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 79 Citations 33,904 241 World Ranking 12173 National Ranking 6347
Genetics D-index 75 Citations 32,306 213 World Ranking 1220 National Ranking 575

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Genetics
  • Internal medicine

Hilary Coon mainly focuses on Genetics, Autism, Genome-wide association study, Copy-number variation and Genetic linkage. Her work on Meta-analysis expands to the thematically related Genetics. She interconnects Intellectual disability, Clinical psychology and Macrocephaly in the investigation of issues within Autism.

The study incorporates disciplines such as Autism spectrum disorder and Haplotype in addition to Genome-wide association study. Her work deals with themes such as Structural variation, Genetic variation, Allele frequency and Genetic architecture, which intersect with Copy-number variation. Her research in Genetic linkage intersects with topics in Genetic marker, Linkage and Pedigree chart.

Her most cited work include:

  • Functional impact of global rare copy number variation in autism spectrum disorders (1592 citations)
  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (1570 citations)
  • Synaptic, transcriptional and chromatin genes disrupted in autism (1544 citations)

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

Genetics, Genetic linkage, Autism, Gene and Autism spectrum disorder are her primary areas of study. Her study in Linkage, Pedigree chart, Locus, Gene mapping and Genotype is carried out as part of her Genetics studies. Her studies deal with areas such as Quantitative trait locus, Chromosome and Genome Scan as well as Linkage.

As a member of one scientific family, Hilary Coon mostly works in the field of Genetic linkage, focusing on Single-nucleotide polymorphism and, on occasion, Internal medicine. As part of the same scientific family, Hilary Coon usually focuses on Autism, concentrating on Copy-number variation and intersecting with Genome-wide association study. Hilary Coon has researched Genome-wide association study in several fields, including Genetic association and Genetic architecture.

She most often published in these fields:

  • Genetics (52.03%)
  • Genetic linkage (25.61%)
  • Autism (24.39%)

What were the highlights of her more recent work (between 2017-2021)?

  • Autism (24.39%)
  • Autism spectrum disorder (14.23%)
  • Genetics (52.03%)

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

Autism, Autism spectrum disorder, Genetics, Gene and Genome-wide association study are her primary areas of study. Hilary Coon combines subjects such as Exome sequencing, Clinical psychology, Cognition and Offspring with her study of Autism. Her Exome sequencing research includes themes of Chromatin, Genomic Segment, Computational biology and Copy-number variation.

Her Autism spectrum disorder research incorporates themes from genomic DNA and Neurodevelopmental disorder. In the subject of general Gene, her work in Genotype is often linked to Completed Suicide, Extended family and Medical examiner, thereby combining diverse domains of study. Her Genome-wide association study study combines topics in areas such as Pleiotropy, Psychiatry, Depression, Cause of death and Genetic association.

Between 2017 and 2021, her most popular works were:

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (373 citations)
  • Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (242 citations)
  • An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. (125 citations)

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

  • Gene
  • Genetics
  • Mutation

Hilary Coon mainly focuses on Autism spectrum disorder, Autism, Genetics, Gene and Genome-wide association study. Her Autism spectrum disorder study combines topics from a wide range of disciplines, such as Sample, Independent living and Clinical psychology. The Autism study combines topics in areas such as Odds ratio, Relative risk, Cognition and Cumulative incidence.

Her study involves Copy-number variation, Mutation and Genome, a branch of Genetics. In her study, which falls under the umbrella issue of Copy-number variation, False discovery rate is strongly linked to Regulation of gene expression. Her Genome-wide association study research is multidisciplinary, incorporating elements of Schizophrenia, Psychiatry, Psychiatric genetics, Pleiotropy and Bipolar disorder.

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

Synaptic, transcriptional and chromatin genes disrupted in autism

Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Nature (2014)

2220 Citations

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
Nature (2010)

2152 Citations

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)

2097 Citations

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)

1546 Citations

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Joseph T. Glessner;Kai Wang;Guiqing Cai;Olena Korvatska.
Nature (2009)

1483 Citations

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia

Cathryn M. Lewis;Douglas F. Levinson;Lesley H. Wise;Lynn E. DeLisi.
American Journal of Human Genetics (2003)

1458 Citations

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

Robert Freedman;Hilary Coon;Marina Myles-Worsley;Avi Orr-Urtreger.
Proceedings of the National Academy of Sciences of the United States of America (1997)

1452 Citations

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan.
Nature (2009)

1071 Citations

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

F. Kyle Satterstrom;F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S. Breen.
Cell (2020)

940 Citations

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

Dalila Pinto;Elsa Delaby;Elsa Delaby;Elsa Delaby;Daniele Merico;Mafalda Barbosa.
American Journal of Human Genetics (2014)

914 Citations

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