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 72 Citations 17,078 206 World Ranking 1373 National Ranking 718

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Internal medicine

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.

His most cited work include:

  • Cleft lip and palate: understanding genetic and environmental influences. (966 citations)
  • Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. (477 citations)
  • A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 (406 citations)

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

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.

He most often published in these fields:

  • Genetics (50.11%)
  • Genome-wide association study (23.94%)
  • Single-nucleotide polymorphism (17.00%)

What were the highlights of his more recent work (between 2018-2021)?

  • Genome-wide association study (23.94%)
  • Genetics (50.11%)
  • Genetic architecture (5.82%)

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

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.

Between 2018 and 2021, his most popular works were:

  • Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. (47 citations)
  • Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration (19 citations)
  • Facial recognition from DNA using face-to-DNA classifiers. (15 citations)

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

  • Gene
  • Internal medicine
  • Genetics

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.

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

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

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

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)

566 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

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)

470 Citations

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)

445 Citations

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)

441 Citations

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)

349 Citations

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)

347 Citations

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)

340 Citations

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