Nathan Kopp

2PUBLICATIONS
2CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (2)

|Dec 28, 2020
Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization.

Nathan Kopp, Ina Amarillo, Julian Martinez-Agosto

|Jul 16, 2018
Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.

Nathan D Kopp, Phoebe C R Parrish, Michael Lugo

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Frequent Collaborators

1 joint publications

Julian Martinez-Agosto

1 joint publications

Fabiola Quintero-Rivera