Daryl A. Scott

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

Marwan Shinawi, P. Liu, Sung Hae L. Kang et al. · Journal of Medical Genetics · 2009 · 593 citations

The Pendred syndrome gene encodes a chloride-iodide transport protein

Daryl A. Scott, Rong Wang, Trisha Kreman et al. · Nature Genetics · 1999 · 564 citations

Pendred Syndrome Gene, Disease Mechanism, Mendelian Disorder +5

Use of Exome Sequencing for Infants in Intensive Care Units

Linyan Meng, Mohan Pammi, Anirudh Saronwala et al. · JAMA Pediatrics · 2017 · 422 citations · Full text

A Pathologic Cascade Leading to Synaptic Dysfunction in  -Synuclein-Induced Neurodegeneration

Daryl A. Scott, Iustin V. Tabarean, Yong Tang et al. · Journal of Neuroscience · 2010 · 357 citations · Full text

<i>Dusp6</i>(<i>Mkp3</i>) is a negative feedback regulator of FGF-stimulated ERK signaling during mouse development

Daryl A. Scott, Ekaterina Hatch, Xiaoyan Tian et al. · Development · 2006 · 281 citations · Full text