Author

Andrew Crispin

Observed name: Andrew W. Crispin

Institution: Boston Children's Hospital

Observed institution: Boston Children's Hospital

OpenAlex ID: A5086730347

Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice

2018 · Inga Hofmann, Mitchell J. Geer, et al. · Blood · 54

A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia

2016 · Daniel A. Lichtenstein, Andrew W. Crispin, et al. · Blood · 39

Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia

2020 · Andrew Crispin, Chaoshe Guo, et al. · Journal of Clinical Investigation · 32

Hscb, a Mitochondrial Iron-Sulfur Cluster Assembly Co-Chaperone, Is a Novel Candidate Gene for Congenital Sideroblastic Anemia

2017 · Andrew Crispin, Paul Schmidt, et al. · Blood · 4

HSCB, a co-chaperone in mitochondrial iron-sulfur cluster biogenesis, is a novel candidate gene for congenital sideroblastic anemia

2017 · Andrew Crispin · OpenBU (Boston University)

Works count: 5

Citation count: 129

H-index: 4

I10-index: 3