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Medication Safety During Anesthesia and the Perioperative Period, 1st ed

Anesthesia and analgesia, 2021-11, Vol.133 (5), p.e55-e55

Morell, Robert C

2021

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Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear

Nature communications, 2015-10, Vol.6 (1), p.8557-8557, Article 8557

2015

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Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea

Scientific reports, 2020-10, Vol.10 (1), p.18100-18100, Article 18100

2020

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A comparative analysis of library prep approaches for sequencing low input translatome samples

BMC genomics, 2018-09, Vol.19 (1), p.696-696, Article 696

2018

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Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis

Frontiers in molecular neuroscience, 2019-12, Vol.12, p.316-316

2019

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Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

American journal of human genetics, 2013-04, Vol.92 (4), p.605-613

2013

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Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouse

Proceedings of the National Academy of Sciences - PNAS, 2017-05, Vol.114 (21), p.E4271-E4280

2017

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Modifier variant of METTL13 suppresses human GAB1-associated profound deafness

The Journal of clinical investigation, 2018-04, Vol.128 (4), p.1509-1522

2018

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Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness

Cell, 2018-07, Vol.174 (3), p.536-548.e21

2018

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G protein–coupled receptor Gpr115 (Adgrf4) is required for enamel mineralization mediated by ameloblasts

The Journal of biological chemistry, 2020-11, Vol.295 (45), p.15328-15341

2020

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Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome

Clinical genetics, 2024-05, Vol.105 (5), p.584-586

2024

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Single-Cell RNA-Sequencing From Mouse Incisor Reveals Dental Epithelial Cell-Type Specific Genes

Frontiers in cell and developmental biology, 2020-09, Vol.8, p.841-841

2020

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Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

American journal of human genetics, 2010-03, Vol.86 (3), p.378-388

2010

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Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea

Frontiers in molecular neuroscience, 2020-02, Vol.13, p.13-13

2020

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TGF-β uncouples glycolysis and inflammation in macrophages and controls survival during sepsis

Science signaling, 2023-08, Vol.16 (797), p.eade0385

2023

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Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria

European journal of human genetics : EJHG, 2022-01, Vol.30 (1), p.42-52

2022

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Genetic causes of moderate to severe hearing loss point to modifiers

Clinical genetics, 2017-04, Vol.91 (4), p.589-598

2017

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Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39

The Journal of neuroscience, 2020-04, Vol.40 (15), p.2976-2992

2020

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The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathy

Human molecular genetics, 2019-05, Vol.28 (9), p.1530-1547

2019

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CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct

Human genetics, 2023-10, Vol.142 (10), p.1499-1517

2023

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A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss

Journal of medical genetics, 2015-08, Vol.52 (8), p.548-552

2015

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Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

American journal of human genetics, 2014-01, Vol.94 (1), p.144-152

2014

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Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2

American journal of human genetics, 2016-02, Vol.98 (2), p.331-338

2016

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Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene Targets

Frontiers in molecular neuroscience, 2021-09, Vol.14, p.718241-718241

2021

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Molecular architecture underlying fluid absorption by the developing inner ear

eLife, 2017-10, Vol.6

2017

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Medication Safety During Anesthesia and the Perioperative Period, 1st ed

Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear

Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea

A comparative analysis of library prep approaches for sequencing low input translatome samples

Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouse

Modifier variant of METTL13 suppresses human GAB1-associated profound deafness

Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness

G protein–coupled receptor Gpr115 (Adgrf4) is required for enamel mineralization mediated by ameloblasts

Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome

Single-Cell RNA-Sequencing From Mouse Incisor Reveals Dental Epithelial Cell-Type Specific Genes

Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea

TGF-β uncouples glycolysis and inflammation in macrophages and controls survival during sepsis

Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria

Genetic causes of moderate to severe hearing loss point to modifiers

Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39

The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathy

CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct

A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss

Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2

Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene Targets

Molecular architecture underlying fluid absorption by the developing inner ear

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