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Model-based deep embedding for constrained clustering analysis of single cell RNA-seq data

Nature communications, 2021-03, Vol.12 (1), p.1873-1873, Article 1873

2021

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Impact of in-scanner head motion on multiple measures of functional connectivity: Relevance for studies of neurodevelopment in youth

NeuroImage (Orlando, Fla.), 2012-03, Vol.60 (1), p.623-632

2012

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Clustering of single-cell multi-omics data with a multimodal deep learning method

Nature communications, 2022-12, Vol.13 (1), p.7705-7705, Article 7705

2022

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Sex differences in the structural connectome of the human brain

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (2), p.823-828

2014

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The role of gene-ambient air pollution interactions in paediatric asthma

European respiratory review, 2022-12, Vol.31 (166), p.220094

2022

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Age-Related Effects and Sex Differences in Gray Matter Density, Volume, Mass, and Cortical Thickness from Childhood to Young Adulthood

The Journal of neuroscience, 2017-05, Vol.37 (20), p.5065-5073

2017

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CLEC16A -An Emerging Master Regulator of Autoimmunity and Neurodegeneration

International journal of molecular sciences, 2023-05, Vol.24 (9), p.8224

2023

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Rare variants create synthetic genome-wide associations

PLoS biology, 2010-01, Vol.8 (1), p.e1000294-e1000294

2010

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SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data

Nucleic acids research, 2011-10, Vol.39 (19), p.e132-e132

2011

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Distinct features of SARS-CoV-2-specific IgA response in COVID-19 patients

The European respiratory journal, 2020-08, Vol.56 (2), p.2001526

2020

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Linked Sex Differences in Cognition and Functional Connectivity in Youth

Cerebral cortex (New York, N.Y. 1991), 2015-09, Vol.25 (9), p.2383-2394

2015

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SOCS-JAK-STAT inhibitors and SOCS mimetics as treatment options for autoimmune uveitis, psoriasis, lupus, and autoimmune encephalitis

Frontiers in immunology, 2023, Vol.14, p.1271102-1271102

2023

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Navigating Complexity in Postural Orthostatic Tachycardia Syndrome

Biomedicines, 2024-08, Vol.12 (8), p.1911

2024

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JAK/STAT inhibitor therapy partially rescues the lipodystrophic autoimmune phenotype in Clec16a KO mice

Scientific reports, 2021-04, Vol.11 (1), p.7372-7372, Article 7372

2021

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Neuroimaging of the Philadelphia Neurodevelopmental Cohort

NeuroImage (Orlando, Fla.), 2014-02, Vol.86, p.544-553

2014

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Genome Research, 2007-11, Vol.17 (11), p.1665-1674

2007

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Candidate gene analyses for acute pain and morphine analgesia after pediatric day surgery: African American versus European Caucasian ancestry and dose prediction limits

The pharmacogenomics journal, 2019-12, Vol.19 (6), p.570-581

2019

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The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort

NeuroImage (Orlando, Fla.), 2016-01, Vol.125, p.903-919

2016

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Neurocognitive growth charting in psychosis spectrum youths

JAMA psychiatry (Chicago, Ill.), 2014-04, Vol.71 (4), p.366

2014

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Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Scientific reports, 2021-01, Vol.11 (1), p.1526-1526, Article 1526

2021

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Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Genome medicine, 2013-03, Vol.5 (3), p.28-28

2013

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Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders

Translational psychiatry, 2021-01, Vol.11 (1), p.69-69, Article 69

2021

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Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism

Nature (London), 2015-12, Vol.528 (7582), p.418-421

2015

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Model-based deep embedding for constrained clustering analysis of single cell RNA-seq data

Impact of in-scanner head motion on multiple measures of functional connectivity: Relevance for studies of neurodevelopment in youth

Clustering of single-cell multi-omics data with a multimodal deep learning method

Sex differences in the structural connectome of the human brain

The role of gene-ambient air pollution interactions in paediatric asthma

Age-Related Effects and Sex Differences in Gray Matter Density, Volume, Mass, and Cortical Thickness from Childhood to Young Adulthood

CLEC16A -An Emerging Master Regulator of Autoimmunity and Neurodegeneration

Rare variants create synthetic genome-wide associations

SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Distinct features of SARS-CoV-2-specific IgA response in COVID-19 patients

Linked Sex Differences in Cognition and Functional Connectivity in Youth

SOCS-JAK-STAT inhibitors and SOCS mimetics as treatment options for autoimmune uveitis, psoriasis, lupus, and autoimmune encephalitis

Frequency of genomic secondary findings among 21,915 eMERGE network participants

Navigating Complexity in Postural Orthostatic Tachycardia Syndrome

JAK/STAT inhibitor therapy partially rescues the lipodystrophic autoimmune phenotype in Clec16a KO mice

Neuroimaging of the Philadelphia Neurodevelopmental Cohort

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Candidate gene analyses for acute pain and morphine analgesia after pediatric day surgery: African American versus European Caucasian ancestry and dose prediction limits

The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort

Neurocognitive growth charting in psychosis spectrum youths

Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders

Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism

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