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98 results on '"Vaudel, Marc"'

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1. Rare copy number variation in autoimmune Addison’s disease

3. Author Correction: Characterization of the genetic architecture of infant and early childhood body mass index

6. Genetic effects on the timing of parturition and links to fetal birth weight

11. Finding haplotypic signatures in proteins

12. Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism

13. Identifying Protein Haplotypes by Mass Spectrometry

17. Characterization of the genetic architecture of infant and early childhood body mass index

26. Spatial Environment Affects HNF4A Mutation-Specific Proteome Signatures and Cellular Morphology in hiPSC-Derived β-Like Cells

27. Spatial Environment Affects HNF4A Mutation-Specific Proteome Signatures and Cellular Morphology in hiPSC-Derived β-Like Cells

28. Spatial Environment Affects HNF4A Mutation-Specific Proteome Signatures and Cellular Morphology in hiPSC-Derived β-Like Cells

31. A proteomics sample metadata representation for multiomics integration and big data analysis

33. A proteomics sample metadata representation for multiomics integration, and big data analysis

34. Characterization of the genetic architecture of BMI in infancy and early childhood reveals age-specific effects and implicates pathways involved in Mendelian obesity

36. iTRAQ Data Interpretation

37. Leptin Receptor Signaling Regulates Protein Synthesis Pathways and Neuronal Differentiation in Pluripotent Stem Cells

40. Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents

41. Autozygosity mapping and time-to-spontaneous delivery in Norwegian parent-offspring trios

42. Proteome and Phosphoproteome Changes Associated with Prognosis in Acute Myeloid Leukemia

43. Dynamic proteome profiling of human pluripotent stem cell-derived pancreatic progenitors

45. Proteome and phosphoproteome changes associated with prognosis in acute myeloid leukemia

46. Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth

50. Roadmap for a precision-medicine initiative in the Nordic region

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