S. Grist

发表

Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1.

R. Karchin, Å. Borg, P. Radice, 2009, Mutation research.

Anonymous DNA probes to human chromosome 16 derived from a flow-purified library.

G. Sutherland, V. Hyland, S. Grist, 1988, American journal of human genetics.

Gene rearrangement in B- and T-lymphoproliferative disease detected by the polymerase chain reaction.

A. Morley, S. Neoh, J. Wan, 1991, Blood.

Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer

J. Craig, G. Suthers, J. Muecke, 2006, Familial Cancer.

The effect of cycle number and target size on polymerase chain reaction amplification of polymorphic repetitive sequences.

A. Morley, D. Turner, S. Grist, 2000, Analytical biochemistry.

Functional characterization of human MutY homolog (hMYH) missense mutation (R231L) that is linked with hMYH-associated polyposis.

G. Suthers, A. Lu, Haibo Bai, 2007, Cancer letters.

Gene rearrangement in B- and T-lymphoproliferative disease detected by the polymerase chain reaction.

A. Morley, S. Neoh, J. Wan, 1991, Blood.

DNA polymorphism analysis in transfusion‐associated graft‐versus‐host disease

A. Morley, R. Seshadri, D. Roxby, 1999, Journal of paediatrics and child health.

Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach

Marc Tischkowitz, Nancy Hamel, Aditi Soni, 2008, European Journal of Human Genetics.

Evaluating DNA sequence variants of unknown biological significance.

G. Suthers, Graeme Suthers, Scott A Grist, 2008, Methods in molecular medicine.

Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis.

Andrej Sali, Rachel Karchin, Rebecca Sutphen, 2007, Cancer research.

Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling

P. Oefner, N. Waddell, S. Grimmond, 2006, Genes, chromosomes & cancer.

In vivo human somatic mutation: frequency and spectrum with age.

A. Morley, D. Turner, S. Grist, 1992, Mutation research.

by the polymerase chain reaction (see comments) Gene rearrangement in B- and T-lymphoproliferative disease detected

J. Wan, A. Morley, M. Brisco, 2013 .

Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing

Daniel J. Park, Katherine M. Tucker, R. Sebra, 2021, npj Breast Cancer.

Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing

Daniel J. Park, R. Sebra, G. Giles, 2021, NPJ breast cancer.

Molecular nature of in vivo mutations in human cells at the autosomal HLA-A locus.

A. Morley, D. Turner, S. Grist, 1990, Cancer research.

Identification of two novel transcobalamin two variants associated with developmental delay and megaloblastic anaemia in infancy.

S. Grist, Jonathan H Lim, R. Hall, 2022, Pathology.

Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16

G. Sutherland, V. Hyland, S. Grist, 1988, Human Genetics.

Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registry.

D. Mackey, I. Goldberg, A. Hewitt, 2013, Ophthalmology.

Leigh Syndrome Caused by the MT-ND5 m.13513G>A Mutation: A Case Presenting with WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia.

D. Thorburn, D. Bratkovic, M. Richardson, 2015, JIMD reports.

Dinucleotide repeat polymorphisms isolated by the polymerase chain reaction.

A. Morley, F. Firgaira, S. Grist, 1993, BioTechniques.

Mutations in human lymphocytes commonly involve gene duplication and resemble those seen in cancer cels.

A. Morley, D. Turner, S. Grist, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Genome-wide association study identifies novel breast cancer susceptibility loci

Lester L. Peters, A. Uitterlinden, D. Cox, 2007, Nature.

Mitochondrial mutations in acute leukaemia

A. Morley, S. Grist, X.-J. Lu, 2004, Leukemia.