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2. Webcam technology on neonatal wards—examining the objective and subjective workload of nurses: a combined observational and survey study

3. Quality of health care for patients with coronary heart disease and comorbid mental disorders: a prospective cohort study

4. Novel genes and sex differences in COVID-19 severity

5. Mapping the human genetic architecture of COVID-19

7. Existence and perceived application of pain management protocols in German neonatal intensive care units

8. Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene

9. Do trained nurses feel more psychologically safe?—Results from a multi‐level modelling approach

10. Personalised depression forecasting using mobile sensor data and ecological momentary assessment

11. Adversarial joint training with self-attention mechanism for robust end-to-end speech recognition

12. The effects of webcams on German neonatal intensive care units – study protocol of a randomised crossover trial (Neo-CamCare)

13. The Wiretap Channel for Capacitive PUF-Based Security Enclosures

14. Towards Constructing HMM Structure for Speech Recognition With Deep Neural Fenonic Baseform Growing

15. Catholic Ownership, Physician Leadership and Operational Strategies: Evidence from German Hospitals

16. What matters most and for whom? A cross-sectional study exploring goals of health professionals in German neonatal intensive care units

17. Improving regional care in the last year of life by setting up a pragmatic evidence-based Plan–Do–Study–Act cycle: results from a cross-sectional survey

18. Patients’ perspectives of facilitators and barriers to patient-centred care: insights from qualitative patient interviews

19. Exploring the differential impact of individual and organizational factors on organizational commitment of physicians and nurses

20. Lightweight End-to-End Speech Enhancement Generative Adversarial Network Using Sinc Convolutions

21. Low-cost limit of classical communication with restricted quantum measurements

22. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

23. Stratified analyses refine association between TLR7 rare variants and severe COVID-19.

24. Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation.

25. TMPRSS2 isoform 1 downregulation by G-quadruplex stabilization induces SARS-CoV-2 replication arrest.

26. Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation.

27. Predicting the pathogenicity of missense variants using features derived from AlphaFold2.

28. Analysis of candidate genes for cleft lip ± cleft palate using murine single-cell expression data.

29. Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.

30. Systematic assays and resources for the functional annotation of non-coding variants.

31. Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations.

33. Detailed stratified GWAS analysis for severe COVID-19 in four European populations.

34. Novel genes and sex differences in COVID-19 severity.

35. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.

36. Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

37. Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding.

38. Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes.

39. Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation.

41. MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration.

42. Genetic Predisposition and the Variable Course of Infectious Diseases.

43. Allele-specific transcription factor binding in a cellular model of orofacial clefting.

44. First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3 , FOXF1 / FOXC2 / FOXL1 , and HNF1B .

45. Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.

46. Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality.

47. LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding.

48. Iron Deficiency Caused by Intestinal Iron Loss-Novel Candidate Genes for Severe Anemia.

49. Extending the allelic spectrum at noncoding risk loci of orofacial clefting.

50. TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19.

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