Publications by authors named "Emily Huber"

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Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Jiawan Sun, Emily Huber, Jean-Hubert Caberg

Cell· December 2025

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Systemic IGF-1 administration prevents traumatic brain injury induced gut permeability, dysmorphia, dysbiosis, and the increased number of immature dentate granule cells.
Lavanya Venkatasamy, Jaclyn Iannucci, Aleksandr Pereverzev, Jonathan Hoar, Emily Huber

Acta Neuropathol Commun· May 2025

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Investigating social connection as a protective factor against exam stress in college students.
Katherine R Mickley Steinmetz, Monica M Gaudier-Diaz, Emily C Huber, Brandon H Edwards, Keely A Muscatell

J Am Coll Health· October 2024

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Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Emily Huber, Jean-Hubert Caberg

medRxiv· August 2024

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Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants.
Corrine Smolen, Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Emily Huber, Jean-Hubert Caberg

Am J Hum Genet· December 2023

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Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variants.
Corrine Smolen, Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Emily Huber, Jean-Hubert Caberg

medRxiv· May 2023

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Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion.
Matthew Jensen, Anastasia Tyryshkina, Lucilla Pizzo, Corrine Smolen, Maitreya Das, Emily Huber

Genome Med· October 2021

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Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevis.
Lucilla Pizzo, Micaela Lasser, Tanzeen Yusuff, Matthew Jensen, Phoebe Ingraham, Emily Huber

PLoS Genet· April 2021

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NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models.
Mayanglambam Dhruba Singh, Matthew Jensen, Micaela Lasser, Emily Huber, Tanzeen Yusuff

PLoS Genet· February 2020

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Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Emily Huber, Jean-Hubert Caberg

Genet Med· April 2019

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Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster.
Janani Iyer, Mayanglambam Dhruba Singh, Matthew Jensen, Payal Patel, Lucilla Pizzo, Emily Huber

Nat Commun· June 2018

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Ellen Hudson: a transformational leader.
Emily Huber

Ky Nurse· May 2015

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