JAMES LUPSKI's research topics

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JAMES LUPSKI

Concepts (1723)

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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, 51 publications between 1991 and 2022, average publication date October 2007. Gene Duplication, 71 publications between 1991 and 2024, average publication date November 2008. Gene Dosage, 61 publications between 1991 and 2022, average publication date February 2009. Gene Rearrangement, 48 publications between 1992 and 2024, average publication date March 2009. Pedigree, 197 publications between 1990 and 2024, average publication date February 2010. Genome, Human, 82 publications between 1992 and 2025, average publication date December 2011. Mutation, 221 publications between 1982 and 2025, average publication date December 2011. Genetic Variation, 57 publications between 1993 and 2024, average publication date April 2012. Alleles, 86 publications between 1992 and 2025, average publication date July 2012. Genetic Diseases, Inborn, 44 publications between 1996 and 2025, average publication date October 2012. Phenotype, 223 publications between 1990 and 2025, average publication date February 2013. Intellectual Disability, 92 publications between 1991 and 2024, average publication date July 2013. Genetic Predisposition to Disease, 80 publications between 1994 and 2024, average publication date August 2015. DNA Copy Number Variations, 87 publications between 2010 and 2024, average publication date November 2015. Genomics, 47 publications between 2003 and 2023, average publication date April 2016. Exome, 74 publications between 2011 and 2025, average publication date January 2017. Neurodevelopmental Disorders, 37 publications between 2016 and 2025, average publication date December 2021.

Charcot-Marie-Tooth Disease
Chromosomes, Human, Pair 17
Abnormalities, Multiple
Chromosome Aberrations
Gene Duplication
Gene Dosage
Gene Rearrangement
Pedigree
Genome, Human
Mutation
Genetic Variation
Alleles
Genetic Diseases, Inborn
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	51	1991	2022	October 2007
Gene Duplication	71	1991	2024	November 2008
Gene Dosage	61	1991	2022	February 2009
Gene Rearrangement	48	1992	2024	March 2009
Pedigree	197	1990	2024	February 2010
Genome, Human	82	1992	2025	December 2011
Mutation	221	1982	2025	December 2011
Genetic Variation	57	1993	2024	April 2012
Alleles	86	1992	2025	July 2012
Genetic Diseases, Inborn	44	1996	2025	October 2012
Phenotype	223	1990	2025	February 2013
Intellectual Disability	92	1991	2024	July 2013
Genetic Predisposition to Disease	80	1994	2024	August 2015
DNA Copy Number Variations	87	2010	2024	November 2015
Genomics	47	2003	2023	April 2016
Exome	74	2011	2025	January 2017
Neurodevelopmental Disorders	37	2016	2025	December 2021

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