RICHARD GIBBS's research topics

RICHARD GIBBS

Concepts (1872)

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Concepts are derived automatically from a person's publications.

The timeline below shows the dates (blue tick marks) of publications associated with RICHARD GIBBS's top concepts. The average publication date for each concept is shown as a red circle, illustrating changes in the primary topics that RICHARD GIBBS has written about over time.

Exons, 43 publications between 1989 and 2023, average publication date May 2008. Sequence Analysis, DNA, 150 publications between 1992 and 2021, average publication date January 2010. Genome, 52 publications between 1996 and 2022, average publication date June 2011. Evolution, Molecular, 44 publications between 1996 and 2020, average publication date August 2012. Genetic Diseases, Inborn, 23 publications between 1988 and 2021, average publication date January 2013. Mutation, 161 publications between 1987 and 2024, average publication date June 2013. Humans, 527 publications between 1987 and 2025, average publication date December 2013. Genome, Human, 70 publications between 1995 and 2024, average publication date January 2014. Polymorphism, Single Nucleotide, 91 publications between 2003 and 2024, average publication date June 2014. Genetic Variation, 76 publications between 1991 and 2024, average publication date June 2014. Pedigree, 87 publications between 1989 and 2023, average publication date August 2014. Exome, 100 publications between 2011 and 2023, average publication date September 2015. Genomics, 87 publications between 2004 and 2024, average publication date September 2015. Genetic Testing, 26 publications between 1989 and 2024, average publication date November 2015. Genetic Predisposition to Disease, 74 publications between 2000 and 2024, average publication date November 2015. Abnormalities, Multiple, 19 publications between 2005 and 2022, average publication date December 2015. Intellectual Disability, 31 publications between 1988 and 2023, average publication date August 2016. High-Throughput Nucleotide Sequencing, 59 publications between 2011 and 2024, average publication date September 2016. Phenotype, 86 publications between 1997 and 2024, average publication date November 2016.

Exons
Sequence Analysis, DNA
Genome
Evolution, Molecular
Genetic Diseases, Inborn
Mutation
Humans
Genome, Human
Polymorphism, Single Nucleotide
Genetic Variation
Pedigree
Exome
Genomics
Genetic Testing
Genetic Predisposition to Disease
Abnormalities, Multiple
Intellectual Disability
High-Throughput Nucleotide Sequencing
Phenotype

To see the data from this visualization as text, click here.

Name	Number of Publications	First Publication Year	Most Recent Publication Year	Average Publication Date
Exons	43	1989	2023	May 2008
Sequence Analysis, DNA	150	1992	2021	January 2010
Genome	52	1996	2022	June 2011
Evolution, Molecular	44	1996	2020	August 2012
Genetic Diseases, Inborn	23	1988	2021	January 2013
Mutation	161	1987	2024	June 2013
Humans	527	1987	2025	December 2013
Genome, Human	70	1995	2024	January 2014
Polymorphism, Single Nucleotide	91	2003	2024	June 2014
Genetic Variation	76	1991	2024	June 2014
Pedigree	87	1989	2023	August 2014
Exome	100	2011	2023	September 2015
Genomics	87	2004	2024	September 2015
Genetic Testing	26	1989	2024	November 2015
Genetic Predisposition to Disease	74	2000	2024	November 2015
Abnormalities, Multiple	19	2005	2022	December 2015
Intellectual Disability	31	1988	2023	August 2016
High-Throughput Nucleotide Sequencing	59	2011	2024	September 2016
Phenotype	86	1997	2024	November 2016

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