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Dagmar Wieczorek | Researchclopedia

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Dagmar Wieczorek

Düsseldorf University Hospital ORCID

332

Works

23,288

Citations

82

h-index

229

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Genomics and Rare Diseases Genetics and Neurodevelopmental Disorders

Affiliations

Scripps Research Institute2022–2022

Hôpital Necker-Enfants Malades2017–2017

MACOM (United States)2024–2024

Karolinska University Hospital2014–2014

University of Cologne2014–2017

Top Works

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Anita Rauch,Dagmar Wieczorek,et al.

20121,063 citations

Chromatin Remodeling and Cancer

RNA modifications and cancer

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Hossein Najmabadi,Hao Hu,et al.

2011982 citations

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

Tetsuya Niihori,Yoko Aoki,et al.

2006598 citations

<scp>SARS</scp> ‐CoV‐2 targets neurons of 3D human brain organoids

Anand Ramani,Lisa Müller,et al.

2020531 citations

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

Sabine Endele,Georg Rosenberger,et al.

2010506 citations

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

Johannes G. Dauwerse,Jill Dixon,et al.

2010366 citations

De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome

Alexander Hoischen,Bregje W.M. van Bon,et al.

2011277 citations

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

Lia Abbasi‐Moheb,Sara Mertel,et al.

2012272 citations

Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation

Sabrina Giglio,Vladimiro Calvari,et al.

2002267 citations