2014 - Fellow of the American Association for the Advancement of Science (AAAS)
His scientific interests lie mostly in Genetics, Candidate gene, Pediatrics, Genome-wide association study and Gene. Genetics is closely attributed to Molecular biology in his research. His work deals with themes such as Frameshift mutation, Heart disease, Proband and Haplotype, which intersect with Candidate gene.
Jeffrey C. Murray interconnects Single-nucleotide polymorphism and Immunology in the investigation of issues within Haplotype. His Pediatrics research includes themes of Pregnancy, Oral cleft, Epidemiology, Obstetrics and Risk factor. His Genome-wide association study research is multidisciplinary, incorporating elements of Evolutionary biology, Bioinformatics, Copy-number variation, Genetic association and Craniofacial.
Genetics, Gene, Single-nucleotide polymorphism, Pediatrics and Internal medicine are his primary areas of study. In his study, which falls under the umbrella issue of Genetics, Restriction fragment length polymorphism is strongly linked to Molecular biology. His Pediatrics research includes elements of Low birth weight, Pregnancy, Gestational age, Epidemiology and Obstetrics.
The various areas that Jeffrey C. Murray examines in his Pregnancy study include Case-control study and Risk factor. His study explores the link between Obstetrics and topics such as Cohort study that cross with problems in Cohort. The Internal medicine study combines topics in areas such as Gastroenterology, Endocrinology and Oncology.
Jeffrey C. Murray mainly investigates Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Gene. Jeffrey C. Murray has included themes like Fetus, Case-control study, Genetic association and Genetic predisposition in his Genome-wide association study study. His Single-nucleotide polymorphism study combines topics from a wide range of disciplines, such as Genotyping, Genetic variation, Pediatrics and Cohort.
His research investigates the connection between Pediatrics and topics such as Immunization that intersect with problems in Pregnancy. His Internal medicine research is multidisciplinary, relying on both Gastroenterology, Endocrinology, Surgery and Oncology. His studies in Candidate gene integrate themes in fields like Ductus arteriosus and Haplotype.
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genotype and Pediatrics. Exome sequencing, Gene, Allele, IRF6 and Heritability are the primary areas of interest in his Genetics study. He combines subjects such as Bioinformatics, Mutation, Case-control study, Genetic association and Candidate gene with his study of Genome-wide association study.
His Case-control study study integrates concerns from other disciplines, such as Odds ratio, Missense mutation and Pregnancy. His research integrates issues of Vascular resistance, Internal medicine, Cohort and Genetic variation in his study of Single-nucleotide polymorphism. His study on Infant newborn is often connected to Quality assurance as part of broader study in Pediatrics.
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Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
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)
Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination
Karl W. Broman;Jeffrey C. Murray;Val C. Sheffield;Raymond L. White.
American Journal of Human Genetics (1998)
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
E. V. Semina;R. Reiter;N. J. Leysens;W. L. M. Alward.
Nature Genetics (1996)
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Shinji Kondo;Brian C. Schutte;Rebecca J. Richardson;Bryan C. Bjork.
Nature Genetics (2002)
Gene/environment causes of cleft lip and/or palate
Clinical Genetics (2002)
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)
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).
JC Murray;KH Buetow;JL Weber;S Ludwigsen.
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)
Pitx2, a Bicoid-Type Homeobox Gene, Is Involved in a Lefty-Signaling Pathway in Determination of Left-Right Asymmetry
Hidefumi Yoshioka;Chikara Meno;Kazuko Koshiba;Minoru Sugihara.
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