SEEMA LALANI's research topics

SEEMA LALANI

Concepts (647)

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

Abnormalities, Multiple, 20 publications between 2002 and 2025, average publication date May 2012. Comparative Genomic Hybridization, 25 publications between 2008 and 2020, average publication date July 2012. Gene Deletion, 11 publications between 2003 and 2019, average publication date October 2012. Chromosome Deletion, 21 publications between 2005 and 2023, average publication date February 2013. Sequence Deletion, 13 publications between 2008 and 2020, average publication date March 2013. Developmental Disabilities, 22 publications between 2006 and 2023, average publication date October 2014. Exons, 11 publications between 2009 and 2022, average publication date May 2015. DNA Copy Number Variations, 24 publications between 2010 and 2021, average publication date February 2016. Heart Defects, Congenital, 20 publications between 2004 and 2023, average publication date June 2016. DNA-Binding Proteins, 16 publications between 2005 and 2023, average publication date November 2016. Genetic Diseases, Inborn, 10 publications between 2013 and 2024, average publication date August 2017. Seizures, 6 publications between 2009 and 2022, average publication date December 2017. Mutation, 28 publications between 2004 and 2025, average publication date December 2017. Phenotype, 42 publications between 2003 and 2026, average publication date January 2018. Intellectual Disability, 22 publications between 2008 and 2024, average publication date May 2018. Genetic Predisposition to Disease, 18 publications between 2012 and 2025, average publication date September 2018. Mutation, Missense, 15 publications between 2004 and 2025, average publication date November 2018. Exome, 22 publications between 2011 and 2026, average publication date March 2019. Neurodevelopmental Disorders, 13 publications between 2015 and 2025, average publication date May 2022.

Abnormalities, Multiple
Comparative Genomic Hybridization
Gene Deletion
Chromosome Deletion
Sequence Deletion
Developmental Disabilities
Exons
DNA Copy Number Variations
Heart Defects, Congenital
DNA-Binding Proteins
Genetic Diseases, Inborn
Seizures
Mutation
Phenotype
Intellectual Disability
Genetic Predisposition to Disease
Mutation, Missense
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
Abnormalities, Multiple	20	2002	2025	May 2012
Comparative Genomic Hybridization	25	2008	2020	July 2012
Gene Deletion	11	2003	2019	October 2012
Chromosome Deletion	21	2005	2023	February 2013
Sequence Deletion	13	2008	2020	March 2013
Developmental Disabilities	22	2006	2023	October 2014
Exons	11	2009	2022	May 2015
DNA Copy Number Variations	24	2010	2021	February 2016
Heart Defects, Congenital	20	2004	2023	June 2016
DNA-Binding Proteins	16	2005	2023	November 2016
Genetic Diseases, Inborn	10	2013	2024	August 2017
Seizures	6	2009	2022	December 2017
Mutation	28	2004	2025	December 2017
Phenotype	42	2003	2026	January 2018
Intellectual Disability	22	2008	2024	May 2018
Genetic Predisposition to Disease	18	2012	2025	September 2018
Mutation, Missense	15	2004	2025	November 2018
Exome	22	2011	2026	March 2019
Neurodevelopmental Disorders	13	2015	2025	May 2022

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