October 05, 2007 preprint Open access PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genome Research DOI: 10.1101/gr.6861907 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 6 stored of 1,926 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals 2023 Nature Communications article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 59 citations Assessment of burden and segregation profiles of CNVs in patients with epilepsy 2022 Annals of Clinical and Translational Neurology article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 6 citations Assessment of burden and segregation profiles of CNVs in patients with epilepsy 2022 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 0 citations 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans 2021 preprint Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 1 citations Technologies for Pharmacogenomics: A Review 2020 Genes article Pharmacology, Toxicology and Pharmaceutics Pharmacogenetics and Drug Metabolism Open access 83 citations Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients 2020 Journal of Bone and Mineral Research article Medicine Bone health and osteoporosis research Open access 19 citations 6 results References 0