Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

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Recent Activity

Detailed stratified GWAS analysis for severe COVID-19 in four European populations.
28 November 2022 by Petra Bacher in 'Human molecular genetics'
Detailed stratified GWAS analysis for severe COVID-19 in four European populations.
28 November 2022 by Kerstin Ludwig in 'Human molecular genetics'
Detailed stratified GWAS analysis for severe COVID-19 in four European populations.
28 November 2022 by Ingo Kurth in 'Human molecular genetics'
Detailed stratified GWAS analysis for severe COVID-19 in four European populations.
28 November 2022 by Per Hoffmann in 'Human molecular genetics'
Detailed stratified GWAS analysis for severe COVID-19 in four European populations.
28 November 2022 by Georg Hemmrich-Stanisak in 'Human molecular genetics'
DYT6 mutated THAP1 is a cell type dependent regulator of the SP1 family.
21 November 2022 by Nicolas Casadei in 'Brain : a journal of neurology'
Novel genes and sex differences in COVID-19 severity.
10 November 2022 by Kerstin Ludwig in 'Human molecular genetics'
Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome.
21 Oktober 2022 by Dagmar Wieczorek in 'Brain : a journal of neurology'
Novel biomarkers of inflammation, kidney function and chronic kidney disease in the general population.
22 September 2022 by Christian Herder in 'Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association'
Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysis.
22 September 2022 by Bruno Huettel in 'Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association'
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
14 September 2022 by Dagmar Wieczorek in 'Brain : a journal of neurology'
Mutations in TAF8 cause a neurodegenerative disorder.
14 September 2022 by Holger Thiele in 'Brain : a journal of neurology'
Intratumoral heterogeneity of MYC drives medulloblastoma metastasis and angiogenesis.
1 September 2022 by Arndt Borkhardt in 'Neuro-oncology'
The discovAIR project: a roadmap towards the Human Lung Cell Atlas.
18 August 2022 by Joachim Schultze in 'The European respiratory journal'
The discovAIR project: a roadmap towards the Human Lung Cell Atlas.
18 August 2022 by Elena De Domenico in 'The European respiratory journal'
Induction of senescence upon loss of the Ash2l core subunit of H3K4 methyltransferase complexes.
12 August 2022 by Ivan Costa in 'Nucleic acids research'
Detailed Transcriptional Landscape of Peripheral Blood Points to Increased Neutrophil Activation in Treatment-Naïve Inflammatory Bowel Disease.
4 August 2022 by Georg Hemmrich-Stanisak in 'Journal of Crohn's & colitis'
Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Patients with Breast Cancer.
2 August 2022 by Tanja Fehm in 'Clinical cancer research : an official journal of the American Association for Cancer Research'
Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach - CORRIGENDUM.
1 August 2022 by Stefan Herms in 'The British journal of psychiatry : the journal of mental science'
Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach - CORRIGENDUM.
1 August 2022 by Per Hoffmann in 'The British journal of psychiatry : the journal of mental science'
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