Matthew Jensen

发表

NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models

S. Girirajan, L. A. Lowery, D. Rincon-Limas, 2020, PLoS genetics.

NCBP2-mediated apoptosis contributes to developmental defects of the schizophrenia-associated 3q29 deletion

S. Girirajan, L. A. Lowery, D. Rincon-Limas, 2019 .

NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and X. laevis models

S. Girirajan, L. A. Lowery, D. Rincon-Limas, 2019, bioRxiv.

Pervasive epistasis in cell proliferation pathways modulates neurodevelopmental defects of autism-associated 16p11.2 deletion

S. Girirajan, J. Badano, Qingyu Wang, 2017, bioRxiv.

A machine-learning approach for accurate detection of copy number variants from exome sequencing

S. Girirajan, Matthew Jensen, Vijay Kumar Pounraja, 2018, bioRxiv.

Functional assessment of the “two-hit” model for neurodevelopmental defects in Drosophila and X. laevis

S. Girirajan, L. A. Lowery, Arjun Krishnan, 2020, bioRxiv.

Artificial gravity partially protects space-induced neurological deficits in Drosophila melanogaster.

S. Girirajan, S. Costes, A. Paul, 2022, Cell reports.

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

J. Rosenfeld, M. Fichera, C. Romano, 2018, Genetics in Medicine.

Rare variants in the genetic background modulate the expressivity of neurodevelopmental disorders

J. Rosenfeld, M. Fichera, C. Romano, 2018, bioRxiv.

Drosophila models of pathogenic copy-number variant genes show global and non-neuronal defects during development

S. Girirajan, Z. Lai, Matthew Jensen, 2019, bioRxiv.

Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders

F. Hormozdiari, Osnat Penn, F. Hormozdiari, 2019, Genome Medicine.

Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity

Santhosh Girirajan, Matthew Jensen, Naomi S Altman, 2016, Scientific Reports.

A machine-learning approach for accurate detection of copy-number variants from exome sequencing

Vijay Kumar, Santhosh Girirajan, Gopal Jayakar, 2018 .

Gene discoveries in autism are biased towards comorbidity with intellectual disability

S. Girirajan, Matthew Jensen, Corrine E Smolen, 2019, Journal of Medical Genetics.

An interaction-based model for neuropsychiatric features of copy-number variants

S. Girirajan, Matthew Jensen, 2018, bioRxiv.

Mapping a shared genetic basis for neurodevelopmental disorders

S. Girirajan, Matthew Jensen, 2017, Genome Medicine.

The chromatin remodeler ISWI acts during Drosophila development to regulate adult sleep

S. Girirajan, M. Deardorff, Matthew Jensen, 2020, Science Advances.

Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion

S. Girirajan, Arjun Krishnan, Matthew Jensen, 2021, Genome Medicine.

Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster

S. Girirajan, J. Badano, Qingyu Wang, 2018, Nature Communications.

A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome.

S. Girirajan, R. Kooy, F. Tassone, 2017, European journal of medical genetics.

Transcriptome Analyses of Heart and Liver Reveal Novel Pathways for Regulating Songbird Migration

I. Albert, C. Praul, A. Sebastian, 2019, Scientific Reports.