106 results on '"Vigeland, Magnus Dehli"'
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2. Correlation between gene expression and MRI STIR signals in patients with chronic low back pain and Modic changes indicates immune involvement
3. Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis
4. Pairwise relatedness testing in the context of inbreeding: expectation and variance of the likelihood ratio
5. Relatedness coefficients in pedigrees with inbred founders
6. Probabilities on Pedigrees
7. Segregation Analysis for Variant Interpretation
8. Realised Relatedness
9. Pedigrees and Marker Data
10. Inference of Pairwise Relatedness
11. Kinship Testing
12. Pedigree Reconstruction
13. Linkage Analysis
14. Coefficients of Relatedness
15. Prerequisites
16. Tropical complete intersection curves
17. Tropical Lines on Cubic Surfaces
18. Smooth tropical surfaces with infinitely many tropical lines
19. The group law on a tropical elliptic curve
20. Investigation of serious crimes using DNA from dust and air
21. Evaluating the statistical power of DNA-based identification, exemplified by ‘The missing grandchildren of Argentina’
22. Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2
23. Two-locus identity coefficients in pedigrees
24. Mixtures with relatives: A pedigree perspective
25. A general approach to power calculation for relationship testing
26. Long-Term Use of Amoxicillin Is Associated with Changes in Gene Expression and DNA Methylation in Patients with Low Back Pain and Modic Changes.
27. Mixtures with relatives and linked markers
28. Tropical Lines on Cubic Surfaces
29. Referee report. For: skater: an R package for SNP-based kinship analysis, testing, and evaluation [version 1; peer review: 1 approved, 1 approved with reservations]
30. THE GROUP LAW ON A TROPICAL ELLIPTIC CURVE
31. Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5
32. Whole‐exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways
33. Two-locus identity coefficients in pedigrees.
34. Smooth tropical surfaces with infinitely many tropical lines
35. Elevated hydroxycholesterols in Norwegian patients with hereditary spastic paraplegia SPG5
36. pedsuite: Easy Installation of the 'ped suite' Packages for Pedigree Analysis
37. A novel somatic mutation inGNB2provides new insights to the pathogenesis of Sturge–Weber syndrome
38. paramlink2: Parametric Linkage Analysis
39. segregatr: Segregation Analysis for Variant Interpretation
40. dvir: Disaster Victim Identification
41. Joint DNA-based Disaster Victim Identification
42. pedbuildr: Pedigree Reconstruction
43. Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis
44. Pairwise relatedness testing in the context of inbreeding: expectation and variance of the likelihood ratio
45. ibdsim2: Simulation of Chromosomal Regions Shared by Family Members
46. forrel: Forensic Pedigree Analysis and Relatedness Inference
47. novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome.
48. pedmut: Mutation Models for Pedigree Likelihood Computations
49. Pathogenic variants inKCTD7perturb neuronal K+fluxes and glutamine transport
50. Mixtures with relatives and linked markers
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