Sally J. Jeffries
Birmingham, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 16 publications
Common variation at 1q23.3, 2p23.3, 2q33.3, and 2p21 influences risk of acute myeloid leukemia.
Journal: Blood
Published: August 19, 2025
Common variation at 1q23.3, 2p23.3, 2q33.3, and 2p21 influences the risk of acute myeloid leukemia.
Journal: Blood
Published: August 19, 2025
Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.
Journal: Nature communications
Published: January 05, 2022
Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.
Journal: Nature communications
Published: January 30, 2020
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.
Journal: Cancer genetics
Published: March 11, 2018
Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.
Journal: Cancer genetics
Published: March 05, 2018
Mutational analysis of disease relapse in patients allografted for acute myeloid leukemia.
Journal: Blood advances
Published: August 23, 2016
Sexual dimorphism in relation to adipose tissue and intrahepatocellular lipid deposition in early infancy.
Journal: International journal of obesity (2005)
Published: October 05, 2014
Last Updated: 09/26/2026