PENGFEI LIU's research topics

PENGFEI LIU

Concepts (334)

Back to Profile

Concepts are derived automatically from a person's publications.

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

Gene Duplication, 6 publications between 2009 and 2015, average publication date April 2012. Charcot-Marie-Tooth Disease, 3 publications between 2010 and 2015, average publication date June 2013. Genomic Instability, 4 publications between 2010 and 2017, average publication date July 2013. Chromosomes, Human, Pair 17, 8 publications between 2010 and 2019, average publication date October 2013. Gene Rearrangement, 10 publications between 2009 and 2019, average publication date December 2013. Developmental Disabilities, 7 publications between 2009 and 2019, average publication date September 2014. Chromosome Duplication, 8 publications between 2011 and 2019, average publication date September 2014. DNA Replication, 7 publications between 2011 and 2019, average publication date December 2014. Smith-Magenis Syndrome, 7 publications between 2011 and 2019, average publication date January 2015. Chromosome Aberrations, 5 publications between 2009 and 2019, average publication date May 2015. DNA Copy Number Variations, 17 publications between 2010 and 2019, average publication date June 2015. Gigantism, 4 publications between 2014 and 2016, average publication date July 2015. Phenotype, 22 publications between 2009 and 2019, average publication date March 2016. Sequence Analysis, DNA, 9 publications between 2011 and 2019, average publication date April 2016. Alleles, 12 publications between 2011 and 2019, average publication date June 2016. Genomic Structural Variation, 3 publications between 2014 and 2019, average publication date August 2016. Intellectual Disability, 8 publications between 2009 and 2019, average publication date October 2016. Genetic Diseases, Inborn, 10 publications between 2012 and 2019, average publication date February 2017. Exome, 12 publications between 2014 and 2019, average publication date August 2017.

Gene Duplication
Charcot-Marie-Tooth Disease
Genomic Instability
Chromosomes, Human, Pair 17
Gene Rearrangement
Developmental Disabilities
Chromosome Duplication
DNA Replication
Smith-Magenis Syndrome
Chromosome Aberrations
DNA Copy Number Variations
Gigantism
Phenotype
Sequence Analysis, DNA
Alleles
Genomic Structural Variation
Intellectual Disability
Genetic Diseases, Inborn
Exome

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
Gene Duplication	6	2009	2015	April 2012
Charcot-Marie-Tooth Disease	3	2010	2015	June 2013
Genomic Instability	4	2010	2017	July 2013
Chromosomes, Human, Pair 17	8	2010	2019	October 2013
Gene Rearrangement	10	2009	2019	December 2013
Developmental Disabilities	7	2009	2019	September 2014
Chromosome Duplication	8	2011	2019	September 2014
DNA Replication	7	2011	2019	December 2014
Smith-Magenis Syndrome	7	2011	2019	January 2015
Chromosome Aberrations	5	2009	2019	May 2015
DNA Copy Number Variations	17	2010	2019	June 2015
Gigantism	4	2014	2016	July 2015
Phenotype	22	2009	2019	March 2016
Sequence Analysis, DNA	9	2011	2019	April 2016
Alleles	12	2011	2019	June 2016
Genomic Structural Variation	3	2014	2019	August 2016
Intellectual Disability	8	2009	2019	October 2016
Genetic Diseases, Inborn	10	2012	2019	February 2017
Exome	12	2014	2019	August 2017

LIU's Networks

Click the

Explore

buttons for more information and interactive visualizations!

Concepts (334)

Explore

Co-Authors (86)

Explore

Similar People (60)

Explore

Same Department

Explore

Physical Neighbors