Search research articles
Contact Us
Filters
Showing results (1-10 of 11) with videos related to
Page
of 2
Sort By:
Biorxiv : the Preprint Server for Biology
|
March 23, 2026
Evolutionary instability drives structural diversity and disease susceptibility at the 16p12.2 locus
Corrine Smolen, Santhosh Girirajan
Cell
|
August 5, 2022
The gene dose makes the disease
Corrine Smolen, Santhosh Girirajan
STAR Protocols
|
May 9, 2026
Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variants
Corrine Smolen, Matthew Jensen, Santhosh Girirajan
Journal of Medical Genetics
|
March 11, 2020
Gene discoveries in autism are biased towards comorbidity with intellectual disability
Matthew 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 deletion
Matthew 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 disorders
Jiawan Sun, Serena Noss, Deepro Banerjee, et al.
Nature Communications
|
April 30, 2026
Functional impact of genetic background on variable expressivity in neurodevelopmental disorders
Jiawan 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 variants
Corrine 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 variants
Corrine Smolen, Matthew Jensen, Lisa Dyer, et al.
Cell
|
October 8, 2025
Genetic modifiers and ascertainment drive variable expressivity of complex disorders
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Biorxiv : the Preprint Server for Biology
|
March 23, 2026
Evolutionary instability drives structural diversity and disease susceptibility at the 16p12.2 locus
Corrine Smolen, Santhosh Girirajan
Cell
|
August 5, 2022
The gene dose makes the disease
Corrine Smolen, Santhosh Girirajan
STAR Protocols
|
May 9, 2026
Protocol for identifying genetic modifiers of phenotypes in individuals with disease-associated variants
Corrine Smolen, Matthew Jensen, Santhosh Girirajan
Journal of Medical Genetics
|
March 11, 2020
Gene discoveries in autism are biased towards comorbidity with intellectual disability
Matthew 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 deletion
Matthew 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 disorders
Jiawan Sun, Serena Noss, Deepro Banerjee, et al.
Nature Communications
|
April 30, 2026
Functional impact of genetic background on variable expressivity in neurodevelopmental disorders
Jiawan 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 variants
Corrine 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 variants
Corrine Smolen, Matthew Jensen, Lisa Dyer, et al.
Cell
|
October 8, 2025
Genetic modifiers and ascertainment drive variable expressivity of complex disorders
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, et al.
Page
of 2