Dagmar Wieczorek

Research.com Recognitions

• 2024 - Research.com Genetics in Germany Leader Award
• 2023 - Research.com Genetics in Germany Leader Award

Overview

Best Publications

• Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment.

  Jonas Schulte-Schrepping;Nico Reusch;Daniela Paclik;Kevin Baßler

  1496
  Citations

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

  Anita Rauch;Dagmar Wieczorek;Elisabeth Graf;Thomas Wieland

  1163
  Citations

• Deep sequencing reveals 50 novel genes for recessive cognitive disorders

  Hossein Najmabadi;Hao Hu;Masoud Garshasbi;Tomasz Zemojtel

  1052
  Citations

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

  Tetsuya Niihori;Yoko Aoki;Yoko Narumi;Giovanni Neri

  671
  Citations

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

  Sabine Endele;Georg Rosenberger;Kirsten Geider;Bernt Popp

  572
  Citations

• SARS-CoV-2 targets neurons of 3D human brain organoids.

  Anand Ramani;Lisa Müller;Philipp Niklas Ostermann;Elke Gabriel

  508
  Citations

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

  Johannes G. Dauwerse;Jill Dixon;Saskia Seland;Claudia A L Ruivenkamp

  415
  Citations

• 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;Thomas Bahmer

  377
  Citations

• Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

  Thilo Dörk;Bernd Dworniczak;Christa Aulehla-Scholz;Dagmar Wieczorek

  306
  Citations

• De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome

  Alexander Hoischen;Bregje W M van Bon;Benjamín Rodríguez-Santiago;Benjamín Rodríguez-Santiago;Christian Gilissen

  305
  Citations

• Mutations in NSUN2 cause autosomal-recessive intellectual disability

  Lia Abbasi-Moheb;Sara Mertel;Melanie Gonsior;Leyla Nouri-Vahid

  288
  Citations

• Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability

  Juliane Hoyer;Arif B. Ekici;Sabine Endele;Bernt Popp

  287
  Citations

• Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I

  Huiling He;Sandya Liyanarachchi;Keiko Akagi;Rebecca Nagy

  267
  Citations

• Oculo-auriculo-vertebral spectrum (OAVS) : clinical evaluation and severity scoring of 53 patients and proposal for a new classification

  Christiane Tasse;Stefan Böhringer;Sven Fischer;Hermann-Josef Lüdecke

  265
  Citations

• CEP152 is a genome maintenance protein disrupted in Seckel syndrome

  Ersan Kalay;Gökhan Yigit;Yakup Aslan;Karen E Brown

  263
  Citations

• Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome

  Jeroen K.J. Van Houdt;Beata Anna Nowakowska;Sérgio B. Sousa;Sérgio B. Sousa;Barbera D.C. Van Schaik

  255
  Citations

• The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

  Fanny Kortüm;Soma Das;Max Flindt;Deborah J Morris-Rosendahl

  246
  Citations

• Diagnostic approach to microcephaly in childhood: a two-center study and review of the literature.

  Maja von der Hagen;Mark Pivarcsi;Juliane Liebe;Horst von Bernuth

  243
  Citations

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

  Sabrina Giglio;Vladimiro Calvari;Giuliana Gregato;Giorgio Gimelli

  229
  Citations

• A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling.

  Dagmar Wieczorek;Nina Bögershausen;Filippo Beleggia;Sabine Steiner-Haldenstätt

  229
  Citations