Patrícia B. S. Celestino-Soper

Analysis of shared heritability in common disorders of the brain

Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane et al. · Science · 2018 · 2K citations · Full text

Life Sciences, Genetics, Psychiatry +17

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus et al. · Neuron · 2011 · 1.3K citations · Full text

Medicine, Genetics, Molecular Genetics +17

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Patrícia B. S. Celestino-Soper, Sara Violante, Emily L. Crawford et al. · Proceedings of the National Academy of Sciences · 2012 · 142 citations

Life Sciences, Genetics, Molecular Genetics +13

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

Patrícia B. S. Celestino-Soper, Chad A. Shaw, Stephan Sanders et al. · Human Molecular Genetics · 2011 · 121 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders

Patrícia B. S. Celestino-Soper, Cindy Skinner, Richard J. Schroer et al. · Molecular Cytogenetics · 2012 · 51 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17