Dagmar Wieczorek - Concepedia

Author

Dagmar Wieczorek

Also Known As

Andreas Walker, Anna C. Aschenbrenner, Crepel, An, D Wieczorek, D. Wieczorek, DAGMAR WIECZOREK, Dagmar Wieczorek, Guntram Borck, Iascone, Maria, Jörn Walter

334

Publications

23K

Citations

H-Index

211

Concepts

All Affiliations

Essen University Hospital Heinrich Heine University Düsseldorf University of Duisburg-Essen Düsseldorf University Hospital Institut für Medizinische Informatik, Biometrie und Epidemiologie

About

Dagmar Wieczorek is an author at Essen University Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	60	113	13.9K
2	Engineering	7	7	327
3	Education	2	2	81
4	Health Sciences	2	2	29
5	Language Studies	1	1	14

Dagmar Wieczorek

201

Publications

20.2K

Citations

H-Index

Page 1

	Year	Citations
Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment Jonas Schulte-Schrepping, Nico Reusch, Daniela Paclik, Cell Covid-19 PandemicHematologyPathologyCovid-19 EpidemiologySevere Covid-19 Is	2020	1.6K
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, The Lancet Genetic MutationsMendelian DisorderGenetic DisorderGeneticsFragile X Spectrum	2012	1.1K
Deep sequencing reveals 50 novel genes for recessive cognitive disorders Hossein Najmabadi, Hao Hu, Masoud Garshasbi, Nature Neurodegenerative DiseasesRecessive Cognitive DisordersGenetic DisorderGeneticsNeuroscience	2011	975
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome Tetsuya Niihori, Yoko Aoki, Yoko Narumi, Nature Genetics Mendelian DisorderGenetic DisorderGermline KrasGeneticsDermatology	2006	593
<scp>SARS</scp> ‐CoV‐2 targets neurons of 3D human brain organoids Anand Ramani, Lisa Müller, Philipp Niklas Ostermann, The EMBO Journal	2020	526
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes Sabine Endele, Georg Rosenberger, Kirsten Geider, Nature Genetics Developmental BiologyMolecular NeuroscienceBrain DevelopmentNeuroanatomyGenetics	2010	502
Longitudinal Multi-omics Analyses Identify Responses of Megakaryocytes, Erythroid Cells, and Plasmablasts as Hallmarks of Severe COVID-19 Joana P. Bernardes, Neha Mishra, Florian Tran, Immunity Erythroid CellsLong CovidImmunologySevere Covid-19Blood Cell	2020	400
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome Johannes G. Dauwerse, Jill Dixon, Saskia Seland, Nature Genetics Mendelian DisorderTreacher CollinsRna PolymerasesGenetic DisorderNatural Sciences	2010	364
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome Alexander Hoischen, Bregje W.M. van Bon, Benjamín Rodríguez‐Santiago, Nature Genetics Somatic VariantAutoimmune DiseaseMendelian DisorderGenetic DisorderGenetics	2011	277
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability Lia Abbasi‐Moheb, Sara Mertel, Melanie Gonsior, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsFragile X SpectrumDisease Gene Identification	2012	269

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