JAMES LUPSKI's research topics

JAMES LUPSKI

Concepts (1737)

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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 JAMES LUPSKI's top concepts. The average publication date for each concept is shown as a red circle, illustrating changes in the primary topics that JAMES LUPSKI has written about over time.

Charcot-Marie-Tooth Disease, 102 publications between 1990 and 2023, average publication date February 2001. Chromosomes, Human, Pair 17, 119 publications between 1990 and 2021, average publication date November 2001. Abnormalities, Multiple, 90 publications between 1991 and 2022, average publication date July 2007. Chromosome Aberrations, 52 publications between 1991 and 2024, average publication date February 2008. Gene Duplication, 71 publications between 1991 and 2024, average publication date November 2008. Gene Rearrangement, 48 publications between 1992 and 2026, average publication date March 2009. Gene Dosage, 62 publications between 1991 and 2025, average publication date May 2009. Pedigree, 204 publications between 1990 and 2026, average publication date September 2010. Genome, Human, 83 publications between 1992 and 2026, average publication date February 2012. Mutation, 227 publications between 1982 and 2026, average publication date April 2012. Genetic Variation, 58 publications between 1993 and 2025, average publication date July 2012. Genetic Diseases, Inborn, 45 publications between 1996 and 2026, average publication date February 2013. Alleles, 91 publications between 1992 and 2026, average publication date April 2013. Phenotype, 229 publications between 1990 and 2026, average publication date June 2013. Intellectual Disability, 94 publications between 1991 and 2026, average publication date October 2013. Genetic Predisposition to Disease, 83 publications between 1994 and 2026, average publication date January 2016. DNA Copy Number Variations, 89 publications between 2010 and 2026, average publication date February 2016. Genomics, 49 publications between 2003 and 2025, average publication date September 2016. Exome, 74 publications between 2011 and 2025, average publication date January 2017. Neurodevelopmental Disorders, 43 publications between 2016 and 2026, average publication date July 2022.

Charcot-Marie-Tooth Disease
Chromosomes, Human, Pair 17
Abnormalities, Multiple
Chromosome Aberrations
Gene Duplication
Gene Rearrangement
Gene Dosage
Pedigree
Genome, Human
Mutation
Genetic Variation
Genetic Diseases, Inborn
Alleles
Phenotype
Intellectual Disability
Genetic Predisposition to Disease
DNA Copy Number Variations
Genomics
Exome
Neurodevelopmental Disorders

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
Charcot-Marie-Tooth Disease	102	1990	2023	February 2001
Chromosomes, Human, Pair 17	119	1990	2021	November 2001
Abnormalities, Multiple	90	1991	2022	July 2007
Chromosome Aberrations	52	1991	2024	February 2008
Gene Duplication	71	1991	2024	November 2008
Gene Rearrangement	48	1992	2026	March 2009
Gene Dosage	62	1991	2025	May 2009
Pedigree	204	1990	2026	September 2010
Genome, Human	83	1992	2026	February 2012
Mutation	227	1982	2026	April 2012
Genetic Variation	58	1993	2025	July 2012
Genetic Diseases, Inborn	45	1996	2026	February 2013
Alleles	91	1992	2026	April 2013
Phenotype	229	1990	2026	June 2013
Intellectual Disability	94	1991	2026	October 2013
Genetic Predisposition to Disease	83	1994	2026	January 2016
DNA Copy Number Variations	89	2010	2026	February 2016
Genomics	49	2003	2025	September 2016
Exome	74	2011	2025	January 2017
Neurodevelopmental Disorders	43	2016	2026	July 2022

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