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Author Details

Richard A Sturm
Frazer Institute, The University of Queensland, Dermatology Research Centre
1985
186
54
PMIDPaper TitleJournal TitlePublished Year
37766469Assessing the genetic risk of nodular melanoma using a candidate gene approach.Br J Dermatol2024
37766469Assessing the genetic risk of nodular melanoma using a candidate gene approach.Br J Dermatol2024
37635363MITF E318K: A rare homozygous case with multiple primary melanoma.Pigment Cell Melanoma Res2024
37635363MITF E318K: A rare homozygous case with multiple primary melanoma.Pigment Cell Melanoma Res2024
36879448The MC1R r allele does not increase melanoma risk in MITF E318K carriers.Br J Dermatol2023
37639774H3K4me3 remodeling induced acquired resistance through O-GlcNAc transferase.Drug Resist Updat2023
37013120Skin cancer excisions and histopathology outcomes when following a contemporary population-based cohort longitudinally with 3D total-body photography.Skin Health Dis2023
36879448The MC1R r allele does not increase melanoma risk in MITF E318K carriers.Br J Dermatol2023
37487699<i>GOLM1</i>: expanding our understanding of melanoma susceptibility.J Med Genet2023
37487699<i>GOLM1</i>: expanding our understanding of melanoma susceptibility.J Med Genet2023
37639774H3K4me3 remodeling induced acquired resistance through O-GlcNAc transferase.Drug Resist Updat2023
37013120Skin cancer excisions and histopathology outcomes when following a contemporary population-based cohort longitudinally with 3D total-body photography.Skin Health Dis2023
34958806Reciprocal Regulation of BRN2 and NOTCH1/2 Signaling Synergistically Drives Melanoma Cell Migration and Invasion.J Invest Dermatol2022
35894802Amelanotic/hypopigmented melanoma in a sibship with oculocutaneous albinism.J Dermatol2022
35626014Genome-Wide Association Study Suggests the Variant rs7551288*A within the <i>DHCR24</i> Gene Is Associated with Poor Overall Survival in Melanoma Patients.Cancers (Basel)2022
37632874The Experience of 3D Total-Body Photography to Monitor Nevi: Results From an Australian General Population-Based Cohort Study.JMIR Dermatol2022
34958806Reciprocal Regulation of BRN2 and NOTCH1/2 Signaling Synergistically Drives Melanoma Cell Migration and Invasion.J Invest Dermatol2022
35349165The Eumelanin Human Skin Colour Scale: a proof-of-concept study.Br J Dermatol2022
35176174Analysis of human leukocyte antigen associations in human papillomavirus-positive and -negative head and neck cancer: Comparison with cervical cancer.Cancer2022
34871578Genome-Scale DNA Methylation Analysis Identifies Repeat Element Alterations that Modulate the Genomic Stability of Melanocytic Nevi.J Invest Dermatol2022
37632874The Experience of 3D Total-Body Photography to Monitor Nevi: Results From an Australian General Population-Based Cohort Study.JMIR Dermatol2022
35349165The Eumelanin Human Skin Colour Scale: a proof-of-concept study.Br J Dermatol2022
35626014Genome-Wide Association Study Suggests the Variant rs7551288*A within the <i>DHCR24</i> Gene Is Associated with Poor Overall Survival in Melanoma Patients.Cancers (Basel)2022
35894802Amelanotic/hypopigmented melanoma in a sibship with oculocutaneous albinism.J Dermatol2022
35176174Analysis of human leukocyte antigen associations in human papillomavirus-positive and -negative head and neck cancer: Comparison with cervical cancer.Cancer2022
34871578Genome-Scale DNA Methylation Analysis Identifies Repeat Element Alterations that Modulate the Genomic Stability of Melanocytic Nevi.J Invest Dermatol2022
32800874The Distinctive Genomic Landscape of Giant Congenital Melanocytic Nevi.J Invest Dermatol2021
33681261On Naevi and Melanomas: Two Sides of the Same Coin?Front Med (Lausanne)2021
33945506The deacylase SIRT5 supports melanoma viability by influencing chromatin dynamics.J Clin Invest2021
33884765Genetic analysis of multiple primary melanomas arising within the boundaries of congenital nevi depigmentosa.Pigment Cell Melanoma Res2021
32800874The Distinctive Genomic Landscape of Giant Congenital Melanocytic Nevi.J Invest Dermatol2021
33681261On Naevi and Melanomas: Two Sides of the Same Coin?Front Med (Lausanne)2021
33884765Genetic analysis of multiple primary melanomas arising within the boundaries of congenital nevi depigmentosa.Pigment Cell Melanoma Res2021
33945506The deacylase SIRT5 supports melanoma viability by influencing chromatin dynamics.J Clin Invest2021
31421127Genes Determining Nevus Count and Dermoscopic Appearance in Australian Melanoma Cases and Controls.J Invest Dermatol2020
31794051The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls.Br J Dermatol2020
31733171Multiple interaction nodes define the postreplication repair response to UV-induced DNA damage that is defective in melanomas and correlated with UV signature mutation load.Mol Oncol2020
32341527Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.Nat Genet2020
32386439CDKN2A testing threshold in a high-risk Australian melanoma cohort: number of primaries, family history and young age of onset impact risk.J Eur Acad Dermatol Venereol2020
32151667Mutation Signatures in Melanocytic Nevi Reveal Characteristics of Defective DNA Repair.J Invest Dermatol2020
32638676Gene Discovery Using Twins.Twin Res Hum Genet2020
32966289Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants.PLoS One2020
31421127Genes Determining Nevus Count and Dermoscopic Appearance in Australian Melanoma Cases and Controls.J Invest Dermatol2020
31794051The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls.Br J Dermatol2020
31733171Multiple interaction nodes define the postreplication repair response to UV-induced DNA damage that is defective in melanomas and correlated with UV signature mutation load.Mol Oncol2020
32638676Gene Discovery Using Twins.Twin Res Hum Genet2020
32966289Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants.PLoS One2020
32151667Mutation Signatures in Melanocytic Nevi Reveal Characteristics of Defective DNA Repair.J Invest Dermatol2020
32386439CDKN2A testing threshold in a high-risk Australian melanoma cohort: number of primaries, family history and young age of onset impact risk.J Eur Acad Dermatol Venereol2020
32341527Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.Nat Genet2020
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Collaborators

Co-authored papers 22
Dermatology Research Centre, UQ Diamantina Institute, The University of Queensland
Co-authored papers 20
Co-authored papers 14
QIMR Berghofer Medical Research Institute
Co-authored papers 12
Ellen and Ronald Caplan Cancer Center, The Wistar Institute
Co-authored papers 7
King's College London
Co-authored papers 4
Institut Curie, PSL Research University, INSERM U1021
Co-authored papers 3
Lions Eye Institute, University of Western Australia
Co-authored papers 3
Ludwig Institute for Cancer Research, University of Oxford
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3
Co-authored papers 2
The University of Queensland
Co-authored papers 2
Cutaneous Biology Research Center, Mass. General Hospital, Harvard Medical School
Co-authored papers 2
Erasmus University Medical Center
Co-authored papers 2
Center for Regenerative Therapies, Technical University Dresden
Co-authored papers 2
Co-authored papers 2
BioMedical Center, University of Iceland
Co-authored papers 2
The Kolling Institute, University of Sydney, and Royal North Shore Hospital
Co-authored papers 2
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
Menzies Institute for Medical Research, University of Tasmania
Co-authored papers 2
National Cancer Institute, National Institutes of Health
Co-authored papers 2
Co-authored papers 2
Medical Research Council Integrative Epidemiology Unit at the University of Bristol
Co-authored papers 2
Co-authored papers 2
Yale School of Medicine
Co-authored papers 2
Co-authored papers 2
Center for Molecular Medicine, University of Georgia
Co-authored papers 1
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 1
National Centre for Biotechnology (CNB-CSIC)
Co-authored papers 1