CHRISTINE ENG's research topics

CHRISTINE ENG

Concepts (487)

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

Fabry Disease, 6 publications between 2003 and 2018, average publication date March 2008. Oligonucleotide Array Sequence Analysis, 7 publications between 2005 and 2013, average publication date June 2009. Genetic Counseling, 6 publications between 2006 and 2017, average publication date March 2012. Prenatal Diagnosis, 10 publications between 2005 and 2025, average publication date January 2013. Chromosome Disorders, 4 publications between 2012 and 2021, average publication date January 2016. Mutation, 23 publications between 2004 and 2021, average publication date February 2016. Abnormalities, Multiple, 8 publications between 2008 and 2021, average publication date February 2016. Genome, Human, 7 publications between 2013 and 2019, average publication date March 2016. Phenotype, 28 publications between 2003 and 2021, average publication date April 2016. Muscle Hypotonia, 6 publications between 2014 and 2019, average publication date May 2016. Genetic Testing, 17 publications between 2006 and 2025, average publication date June 2016. Sequence Analysis, DNA, 19 publications between 2012 and 2019, average publication date June 2016. Exome, 37 publications between 2012 and 2024, average publication date April 2017. Intellectual Disability, 15 publications between 2012 and 2021, average publication date May 2017. DNA Copy Number Variations, 9 publications between 2013 and 2020, average publication date June 2017. High-Throughput Nucleotide Sequencing, 13 publications between 2015 and 2020, average publication date August 2017. Genetic Diseases, Inborn, 14 publications between 2013 and 2025, average publication date September 2017. Alleles, 13 publications between 2016 and 2019, average publication date October 2017. Rare Diseases, 4 publications between 2018 and 2023, average publication date December 2020.

Fabry Disease
Oligonucleotide Array Sequence Analysis
Genetic Counseling
Prenatal Diagnosis
Chromosome Disorders
Mutation
Abnormalities, Multiple
Genome, Human
Phenotype
Muscle Hypotonia
Genetic Testing
Sequence Analysis, DNA
Exome
Intellectual Disability
DNA Copy Number Variations
High-Throughput Nucleotide Sequencing
Genetic Diseases, Inborn
Alleles
Rare Diseases

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
Fabry Disease	6	2003	2018	March 2008
Oligonucleotide Array Sequence Analysis	7	2005	2013	June 2009
Genetic Counseling	6	2006	2017	March 2012
Prenatal Diagnosis	10	2005	2025	January 2013
Chromosome Disorders	4	2012	2021	January 2016
Mutation	23	2004	2021	February 2016
Abnormalities, Multiple	8	2008	2021	February 2016
Genome, Human	7	2013	2019	March 2016
Phenotype	28	2003	2021	April 2016
Muscle Hypotonia	6	2014	2019	May 2016
Genetic Testing	17	2006	2025	June 2016
Sequence Analysis, DNA	19	2012	2019	June 2016
Exome	37	2012	2024	April 2017
Intellectual Disability	15	2012	2021	May 2017
DNA Copy Number Variations	9	2013	2020	June 2017
High-Throughput Nucleotide Sequencing	13	2015	2020	August 2017
Genetic Diseases, Inborn	14	2013	2025	September 2017
Alleles	13	2016	2019	October 2017
Rare Diseases	4	2018	2023	December 2020

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