JAMES LUPSKI's research topics

JAMES LUPSKI

Concepts (1673)

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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, 101 publications between 1990 and 2023, average publication date February 2001. Chromosomes, Human, Pair 17, 115 publications between 1990 and 2021, average publication date November 2001. Abnormalities, Multiple, 87 publications between 1991 and 2022, average publication date September 2007. Gene Duplication, 66 publications between 1991 and 2020, average publication date May 2008. Gene Rearrangement, 46 publications between 1992 and 2020, average publication date January 2009. Gene Dosage, 60 publications between 1991 and 2022, average publication date March 2009. Pedigree, 186 publications between 1990 and 2023, average publication date January 2010. Genome, Human, 78 publications between 1992 and 2022, average publication date July 2011. Mutation, 212 publications between 1982 and 2023, average publication date September 2011. Genetic Variation, 56 publications between 1993 and 2021, average publication date February 2012. Alleles, 81 publications between 1992 and 2023, average publication date February 2012. Genetic Diseases, Inborn, 43 publications between 1996 and 2021, average publication date June 2012. Phenotype, 207 publications between 1990 and 2024, average publication date July 2012. Intellectual Disability, 87 publications between 1991 and 2024, average publication date November 2012. Genetic Predisposition to Disease, 75 publications between 1994 and 2023, average publication date May 2015. DNA Copy Number Variations, 86 publications between 2010 and 2024, average publication date October 2015. Exome, 72 publications between 2011 and 2022, average publication date November 2016. Microcephaly, 28 publications between 2005 and 2024, average publication date December 2016. Genetic Association Studies, 46 publications between 2010 and 2022, average publication date August 2017. Neurodevelopmental Disorders, 31 publications between 2016 and 2024, average publication date June 2021.

Charcot-Marie-Tooth Disease
Chromosomes, Human, Pair 17
Abnormalities, Multiple
Gene Duplication
Gene Rearrangement
Gene Dosage
Pedigree
Genome, Human
Mutation
Genetic Variation
Alleles
Genetic Diseases, Inborn
Phenotype
Intellectual Disability
Genetic Predisposition to Disease
DNA Copy Number Variations
Exome
Microcephaly
Genetic Association Studies
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	101	1990	2023	February 2001
Chromosomes, Human, Pair 17	115	1990	2021	November 2001
Abnormalities, Multiple	87	1991	2022	September 2007
Gene Duplication	66	1991	2020	May 2008
Gene Rearrangement	46	1992	2020	January 2009
Gene Dosage	60	1991	2022	March 2009
Pedigree	186	1990	2023	January 2010
Genome, Human	78	1992	2022	July 2011
Mutation	212	1982	2023	September 2011
Genetic Variation	56	1993	2021	February 2012
Alleles	81	1992	2023	February 2012
Genetic Diseases, Inborn	43	1996	2021	June 2012
Phenotype	207	1990	2024	July 2012
Intellectual Disability	87	1991	2024	November 2012
Genetic Predisposition to Disease	75	1994	2023	May 2015
DNA Copy Number Variations	86	2010	2024	October 2015
Exome	72	2011	2022	November 2016
Microcephaly	28	2005	2024	December 2016
Genetic Association Studies	46	2010	2022	August 2017
Neurodevelopmental Disorders	31	2016	2024	June 2021

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