EDITORIAL
Published on 09 Sep 2022
Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases
doi 10.3389/fgene.2022.1022918
- 837 views
- Frontiers in Genetics
- Human and Medical Genomics
- Research Topics
- Chromosome Structural Variants: Epidemiology, Identification and Contribution to Human Diseases
Chromosome Structural Variants: Epidemiology, Identification and Contribution to Human Diseases
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Articles
ORIGINAL RESEARCH
Published on 02 Jun 2022
Combining Z-Score and Maternal Copy Number Variation Analysis Increases the Positive Rate and Accuracy in Non-Invasive Prenatal Testing
doi 10.3389/fgene.2022.887176
- 3,205 views
- 4 citations
ORIGINAL RESEARCH
Published on 14 Apr 2022
Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders
doi 10.3389/fgene.2022.803088
- 2,810 views
- 1 citation
ORIGINAL RESEARCH
Published on 23 Mar 2022
Copy Number Variation Analysis of Euploid Pregnancy Loss
doi 10.3389/fgene.2022.766492
- 1,970 views
- 7 citations
CORRECTION
Published on 25 Feb 2022
Corrigendum: SVInterpreter: A Comprehensive Topologically Associated Domain Based Clinical Outcome Prediction Tool for Balanced and Unbalanced Structural Variants
doi 10.3389/fgene.2022.868306
- 639 views
ORIGINAL RESEARCH
Published on 24 Feb 2022
Profile of Chromosomal Alterations, Chromosomal Instability and Clonal Heterogeneity in Colombian Farmers Exposed to Pesticides
doi 10.3389/fgene.2022.820209
- 2,555 views
- 4 citations
ORIGINAL RESEARCH
Published on 21 Dec 2021
Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees
doi 10.3389/fgene.2021.731815
- 2,897 views
- 2 citations
TECHNOLOGY AND CODE
Published on 01 Dec 2021
SVInterpreter: A Comprehensive Topologically Associated Domain-Based Clinical Outcome Prediction Tool for Balanced and Unbalanced Structural Variants
doi 10.3389/fgene.2021.757170
- 3,344 views
- 4 citations
ORIGINAL RESEARCH
Published on 04 Nov 2021
Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project
doi 10.3389/fgene.2021.752390
- 2,969 views
- 4 citations
ORIGINAL RESEARCH
Published on 20 Sep 2021
Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis
doi 10.3389/fgene.2021.742325
- 2,770 views
- 9 citations
ORIGINAL RESEARCH
Published on 26 Aug 2021
Chromoanagenesis Event Underlies a de novo Pericentric and Multiple Paracentric Inversions in a Single Chromosome Causing Coffin–Siris Syndrome
doi 10.3389/fgene.2021.708348
- 2,996 views
- 7 citations
METHODS
Published on 18 Mar 2021
stLFRsv: A Germline Structural Variant Analysis Pipeline Using Co-barcoded Reads
doi 10.3389/fgene.2021.636239
- 3,495 views
- 6 citations
Published in
Frontiers in Genetics
- Human and Medical Genomics
Impact
- 34kTopic views
- 24kArticle views
- 7,988Article downloads