Her main research concerns Genetics, Locus, Genotype, Genetic linkage and Immunology. Her research in Genetic association, Single-nucleotide polymorphism, Gene, Candidate gene and Pedigree chart are components of Genetics. In the subject of general Gene, her work in Gene product, Frameshift mutation, Gene family and Positional cloning is often linked to ELAC2, thereby combining diverse domains of study.
Her work deals with themes such as Genome-wide association study, Genetic predisposition, Family history, Linkage disequilibrium and Chronic lymphocytic leukemia, which intersect with Locus. Her Genotype research is multidisciplinary, incorporating perspectives in Internal medicine and Allele. Her Genetic linkage research is multidisciplinary, incorporating elements of Prostate, Genome, Disease, Genetic determinism and Linkage.
Genetics, Internal medicine, Single-nucleotide polymorphism, Pedigree chart and Gene are her primary areas of study. Genetic linkage, Locus, Linkage, Haplotype and Genetic association are the core of her Genetics study. Nicola J. Camp combines subjects such as Disease, Genetic predisposition and Gene mapping with her study of Locus.
Her Internal medicine study which covers Oncology that intersects with Breast cancer. Her Pedigree chart study integrates concerns from other disciplines, such as Chromosome and Genomic Segment. Her Gene study frequently draws connections to adjacent fields such as Computational biology.
Nicola J. Camp focuses on Internal medicine, Oncology, Gene, Genetics and Breast cancer. Many of her studies on Internal medicine involve topics that are commonly interrelated, such as Genome-wide association study. In her work, Transcriptome and In silico is strongly intertwined with Computational biology, which is a subfield of Gene.
Genetic association, Leukemia, Genomic Segment and Germline mutation are among the areas of Genetics where the researcher is concentrating her efforts. Her research integrates issues of Gene expression, Proportional hazards model, Disease and Locus in her study of Breast cancer. Her study brings together the fields of Haplotype and Locus.
Nicola J. Camp spends much of her time researching Internal medicine, Genome-wide association study, Odds ratio, Chronic lymphocytic leukemia and Gene. In her study, which falls under the umbrella issue of Internal medicine, Breast cancer and Genetic testing is strongly linked to Oncology. Her Genome-wide association study study contributes to a more complete understanding of Genetics.
The concepts of her Chronic lymphocytic leukemia study are interwoven with issues in Follicular lymphoma, Lymphoma and Genotype. Her research investigates the connection between Allele and topics such as Genetic architecture that intersect with issues in Single-nucleotide polymorphism. Her research in B cell intersects with topics in SNP and Locus.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
A Variant of the HTRA1 Gene Increases Susceptibility to Age-Related Macular Degeneration
Zhenglin Yang;Nicola J. Camp;Hui Sun;Zongzhong Tong.
A candidate prostate cancer susceptibility gene at chromosome 17p.
Sean V. Tavtigian;Jacques Simard;David H F Teng;Vicki Abtin.
Nature Genetics (2001)
Quantitative Trait Loci
Nicola J. Camp;Angela Cox.
Interleukin-1 Receptor Antagonist Gene Polymorphism and Coronary Artery Disease
Sheila E. Francis;Nicola J. Camp;Rachael M. Dewberry;Julian Gunn.
Predisposition locus for major depression at chromosome 12q22-12q23.2.
Victor Abkevich;Nicola J. Camp;Charles H. Hensel;Chris D. Neff.
American Journal of Human Genetics (2003)
An analysis of linkage disequilibrium in the interleukin-1 gene cluster, using a novel grouping method for multiallelic markers.
Angela Cox;Nicola J. Camp;Martin J.H. Nicklin;Francesco S. di Giovine.
American Journal of Human Genetics (1998)
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Sonja I. Berndt;Christine F. Skibola;Christine F. Skibola;Vijai Joseph;Nicola J. Camp.
Nature Genetics (2013)
Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees
Hilary Coon;Michele E Villalobos;Reid J Robison;Nicola J Camp.
Molecular Autism (2010)
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)
Jianfeng Xu;Ethan M. Lange;Ethan M. Lange;Lingyi Lu;Siqun L. Zheng.
Human Genetics (2013)
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32
Lucia Conde;Eran Halperin;Nicholas K. Akers;Kevin M. Brown.
Nature Genetics (2010)
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