · 685 citations

Ataxia-telangiectasia Gene, Genetic Disorder, Genetics +4

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

Ethylin Wang Jabs, Ulrich Müller, Xiang Li et al. · Cell · 1993 · 678 citations

Sclerostin, Developmental Biology, Genetic Disorder +6

Prevalence and causes of amblyopia in an adult population

Karin Attebo, Paul Mitchell, Robert G. Cumming et al. · Ophthalmology · 1998 · 462 citations

Visual Impairment, Eye Tracking, Adult Population +1

Direct Evidence for a Bone Marrow Origin of the Alveolar Macrophage in Man

E. Donnall Thomas, R Ramberg, George E. Sale et al. · Science · 1976 · 378 citations

Immunology, Pathology, Pulmonary Alveolar Proteinosis +18