Robert J. Morell

Also affiliated with National Institute on Deafness and Other Communication Disorders

NeuroscienceBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 28 papers. Top paper: “Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F”.

Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

The American Journal of Human Genetics(2001)10.1086/321277

N/A

0.905DataRank · unranked

417 citations

Saima Riazuddin, Steve L. Bernstein, Zahoor Ahmed, Shaheen Khan, Andrew J. Griffith +5 more

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)10.3389/fnmol.2021.718241

N/A

0.564DataRank · unranked

42 citations

Rafal T. Olszewski, Soumya Korrapati, Katharine Fernandez, Erich T. Boger, Tracy S. Fitzgerald +4 more

Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

Clinical Genetics(2023)10.1111/cge.14312

N/A

0.477DataRank · unranked

23 citations

Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy Turriff, Keith Pelstring +22 more

Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40

Brain(2023)10.1093/brain/awad314

N/A

0.406DataRank · unranked

14 citations

Thomas Scerri, Adam P. Vogel, Christopher A. Reid, Mara Quach, Victoria E. Jackson +28 more

GZMK+CD8+ T cells target a specific acinar cell type in Sjögren's disease

Annals of the Rheumatic Diseases(2025)10.1016/j.ard.2025.08.014

N/A

0.385DataRank · unranked

12 citations

Paola Pérez, Anson T. Ku, Bruno Fernandes Matuck, Khoa Huynh, Shunsuke Sakai +38 more

Dexamethasone-eluting cochlear implants reduce inflammation and foreign body response in human and murine cochleae

Scientific Reports(2025)10.1038/s41598-025-10739-y

N/A

0.345DataRank · unranked

9 citations

Brian Mostaert, Peter Eckard, Shakila Mahmuda Fatima, Rachel A. Scheperle, Ibrahim Razu +16 more

Molecular differences between young and mature stria vascularis from organotypic explants and transcriptomics

iScience(2025)10.1016/j.isci.2025.111832

N/A

0.292DataRank · unranked

6 citations

Ryosuke Yamamoto, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell, Michael Hoa +2 more

Mutations in ZBTB20 in individuals with persistent stuttering

medRxiv(2022)10.1101/2022.11.03.22281471

N/A

0.208DataRank · unranked

3 citations

Muhammad Hashim Raza, Tae‐Un Han, Terra D. Barnes, Philip Shaw, Gustavo Sudre +4 more

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

Journal of Neuroscience(2020)10.1523/jneurosci.2278-19.2020

N/A

0DataRank · unranked

34 citations

Rafal T. Olszewski, Risa Tona, Samuel Leitess, Talah Wafa, Ian Taukulis +13 more

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

European Journal of Human Genetics(2021)10.1038/s41431-021-00984-w

N/A

0DataRank · unranked

16 citations

Rabia Faridi, Parna Chattaraj, Rizwan Yousaf, Risa Tona, Samuel Okorie +10 more

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

Science Signaling(2023)10.1126/scisignal.ade0385

N/A

0DataRank · unranked

91 citations

Chen Yao, Tyrone Dowdy, Wenwen Jin, Yun-Ji Lim, Liliana Catherine Patiño +14 more

Issue Information

Human Mutation(2018)10.1002/humu.23568

N/A

0DataRank · unranked

0 citations

R. Donald Harvey, Tracy Dudding‐Byth, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel +135 more

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

Human Genetics(2023)10.1007/s00439-023-02581-x

N/A

0DataRank · unranked

13 citations

Cristina Fenollar‐Ferrer, Hyun Jae Lee, Parna Chattaraj, Iván A. López, Kyungreem Han +7 more

GZMK+CD8+ T cells Target a Specific Acinar Cell Type in Sjögren’s Disease

Research Square(2023)10.21203/rs.3.rs-3601404/v1

N/A

0DataRank · unranked

19 citations

Thomas Pranzatelli, Paola Pérez, Anson T. Ku, Bruno Fernandes Matuck, Khoa Huynh +37 more

Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient mice

Research Square(2023)10.21203/rs.3.rs-3310464/v1

N/A

0DataRank · unranked

0 citations

Rizwan Yousaf, Sayaka Inagaki, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell +9 more

Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome

Clinical Genetics(2024)10.1111/cge.14514

N/A

0DataRank · unranked

6 citations

Pamela Stratton, Noemi Salmeri, Robert J. Morell, Asma Ali Khan, Muhammad A. Usmani +4 more

Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1-Deficient Mice

Genes(2024)10.3390/genes15070845

N/A

0DataRank · unranked

2 citations

Rizwan Yousaf, Sayaka Inagaki, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell +9 more

GZMK+CD8+ T cells Target A Specific Acinar Cell Type in Sjögren’s Disease

Research Square(2024)10.21203/rs.3.rs-3601404/v2

N/A

0DataRank · unranked

5 citations

Paola Pérez, Anson T. Ku, Bruno Fernandes Matuck, Khoa Huynh, Shunsuke Sakai +38 more

Molecular differences between neonatal and adult stria vascularis from organotypic explants and transcriptomics

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.24.590986

N/A

0DataRank · unranked

1 citations

Ryosuke Yamamoto, Rafal T. Olszewski, Shoujun Gu, Robert J. Morell, Michael Hoa +2 more

Activin A activation of Smad3 mitigates innate inflammation in mouse models of psoriasis and sepsis

Journal of Clinical Investigation(2025)10.1172/jci187063

N/A

0DataRank · unranked

9 citations

Yun-Ji Lim, Wenwen Jin, Na Liu, Liliana Catherine Patiño, Weiwei Chen +7 more

Neurotrophin signaling is a central mechanism of salivary dysfunction after irradiation that disrupts myoepithelial cells

npj Regenerative Medicine(2023)10.1038/s41536-023-00290-7

N/A

0DataRank · unranked

27 citations

Vaishali Patel, Marit H. Aure, Mary Pasquale, NIDCD/NIDCR Genomics and Computational Biology Core, Robert J. Morell +12 more

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

Frontiers in Cell and Developmental Biology(2020)10.3389/fcell.2020.00841

N/A

0DataRank · unranked

75 citations

Kan Saito, Daniel Martı́n, Erich T. Boger, Craig Rhodes, Keigo Yoshizaki +6 more

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

Scientific Reports(2020)10.1038/s41598-020-75238-8

N/A

0DataRank · unranked

53 citations

Rafal T. Olszewski, Ian Taukulis, Zheng Wei, Daniel Martı́n, Robert J. Morell +2 more

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)10.3389/fnmol.2020.00013

N/A

0DataRank · unranked

56 citations

Rafal T. Olszewski, Xiaoyi Li, Ian Taukulis, Shoujun Gu, Alvin DeTorres +7 more

Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

Genes(2020)10.3390/genes11101122

N/A

0DataRank · unranked

20 citations

Iván A. López, Cristina Fenollar‐Ferrer, Rabia Faridi, Claudio Anselmi, Asma Ali Khan +10 more

Cell-Specific Transcriptional Responses to Heat Shock in the Mouse Utricle Epithelium

Frontiers in Cellular Neuroscience(2020)10.3389/fncel.2020.00123

N/A

0DataRank · unranked

19 citations

Matthew Ryals, Lindsey May, Daniel Martı́n, Nora C. Welsh, Erich T. Boger +4 more

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

Journal of Biological Chemistry(2020)10.1074/jbc.ra120.014281

N/A

0DataRank · unranked

19 citations

Keigo Yoshizaki, Kan Saito, T Ikeuchi, Tsutomu Iwamoto, Craig Rhodes +12 more

Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome

Clinical Genetics(2020)10.1111/cge.13868

N/A

0DataRank · unranked

37 citations

Rabia Faridi, Kelly King, Christopher Zalewski, Rizwan Yousaf, Julie M. Schultz +9 more