What is he best known for?
The fields of study he is best known for:
- Cancer
- Internal medicine
- Gene
His primary areas of investigation include Breast cancer, Internal medicine, Cancer, Oncology and Genetics.
D. Gareth Evans combines subjects such as Cancer research, Genetic predisposition, Gynecology and Single-nucleotide polymorphism, Genotype with his study of Breast cancer.
His work is dedicated to discovering how Cancer, Genetic counseling are connected with Family history and other disciplines.
His Oncology study also includes fields such as
- Prospective cohort study, which have a strong connection to Obstetrics,
- Gene mutation which intersects with area such as Estrogen receptor.
D. Gareth Evans works mostly in the field of Risk factor, limiting it down to concerns involving Relative risk and, occasionally, Neurofibromatosis.
His Ovarian cancer research includes elements of Serous fluid and Cohort study.
His most cited work include:
- Genome-wide association study identifies novel breast cancer susceptibility loci (2045 citations)
- Association of Risk-Reducing Surgery in BRCA1 or BRCA2 Mutation Carriers With Cancer Risk and Mortality (965 citations)
- Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations (902 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Breast cancer, Internal medicine, Oncology, Cancer and Genetics.
His Breast cancer study integrates concerns from other disciplines, such as Prospective cohort study, Gynecology, Family history and Family medicine.
His biological study deals with issues like Germline mutation, which deal with fields such as Germline.
His work in Oncology addresses issues such as Cohort, which are connected to fields such as Cohort study.
His Cancer research includes themes of Cancer research and Risk factor.
Mutation, Allele, Single-nucleotide polymorphism, Genotype and Genome-wide association study are among the areas of Genetics where D. Gareth Evans concentrates his study.
He most often published in these fields:
- Breast cancer (56.96%)
- Internal medicine (43.77%)
- Oncology (35.36%)
What were the highlights of his more recent work (between 2019-2021)?
- Internal medicine (43.77%)
- Breast cancer (56.96%)
- Oncology (35.36%)
In recent papers he was focusing on the following fields of study:
D. Gareth Evans mainly focuses on Internal medicine, Breast cancer, Oncology, Cancer and Family medicine.
In his study, which falls under the umbrella issue of Internal medicine, Medical genetics, Li–Fraumeni syndrome, Bioinformatics and Germline mutation is strongly linked to Germline.
His studies deal with areas such as Proportional hazards model, Cohort study and Obstetrics as well as Breast cancer.
His studies examine the connections between Oncology and genetics, as well as such issues in PALB2, with regards to CHEK2.
His Cancer study frequently links to other fields, such as Gene.
D. Gareth Evans has researched Family medicine in several fields, including Underserved Population and Breast screening.
Between 2019 and 2021, his most popular works were:
- Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (96 citations)
- Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (96 citations)
- Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families (68 citations)
In his most recent research, the most cited papers focused on:
- Cancer
- Internal medicine
- Gene
D. Gareth Evans focuses on Internal medicine, Breast cancer, Oncology, Lynch syndrome and Family medicine.
D. Gareth Evans frequently studies issues relating to Germline and Internal medicine.
The various areas that D. Gareth Evans examines in his Breast cancer study include Odds ratio, Cohort study and Hazard ratio.
His Oncology research is multidisciplinary, incorporating perspectives in Single-nucleotide polymorphism, Genetic association, Cohort and PALB2.
His Lynch syndrome research focuses on Endometrial cancer and how it connects with MLH1, MSH2, Colorectal cancer, MSH6 and Genetic counseling.
His research integrates issues of Young adult, Phenotype, Malignancy and Genomics in his study of Cancer.
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