Ingrid Bader

Genetics of intellectual disability in consanguineous families

Hao Hu, Kimia Kahrizi, Luciana Musante et al. · Molecular Psychiatry · 2018 · 206 citations

Intellectual Impairment, Complex Trait Genetics, Genetic Disorder +5

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Anne Gregor, Beate Albrecht, Ingrid Bader et al. · BMC Medical Genetics · 2011 · 121 citations · Full text

<i>CAD</i>mutations and uridine-responsive epileptic encephalopathy

Johannes Koch, Johannes A. Mayr, Bader Alhaddad et al. · Brain · 2016 · 121 citations · Full text

Pyrimidine Biosynthesis, Uridine-responsive Epileptic Encephalopathy, Genetics +18

X-linked Retinitis Pigmentosa:<i>RPGR</i>Mutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15

Ingrid Bader, Oliver Brandau, Helene Achatz et al. · Investigative Ophthalmology & Visual Science · 2003 · 116 citations

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok, Justine Rousseau, Joanna Twist et al. · Nature Communications · 2018 · 116 citations · Full text

Brain Development, Genetics, Molecular Biology +25