Her work often combines Genetics and Evolutionary biology studies. She combines Evolutionary biology and Genetics in her research. Many of her studies on Gene apply to SNP as well. Heather M. Stringham carries out multidisciplinary research, doing studies in Genome-wide association study and Genome. Heather M. Stringham applies her multidisciplinary studies on Genome and Genome-wide association study in her research. Heather M. Stringham performs integrative study on Genotype and Genotyping. In her work, she performs multidisciplinary research in Single-nucleotide polymorphism and Bioinformatics. While working on this project, she studies both Bioinformatics and Single-nucleotide polymorphism. Her study ties her expertise on Body mass index together with the subject of Endocrinology.
Heather M. Stringham connects Genetics with Quantitative trait locus in her research. She performs multidisciplinary study in the fields of Gene and Locus (genetics) via her papers. Heather M. Stringham performs multidisciplinary study on Locus (genetics) and Genotype in her works. Her work on Genotype is being expanded to include thematically relevant topics such as SNP. She integrates several fields in her works, including Endocrinology and Internal medicine. She brings together Internal medicine and Endocrinology to produce work in her papers. Her research on Single-nucleotide polymorphism often connects related areas such as SNP. She merges many fields, such as Genome-wide association study and Genetic architecture, in her writings. She merges Genetic architecture with Genome-wide association study in her study.
As part of her studies on Genetics, Heather M. Stringham often connects relevant areas like Nonsynonymous substitution. Heather M. Stringham regularly ties together related areas like Genome in her Nonsynonymous substitution studies. Heather M. Stringham performs multidisciplinary study in Genome and Copy-number variation in her work. She performs multidisciplinary studies into Copy-number variation and Single-nucleotide polymorphism in her work. Many of her studies involve connections with topics such as Missing heritability problem and Single-nucleotide polymorphism. Heather M. Stringham conducted interdisciplinary study in her works that combined Missing heritability problem and Heritability. While working on this project, Heather M. Stringham studies both Heritability and Genetic architecture. In her research, she performs multidisciplinary study on Genetic architecture and Genome-wide association study. Genome-wide association study and 1000 Genomes Project are two areas of study in which Heather M. Stringham engages in interdisciplinary work.
Heather M. Stringham undertakes interdisciplinary study in the fields of Gene and Nonsynonymous substitution through her research. Her Nonsynonymous substitution study frequently links to related topics such as Genome. Heather M. Stringham undertakes interdisciplinary study in the fields of Genome and Genetic variation through her research. Heather M. Stringham integrates Genetic variation with Genetics in her research. In her articles, Heather M. Stringham combines various disciplines, including Genetics and Computational biology. She integrates many fields in her works, including Computational biology and Gene. In her papers, she integrates diverse fields, such as Locus (genetics) and Genotype. Heather M. Stringham integrates many fields, such as Genotype and Locus (genetics), in her works. She performs integrative Single-nucleotide polymorphism and Expression quantitative trait loci research in her work.
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Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
Siddhartha Jaiswal;Pierre Fontanillas;Jason Flannick;Jason Flannick;Alisa Manning.
The New England Journal of Medicine (2014)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Laura J. Scott;Karen L. Mohlke;Lori L. Bonnycastle;Cristen J. Willer.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena.
Nature Genetics (2010)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
E Zeggini;L J Scott;R Saxena;B F Voight.
Nature Genetics (2008)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight;Benjamin F. Voight;Laura J. Scott;Valgerdur Steinthorsdottir;Andrew P. Morris.
Nature Genetics (2010)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud.
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira.
Nature Genetics (2012)
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