Murat Günel

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Stephan Sanders, Michael T. Murtha, Abha R. Gupta et al. · Nature · 2012 · 2.1K citations

Neurodevelopmental Disorders, Syndromic Autism, Whole-exome Sequencing +9

Human Hypertension Caused by Mutations in WNK Kinases

Frederick H. Wilson, Sandra Disse-Nicodème, Keith A. Choate et al. · Science · 2001 · 1.5K citations

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

Neurodevelopmental Disorders, Williams Syndrome Region, Syndromic Autism +10

Neuroinvasion of SARS-CoV-2 in human and mouse brain

Eric Song, Ce Zhang, Benjamin Israelow et al. · The Journal of Experimental Medicine · 2020 · 1K citations · Full text

Long Covid, Neurovirology, Medicine +15

Sequence Variants in <i>SLITRK1</i> Are Associated with Tourette's Syndrome

Jesse F. Abelson, Kenneth Y. Kwan, Brian J. O’Roak et al. · Science · 2005 · 943 citations

Genetics, Molecular Genetics, Synaptic Signaling +16