Eric Morrow

Brown University, Providence, RI 
"Eric Morrow"
Mean distance: 14.27 (cluster 32)
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Kavanaugh BC, Schremp CA, Jones RN, et al. (2021) Moderators of Age of Diagnosis in > 20,000 Females with Autism in Two Large US Studies. Journal of Autism and Developmental Disorders
Ma L, Prada AM, Schmidt M, et al. (2021) Generation of pathogenic TPP1 mutations in human stem cells as a model for neuronal ceroid lipofuscinosis type 2 disease. Stem Cell Research. 53: 102323
Lizarraga SB, Ma L, Maguire AM, et al. (2021) Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13
Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, et al. (2020) Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045
Moreno-De-Luca D, Kavanaugh BC, Best CR, et al. (2020) Clinical Genetic Testing in Autism Spectrum Disorder in a Large Community-Based Population Sample. Jama Psychiatry
McCormick CEB, Kavanaugh BC, Sipsock D, et al. (2020) Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study. Autism Research : Official Journal of the International Society For Autism Research
Ouyang Q, Joesch-Cohen L, Mishra S, et al. (2019) Functional Assessment of the Mouse Homologue of the Human Ala-9-Ser NHE6 Variant. Eneuro
Ouyang Q, Kavanaugh BC, Joesch-Cohen L, et al. (2019) GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. Human Genetics
Kavanaugh BC, Warren EB, Baytas O, et al. (2019) Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification. American Journal of Medical Genetics. Part A
Warren EB, Morrow EM. (2019) Mitochondrial Function in 22q11 Deletion Syndrome. Neuron. 102: 1089-1091
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