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Corrine Smolen

Showing results (1-10 of 11) with videos related to

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Biorxiv : the Preprint Server for Biology|March 23, 2026
Evolutionary instability drives structural diversity and disease susceptibility at the 16p12.2 locusCorrine Smolen, Santhosh Girirajan
Cell|August 5, 2022
The gene dose makes the diseaseCorrine Smolen, Santhosh Girirajan
STAR Protocols|May 9, 2026
Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variantsCorrine Smolen, Matthew Jensen, Santhosh Girirajan
Journal of Medical Genetics|March 11, 2020
Gene discoveries in autism are biased towards comorbidity with intellectual disabilityMatthew Jensen, Corrine Smolen, Santhosh Girirajan
Genome Medicine|October 18, 2021
Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletionMatthew Jensen, Anastasia Tyryshkina, Lucilla Pizzo, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
An integrated framework for functional dissection of variable expressivity in genetic disordersJiawan Sun, Serena Noss, Deepro Banerjee, et al.
Nature Communications|April 30, 2026
Functional impact of genetic background on variable expressivity in neurodevelopmental disordersJiawan Sun, Serena Noss, Corrine Smolen, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
American Journal of Human Genetics|November 18, 2023
Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
Cell|October 8, 2025
Genetic modifiers and ascertainment drive variable expressivity of complex disordersMatthew Jensen, Corrine Smolen, Anastasia Tyryshkina, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Biorxiv : the Preprint Server for Biology|March 23, 2026
Evolutionary instability drives structural diversity and disease susceptibility at the 16p12.2 locusCorrine Smolen, Santhosh Girirajan
Cell|August 5, 2022
The gene dose makes the diseaseCorrine Smolen, Santhosh Girirajan
STAR Protocols|May 9, 2026
Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variantsCorrine Smolen, Matthew Jensen, Santhosh Girirajan
Journal of Medical Genetics|March 11, 2020
Gene discoveries in autism are biased towards comorbidity with intellectual disabilityMatthew Jensen, Corrine Smolen, Santhosh Girirajan
Genome Medicine|October 18, 2021
Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletionMatthew Jensen, Anastasia Tyryshkina, Lucilla Pizzo, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
An integrated framework for functional dissection of variable expressivity in genetic disordersJiawan Sun, Serena Noss, Deepro Banerjee, et al.
Nature Communications|April 30, 2026
Functional impact of genetic background on variable expressivity in neurodevelopmental disordersJiawan Sun, Serena Noss, Corrine Smolen, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
American Journal of Human Genetics|November 18, 2023
Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
Cell|October 8, 2025
Genetic modifiers and ascertainment drive variable expressivity of complex disordersMatthew Jensen, Corrine Smolen, Anastasia Tyryshkina, et al.
Pageof 2