D-Index & Metrics Best Publications

D-Index & Metrics

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 112 Citations 56,134 334 World Ranking 265 National Ranking 162

Research.com Recognitions

Awards & Achievements

2018 - Fellow of the American Academy of Arts and Sciences

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Genetics

His primary areas of investigation include Genetics, Autism, Locus, Gene and Genetic linkage. His research on Genetics often connects related topics like Molecular biology. His study in Molecular biology is interdisciplinary in nature, drawing from both Complementary DNA, Duchenne muscular dystrophy and Exon.

His Autism research integrates issues from Single-nucleotide polymorphism and Intellectual disability. His Genetic linkage research also works with subjects such as

  • Quantitative trait locus together with Genetic heterogeneity,
  • Genetic determinism together with Linkage. His Genome-wide association study study combines topics in areas such as CNTNAP2, Allele and Genetic association.

His most cited work include:

  • Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. (1976 citations)
  • 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)

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

Genetics, Transplantation, Immunology, Surgery and Gene are his primary areas of study. Anthony P. Monaco regularly links together related areas like Autism in his Genetics studies. His biological study spans a wide range of topics, including Single-nucleotide polymorphism and Candidate gene.

His studies deal with areas such as Immunosuppression, Kidney and Pathology as well as Transplantation. His Gene study frequently draws connections to other fields, such as Molecular biology. Anthony P. Monaco has included themes like Gastroenterology and Diabetes mellitus, Endocrinology in his Internal medicine study.

He most often published in these fields:

  • Genetics (35.18%)
  • Transplantation (22.90%)
  • Immunology (19.14%)

What were the highlights of his more recent work (between 2005-2021)?

  • Genetics (35.18%)
  • Autism (7.63%)
  • Genome-wide association study (5.20%)

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

His scientific interests lie mostly in Genetics, Autism, Genome-wide association study, Dyslexia and Transplantation. His research related to Single-nucleotide polymorphism, Copy-number variation, Candidate gene, Locus and Gene might be considered part of Genetics. His work is dedicated to discovering how Candidate gene, Genetic association are connected with Genetic linkage and other disciplines.

Many of his studies involve connections with topics such as Intellectual disability and Autism. His Genome-wide association study research includes themes of Schizophrenia, Bipolar disorder, Specific language impairment, Genomics and Allele. The Reading disability research he does as part of his general Dyslexia study is frequently linked to other disciplines of science, such as Clinical psychology and Cognition, therefore creating a link between diverse domains of science.

Between 2005 and 2021, his most popular works were:

  • 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)
  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (1570 citations)

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

  • Gene
  • Internal medicine
  • Genetics

Anthony P. Monaco mostly deals with Genetics, Autism, Genome-wide association study, Single-nucleotide polymorphism and Copy-number variation. His Genetics study frequently draws connections to adjacent fields such as Specific language impairment. His Specific language impairment study incorporates themes from CNTNAP2 and Communication disorder.

His Copy-number variation research includes elements of Genetic variation, Bioinformatics and Genetic architecture. The concepts of his Locus study are interwoven with issues in Heterologous, Immunology, Lymphocyte and Immunologic Tolerance. His Genetic association research is multidisciplinary, incorporating perspectives in Psychiatric genetics and Genomics.

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

Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.

M. Koenig;E.P. Hoffman;C.J. Bertelson;A.P. Monaco.
Cell (1987)

2784 Citations

A forkhead-domain gene is mutated in a severe speech and language disorder

Cecilia S. L. Lai;Simon E. Fisher;Jane A. Hurst;Faraneh Vargha-Khadem.
Nature (2001)

2577 Citations

Molecular evolution of FOXP2, a gene involved in speech and language

Wolfgang Enard;Molly Przeworski;Simon E. Fisher;Cecilia S. L. Lai.
Nature (2002)

2082 Citations

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

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

1898 Citations

The Complete Sequence of Dystrophin Predicts a Rod-Shaped Cytoskeletal Protein

M. Koenig;M. Koenig;A.P. Monaco;A.P. Monaco;L.M. Kunkel;L.M. Kunkel;L.M. Kunkel.
Cell (1988)

1866 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)

1708 Citations

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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

1454 Citations

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.

Anthony P. Monaco;Corlee J. Bertelson;Corlee J. Bertelson;Sabina Liechti-Gallati;Hans Moser.
Genomics (1988)

1382 Citations

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.

Anthony P. Monaco;Anthony P. Monaco;Rachael L. Neve;Rachael L. Neve;Chris Colletti-Feener;Corlee J. Bertelson.
Nature (1986)

1258 Citations

Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location

B. Royerpokora;L. M. Kunkel;A. P. Monaco;S. C. Goff.
Nature (1986)

976 Citations

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