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Aerosol delivery of SARS-CoV-2 human monoclonal antibodies in macaques limits viral replication and lung pathology.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-42440-x
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- Article
Shared and Distinct Functional Effects of Patient-Specific Tbr1 Mutations on Cortical Development.
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- Journal of Neuroscience, 2022, v. 42, n. 37, p. 7166, doi. 10.1523/JNEUROSCI.0409-22.2022
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- Article
Validation of Autism Diagnosis and Clinical Data in the SPARK Cohort.
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- Journal of Autism & Developmental Disorders, 2022, v. 52, n. 8, p. 3383, doi. 10.1007/s10803-021-05218-y
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- Article
High-content single-cell combinatorial indexing.
- Published in:
- Nature Biotechnology, 2021, v. 39, n. 12, p. 1574, doi. 10.1038/s41587-021-00962-z
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- Publication type:
- Article
Neutralization of SARS-CoV-2 variants by convalescent and BNT162b2 vaccinated serum.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25479-6
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- Publication type:
- Article
Autism and attention-deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1.
- Published in:
- 2021
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- journal article
Autism questionnaire scores do not only rise because of autism.
- Published in:
- Developmental Medicine & Child Neurology, 2021, v. 63, n. 2, p. 235, doi. 10.1111/dmcn.14725
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- Article
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes.
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- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0093-8
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- Article
Highly scalable generation of DNA methylation profiles in single cells.
- Published in:
- Nature Biotechnology, 2018, v. 36, n. 5, p. 428, doi. 10.1038/nbt.4112
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- Article
Current Perspectives in Autism Spectrum Disorder: From Genes to Therapy.
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- Journal of Neuroscience, 2016, v. 36, n. 45, p. 11402, doi. 10.1523/JNEUROSCI.2335-16.2016
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- Publication type:
- Article
Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology.
- Published in:
- Frontiers in Neuroscience, 2015, p. 1, doi. 10.3389/fnins.2015.00477
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- Article
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.
- Published in:
- 2015
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- Publication type:
- journal article
Refining analyses of copy number variation identifies specific genes associated with developmental delay.
- Published in:
- Nature Genetics, 2014, v. 46, n. 10, p. 1063, doi. 10.1038/ng.3092
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- Publication type:
- Article
MIPgen: optimized modeling and design of molecular inversion probes for targeted resequencing.
- Published in:
- Bioinformatics, 2014, v. 30, n. 18, p. 2670, doi. 10.1093/bioinformatics/btu353
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- Publication type:
- Article
De novo TBR1 mutations in sporadic autism disrupt protein functions.
- Published in:
- Nature Communications, 2014, v. 5, n. 9, p. 4954, doi. 10.1038/ncomms5954
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- Publication type:
- Article
Whole-Genome Sequencing of Individuals from a Founder Population Identifies Candidate Genes for Asthma.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104396
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- Article
A general framework for estimating the relative pathogenicity of human genetic variants.
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- Nature Genetics, 2014, v. 46, n. 3, p. 310, doi. 10.1038/ng.2892
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- Publication type:
- Article
GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
- Published in:
- Nature Genetics, 2013, v. 45, n. 9, p. 1073, doi. 10.1038/ng.2727
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- Publication type:
- Article
Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions.
- Published in:
- Nature Methods, 2013, v. 10, n. 9, p. 903, doi. 10.1038/nmeth.2572
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- Publication type:
- Article
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
- Published in:
- Nature Genetics, 2013, v. 45, n. 7, p. 825, doi. 10.1038/ng.2646
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- Article
Estimating the human mutation rate using autozygosity in a founder population.
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- Nature Genetics, 2012, v. 44, n. 11, p. 1277, doi. 10.1038/ng.2418
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- Publication type:
- Article
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
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- Nature Genetics, 2012, v. 44, n. 8, p. 934, doi. 10.1038/ng.2331
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- Publication type:
- Article
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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- Nature, 2012, v. 485, n. 7397, p. 246, doi. 10.1038/nature10989
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- Article
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.
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- Nature Genetics, 2012, v. 44, n. 4, p. 440, doi. 10.1038/ng.1091
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- Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
- Published in:
- 2012
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- Correction notice
Detection of structural variants and indels within exome data.
- Published in:
- Nature Methods, 2012, v. 9, n. 2, p. 176, doi. 10.1038/nmeth.1810
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- Publication type:
- Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
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- Nature Genetics, 2011, v. 43, n. 6, p. 585, doi. 10.1038/ng.835
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- Publication type:
- Article
Rare independent mutations in renal salt handling genes contribute to blood pressure variation.
- Published in:
- Nature Genetics, 2008, v. 40, n. 5, p. 592, doi. 10.1038/ng.118
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- Publication type:
- Article
Autism genetics: strategies, challenges, and opportunities.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2008, v. 1, n. 1, p. 4, doi. 10.1002/aur.3
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- Publication type:
- Article