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
Medicine D-index 72 Citations 21,477 328 World Ranking 16232 National Ranking 8275
Genetics D-index 72 Citations 21,294 316 World Ranking 1407 National Ranking 665

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Mutation
  • Genetics

Her main research concerns Genetics, Genetic linkage, Locus, Prostate cancer and Genome-wide association study. All of her Genetics and Gene, Genetic association, Allele, Haplotype and Germline mutation investigations are sub-components of the entire Genetics study. The various areas that Joan E. Bailey-Wilson examines in her Genetic linkage study include Genetic determinism, Genotype and Pedigree chart.

Her Locus research incorporates elements of Microsatellite, Lung cancer and Gene mapping. Her work is dedicated to discovering how Prostate cancer, Allele frequency are connected with Ensemble learning, Mutation and Exome sequencing and other disciplines. Genome-wide association study is a primary field of her research addressed under Single-nucleotide polymorphism.

Her most cited work include:

  • Replicating genotype–phenotype associations (1216 citations)
  • Major Susceptibility Locus for Prostate Cancer on Chromosome 1 Suggested by a Genome-Wide Search (709 citations)
  • Evidence for a prostate cancer susceptibility locus on the X chromosome. (632 citations)

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

Her primary scientific interests are in Genetics, Genetic linkage, Linkage, Locus and Internal medicine. Genetics is a component of her Single-nucleotide polymorphism, Genome-wide association study, Prostate cancer, Allele and Genotype studies. The Genetic linkage study which covers Haplotype that intersects with Candidate gene.

Her Linkage research integrates issues from Genetic analysis, Statistics, Type I and type II errors, Microsatellite and Computational biology. Her study in Locus is interdisciplinary in nature, drawing from both Genetic marker, Genome, Human genetics and Gene mapping. Joan E. Bailey-Wilson has included themes like Endocrinology and Oncology in her Internal medicine study.

She most often published in these fields:

  • Genetics (66.96%)
  • Genetic linkage (27.83%)
  • Linkage (19.71%)

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

  • Genetics (66.96%)
  • Genome-wide association study (15.36%)
  • Exome (7.54%)

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

Joan E. Bailey-Wilson mainly focuses on Genetics, Genome-wide association study, Exome, Candidate gene and Lung cancer. Her study in Genetic linkage, Exome sequencing, Gene, Haplotype and Allele frequency falls within the category of Genetics. Her research in Haplotype intersects with topics in Microsatellite and Linkage.

Her study explores the link between Genome-wide association study and topics such as Genetic association that cross with problems in Functional data analysis, Type I and type II errors, Computational biology and Statistics. Her Lung cancer research includes elements of Cancer, Disease and 1000 Genomes Project. Her research integrates issues of Germline mutation, Oncology and Germline in her study of Cancer.

Between 2014 and 2021, her most popular works were:

  • REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants (546 citations)
  • Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm (322 citations)
  • High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets (122 citations)

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

  • Gene
  • Mutation
  • Genetics

Genetics, Genome-wide association study, Genetic association, Exome and Exome sequencing are her primary areas of study. The study of Genetics is intertwined with the study of Disease in a number of ways. Joan E. Bailey-Wilson usually deals with Genome-wide association study and limits it to topics linked to 1000 Genomes Project and Oncology, CDKN2A, Imputation, Squamous carcinoma and Adenocarcinoma.

In her research on the topic of Genetic association, Keratoconus, Astigmatism and Heritability is strongly related with Statistics. Her studies deal with areas such as Whole genome sequencing, Massive parallel sequencing and Mutation as well as Exome. She interconnects Allele frequency and DNA sequencing in the investigation of issues within Exome sequencing.

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

Replicating genotype–phenotype associations

Stephen J. Chanock;Teri Manolio;Michael Boehnke;Eric Boerwinkle.
Nature (2007)

1570 Citations

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

Nilah M M. Ioannidis;Joseph H H. Rothstein;Joseph H H. Rothstein;Vikas Pejaver;Sumit Middha.
American Journal of Human Genetics (2016)

1050 Citations

Major Susceptibility Locus for Prostate Cancer on Chromosome 1 Suggested by a Genome-Wide Search

Jeffrey R. Smith;Diha Freije;John D. Carpten;Henrik Grönberg;Henrik Grönberg.
Science (1996)

1032 Citations

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

J.D. Carpten;C.M. Robbins;A. Villablanca;L. Forsberg.
Nature Genetics (2002)

744 Citations

Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases

Kevin G. Becker;Richard M. Simon;Joan E. Bailey-Wilson;Boris Freidlin.
Proceedings of the National Academy of Sciences of the United States of America (1998)

731 Citations

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1.

J. Carpten;N. Nupponen;S. Isaacs;R. Sood.
Nature Genetics (2002)

654 Citations

Evidence for a prostate cancer susceptibility locus on the X chromosome.

Jianfeng Xu;Deborah Meyers;Diha Freije;Sarah Isaacs.
Nature Genetics (1998)

636 Citations

Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource

Henry T. Lynch;William Kimberling;William A. Albano;Jane F. Lynch.
Cancer (1985)

562 Citations

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Virginie J M Verhoeven;Pirro G Hysi;Robert Wojciechowski;Robert Wojciechowski;Qiao Fan.
Nature Genetics (2013)

453 Citations

Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

Jianfeng Xu;S. Lilly Zheng;Akira Komiya;Josyf C. Mychaleckyj.
Nature Genetics (2002)

427 Citations

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