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Author Details
Full Name
Richard A Sturm
Affiliation
Frazer Institute, The University of Queensland, Dermatology Research Centre
ORCID
Career Start Year
1985
Papers
186
H Index
54
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37766469
Assessing the genetic risk of nodular melanoma using a candidate gene approach.
Br J Dermatol
2024
37766469
Assessing the genetic risk of nodular melanoma using a candidate gene approach.
Br J Dermatol
2024
37635363
MITF E318K: A rare homozygous case with multiple primary melanoma.
Pigment Cell Melanoma Res
2024
37635363
MITF E318K: A rare homozygous case with multiple primary melanoma.
Pigment Cell Melanoma Res
2024
36879448
The MC1R r allele does not increase melanoma risk in MITF E318K carriers.
Br J Dermatol
2023
37639774
H3K4me3 remodeling induced acquired resistance through O-GlcNAc transferase.
Drug Resist Updat
2023
37013120
Skin cancer excisions and histopathology outcomes when following a contemporary population-based cohort longitudinally with 3D total-body photography.
Skin Health Dis
2023
36879448
The MC1R r allele does not increase melanoma risk in MITF E318K carriers.
Br J Dermatol
2023
37487699
<i>GOLM1</i>: expanding our understanding of melanoma susceptibility.
J Med Genet
2023
37487699
<i>GOLM1</i>: expanding our understanding of melanoma susceptibility.
J Med Genet
2023
37639774
H3K4me3 remodeling induced acquired resistance through O-GlcNAc transferase.
Drug Resist Updat
2023
37013120
Skin cancer excisions and histopathology outcomes when following a contemporary population-based cohort longitudinally with 3D total-body photography.
Skin Health Dis
2023
34958806
Reciprocal Regulation of BRN2 and NOTCH1/2 Signaling Synergistically Drives Melanoma Cell Migration and Invasion.
J Invest Dermatol
2022
35894802
Amelanotic/hypopigmented melanoma in a sibship with oculocutaneous albinism.
J Dermatol
2022
35626014
Genome-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
37632874
The Experience of 3D Total-Body Photography to Monitor Nevi: Results From an Australian General Population-Based Cohort Study.
JMIR Dermatol
2022
34958806
Reciprocal Regulation of BRN2 and NOTCH1/2 Signaling Synergistically Drives Melanoma Cell Migration and Invasion.
J Invest Dermatol
2022
35349165
The Eumelanin Human Skin Colour Scale: a proof-of-concept study.
Br J Dermatol
2022
35176174
Analysis of human leukocyte antigen associations in human papillomavirus-positive and -negative head and neck cancer: Comparison with cervical cancer.
Cancer
2022
34871578
Genome-Scale DNA Methylation Analysis Identifies Repeat Element Alterations that Modulate the Genomic Stability of Melanocytic Nevi.
J Invest Dermatol
2022
37632874
The Experience of 3D Total-Body Photography to Monitor Nevi: Results From an Australian General Population-Based Cohort Study.
JMIR Dermatol
2022
35349165
The Eumelanin Human Skin Colour Scale: a proof-of-concept study.
Br J Dermatol
2022
35626014
Genome-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
35894802
Amelanotic/hypopigmented melanoma in a sibship with oculocutaneous albinism.
J Dermatol
2022
35176174
Analysis of human leukocyte antigen associations in human papillomavirus-positive and -negative head and neck cancer: Comparison with cervical cancer.
Cancer
2022
34871578
Genome-Scale DNA Methylation Analysis Identifies Repeat Element Alterations that Modulate the Genomic Stability of Melanocytic Nevi.
J Invest Dermatol
2022
32800874
The Distinctive Genomic Landscape of Giant Congenital Melanocytic Nevi.
J Invest Dermatol
2021
33681261
On Naevi and Melanomas: Two Sides of the Same Coin?
Front Med (Lausanne)
2021
33945506
The deacylase SIRT5 supports melanoma viability by influencing chromatin dynamics.
J Clin Invest
2021
33884765
Genetic analysis of multiple primary melanomas arising within the boundaries of congenital nevi depigmentosa.
Pigment Cell Melanoma Res
2021
32800874
The Distinctive Genomic Landscape of Giant Congenital Melanocytic Nevi.
J Invest Dermatol
2021
33681261
On Naevi and Melanomas: Two Sides of the Same Coin?
Front Med (Lausanne)
2021
33884765
Genetic analysis of multiple primary melanomas arising within the boundaries of congenital nevi depigmentosa.
Pigment Cell Melanoma Res
2021
33945506
The deacylase SIRT5 supports melanoma viability by influencing chromatin dynamics.
J Clin Invest
2021
31421127
Genes Determining Nevus Count and Dermoscopic Appearance in Australian Melanoma Cases and Controls.
J Invest Dermatol
2020
31794051
The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls.
Br J Dermatol
2020
31733171
Multiple 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 Oncol
2020
32341527
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.
Nat Genet
2020
32386439
CDKN2A 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 Venereol
2020
32151667
Mutation Signatures in Melanocytic Nevi Reveal Characteristics of Defective DNA Repair.
J Invest Dermatol
2020
32638676
Gene Discovery Using Twins.
Twin Res Hum Genet
2020
32966289
Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants.
PLoS One
2020
31421127
Genes Determining Nevus Count and Dermoscopic Appearance in Australian Melanoma Cases and Controls.
J Invest Dermatol
2020
31794051
The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls.
Br J Dermatol
2020
31733171
Multiple 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 Oncol
2020
32638676
Gene Discovery Using Twins.
Twin Res Hum Genet
2020
32966289
Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants.
PLoS One
2020
32151667
Mutation Signatures in Melanocytic Nevi Reveal Characteristics of Defective DNA Repair.
J Invest Dermatol
2020
32386439
CDKN2A 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 Venereol
2020
32341527
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.
Nat Genet
2020
1 - 50 of 372
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row(s) 1 - 30 of 30
Collaborators
Nicholas G Martin
Co-authored papers
22
Aaron G Smith
Dermatology Research Centre, UQ Diamantina Institute, The University of Queensland
Co-authored papers
20
Grant W Montgomery
Co-authored papers
14
Nicholas K Hayward
QIMR Berghofer Medical Research Institute
Co-authored papers
12
Meenhard Herlyn
Ellen and Ronald Caplan Cancer Center, The Wistar Institute
Co-authored papers
7
Tim D Spector
King's College London
Co-authored papers
4
Lionel Larue
Institut Curie, PSL Research University, INSERM U1021
Co-authored papers
3
David A Mackey
Lions Eye Institute, University of Western Australia
Co-authored papers
3
Colin R Goding
Ludwig Institute for Cancer Research, University of Oxford
Co-authored papers
3
Sarah E Medland
Co-authored papers
3
Matthew A Brown
Co-authored papers
3
Leonie C Jacobs
Co-authored papers
2
Reuben S Q Kim
The University of Queensland
Co-authored papers
2
David E Fisher
Cutaneous Biology Research Center, Mass. General Hospital, Harvard Medical School
Co-authored papers
2
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers
2
Christian Praetorius
Center for Regenerative Therapies, Technical University Dresden
Co-authored papers
2
Scott D Gordon
Co-authored papers
2
Eir??kur Steingr??msson
BioMedical Center, University of Iceland
Co-authored papers
2
David J Hunter
The Kolling Institute, University of Sydney, and Royal North Shore Hospital
Co-authored papers
2
William J Pavan
National Human Genome Research Institute, National Institutes of Health
Co-authored papers
2
Alex W Hewitt
Menzies Institute for Medical Research, University of Tasmania
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National Cancer Institute, National Institutes of Health
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