What is she best known for?
The fields of study she is best known for:
Her primary areas of study are Genetics, Cancer, Breast cancer, Internal medicine and Colorectal cancer.
Genetics is a component of her Genome-wide association study, Germline mutation, Locus, Allele and DNA mismatch repair studies.
Annika Lindblom interconnects Odds ratio, Genetic variation, Genetic predisposition and Genetic association in the investigation of issues within Genome-wide association study.
The various areas that she examines in her Breast cancer study include TOX3, Single-nucleotide polymorphism and Cancer research.
Her research on Internal medicine often connects related areas such as Oncology.
Her work deals with themes such as Carcinogenesis, Gene, Adenoma and Gastroenterology, which intersect with Colorectal cancer.
Her most cited work include:
- Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families (2565 citations)
- Revised Bethesda Guidelines for Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) and Microsatellite Instability (2320 citations)
- Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer (1835 citations)
What are the main themes of her work throughout her whole career to date?
Her primary scientific interests are in Internal medicine, Breast cancer, Oncology, Genetics and Cancer.
Her study focuses on the intersection of Breast cancer and fields such as Single-nucleotide polymorphism with connections in the field of Haplotype.
She has researched Oncology in several fields, including Bioinformatics, Confidence interval, Disease, Endometrial cancer and Risk factor.
Her studies in Genome-wide association study, Locus, Gene, Allele and Germline mutation are all subfields of Genetics research.
Her Genome-wide association study research is multidisciplinary, incorporating perspectives in Candidate gene, Genetic association and Genetic predisposition.
Her research integrates issues of Mutation, Gynecology, Genetic counseling and Pathology in her study of Cancer.
She most often published in these fields:
- Internal medicine (52.70%)
- Breast cancer (42.97%)
- Oncology (43.51%)
What were the highlights of her more recent work (between 2017-2021)?
- Internal medicine (52.70%)
- Oncology (43.51%)
- Colorectal cancer (39.73%)
In recent papers she was focusing on the following fields of study:
Annika Lindblom mainly focuses on Internal medicine, Oncology, Colorectal cancer, Cancer and Breast cancer.
Her study in Oncology is interdisciplinary in nature, drawing from both Prostate cancer, Ovarian cancer, Primary tumor, Endometrial cancer and Family history.
Colorectal cancer is a subfield of Genetics that Annika Lindblom explores.
Her Cancer study integrates concerns from other disciplines, such as Lower risk and Gene.
Her Breast cancer research integrates issues from Medical genetics, Germline mutation, Proportional hazards model and Cancer research.
Her work in Lynch syndrome covers topics such as MSH6 which are related to areas like MLH1 and MSH2.
Between 2017 and 2021, her most popular works were:
- Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (257 citations)
- Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database (196 citations)
- Discovery of common and rare genetic risk variants for colorectal cancer (131 citations)
In her most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Internal medicine, Oncology, Colorectal cancer, Cancer and Genome-wide association study.
Her work on Odds ratio, Cancer prevention, Aspirin and Family history as part of general Internal medicine research is frequently linked to Risk assessment, thereby connecting diverse disciplines of science.
Her biological study spans a wide range of topics, including Confidence interval, Ovarian cancer, Breast cancer, Endometrial cancer and Cohort.
Her Breast cancer study combines topics from a wide range of disciplines, such as Germline mutation and Prostate cancer.
Particularly relevant to Lynch syndrome is her body of work in Cancer.
Her Genome-wide association study study combines topics in areas such as Medical genetics, Disease and Hazard ratio.
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