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51. Somatic mutations of esophageal adenocarcinoma: a comparison between Black and White patients

52. Break-induced replication underlies formation of inverted triplications and generates unexpected diversity in haplotype structures

53. Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis

55. Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

56. Insights into genetics, human biology and disease gleaned from family based genomic studies

57. Butterfly genome reveals promiscuous exchange of mimicry adaptations among species

58. A high-resolution map of human evolutionary constraint using 29 mammals.

59. Genetic Sex Validation for Sample Tracking in Clinical Testing

61. The Genome Sequence of Drosophila melanogaster

62. Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease

63. Comparative genome sequencing of drosophila pseudoobscura: Chromosomal, gene and cis-element evolution

64. Sooty mangabey genome sequence provides insight into AIDS resistance in a natural SIV host

65. Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis

66. Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers

67. Hemimetabolous genomes reveal molecular basis of termite eusociality

68. Frequency and spectrum of clinically significant molecular alterations detected by tumor gene panel testing for pediatric cancer patients in the Texas KidsCanSeq study.

69. INTRA- AND INTER-HOST EVOLUTION OF HUMAN NOROVIRUS IN HEALTHY ADULTS

70. Longitudinal host transcriptional responses to SARS-CoV-2 infection in adults with extremely high viral load

71. Examining intra-host genetic variation of RSV by short read high-throughput sequencing

72. Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk

73. Data from Proteogenomic Markers of Chemotherapy Resistance and Response in Triple-Negative Breast Cancer

74. Supplementary Table from Proteogenomic Markers of Chemotherapy Resistance and Response in Triple-Negative Breast Cancer

75. Supplementary Figure from Proteogenomic Markers of Chemotherapy Resistance and Response in Triple-Negative Breast Cancer

76. Data from Integrative Genomic Characterization of Oral Squamous Cell Carcinoma Identifies Frequent Somatic Drivers

77. Supplementary Text from Integrative Genomic Characterization of Oral Squamous Cell Carcinoma Identifies Frequent Somatic Drivers

78. The genomic landscape of familial glioma

80. Functional Genomics of Gastrointestinal Escherichia coli Isolated from Patients with Cancer and Diarrhea

81. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma

82. Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome

83. Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

84. De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

85. Supplemental Figure 1 from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

86. Supplemental Tables S1-S4 and S6-S13 from Mutational Landscape of Aggressive Cutaneous Squamous Cell Carcinoma

87. Data from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

88. Supplemental Table 2 from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

89. Supplemental Figure 2 from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

90. Supplemental Table 3 from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

91. Supplemental Table 1 from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

92. Supplemental Figure 4 from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

93. Supplemental Figure 3 from Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse

94. Supplemental Table S5 from Mutational Landscape of Aggressive Cutaneous Squamous Cell Carcinoma

95. Supplemental Figures and Methods from Mutational Landscape of Aggressive Cutaneous Squamous Cell Carcinoma

96. Modeling nonsegmented negative-strand RNA virus (NNSV) transcription with ejective polymerase collisions and biased diffusion

98. A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

99. Combined burden and functional impact tests for cancer driver discovery using DriverPower

100. Integrative pathway enrichment analysis of multivariate omics data

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