Author

Süleyman Gülsüner

University of WashingtonORCID 0000-0002-3897-1238Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amal Abu RayyaniD· 1 shared Amihood Singer· 1 shared Amir PelegiD· 1 shared Asgeir Orn ArnthorssoniD· 1 shared Bella DavidoviD· 1 shared Chana VinkleriD· 1 shared Doaa Ali‐Naffaa· 1 shared Dorit LeviD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Amal Abu RayyanORCID

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1 paper

Recent·Most cited

GeneticsClinical GeneticsPeer-reviewedJul 20, 2020

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

Zippora Brownstein, Süleyman Gülsüner, Tom Walsh…·Karen B. Avraham

The paper identifies genetic causes of inherited hearing loss in the Israeli Jewish population, finding a novel deafness gene ATOH1 and demonstrating the effectiveness of targeted genomic sequencing.

31 citations

humanwhole-exome sequencing

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