Dagmar Wieczorek

Dagmar Wieczorek publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Dagmar Wieczorek sits on this spectrum.

Dagmar Wieczorek D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Dagmar Wieczorek sits on this spectrum.

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