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52. Polygenic risk heterogeneity among focal epilepsies

53. Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

54. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

55. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

59. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

60. Analysis of shared heritability in common disorders of the brain

62. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

63. Diagnostic implications of genetic copy number variation in epilepsy plus

64. Identification and quantification of oligogenic loss-of-function disorders

65. Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome:a case-control study

66. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

67. Variant Score Ranker—a web application for intuitive missense variant prioritization

69. Clinical sequencing yield in epilepsy, autism spectrum disorder, and intellectual disability: A systematic review and meta‐analysis.

70. Carbamazepine- and oxcarbazepine-induced hyponatremia in people with epilepsy

71. Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy

72. Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study

73. Genetic variants in the bipolar disorder risk locus SYNE1that affect CPG2 expression and protein function

74. Pitfalls in genetic testing : the story of missed SCN1A mutations

78. Molekulargenetische Exploration der idiopathisch generalisierten Epilepsien

79. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

80. 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

81. Association of ultra-rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study

82. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

83. Diagnostic implications of genetic copy number variation in epilepsy plus

84. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

85. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

86. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1,2q22.3 and 17q21.32

87. Genome-wide association study of copy number variations in Parkinson's disease.

88. The genomic landscape across 474 surgically accessible epileptogenic human brain lesions.

89. A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies.

90. Analysis of shared heritability in common disorders of the brain.

91. Pitfalls in genetic testing: the story of missed SCN1A mutations.

92. Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests.

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