D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 92 Citations 33,138 293 World Ranking 593 National Ranking 339

Research.com Recognitions

Awards & Achievements

2014 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Mutation

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.

His most cited work include:

  • The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (455 citations)
  • Disruption of an AP-2 alpha binding site in an IRF6 enhancer is associated with cleft lip (348 citations)
  • Noninvasive Whole-Genome Sequencing of a Human Fetus (334 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Genetics (46.65%)
  • Gene (17.57%)
  • Single-nucleotide polymorphism (14.23%)

What were the highlights of his more recent work (between 2014-2021)?

  • Genetics (46.65%)
  • Genome-wide association study (10.25%)
  • Single-nucleotide polymorphism (14.23%)

In recent papers he was focusing on the following fields of study:

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.

Between 2014 and 2021, his most popular works were:

  • The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (455 citations)
  • A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 (89 citations)
  • Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology (85 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Mutation

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.

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.

Best Publications

Genetic studies of body mass index yield new insights for obesity biology

Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Nature (2015)

2711 Citations

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)

1306 Citations

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)

1215 Citations

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)

959 Citations

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)

888 Citations

Gene/environment causes of cleft lip and/or palate

JC Murray.
Clinical Genetics (2002)

873 Citations

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)

681 Citations

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).

JC Murray;KH Buetow;JL Weber;S Ludwigsen.
Science (1994)

672 Citations

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)

501 Citations

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.
Cell (1998)

497 Citations

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