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Your search keyword '"Landers, John E."' showing total 431 results

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51. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

52. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

53. Social Support in Marriage.

54. Reduced Expression of the Kinesin-Associated Protein 3 (KIFAP3) Gene Increases Survival in Sporadic Amyotrophic Lateral Sclerosis

55. Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

56. TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations

60. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

61. Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis

62. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

63. The Effect of SMN Gene Dosage on ALS Risk and Disease Severity

64. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

65. The effect of SMN gene dosage on ALS risk and disease severity

66. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

68. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome-wide meta-analysis

69. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories

70. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

71. Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS

72. Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia

73. ATXN2 intermediate expansions in amyotrophic lateral sclerosis.

74. Role of Lysosomal Gene Variants in Modulating GBA‐Associated Parkinson's Disease Risk.

75. The distinct genetic pattern of ALS in Turkey and novel mutations

76. Novel mutations support a role for Profilin 1 in the pathogenesis of ALS

77. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

78. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

81. Angiogenin Variants in Parkinson Disease and Amyotrophic Lateral Sclerosis

82. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

83. A large genome scan for rare CNVs in amyotrophic lateral sclerosis

84. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

87. Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort

88. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

89. Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort

90. Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort

91. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

96. Rare variants in MYH15 modify amyotrophic lateral sclerosis risk

97. Quantitative proteomics identifies proteins that resist translational repression and become dysregulated in ALS-FUS

98. Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis

99. Mutations in the Sphingolipid Pathway Gene SPTLC1 are a Cause of Amyotrophic Lateral Sclerosis

100. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

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