Genetic basis of neurodevelopmental disorders in 103 Jordanian families
Tawfiq Froukh(Philadelphia University), Rebecca Buchert(Institute of Human Genetics), Beate Kootz(University of Tübingen), Sana' A. S. Al Hait(Jordan Hospital), Moath Hamadallah(The Farah Hospital), Ayman J. Alfrook(Jordan Hospital), Julia Sommerfeld(University of Tübingen), Philipp Alexander Koch(University of Tübingen), Anis Al‐Nazer(Philadelphia University), Lucia Laugwitz(University Children's Hospital Tübingen), Aya Baraghiti(Philadelphia University), Angelika Rieß(University of Tübingen), Johannes Hanselmann(University of Tübingen), Wael Al‐Ameri(Jordan Hospital), Olaf Rieß(University of Tübingen), Tala Issa(Philadelphia University), Rami Abou Jamra(Leipzig University), Omar Nafie(Mutah University), Marc Sturm(University of Tübingen), Peter Bauer(Centogene (Germany)), Linda Sofan(Philadelphia University), Tobias B. Haack(Technical University of Munich)
Cited by 30
Related Papers
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
Mortality after surgery in Europe: a 7 day cohort study
|The Lancet|2012|1.4k
14-3-3 proteins in the nervous system
|Nature reviews. Neuroscience|2003|625
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease
|Human Molecular Genetics|2005|566
<i>SNCA</i> variants are associated with increased risk for multiple system atrophy
|Annals of Neurology|2009|283