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Author Details
Full Name
Juergen K V Reichardt
Affiliation
Australian Institute of Tropical Health and Medicine, James Cook University
ORCID
Career Start Year
1982
Papers
133
H Index
35
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37488607
COVID-19 annual update: a narrative review.
Hum Genomics
2023
36171619
J'Accuse⿦.. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing.
Hum Genomics
2022
35650595
COVID-19 2022 update: transition of the pandemic to the endemic phase.
Hum Genomics
2022
33252176
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals.
Hum Mutat
2021
33612096
Standardized nomenclature and open science in Human Genomics.
Hum Genomics
2021
34429158
Update on human genetic susceptibility to COVID-19: susceptibility to virus and response.
Hum Genomics
2021
34537084
Correction to: Update on human genetic susceptibility to COVID-19: susceptibility to virus and response.
Hum Genomics
2021
33966626
COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policy.
Hum Genomics
2021
31371789
Meeting report: The Human Genome Meeting (HGM) 2019 in Seoul, Korea.
Eur J Hum Genet
2020
31873296
A call for global action for rare diseases in Africa.
Nat Genet
2020
33357238
COVID-19 update: the first 6 months of the pandemic.
Hum Genomics
2020
33381478
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations.
Front Pediatr
2020
32641116
Human genetics and genomics meetings going virtual: practical lessons learned from two international meetings in early 2020.
Hum Genomics
2020
32522249
Genomics of COVID-19: molecular mechanisms going from susceptibility to severity of the disease.
Hum Genomics
2020
32398162
COVID-19 vulnerability: the potential impact of genetic susceptibility and airborne transmission.
Hum Genomics
2020
30961828
The Gut-Brain Axis, Paving the Way to Brain Cancer.
Trends Cancer
2019
31822297
Human genetics and genomics research in Ecuador: historical survey, current state, and future directions.
Hum Genomics
2019
31370887
Meeting report: the Human Genome Meeting (HGM) 2019 in Seoul, Korea.
Hum Genomics
2019
29228205
Associations between polymorphisms in genes related to estrogen metabolism and function and prostate cancer risk: results from the Prostate Cancer Prevention Trial.
Carcinogenesis
2018
29636189
Reflections of a Biomedical Scientist on Four Continents in Interdisciplinary Research.
Trends Genet
2018
26768750
Identification of genomic aberrations in hemangioblastoma by droplet digital PCR and SNP microarray highlights novel candidate genes and pathways for pathogenesis.
BMC Genomics
2016
26589415
Serum androgens and prostate cancer risk: results from the placebo arm of the Prostate Cancer Prevention Trial.
Cancer Causes Control
2016
27556862
Zinc enhances temozolomide cytotoxicity in glioblastoma multiforme model systems.
Oncotarget
2016
27164191
Association of androgen metabolism gene polymorphisms with prostate cancer risk and androgen concentrations: Results from the Prostate Cancer Prevention Trial.
Cancer
2016
25421747
Single nucleotide differences (SNDs) continue to contaminate the dbSNP database with consequences for human genomics and health.
Hum Mutat
2015
26537019
Genomics is changing personal healthcare and medicine: the dawn of iPH (individualized preventive healthcare).
Hum Genomics
2015
26075443
Schwannomas exhibit distinct size-dependent gene-expression patterns.
Future Oncol
2015
25955319
Finasteride concentrations and prostate cancer risk: results from the Prostate Cancer Prevention Trial.
PLoS One
2015
25733274
Effect of finasteride on serum androstenedione and risk of prostate cancer within the prostate cancer prevention trial: differential effect on high- and low-grade disease.
Urology
2015
24824408
Androgen receptor CAG repeat length and TMPRSS2:ETS prostate cancer risk: results From the Prostate Cancer Prevention Trial.
Urology
2014
24980480
Novel age-dependent targets in vestibular schwannomas.
Hum Genomics
2014
23039322
Type and location of isocitrate dehydrogenase mutations influence clinical characteristics and disease outcome of acute myeloid leukemia.
Leuk Lymphoma
2013
23532445
In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria.
J Inherit Metab Dis
2013
22879203
Associations of serum sex steroid hormone and 5α-androstane-3α,17β-diol glucuronide concentrations with prostate cancer risk among men treated with finasteride.
Cancer Epidemiol Biomarkers Prev
2012
22973298
Translesion DNA polymerases and cancer.
Front Genet
2012
22716497
Current progress in using vitamin D and its analogs for cancer prevention and treatment.
Expert Rev Anticancer Ther
2012
21667068
Serum estrogen levels and prostate cancer risk in the prostate cancer prevention trial: a nested case-control study.
Cancer Causes Control
2011
21771722
Repeat polymorphisms in estrogen metabolism genes and prostate cancer risk: results from the Prostate Cancer Prevention Trial.
Carcinogenesis
2011
21974670
Information symmetries in irreversible processes.
Chaos
2011
19639008
The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutations.
Heredity (Edinb)
2010
21149329
Transition of a clinical trial into translational research: the prostate cancer prevention trial experience.
Cancer Prev Res (Phila)
2010
21142863
Finasteride metabolism and pharmacogenetics: new approaches to personalized prevention of prostate cancer.
Future Oncol
2010
21217827
Modeling single nucleotide polymorphisms in the human AKR1C1 and AKR1C2 genes: implications for functional and genotyping analyses.
PLoS One
2010
20952028
Androgen receptor CAG repeat length and association with prostate cancer risk: results from the prostate cancer prevention trial.
J Urol
2010
20519274
Differential expression of steroid 5alpha-reductase isozymes and association with disease severity and angiogenic genes predict their biological role in prostate cancer.
Endocr Relat Cancer
2010
19877174
Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies.
Hum Mutat
2010
18623241
Genomic analysis of cancer tissue reveals that somatic mutations commonly occur in a specific motif.
Hum Mutat
2009
19797393
PCR-free method detects high frequency of genomic instability in prostate cancer.
Nucleic Acids Res
2009
19416875
The future of the human SNP identification: which individuals to sequence?
Proc Natl Acad Sci U S A
2009
19255933
A family-based study does not support the association of a functional polymorphism in the gene for endothelial nitric oxide synthase with risk for rheumatoid arthritis.
Scand J Rheumatol
2009
1 - 50 of 133
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