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Identification of a Novel DNAAF3 Variant in a 54-Year-Old Patient With Newly Diagnosed Primary Ciliary Dyskinesia (PCD)
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Clinical and Genetic Study of a Pseudo‐Dominant Primary Ciliary Dyskinesia Pedigree: The First DNAAF1‐Associated Family Reported in Chinese Population
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Two Distinct Clinical Presentations of Primary Ciliary Dyskinesia (PCD): Diagnostic Utility of Whole-Exome Sequencing in a Genetically Heterogeneous Disorder
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Building capacity for diagnosis of Primary Ciliary Dyskinesia in South Africa: a descriptive study
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Association of genetic variants and the susceptibility to abnormal involuntary movements and tardive dyskinesia (TD) in Xhosa schizophrenia patients
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A Novel Approach to Interrogating Whole Genome Sequencing Data to Optimise Clinical Utility
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Mitochondrial genome sequence of Bleeker, 1849 (Syngnathiformes, Syngnathidae) and its phylogenetic placement
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Multiple instance fine-mapping: Predicting causal regulatory variants with a deep sequence model
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Comparison between genomic alterations in mouse, pig, and human through whole-genome sequencing
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Full-length transcriptome sequencing and identification of skin colour-associated genes in red tilapia
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Sequence context and methylation interact to shape germline mutation rate variation at CpG sites
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Correction to: Draft genome sequences of , , and isolated from onion bulbs () displaying symptoms of bacterial rot
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Identification and complete genome sequence analysis of aconitum virus 2 from Hebei infecting Debx
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Genotype-by-sequencing of global hyacinth bean () collections provides genomic resources for crop conservation and improvement
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Telomeric repeat diversity across Nepomorpha (Hemiptera, Heteroptera) revealed by whole-genome sequencing data
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Retraction: Constraints on the evolution of toxin-resistant Na,K-ATPases have limited dependence on sequence divergence
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Development of a high-throughput diagnostic screening tool to monitor the status of amitraz resistance and genotype in the cattle tick, Rhipicephalus microplus
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The regulation of Xrp1 expression by uORFs and main ORF sequences and its function in Drosophila disease models
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Three Unrelated Children With Childhood Apraxia of Speech: Exome Sequencing and Functional Gene Analysis Imply a Role of Laminin-511 in Early Neurodevelopment
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Prenatal Etiology Diagnosis of Rare Compound Heterozygous PROC Gene Variants in a Fetus With Ocular Ultrasonic Anomaly Using Whole Exome Sequencing
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Photoperiodic patterns in miRNA-mRNA pairs and tRNA fragments revealed by time-course co-sequencing in Arabidopsis
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Characterization of long noncoding RNAs, microRNAs, and piwiRNAs in reef-building corals
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Novel Generation-Skipping Inheritance Pattern of Marfan Syndrome Due to FBN1 Insertional Translocation: Diagnostic Utility of FISH and Implications for Genetic Counseling
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FEMA-Long: Modeling unstructured covariances for discovery of time-dependent effects in large-scale longitudinal datasets
