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51. Common variants associated with plasma triglycerides and risk for coronary artery disease

52. Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene

53. Sh3tc2 deficiency affects neuregulin-1/ErbB signaling

54. Discovery and refinement of loci associated with lipid levels

55. FTO genotype is associated with phenotypic variability of body mass index

56. [Bio-informatic and personalized medicine: Switzerland is pioneer]

57. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

58. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

59. KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

60. Genetic testing in patients with obesity

61. A Multi-SNP Locus-Association Method Reveals a Substantial Fraction of the Missing Heritability

62. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

63. Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma

64. Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability

65. Methods for testing association between uncertain genotypes and quantitative traits

66. Genome-wide association study identifies two loci strongly affecting transferrin glycosylation

67. 4. Coordinating variant interpretation knowledgebases improves clinical interpretation of genomic variants in cancers

68. Hundreds of variants clustered in genomic loci and biological pathways affect human height

69. Fine mapping ofAHI1as a schizophrenia susceptibility gene: from association to evolutionary evidence

70. Familial occurrence of an association of multiple intestinal atresia and choanal atresia: A new syndrome?

71. Mutation screening of the glutamate cysteine ligase modifier (GCLM) gene in patients with schizophrenia

72. Genome-wide association study identifies eight loci associated with blood pressure

73. The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt/β-catenin pathway

74. Mapping of bovine prolactin and rhodopsin genes in hybrid somatic cells

75. The bovine gene map

76. Restriction fragment length polymorphisms in dairy and beef cattle at the growth hormone and prolactin loci*

77. Limb-Girdle Muscular Dystrophy Type 2A Can Result from Accelerated Autoproteolytic Inactivation of Calpain 3

78. Calpain 3, the 'gatekeeper' of proper sarcomere assembly, turnover and maintenance

79. Calcium phosphate transfection generates mammalian recombinant cell lines with higher specific productivity than polyfection

80. Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular origin

81. Automated four-color interphase fluorescence in situ hybridization approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid acute lymphoblastic leukemia

82. Subtelomeric 6p deletion: Clinical and array-CGH characterization in two patients

83. A modular approach for integrative analysis of large-scale gene-expression and drug-response data

84. CNVs and genetic medicine (excitement and consequences of a rediscovery)

85. Computational Problems in Perfect Phylogeny Haplotyping: Typing without Calling the Allele

86. Promoter polymorphisms and allelic imbalance in ABCB1 expression

87. Cell-permeable peptides induce dose- and length-dependent cytotoxic effects

88. Genome-wide prediction of matrix attachment regions that increase gene expression in mammalian cells

89. Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markers

90. Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

92. Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)

93. SREBP-1c expression in Schwann cells is affected by diabetes and nutritional status

94. Recommendations for locus-specific databases and their curation

95. Copy number variations and cognitive phenotypes in unselected populations

96. A single epidermal stem cell strategy for safe ex vivo gene therapy

97. Genome-wide Association Studies Identify Genetic Loci Associated with Albuminuria in Diabetes

98. A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology

99. When to refer for neurogenetic assessment

100. The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males

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