Julia Wickert

Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy

Steffen Syrbe, Frederike L. Harms, Elena Parrini et al. · Brain · 2017 · 96 citations · Full text

Neurogenomics, Brain Development, Neurological Disorder +23

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?

Moneef Shoukier, Nina Klein, Bernd Auber et al. · Clinical Genetics · 2012 · 67 citations · Full text

Array Cgh, Genetics, Genetic Epidemiology +17

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

Aurélie Méneret, Christel Depienne, Florence Riant et al. · PubMed · 2014 · 62 citations

A 16q12 microdeletion in a boy with severe psychomotor delay, craniofacial dysmorphism, brain and limb malformations, and a heart defect

Moneef Shoukier, Julia Wickert, Julia Schröder et al. · American Journal of Medical Genetics Part A · 2011 · 42 citations

Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients

Katta M. Girisha, Abdul Mueed Bidchol, Luitgard Graul‐Neumann et al. · BMC Medical Genetics · 2016 · 30 citations · Full text