Stuart H. Orkin

Isolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinase.

A. Michelson, A. Markham, S. Orkin, 1983, Proceedings of the National Academy of Sciences of the United States of America.

The histone demethylase UTX regulates the lineage-specific epigenetic program of invariant natural killer T cells

S. Orkin, Guocheng Yuan, P. Das, 2016, Nature Immunology.

Thalassemia due to a mutation in the cleavage‐polyadenylation signal of the human beta‐globin gene.

S. Orkin, S. Antonarakis, H. Kazazian, 1985, The EMBO journal.

Chronic granulomatous disease.

S. Orkin, M. Dinauer, Stuart H. Orkin, 1992, Annual review of medicine.

The molecular genetics of thalassemia.

S. Orkin, D. Nathan, Stuart H. Orkin, 1981, Advances in human genetics.

Restriction site polymorphism in the phosphoglycerate kinase gene on the X chromosome

A. Michelson, S. Orkin, S. Antonarakis, 2004, Human Genetics.

A downstream element in the human beta-globin promoter: evidence of extended sequence-specific transcription factor IID contacts.

B. A. Lewis, T. Kim, S. Orkin, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Inactivation of an acceptor RNA splice site by a short deletion in beta-thalassemia.

S. Orkin, H. Kazazian, H. Kazazian, 1983, The Journal of biological chemistry.

ATA box transcription mutation in β-thalassemia

S. Orkin, P. Giardina, S. C. Goff, 1983 .