Elliot Stolerman

5PUBLICATIONS
15CO-AUTHORS
Flight dynamicsGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Jun 01, 2023
Clinical case report: mosaic ANK3 pathogenic variant in a patient with autism spectrum disorder and neurodevelopmental delay.

Xiaolan Fang, Timothy Fee, Jessica Davis

|Apr 11, 2023
RNA analysis of intronic variants in the LAMA2 gene detected by whole genome sequencing confirms a rare dual diagnosis of incontinentia pigmenti with limb-girdle muscular dystrophy.

Camerun Washington, Elliot S Stolerman, Jessica A Cooley-Coleman

|Dec 21, 2021
De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability.

Audrey Schalk, Margot A Cousin, Nikita R Dsouza

|Jul 01, 2021
Tenorio syndrome: Description of 14 novel cases and review of the clinical and molecular features.

Jair Antonio Tenorio-Castaño, Pedro Arias, Alberto Fernández-Jaén

|May 25, 2019
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.

Elliot S Stolerman, Elizabeth Francisco, Jennifer L Stallworth

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Frequent Collaborators

1 joint publications

Raymond J Louie

1 joint publications

Antonio Federico Martínez-Monseny

1 joint publications

Camerun Washington

1 joint publications

Xiaolan Fang