Evangeline Kurtz-Nelson

6PUBLICATIONS
48CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Memory and attentionDevelopmental genetics (incl. sex determination)Neurology and neuromuscular diseases
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Publications (6)

|Jan 12, 2026
Whole exome sequencing facilitates early neurodevelopmental diagnosis in an outpatient clinic.

Casaundra Gutowski, Molly Lombard, Evangeline Kurtz-Nelson

|Jul 31, 2024
Visual and auditory attention in individuals with DYRK1A and SCN2A disruptive variants.

Caitlin M Hudac, Kelsey Dommer, Monique Mahony

|Sep 07, 2023
Rhythmic attentional sampling in autism.

Xiaoxu Fan, Tamar Kolodny, Kristin M Woodard

|Jul 27, 2023
Characterizing the autism spectrum phenotype in DYRK1A-related syndrome.

Evangeline C Kurtz-Nelson, Hannah M Rea, Aiva C Petriceks

|Aug 17, 2022
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders.

Xiangbin Jia, Shujie Zhang, Senwei Tan

|Jun 05, 2021
The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects.

Mireia Coll-Tané, Naihua N Gong, Samuel J Belfer

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Frequent Collaborators

3 joint publications

Evan E Eichler

2 joint publications

Emily Neuhaus

2 joint publications

Caitlin M Hudac

1 joint publications

Mireia Coll-Tané