John L. Hopper
Researcher Next ID · RN-025657
Researcher · Biochemistry, Genetics and Molecular Biology
Melbourne, Australia
- Works count
- 1,936
- Citation count
- 81,372
- H-index
- 137
- i10-index
- 919
Research interests
Publications
Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
Nature Communications · 2020 · 10.1038/s41467-020-17117-4
Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
Nature Communications · 2020 · 10.1038/s41467-020-17117-4
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Genetics in Medicine · 2019 · https://doi.org/10.1038/s41436-019-0596-9
Cancer Risks Associated With GermlinePALB2Pathogenic Variants: An International Study of 524 Families
Journal of Clinical Oncology · 2019 · 10.1200/jco.19.01907
Childhood predictors of lung function trajectories and future COPD risk: a prospective cohort study from the first to the sixth decade of life
The Lancet Respiratory Medicine · 2018 · 10.1016/s2213-2600(18)30100-0
Discovery of common and rare genetic risk variants for colorectal cancer
Nature Genetics · 2018 · https://doi.org/10.1038/s41588-018-0286-6
Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
JAMA · 2017 · https://doi.org/10.1001/jama.2017.7112
Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
Cancer Epidemiology Biomarkers & Prevention · 2016 · 10.1158/1055-9965.epi-16-0693
Identification of Lynch Syndrome Among Patients With Colorectal Cancer
JAMA · 2012 · 10.1001/jama.2012.13088
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Nature · 2011 · 10.1038/nature10630
Genome-wide association study identifies three loci associated with melanoma risk
Nature Genetics · 2009 · 10.1038/ng.411
The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations
Gastroenterology · 2008 · 10.1053/j.gastro.2008.04.026
Multiple newly identified loci associated with prostate cancer susceptibility
Nature Genetics · 2008 · https://doi.org/10.1038/ng.90
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
Nature Genetics · 2008 · 10.1038/ng.111
Iron-Overload–Related Disease inHFEHereditary Hemochromatosis
New England Journal of Medicine · 2008 · https://doi.org/10.1056/nejmoa073286
The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
British Journal of Cancer · 2008 · https://doi.org/10.1038/sj.bjc.6604305
Mammographic breast density as an intermediate phenotype for breast cancer
The Lancet Oncology · 2005 · 10.1016/s1470-2045(05)70390-9
Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency
JAMA · 2005 · 10.1001/jama.293.16.1979
Heritability of Mammographic Density, a Risk Factor for Breast Cancer
New England Journal of Medicine · 2002 · 10.1056/nejmoa013390
Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors
Journal of Clinical Oncology · 2002 · 10.1200/jco.2002.20.4.1043
Preoperative MRI predicts outcome of temporal lobectomy
Neurology · 1995 · 10.1212/wnl.45.7.1358
Genetics of Asthma and Hay Fever in Australian Twins
American Review of Respiratory Disease · 1990 · 10.1164/ajrccm/142.6_pt_1.1351
Reduced Bone Mass in Daughters of Women with Osteoporosis
New England Journal of Medicine · 1989 · 10.1056/nejm198903023200903
Genetic determinants of bone mass in adults. A twin study.
Journal of Clinical Investigation · 1987 · https://doi.org/10.1172/jci113125
Extensions to multivariate normal models for pedigree analysis
Annals of Human Genetics · 1982 · 10.1111/j.1469-1809.1982.tb01588.x
Current projects
No projects listed.