Sandra Hanks
CURE International UK(GB)Institute of Cancer Research(GB)
Publications by Year
Research Areas
Renal and related cancers, Microtubule and mitosis dynamics, DNA Repair Mechanisms, Epigenetics and DNA Methylation, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene(2006)986 cited
- → Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer(2006)641 cited
- → Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B(2004)606 cited
- → DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome(2011)361 cited
- → Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability(2014)353 cited
- → NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes(2003)301 cited
- → Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer(2012)257 cited
- → Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis(2003)240 cited
- → Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor(2008)197 cited
- → Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height(2011)169 cited