Found: 55
Select item for more details and to access through your institution.
Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility.
- Published in:
- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-015-0058-7
- By:
- Publication type:
- Article
Identification of polymorphic SVA retrotransposons using a mobile element scanning method for SVA (ME-Scan-SVA).
- Published in:
- Mobile DNA, 2016, v. 7, p. 1, doi. 10.1186/s13100-016-0072-x
- By:
- Publication type:
- Article
Common genetic risk factors in ASD and ADHD co-occurring families.
- Published in:
- Human Genetics, 2023, v. 142, n. 2, p. 217, doi. 10.1007/s00439-022-02496-z
- By:
- Publication type:
- Article
Predicting embryonic aneuploidy rate in IVF patients using whole-exome sequencing.
- Published in:
- Human Genetics, 2022, v. 141, n. 10, p. 1615, doi. 10.1007/s00439-022-02450-z
- By:
- Publication type:
- Article
Transposable Elements in Bats Show Differential Accumulation Patterns Determined by Class and Functionality.
- Published in:
- Life (2075-1729), 2022, v. 12, n. 8, p. 1190, doi. 10.3390/life12081190
- By:
- Publication type:
- Article
Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidy.
- Published in:
- Molecular Human Reproduction, 2017, v. 23, n. 6, p. 406, doi. 10.1093/molehr/gax018
- By:
- Publication type:
- Article
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.
- Published in:
- Nature Biotechnology, 2014, v. 32, n. 7, p. 663, doi. 10.1038/nbt.2895
- By:
- Publication type:
- Article
A genetic mechanism for Tibetan high-altitude adaptation.
- Published in:
- Nature Genetics, 2014, v. 46, n. 9, p. 951, doi. 10.1038/ng.3067
- By:
- Publication type:
- Article
Characterization of the primate TRIM gene family reveals the recent evolution in primates.
- Published in:
- Molecular Genetics & Genomics, 2020, v. 295, n. 5, p. 1281, doi. 10.1007/s00438-020-01698-2
- By:
- Publication type:
- Article
PrecisionProDB: improving the proteomics performance for precision medicine.
- Published in:
- Bioinformatics, 2021, v. 37, n. 19, p. 3361, doi. 10.1093/bioinformatics/btab218
- By:
- Publication type:
- Article
Shared and Unique Signals of High-Altitude Adaptation in Geographically Distinct Tibetan Populations.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0088252
- By:
- Publication type:
- Article
Ancestry of the Iban Is Predominantly Southeast Asian: Genetic Evidence from Autosomal, Mitochondrial, and Y Chromosomes.
- Published in:
- PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0016338
- By:
- Publication type:
- Article
MACSNVdb: a high-quality SNV database for interspecies genetic divergence investigation among macaques.
- Published in:
- Database: The Journal of Biological Databases & Curation, 2020, v. 2020, p. 1, doi. 10.1093/database/baaa027
- By:
- Publication type:
- Article
Alu repeats increase local recombination rates.
- Published in:
- BMC Genomics, 2009, v. 10, p. 530, doi. 10.1186/1471-2164-10-530
- By:
- Publication type:
- Article
Whole-Genome Sequencing of Tibetan Macaque (Macaca thibetana) Provides New Insight into the Macaque Evolutionary History.
- Published in:
- Molecular Biology & Evolution, 2014, v. 31, n. 6, p. 1475, doi. 10.1093/molbev/msu104
- By:
- Publication type:
- Article
Crohn’s Disease and Genetic Hitchhiking at IBD5.
- Published in:
- Molecular Biology & Evolution, 2012, v. 29, n. 1, p. 101, doi. 10.1093/molbev/msr151
- By:
- Publication type:
- Article
Exome sequencing links CEP120 mutation to maternally derived aneuploid conception risk.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells.
- Published in:
- eLife, 2024, p. 1, doi. 10.7554/eLife.82809
- By:
- Publication type:
- Article
Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells.
- Published in:
- eLife, 2024, p. 1, doi. 10.7554/eLife.82809
- By:
- Publication type:
- Article
Integrated Mobile Element Scanning (ME-Scan) method for identifying multiple types of polymorphic mobile element insertions.
- Published in:
- Mobile DNA, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13100-020-00207-x
- By:
- Publication type:
- Article
Can-SINE dynamics in the giant panda and three other Caniformia genomes.
- Published in:
- Mobile DNA, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13100-018-0137-0
- By:
- Publication type:
- Article
Limited Distribution of a Cardiomyopathy-Associated Variant in India.
- Published in:
- Annals of Human Genetics, 2010, v. 74, n. 2, p. 184, doi. 10.1111/j.1469-1809.2010.00561.x
- By:
- Publication type:
- Article
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.
- Published in:
- Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00428
- By:
- Publication type:
- Article
Effect of interleukin-6 polymorphism on risk of preterm birth within population strata: a meta-analysis.
- Published in:
- BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-30
- By:
- Publication type:
- Article
Genetic analysis of ancestry, admixture and selection in Bolivian and Totonac populations of the New World.
- Published in:
- BMC Genetics, 2012, v. 13, n. 1, p. 39, doi. 10.1186/1471-2156-13-39
- By:
- Publication type:
- Article
Modeling the Amplification Dynamics of Human Alu Retrotransposons.
- Published in:
- PLoS Computational Biology, 2005, v. 1, n. 4, p. 333, doi. 10.1371/journal.pcbi.0010044
- By:
- Publication type:
- Article
Genomics and epigenetics guided identification of tissue-specific genomic safe harbors.
- Published in:
- Genome Biology, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s13059-022-02770-3
- By:
- Publication type:
- Article
Genomic Copy Number Variation Study of Nine Macaca Species Provides New Insights into Their Genetic Divergence, Adaptation, and Biomedical Application.
- Published in:
- Genome Biology & Evolution, 2020, v. 12, n. 12, p. 2211, doi. 10.1093/gbe/evaa200
- By:
- Publication type:
- Article
Whole Genome Sequencing and Assembly of the Asian Honey Bee Apis dorsata.
- Published in:
- Genome Biology & Evolution, 2020, v. 12, n. 1, p. 3677, doi. 10.1093/gbe/evz277
- By:
- Publication type:
- Article
Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis.
- Published in:
- Genome Biology & Evolution, 2015, v. 7, n. 6, p. 1664, doi. 10.1093/gbe/evv099
- By:
- Publication type:
- Article
Variation in piRNA and Transposable Element Content in Strains of Drosophila melanogaster.
- Published in:
- Genome Biology & Evolution, 2014, v. 6, n. 10, p. 2786, doi. 10.1093/gbe/evu217
- By:
- Publication type:
- Article
Apparent Variation in Neanderthal Admixture among African Populations is Consistent with Gene Flow from Non-African Populations.
- Published in:
- Genome Biology & Evolution, 2013, v. 5, n. 11, p. 2075, doi. 10.1093/gbe/evt160
- By:
- Publication type:
- Article
Extremely low-coverage whole genome sequencing in South Asians captures population genomics information.
- Published in:
- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3767-6
- By:
- Publication type:
- Article
Correction to: Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
SINEs of a Nearly Perfect Character.
- Published in:
- Systematic Biology, 2006, v. 55, n. 6, p. 928, doi. 10.1080/10635150600865419
- By:
- Publication type:
- Article
SIRT7 mediates L1 elements transcriptional repression and their association with the nuclear lamina.
- Published in:
- Nucleic Acids Research, 2019, v. 47, n. 15, p. 7870, doi. 10.1093/nar/gkz519
- By:
- Publication type:
- Article
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06159-4
- By:
- Publication type:
- Article
Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 7, p. 1, doi. 10.1371/journal.pgen.1003634
- By:
- Publication type:
- Article
A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 8, p. 1, doi. 10.1371/journal.pgen.1002236
- By:
- Publication type:
- Article
Cover Image.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 5, p. i, doi. 10.1002/pd.5950
- By:
- Publication type:
- Article
Origins and mechanisms leading to aneuploidy in human eggs.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Using whole-exome sequencing to investigate the genetic bases of lysosomal storage diseases of unknown etiology.
- Published in:
- Human Mutation, 2017, v. 38, n. 11, p. 1491, doi. 10.1002/humu.23291
- By:
- Publication type:
- Article
Assessing the Expression of Long INterspersed Elements (LINEs) via Long-Read Sequencing in Diverse Human Tissues and Cell Lines.
- Published in:
- Genes, 2023, v. 14, n. 10, p. 1893, doi. 10.3390/genes14101893
- By:
- Publication type:
- Article
Transposable Elements Shape the Genome Diversity and the Evolution of Noctuidae Species.
- Published in:
- Genes, 2023, v. 14, n. 6, p. 1244, doi. 10.3390/genes14061244
- By:
- Publication type:
- Article
MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.
- Published in:
- Genes, 2022, v. 13, n. 8, p. 1329, doi. 10.3390/genes13081329
- By:
- Publication type:
- Article
Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-020-02101-4
- By:
- Publication type:
- Article
Evaluating nanopore sequencing data processing pipelines for structural variation identification.
- Published in:
- Genome Biology, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s13059-019-1858-1
- By:
- Publication type:
- Article
Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 17, p. 13248, doi. 10.3390/ijms241713248
- By:
- Publication type:
- Article
A comprehensive analysis of piRNAs from adult human testis and their relationship with genes and mobile elements.
- Published in:
- BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-545
- By:
- Publication type:
- Article
Mobile element scanning (ME-Scan) by targetedhigh-throughput sequencing.
- Published in:
- BMC Genomics, 2010, v. 11, p. 410, doi. 10.1186/1471-2164-11-410
- By:
- Publication type:
- Article