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QAPA: a new method for the systematic analysis of alternative polyadenylation from RNA-seq data

Genome Biology, 2018-03, Vol.19 (1), p.45-45, Article 45

2018

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An Assistive Control Approach for a Lower-Limb Exoskeleton to Facilitate Recovery of Walking Following Stroke

IEEE transactions on neural systems and rehabilitation engineering, 2015-05, Vol.23 (3), p.441-449

2015

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Differential contribution of transcriptomic regulatory layers in the definition of neuronal identity

Nature communications, 2021-01, Vol.12 (1), p.335-335, Article 335

2021

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Genetic interaction mapping and exon-resolution functional genomics with a hybrid Cas9-Cas12a platform

Nature biotechnology, 2020-05, Vol.38 (5), p.638-648

2020

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An Approach for the Cooperative Control of FES With a Powered Exoskeleton During Level Walking for Persons With Paraplegia

IEEE transactions on neural systems and rehabilitation engineering, 2016-04, Vol.24 (4), p.455-466

2016

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Germ-line DNA copy number variation frequencies in a large North American population

Human genetics, 2007-11, Vol.122 (3-4), p.345-353

2007

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Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome

American journal of human genetics, 2010-10, Vol.87 (4), p.553-559

2010

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Identifying human pre-mRNA cleavage and polyadenylation factors by genome-wide CRISPR screens using a dual fluorescence readthrough reporter

Nucleic acids research, 2024-05, Vol.52 (8), p.4483-4501

2024

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A Preliminary Assessment of Legged Mobility Provided by a Lower Limb Exoskeleton for Persons With Paraplegia

IEEE transactions on neural systems and rehabilitation engineering, 2014-05, Vol.22 (3), p.482-490

2014

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RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression

Genome research, 2011-04, Vol.21 (4), p.545-554

2011

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Time of day is an inaccurate surrogate marker for sleep-wake state in an epilepsy monitoring unit

Epilepsy research, 2021-01, Vol.169, p.106524-106524, Article 106524

2021

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Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing

Human mutation, 2010-08, Vol.31 (8), p.918-923

2010

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Cytochrome b Mutations That Modify the Ubiquinol-binding Pocket of the Cytochrome bc1 Complex and Confer Anti-malarial Drug Resistance in Saccharomyces cerevisiae

The Journal of biological chemistry, 2005-04, Vol.280 (17), p.17142-17148

2005

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Volitional Control of a Prosthetic Knee Using Surface Electromyography

IEEE transactions on biomedical engineering, 2011-01, Vol.58 (1), p.144-151

2011

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An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms

Genome research, 2017-10, Vol.27 (10), p.1759-1768

2017

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Identification of gene fusion transcripts by transcriptome sequencing in BRCA1-mutated breast cancers and cell lines

BMC medical genomics, 2011-10, Vol.4 (1), p.75-75, Article 75

2011

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Efficient and Accurate Quantitative Profiling of Alternative Splicing Patterns of Any Complexity on a Laptop

Molecular cell, 2018-10, Vol.72 (1), p.187-200.e6

2018

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Novel Mutations in SCO1 as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis

Human mutation, 2013-10, Vol.34 (10), p.1366-1370

2013

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Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype

Journal of medical genetics, 2011-09, Vol.48 (9), p.602-605

2011

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Oncogenic Activation of the RNA Binding Protein NELFE and MYC Signaling in Hepatocellular Carcinoma

Cancer cell, 2017-07, Vol.32 (1), p.101-114.e8

2017

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Multilayered Control of Alternative Splicing Regulatory Networks by Transcription Factors

Molecular cell, 2017-02, Vol.65 (3), p.539-553.e7

2017

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Regulation of alternative polyadenylation by the C2H2-zinc-finger protein Sp1

Molecular cell, 2022-09, Vol.82 (17), p.3135-3150.e9

2022

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RNAcompete methodology and application to determine sequence preferences of unconventional RNA-binding proteins

Methods (San Diego, Calif.), 2017-04, Vol.118-119, p.3-15

2017

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Shifts in Ribosome Engagement Impact Key Gene Sets in Neurodevelopment and Ubiquitination in Rett Syndrome

Cell reports (Cambridge), 2020-03, Vol.30 (12), p.4179-4196.e11

2020

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RNAcompete-S: Combined RNA sequence/structure preferences for RNA binding proteins derived from a single-step in vitro selection

Methods (San Diego, Calif.), 2017-08, Vol.126, p.18-28

2017

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QAPA: a new method for the systematic analysis of alternative polyadenylation from RNA-seq data

An Assistive Control Approach for a Lower-Limb Exoskeleton to Facilitate Recovery of Walking Following Stroke

Differential contribution of transcriptomic regulatory layers in the definition of neuronal identity

Genetic interaction mapping and exon-resolution functional genomics with a hybrid Cas9-Cas12a platform

An Approach for the Cooperative Control of FES With a Powered Exoskeleton During Level Walking for Persons With Paraplegia

Germ-line DNA copy number variation frequencies in a large North American population

Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome

Identifying human pre-mRNA cleavage and polyadenylation factors by genome-wide CRISPR screens using a dual fluorescence readthrough reporter

A Preliminary Assessment of Legged Mobility Provided by a Lower Limb Exoskeleton for Persons With Paraplegia

RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression

Time of day is an inaccurate surrogate marker for sleep-wake state in an epilepsy monitoring unit

Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing

Cytochrome b Mutations That Modify the Ubiquinol-binding Pocket of the Cytochrome bc1 Complex and Confer Anti-malarial Drug Resistance in Saccharomyces cerevisiae

Volitional Control of a Prosthetic Knee Using Surface Electromyography

An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms

Identification of gene fusion transcripts by transcriptome sequencing in BRCA1-mutated breast cancers and cell lines

Efficient and Accurate Quantitative Profiling of Alternative Splicing Patterns of Any Complexity on a Laptop

Novel Mutations in SCO1 as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis

Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype

Oncogenic Activation of the RNA Binding Protein NELFE and MYC Signaling in Hepatocellular Carcinoma

Multilayered Control of Alternative Splicing Regulatory Networks by Transcription Factors

Regulation of alternative polyadenylation by the C2H2-zinc-finger protein Sp1

RNAcompete methodology and application to determine sequence preferences of unconventional RNA-binding proteins

Shifts in Ribosome Engagement Impact Key Gene Sets in Neurodevelopment and Ubiquitination in Rett Syndrome

RNAcompete-S: Combined RNA sequence/structure preferences for RNA binding proteins derived from a single-step in vitro selection

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