His primary scientific interests are in Genome-wide association study, Genetics, Single-nucleotide polymorphism, Prostate cancer and Breast cancer. Fredrick R. Schumacher combines subjects such as Cancer, Internal medicine, Case-control study and Genetic association with his study of Genome-wide association study. His study in Genetics is interdisciplinary in nature, drawing from both Odds ratio and Population genetics.
His Single-nucleotide polymorphism study frequently involves adjacent topics like Bioinformatics. His Prostate cancer research is multidisciplinary, relying on both Allele and Oncology. His work in the fields of Estrogen receptor overlaps with other areas such as Risk assessment.
Fredrick R. Schumacher focuses on Genome-wide association study, Internal medicine, Single-nucleotide polymorphism, Oncology and Prostate cancer. The study of Genetics and Genotype are components of his Genome-wide association study research. His work deals with themes such as Genotyping and Bioinformatics, which intersect with Single-nucleotide polymorphism.
The study incorporates disciplines such as Prospective cohort study, Gynecology, Family history and Cohort in addition to Oncology. His Prostate cancer research is classified as research in Cancer. His Breast cancer research includes themes of Genetic predisposition and Pathology.
His primary areas of study are Internal medicine, Oncology, Genome-wide association study, Prostate cancer and Colorectal cancer. In general Internal medicine study, his work on Hazard ratio and PROSTATE CANCER SUSCEPTIBILITY often relates to the realm of Published Erratum and Impact study, thereby connecting several areas of interest. His biological study spans a wide range of topics, including Cancer, Breast cancer, Allele and Germline.
His Breast cancer research is multidisciplinary, incorporating elements of Odds ratio and Epidemiology. His Genome-wide association study research incorporates elements of Case-control study and Genetic association. His Prostate cancer research includes elements of Prostate and Computational biology.
Fredrick R. Schumacher mainly focuses on Genome-wide association study, Internal medicine, Oncology, Case-control study and Prostate cancer. His studies deal with areas such as Expression quantitative trait loci and Genetic association as well as Genome-wide association study. His work in Breast cancer, Cancer and Odds ratio are all subfields of Internal medicine research.
In his research, Family history and Cohort is intimately related to Cohort study, which falls under the overarching field of Case-control study. As a member of one scientific family, Fredrick R. Schumacher mostly works in the field of Genetics, focusing on Meta-analysis and, on occasion, Haplotype, Genetic architecture, SNP and Imputation. His studies in Single-nucleotide polymorphism integrate themes in fields like Proportional hazards model, Epidemiology of cancer, Estrogen receptor and Hazard ratio.
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Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
Meredith Yeager;Nick Orr;Richard B Hayes;Kevin B Jacobs.
Nature Genetics (2007)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)
Multiple loci identified in a genome-wide association study of prostate cancer
Gilles Thomas;Kevin B Jacobs;Meredith Yeager;Meredith Yeager;Peter Kraft.
Nature Genetics (2008)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Nature (2017)
Identification of ten loci associated with height highlights new biological pathways in human growth.
Guillaume Lettre;Guillaume Lettre;Anne U Jackson;Christian Gieger;Fredrick R Schumacher;Fredrick R Schumacher.
Nature Genetics (2008)
MicroRNA related polymorphisms and breast cancer risk
Sofia Khan;Dario Greco;Dario Greco;Kyriaki Michailidou;Roger L. Milne;Roger L. Milne.
PLOS ONE (2014)
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Stig E. Bojesen;Stig E. Bojesen;Karen A. Pooley;Sharon E. Johnatty;Jonathan Beesley.
Nature Genetics (2013)
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Rosalind A. Eeles;Ali Amin Al Olama;Sara Benlloch;Edward J. Saunders.
Nature Genetics (2013)
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