Jennifer G. Mulle

Emory University School of Medicine

United States

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Articles (17)

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2024

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2024

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2021

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2021

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2020

Collaborators (10)

Ryan Purcell

Assistant Professor

Emory University School of Medicine

UNITED STATES

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Gary Bassell

Charles Howard Candler Professor and Chair, Department of Cell Biology

Emory University School of Medicine

UNITED STATES

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Ewa Mojs

POLAND

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Bonnie L. Firestein

UNITED STATES

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Adrianna Mostowska

Poznan University of Medical Sciences

POLAND

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Justyna Dąbrowska

Poznan University of Medical Sciences

POLAND

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Victor Faundez

Professor and Vice Chair

Emory University

UNITED STATES

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Stormi White

Assistant Professor

Emory University

UNITED STATES

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Ploski R

POLAND

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Rossana Sanchez Russo

Assistant Professor of Human Genetics

Emory University

UNITED STATES

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Jennifer G. Mulle

Research Interests

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Articles (17)

Adaptive behaviour deficits in individuals with 3q29 deletion syndrome

Behavioral Phenotypes and Comorbidity in 3q29 Deletion Syndrome: Results from the 3q29 Registry

Psychosis spectrum symptoms among individuals with schizophrenia-associated copy number variants and evidence of cerebellar correlates of symptom severity

Scaled and Efficient Derivation of Loss of Function Alleles in Risk Genes for Neurodevelopmental and Psychiatric Disorders in Human iPSC

Structural deviations of the posterior fossa and the cerebellum and their cognitive links in a neurodevelopmental deletion syndrome

Visual-Motor Integration Deficits in 3q29 Deletion Syndrome

Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion

Identification of a new familial case of 3q29 deletion syndrome associated with cleft lip and palate via whole‐exome sequencing

A distinct cognitive profile in individuals with 3q29 deletion syndrome

Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion

Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion

High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing

Identification of a new familial case of 3q29 deletion syndrome associated with cleft lip and palate via whole-exome sequencing

Symptoms of Pediatric Feeding Disorders Among Individuals with 3q29 Deletion Syndrome: A Case-Control Study

Craniofacial features of 3q29 deletion syndrome: Application of next‐generation phenotyping technology

Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders

New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry

Collaborators (10)

Ryan Purcell

Gary Bassell

Ewa Mojs

Bonnie L. Firestein

Adrianna Mostowska

Justyna Dąbrowska

Victor Faundez

Stormi White

Ploski R

Rossana Sanchez Russo

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