Karen B. Avraham

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 4%percentile

0.929Author DataRank

Indexed papers

2in 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 2 indexed papers 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Clinical Genetics(2020)10.1111/cge.13817

Top 22%

0.929DataRank

Top 22%29 citations

Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov +45 more

Papers

Driven by 20 papers — median percentile 78. Top paper: “Mapping of Unconventional Myosins in Mouse and Human”.

Mapping of Unconventional Myosins in Mouse and Human

Genomics(1996)10.1006/geno.1996.0488

N/A

5.4DataRank · unranked

78 citations

Joseph F. Skowron, Debra J. Gilbert, Karen B. Avraham, William L. Perry, William M. Bement +10 more

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Clinical Genetics(2020)10.1111/cge.13817

Top 22%

0.929DataRank

Top 22%29 citations

Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov +45 more

Striatin Is Required for Hearing and Affects Inner Hair Cells and Ribbon Synapses

Frontiers in Cell and Developmental Biology(2020)10.3389/fcell.2020.00615

N/A

0DataRank · unranked

9 citations

Shahar Taiber, Michal Caspi, Tal Koffler-Brill, Amiel A. Dror, Ronen Siman-Tov +7 more

Identification and characterization of key long non-coding RNAs in the mouse cochlea

RNA Biology(2020)10.1080/15476286.2020.1836456

N/A

0DataRank · unranked

7 citations

Shahar Taiber, Alejandro Anaya, Mor Bordeynik‐Cohen, Einat Rosen, Likhitha Kolla +6 more

Striatin is required for hearing and affects inner hair cells and ribbon synapses

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.11.987396

N/A

0DataRank · unranked

3 citations

Shahar Taiber, Michal Caspi, Tal Koffler-Brill, Amiel A. Dror, Moran Rubinstein +4 more

Homozygote loss-of-function variants in the human COCH gene underlie hearing loss

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.29.178053

N/A

0DataRank · unranked

1 citations

Elena Chervinsky, Prathamesh T. Nadar‐Ponniah, Eran Cohen‐Barak, Shahar Taiber, Morad Khayat +3 more

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w

N/A

0DataRank · unranked

17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

medRxiv(2021)10.1101/2021.01.27.21250652

N/A

0DataRank · unranked

8 citations

Marina T. DiStefano, Andrea M. Oza, Madeline Y. Hughes, Emma H. Wilcox, Sarah E. Hemphill +18 more

A nesprin-4/kinesin-1 cargo model for nuclear positioning in cochlear outer hair cells

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.10.463824

N/A

0DataRank · unranked

2 citations

Oren Gozlan, Roie Cohen, Leonardo R. Andrade, Ellen F. Gregory, Daniel A. Starr +7 more

A mouse model for benign paroxysmal positional vertigo with genetic predisposition for displaced otoconia

Genes Brain & Behavior(2020)10.1111/gbb.12635

N/A

0DataRank · unranked

17 citations

Shahar Taiber, Eyal Sela, Ophir Handzel, Karen B. Avraham, Amiel A. Dror

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

Human Genetics(2022)10.1007/s00439-022-02444-x

N/A

0DataRank · unranked

26 citations

Cindy Penney, Darren D. O’Rielly, Anne Griffin, Lara Kamal, Zippora Brownstein +23 more

The Genomics of Auditory Function and Disease

Annual Review of Genomics and Human Genetics(2022)10.1146/annurev-genom-121321-094136

N/A

0DataRank · unranked

21 citations

Kathleen Gwilliam, Ronna Hertzano, Karen B. Avraham, Shahar Taiber

A Nesprin-4/kinesin-1 cargo model for nuclear positioning in cochlear outer hair cells

Frontiers in Cell and Developmental Biology(2022)10.3389/fcell.2022.974168

N/A

0DataRank · unranked

19 citations

Oren Gozlan, Roie Cohen, Leonardo R. Andrade, Ellen F. Gregory, Daniel A. Starr +7 more

The long and short: Non-coding RNAs in the mammalian inner ear

Hearing Research(2022)10.1016/j.heares.2022.108666

N/A

0DataRank · unranked

15 citations

Yael Noy, Karen B. Avraham, Tal Koffler-Brill

SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice

Journal of Medical Genetics(2023)10.1136/jmg-2023-109264

N/A

0DataRank · unranked

6 citations

Matan M. Jean, Yael Noy, Daniel Halpérin, Yuval Yogev, Ohad Wormser +11 more

A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss

Human Molecular Genetics(2023)10.1093/hmg/ddad066

N/A

0DataRank · unranked

1 citations

Ryan J. Carlson, Grace Rabie, Ming K. Lee, Süleyman Gülsüner, Tom Walsh +4 more

Using multi-scale genomics to associate poorly annotated genes with rare diseases

Genome Medicine(2024)10.1186/s13073-023-01276-2

N/A

0DataRank · unranked

7 citations

Dana Sherill-Rofe, Lara Kamal, Idit Bloch, Fouad Zahdeh, Elad Sharon +11 more

A mouse model of GRIN2D developmental and epileptic encephalopathy recapitulates the human disease

Brain(2025)10.1093/brain/awaf149

N/A

0DataRank · unranked

3 citations

Jolan Nassir, Danielle Galber, Shir Quinn, Roni Gal, Mor Ovadia +9 more

Repair of Noise-Induced Damage to Stereocilia F-actin Cores is Facilitated by XIRP2

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.10.455815

N/A

0DataRank · unranked

1 citations

Jun-Sub Im, Masaki Nakahata, Terence E. Imbery, Sihan Li, Daxin Chen +7 more

Homozygote loss-of-function variants in the human COCH gene underlie hearing loss

European Journal of Human Genetics(2020)10.1038/s41431-020-00724-6

N/A

0DataRank · unranked

11 citations

Elena Chervinsky, Prathamesh T. Nadar‐Ponniah, Eran Cohen‐Barak, Shahar Taiber, Morad Khayat +3 more

Karen B. Avraham

Indexed papers

Top data-sharing exemplar

Papers