Cristina Fenollar‐Ferrer

Also affiliated with National Institute on Deafness and Other Communication Disorders, Florida Atlantic University

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 20 papers. Top paper: “Disrupted Choline Clearance and Sustained Acetylcholine Release In Vivo by a Common Choline Transporter Coding Variant Associated with Poor Attentional Control in Humans”.

Disrupted Choline Clearance and Sustained Acetylcholine Release In Vivo by a Common Choline Transporter Coding Variant Associated with Poor Attentional Control in Humans

Journal of Neuroscience(2022)10.1523/jneurosci.1334-21.2022

N/A

0.486DataRank · unranked

8 citations

Cassandra Avila, Sarah Klausner, Vinay Parikh, Cristina Fenollar‐Ferrer, Randy Blakely +2 more

Variants of human CLDN9 cause mild to profound hearing loss

Human Mutation(2021)10.1002/humu.24260

N/A

0.476DataRank · unranked

6 citations

Christophe Philippe, Inna A. Belyantseva, Yoko Nakano, Cristina Fenollar‐Ferrer, Risa Tona +19 more

Glial swip-10 controls systemic mitochondrial function, oxidative stress, and neuronal viability via copper ion homeostasis

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2320611121

N/A

0.455DataRank · unranked

14 citations

Vrinda Kalia, Cristina Fenollar‐Ferrer, Chelsea L. Gibson, Zayna Gichi, André Rajoo +10 more

Taperin bundles F-actin at stereocilia pivot points enabling optimal lifelong mechanosensitivity

The Journal of Cell Biology(2025)10.1083/jcb.202408026

N/A

0.312DataRank · unranked

7 citations

C S C Liu, Abigail K. Dragich, Takushi Miyoshi, Sayaka Inagaki, Ayesha Imtiaz +35 more

Tentonin 3 is a pore-forming subunit of a slow inactivation mechanosensitive channel

Cell Reports(2024)10.1016/j.celrep.2024.114334

N/A

0.241DataRank · unranked

4 citations

Hyunil Ryu, Su-Jin Lim, Thien-Luan Nguyen, Sungwook Yang, Sumin Kang +11 more

Interaction between the TBC1D24 TLDc domain and the KIBRA C2 domain is disrupted by two epilepsy-associated TBC1D24 missense variants

Journal of Biological Chemistry(2024)10.1016/j.jbc.2024.107725

N/A

0.167DataRank · unranked

2 citations

Sayaka Inagaki, Yasuko Ishibashi, Rabia Faridi, Rizwan Yousaf, Isabelle Roux +6 more

Psychomotor Impairments and Therapeutic Implications Revealed by a Mutation Associated with Infantile Parkinsonism-Dystonia

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.09.434693

N/A

0DataRank · unranked

0 citations

Mary Hongying Cheng, Josep Font, Alexandra C. Schwartz, Kaitlyn V. Ledwitch, Amanda M. Duran +14 more

Disrupted choline clearance and sustained acetylcholine release in vivo by a common choline transporter coding variant associated with poor attentional control in humans

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.27.450076

N/A

0DataRank · unranked

0 citations

Cassandra Avila, Sarah Klausner, Vinay Parikh, Cristina Fenollar‐Ferrer, Randy Blakely +2 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

Autoregulation of a trimeric transporter involves the cytoplasmic domains of both adjacent subunits

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.05.494857

N/A

0DataRank · unranked

0 citations

Richard T. Bradshaw, Caroline Koshy, Paul Suhwan Lee, Cristina Fenollar‐Ferrer, Veronika Heinz +3 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

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

SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sac

Science Advances(2024)10.1126/sciadv.adm8663

N/A

0DataRank · unranked

3 citations

Cristina Fenollar‐Ferrer, Kevin Isgrig, Ya-Xian Wang, Kerstin Valente, Juleh Eide +9 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

Insights into autoregulation of a membrane protein complex by its cytoplasmic domains

Biophysical Journal(2022)10.1016/j.bpj.2022.12.021

N/A

0DataRank · unranked

1 citations

Richard T. Bradshaw, Caroline Koshy, Paul Suhwan Lee, Cristina Fenollar‐Ferrer, Veronika Heinz +3 more

PLD2–PI(4,5)P2 interactions in fluid phase membranes: Structural modeling and molecular dynamics simulations

PLoS ONE(2020)10.1371/journal.pone.0236201

N/A

0DataRank · unranked

9 citations

Richard W. Pastor, Cristina Fenollar‐Ferrer, Kyungreem Han

Lysosomal SLC46A3 modulates hepatic cytosolic copper homeostasis

Nature Communications(2021)10.1038/s41467-020-20461-0

N/A

0DataRank · unranked

56 citations

Tsutomu Matsubara, Jaekwon Lee, Cristina Fenollar‐Ferrer, Kyungreem Han, Donghwan Kim +8 more

New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder

Human Genetics(2021)10.1007/s00439-021-02319-7

N/A

0DataRank · unranked

52 citations

Alessandro Rea, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, Shoujun Gu, Zunaira Munir +7 more

Psychomotor impairments and therapeutic implications revealed by a mutation associated with infantile Parkinsonism-Dystonia

eLife(2021)10.7554/elife.68039

N/A

0DataRank · unranked

23 citations

Mary Hongying Cheng, Josep Font, Alexandra C. Schwartz, Kaitlyn V. Ledwitch, Amanda M. Duran +14 more

Serotonin Transporter Ala276 Mouse: Novel Model to Assess the Neurochemical and Behavioral Impact of Thr276 Phosphorylation In Vivo

Neurochemical Research(2021)10.1007/s11064-021-03299-w

N/A

0DataRank · unranked

5 citations

Meagan A. Quinlan, Krista C. Paffenroth, Fiona E. Harrison, Cristina Fenollar‐Ferrer, Rania M. Katamish +4 more