Katherina Walz

Also affiliated with Austral University, Dr. John T. Macdonald Foundation, Sylvester Comprehensive Cancer Center

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 9 papers. Top paper: “Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development”.

Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development

Journal of Clinical Investigation(2020)10.1172/jci136951

N/A

0DataRank · unranked

18 citations

Clemer Abad, Filiz Başak Cengiz, Serhat Seyhan, Armağan İncesulu, Shengru Guo +14 more

Bromodomain Protein BRD4 Is Essential for Hair Cell Function and Survival

Frontiers in Cell and Developmental Biology(2020)10.3389/fcell.2020.576654

N/A

0DataRank · unranked

6 citations

Clemer Abad, Marie E. Maloof, Nagi G. Ayad, Juan I. Young, Xue Zhong Liu +2 more

Generation and characterization of a P2rx2 V60L mouse model for DFNA41

Human Molecular Genetics(2021)10.1093/hmg/ddab077

N/A

0DataRank · unranked

9 citations

Clemer Abad, Zheng‐Yi Chen, Juan I. Young, Channabasavaiah B. Gurumurthy, Katherina Walz +2 more

Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2204084119

N/A

0DataRank · unranked

9 citations

María Lachgar, Mangesh Deokar, Mohammad Faraz Zafeer, Clemer Abad, Müzeyyen Yıldırım Baylan +16 more

SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights

Brain(2024)10.1093/brain/awae079

N/A

0DataRank · unranked

10 citations

Clemer Abad, Maike F. Dohrn, Jian J. Li, Ethan Kim Tieu, Jessica Medina +9 more

Extreme Phenotypic Variability of ACTG1‐Related Disorders in Hearing Loss

Advanced Genetics(2024)10.1002/ggn2.202400040

N/A

0DataRank · unranked

2 citations

Memoona Ramzan, L.A. Calderón, Franco Salvatore, Maria Agustina De Rosa, Stephanie Bivona +12 more

Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2

European Journal of Human Genetics(2024)10.1038/s41431-024-01562-6

N/A

0DataRank · unranked

6 citations

Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Özgül M. Alper +9 more

Single-dose genome editing therapy rescues auditory and vestibular functions in adult mice with DFNA41 deafness

Journal of Clinical Investigation(2025)10.1172/jci187872

N/A

0DataRank · unranked

3 citations

Wenliang Zhu, Stewart Silver, Ariel Miura Armstrong, Fletcher S. Robbins, Arun Prabhu Rameshbabu +9 more

Carboxypeptidase D deficiency causes hearing loss amenable to treatment

Journal of Clinical Investigation(2025)10.1172/jci192090

N/A

0DataRank · unranked

1 citations

Natalie Ortiz-Vega, Mohammad Faraz Zafeer, Amanda G. Lobato, Tahir Atık, Clemer Abad +25 more