Agne Liedén

TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons

Xavier Caubit, Paolo Gubellini, Joris Andrieux et al. · Nature Genetics · 2016 · 141 citations · Full text

Neurodevelopmental Disorders, Molecular Neuroscience, Neurological Disorder +14

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson et al. · Genome Medicine · 2019 · 139 citations · Full text

Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis

M.C.G. Winge, Kassahun Desalegn Bilcha, Agne Liedén et al. · British Journal of Dermatology · 2011 · 112 citations

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability

Paul R. Kasher, Katherine E. Schertz, Megan Thomas et al. · The American Journal of Human Genetics · 2016 · 73 citations · Full text

Obesity, Metabolic Syndrome, Developmental Biology +7

Loss-of-function Variants of the Filaggrin Gene are Associated with Atopic Eczema and Associated Phenotypes in Swedish Families

Elisabeth Ekelund, Agne Liedén, Jenny Link et al. · Acta Dermato Venereologica · 2008 · 68 citations · Full text

Asthma, Environmental Allergy, Severe Eczema Phenotype +17