ELIZABETH ROEDER's research topics

ELIZABETH ROEDER

Concepts (328)

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

Chromosomes, Human, X, 3 publications between 2007 and 2012, average publication date May 2010. Chromosome Deletion, 7 publications between 2007 and 2014, average publication date August 2010. Chromosomes, Human, Pair 16, 5 publications between 1998 and 2018, average publication date December 2010. Beckwith-Wiedemann Syndrome, 1 publications between 2012 and 2012, average publication date August 2012. Cerebellar Neoplasms, 1 publications between 2012 and 2012, average publication date August 2012. Spinal Cord Neoplasms, 1 publications between 2012 and 2012, average publication date August 2012. Abnormalities, Multiple, 13 publications between 2000 and 2021, average publication date August 2012. Facies, 5 publications between 2003 and 2021, average publication date November 2012. Craniofacial Abnormalities, 5 publications between 2005 and 2021, average publication date December 2012. Microcephaly, 7 publications between 2004 and 2023, average publication date February 2013. Phenotype, 21 publications between 2003 and 2023, average publication date October 2014. Developmental Disabilities, 9 publications between 2005 and 2023, average publication date October 2014. DNA Copy Number Variations, 6 publications between 2010 and 2018, average publication date June 2015. Mutation, 13 publications between 2003 and 2023, average publication date December 2016. Intellectual Disability, 17 publications between 2007 and 2023, average publication date March 2017. Mutation, Missense, 8 publications between 2006 and 2023, average publication date July 2017. De Lange Syndrome, 4 publications between 2014 and 2023, average publication date December 2017. Movement Disorders, 3 publications between 2016 and 2023, average publication date February 2020. Neurodevelopmental Disorders, 10 publications between 2017 and 2023, average publication date April 2020. Genetic Association Studies, 6 publications between 2019 and 2023, average publication date December 2020.

Chromosomes, Human, X
Chromosome Deletion
Chromosomes, Human, Pair 16
Beckwith-Wiedemann Syndrome
Cerebellar Neoplasms
Spinal Cord Neoplasms
Abnormalities, Multiple
Facies
Craniofacial Abnormalities
Microcephaly
Phenotype
Developmental Disabilities
DNA Copy Number Variations
Mutation
Intellectual Disability
Mutation, Missense
De Lange Syndrome
Movement Disorders
Neurodevelopmental Disorders
Genetic Association Studies

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
Chromosomes, Human, X	3	2007	2012	May 2010
Chromosome Deletion	7	2007	2014	August 2010
Chromosomes, Human, Pair 16	5	1998	2018	December 2010
Beckwith-Wiedemann Syndrome	1	2012	2012	August 2012
Cerebellar Neoplasms	1	2012	2012	August 2012
Spinal Cord Neoplasms	1	2012	2012	August 2012
Abnormalities, Multiple	13	2000	2021	August 2012
Facies	5	2003	2021	November 2012
Craniofacial Abnormalities	5	2005	2021	December 2012
Microcephaly	7	2004	2023	February 2013
Phenotype	21	2003	2023	October 2014
Developmental Disabilities	9	2005	2023	October 2014
DNA Copy Number Variations	6	2010	2018	June 2015
Mutation	13	2003	2023	December 2016
Intellectual Disability	17	2007	2023	March 2017
Mutation, Missense	8	2006	2023	July 2017
De Lange Syndrome	4	2014	2023	December 2017
Movement Disorders	3	2016	2023	February 2020
Neurodevelopmental Disorders	10	2017	2023	April 2020
Genetic Association Studies	6	2019	2023	December 2020

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Concepts (328)

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