Mathew Nightingale
Dalhousie University(CA)
Publications by Year
Research Areas
Multiple Myeloma Research and Treatments, Ubiquitin and proteasome pathways, Retinal and Macular Surgery, Hereditary Neurological Disorders, Peptidase Inhibition and Analysis
Most-Cited Works
- → Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia(2009)246 cited
- → Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4(2010)195 cited
- → Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome(2011)171 cited
- → Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma(2006)161 cited
- → Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in multiple myeloma(2007)138 cited
- → Phenotypic Overlap Between Familial Exudative Vitreoretinopathy and Microcephaly, Lymphedema, and Chorioretinal Dysplasia Caused byKIF11Mutations(2014)135 cited
- → Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2(2009)92 cited
- → Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease(2010)70 cited
- → Germline Mutations in MAP3K6 Are Associated with Familial Gastric Cancer(2014)68 cited
- Mutations in a novel serine protease PRSS56 in families with nanophthalmos.(2011)