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Prevalence of Creatine Deficiency Syndromes (CDS) and impact of genotypic variability of CDS genes in children with Autism Spectrum Disorder (ASD)

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Prevalence of Creatine Deficiency Syndromes (CDS) and impact of genotypic variability of CDS genes in children with Autism Spectrum Disorder (ASD), , , , , , , and . (2013)VikNGS: a C++ variant integration kit for next generation sequencing association analysis., , , , , and . Bioinform., 36 (4): 1283-1285 (2020)Copy number variation: New insights in genome diversity, , , , , , , , , and 3 other author(s). Genome Research, (2006)Application Domains: The Human Genome Project., and . Essentials of Genomics and Bioinformatics, Wiley, (2002)Genescript: DNA Sequence Annotation Pipeline., , , and . Bioinform., 19 (9): 1177-1178 (2003)Detection of large-scale variation in the human genome, , , , , , , and . Nature Genetics, 36 (9): 949--951 (2004)The human splicing code reveals new insights into the genetic determinants of disease, , , , , , , , , and 7 other author(s). Science, 347 (6218): 1254806+ (Jan 9, 2015)A Scan Statistic to Extract Causal Gene Clusters from Case-Control Genome-wide Rare CNV Data., , , , , , and . BMC Bioinform., (2011)The Database of Genomic Variants: a curated collection of structural variation in the human genome., , , , and . Nucleic Acids Res., 42 (Database-Issue): 986-992 (2014)