His primary scientific interests are in Genetics, Genome-wide association study, Gene, Genetic association and Genotype. His IRF6, Allele, Single-nucleotide polymorphism, Missense mutation and Genetic linkage study are his primary interests in Genetics. His studies examine the connections between Missense mutation and genetics, as well as such issues in Candidate gene, with regards to International HapMap Project.
His studies deal with areas such as Bioinformatics, Genomics, Quantitative trait locus, Human genetics and Craniofacial as well as Genome-wide association study. His Gene research includes elements of Molecular biology, Dopamine, Physiology and Attention deficit hyperactivity disorder. His Genetic association study combines topics in areas such as Data science, Life course approach, Mendelian inheritance and Confidence interval.
Mary L. Marazita mainly investigates Genetics, Genome-wide association study, Single-nucleotide polymorphism, Locus and Gene. His study involves Candidate gene, Genetic association, Genotype, Genetic linkage and Allele, a branch of Genetics. His Genome-wide association study study combines topics from a wide range of disciplines, such as Phenotype, IRF6, Craniofacial and Bioinformatics.
His research integrates issues of Internal medicine, Genotyping, Genetic variation and Haplotype in his study of Single-nucleotide polymorphism. His study in Locus is interdisciplinary in nature, drawing from both Genetic heterogeneity and Genetic architecture. Particularly relevant to Genome is his body of work in Gene.
Mary L. Marazita spends much of his time researching Genome-wide association study, Genetics, Genetic architecture, Craniofacial and Locus. His Genome-wide association study study is concerned with Single-nucleotide polymorphism in general. His Single-nucleotide polymorphism research is multidisciplinary, incorporating perspectives in Young adult and Genetic variants.
His study in Gene, Genome, Whole genome sequencing, Heritability and SNP is done as part of Genetics. Mary L. Marazita works mostly in the field of Locus, limiting it down to topics relating to Genotype and, in certain cases, Gestational age, Bioinformatics, Gestation, Fetus and Quantitative trait locus. His study looks at the intersection of Allele and topics like Family history with IRF6 and Non syndromic.
Mary L. Marazita mainly focuses on Genome-wide association study, Genetics, Genetic architecture, Craniofacial and Locus. Mary L. Marazita has included themes like SNP, Mendelian Randomization Analysis, Confidence interval and Genomics in his Genome-wide association study study. In Genomics, he works on issues like Neural crest, which are connected to Genetic association.
His study in Whole genome sequencing, Genome, Quantitative trait locus and Heritability is carried out as part of his Genetics studies. The concepts of his Genetic architecture study are interwoven with issues in Cranial neural crest, Evolutionary biology and Candidate gene. His study focuses on the intersection of Locus and fields such as Genotype with connections in the field of Allele, Fetus and Gestation.
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Cleft lip and palate: understanding genetic and environmental influences.
Michael J. Dixon;Mary L. Marazita;Terri H. Beaty;Jeffrey C. Murray.
Nature Reviews Genetics (2011)
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
Theresa M. Zucchero;Margaret E. Cooper;Brion S. Maher;Sandra Daack-Hirsch.
The New England Journal of Medicine (2004)
Genetic epidemiological studies of early-onset deafness in the U.S. school-age population
Mary L. Marazita;Lynn M. Ploughman;Brenda Rawlings;Elizabeth Remington.
American Journal of Medical Genetics (1993)
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
Terri H. Beaty;Jeffrey C. Murray;Mary L. Marazita;Ronald G. Munger.
Nature Genetics (2010)
Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b
Debra E. Weese-Mayer;Elizabeth M. Berry-Kravis;Lili Zhou;Brion S. Maher.
American Journal of Medical Genetics (2003)
Detectable clonal mosaicism from birth to old age and its relationship to cancer
Cathy C. Laurie;Cecelia A Laurie;Kenneth Rice;Kimberly F. Doheny.
Nature Genetics (2012)
Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip
Fedik Rahimov;Mary L Marazita;Axel Visel;Margaret E Cooper.
Nature Genetics (2008)
The PhenX Toolkit: Get the Most From Your Measures
Carol M. Hamilton;Lisa C. Strader;Joseph G. Pratt;Deborah Maiese.
American Journal of Epidemiology (2011)
Anthropometric precision and accuracy of digital three-dimensional photogrammetry: comparing the Genex and 3dMD imaging systems with one another and with direct anthropometry.
Seth M. Weinberg;Sybill Naidoo;Daniel P. Govier;Rick A. Martin.
Journal of Craniofacial Surgery (2006)
Maternal Serum 25-Hydroxyvitamin D Concentrations Are Associated with Small-for-Gestational Age Births in White Women
Lisa M. Bodnar;Janet M. Catov;Joseph M. Zmuda;Margaret E. Cooper.
Journal of Nutrition (2010)
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