2023 - Research.com Genetics in Germany Leader Award
Her primary areas of investigation include Genetics, Mutation, Missense mutation, Gene and Genetic heterogeneity. All of her Genetics and Exome sequencing, Intellectual disability, Candidate gene, Phenotype and Haploinsufficiency investigations are sub-components of the entire Genetics study. Dagmar Wieczorek studied Mutation and Molecular biology that intersect with Mutant, GSK-3 and Megalencephaly.
Her Missense mutation study combines topics in areas such as Chromatin remodeling, Noonan syndrome, Frameshift mutation and PTPN11. Dagmar Wieczorek works mostly in the field of Gene, limiting it down to topics relating to Consanguinity and, in certain cases, Candidate Disease Gene, Methylenetetrahydrofolate reductase, Sequence analysis, Disease gene identification and Deep sequencing. Her research in Genetic heterogeneity intersects with topics in RNA, Family history and Bioinformatics.
The scientist’s investigation covers issues in Genetics, Intellectual disability, Missense mutation, Mutation and Phenotype. Her work is connected to Gene, Exome sequencing, Microcephaly, Frameshift mutation and Haploinsufficiency, as a part of Genetics. Dagmar Wieczorek combines subjects such as Allele and Craniofacial with her study of Microcephaly.
In Intellectual disability, Dagmar Wieczorek works on issues like Medical genetics, which are connected to Human genetics. In her study, Short stature is inextricably linked to Genetic heterogeneity, which falls within the broad field of Missense mutation. Her studies in Phenotype integrate themes in fields like Neurodevelopmental disorder and Genotype.
Her main research concerns Genetics, Phenotype, Missense mutation, Intellectual disability and Neuroscience. Her Genetics research is multidisciplinary, relying on both Short stature and Developmental disorder. Her Phenotype research is multidisciplinary, incorporating elements of Degeneration, Pons, Disease and Hypoplasia.
The Missense mutation study combines topics in areas such as Autism spectrum disorder, Muscular hypotonia, Pediatrics and Frameshift mutation. Her Frameshift mutation study deals with Autism intersecting with Genotype. Her biological study spans a wide range of topics, including Exome sequencing, Haploinsufficiency and Macrocephaly.
Neuroscience, Soma, Human brain, Organoid and Central nervous system are her primary areas of study. The study incorporates disciplines such as Stem cell and Neural stem cell in addition to Neuroscience. Her Neural stem cell research integrates issues from Inhibitory postsynaptic potential, GABAergic, Glutamatergic and Biological neural network.
Her Soma research incorporates a variety of disciplines, including Hyperphosphorylation and Severe acute respiratory syndrome coronavirus 2. Her study ties her expertise on Neurodegeneration together with the subject of Neurotropic virus. Her Neurodegeneration study is focused on Internal medicine in general.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch;Dagmar Wieczorek;Elisabeth Graf;Thomas Wieland.
The Lancet (2012)
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
Hossein Najmabadi;Hao Hu;Masoud Garshasbi;Tomasz Zemojtel.
Nature (2011)
Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment.
Jonas Schulte-Schrepping;Nico Reusch;Daniela Paclik;Kevin Baßler.
Cell (2020)
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome
Tetsuya Niihori;Yoko Aoki;Yoko Narumi;Giovanni Neri.
Nature Genetics (2006)
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
Sabine Endele;Georg Rosenberger;Kirsten Geider;Bernt Popp.
Nature Genetics (2010)
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.
Nature Genetics (2011)
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
Thilo Dörk;Bernd Dworniczak;Christa Aulehla-Scholz;Dagmar Wieczorek.
Human Genetics (1997)
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.
Nature Genetics (2011)
CEP152 is a genome maintenance protein disrupted in Seckel syndrome
Ersan Kalay;Gökhan Yigit;Yakup Aslan;Karen E Brown.
Nature Genetics (2011)
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.
American Journal of Human Genetics (2012)
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