His scientific interests lie mostly in Genetics, Genome-wide association study, Single-nucleotide polymorphism, Allele and Cancer. Genetics is closely attributed to Odds ratio in his research. His studies in Odds ratio integrate themes in fields like Lung cancer, Oncology and Case-control study.
As part of the same scientific family, Patrick Sulem usually focuses on Oncology, concentrating on Internal medicine and intersecting with Endocrinology. His work carried out in the field of Genome-wide association study brings together such families of science as Immunology, Frameshift mutation, Menarche, Locus and Genetic variation. His Single-nucleotide polymorphism research is multidisciplinary, incorporating elements of Chromosome and Genome.
Patrick Sulem mostly deals with Genetics, Genome-wide association study, Internal medicine, Allele and Single-nucleotide polymorphism. Patrick Sulem has researched Genome-wide association study in several fields, including Odds ratio, Missense mutation, Bioinformatics, Genetic association and Locus. He combines subjects such as Lung cancer and Case-control study with his study of Odds ratio.
His Internal medicine research is multidisciplinary, relying on both Endocrinology, Type 2 diabetes, Oncology and Cardiology. His biological study spans a wide range of topics, including Menarche, Immunology and Disease. His research brings together the fields of Polymorphism and Single-nucleotide polymorphism.
Patrick Sulem spends much of his time researching Genome-wide association study, Internal medicine, Genetics, Missense mutation and Gene. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Cancer, Case-control study, Atrial fibrillation and Bioinformatics. His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology, Oncology and Cardiology.
His work in the fields of Allele and Y chromosome overlaps with other areas such as Offspring. His studies deal with areas such as Phenotype and Confounding as well as Allele. His Missense mutation research incorporates themes from Loss function, Gastroenterology, Bile acid, Asthma and Genetic association.
His primary areas of investigation include Genetics, Genome-wide association study, Internal medicine, Gene and Severe acute respiratory syndrome coronavirus 2. His Genetics study incorporates themes from Disease and Genetic diversity. In his study, T cell and Pathogenesis is inextricably linked to Missense mutation, which falls within the broad field of Genome-wide association study.
Within one scientific family, Patrick Sulem focuses on topics pertaining to Endocrinology under Internal medicine, and may sometimes address concerns connected to Coronary artery disease. His work on Genetic marker and Candidate gene as part of his general Gene study is frequently connected to SGCG and PITX2, thereby bridging the divide between different branches of science. His research integrates issues of Lipoprotein lipase, Homeostasis, Genotype, Allele frequency and Meta-analysis in his study of Odds ratio.
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Erratum: Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer (Nature Genetics (2009) 41 (991-995))
Xifeng Wu;Yuanqing Ye;Lambertus A. Kiemeney;Patrick Sulem.
Nature Genetics (2009)
Rate of de novo mutations and the importance of father’s age to disease risk
Augustine Kong;Michael L. Frigge;Gisli Masson;Soren Besenbacher;Soren Besenbacher.
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.
Thorgeir E Thorgeirsson;Frank Geller;Patrick Sulem;Thorunn Rafnar.
A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
Thorlakur Jonsson;Jasvinder K. Atwal;Stacy Steinberg;Jon Snaedal.
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Gudmar Thorleifsson;G Bragi Walters;Daniel F Gudbjartsson;Valgerdur Steinthorsdottir.
Nature Genetics (2009)
Spread of SARS-CoV-2 in the Icelandic Population.
Daniel F Gudbjartsson;Agnar Helgason;Hakon Jonsson;Olafur T Magnusson.
The New England Journal of Medicine (2020)
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
Julius Gudmundsson;Patrick Sulem;Andrei Manolescu;Laufey T Amundadottir.
Nature Genetics (2007)
Variants conferring risk of atrial fibrillation on chromosome 4q25
Daniel F Gudbjartsson;David O Arnar;Anna Helgadottir;Solveig Gretarsdottir.
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
Bhairavi Swaminathan;Guðmar Thorleifsson;Magnus Jöud;Mina Ali.
Nature Communications (2015)
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.
Simon N Stacey;Andrei Manolescu;Patrick Sulem;Thorunn Rafnar.
Nature Genetics (2007)
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