Mahdi Sarmady
4PUBLICATIONS
16CO-AUTHORS
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Publications (4)
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|Dec 10, 2025
Whole Genome Sequencing Improves the Identification of Pathogenic and Novel Variation in Nonsyndromic Hearing Loss.Stefan Rentas, Ramakrishnan Rajagopalan, Tolga Ayazseven
|Sep 26, 2024
Targeted and complete genomic sequencing of the major histocompatibility complex in haplotypic form of individual heterozygous samples.Taishan Hu, Timothy L Mosbruger, Nikolaos G Tairis
|Jan 11, 2019
Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach.Chao Wu, Batsal Devkota, Perry Evans
|Sep 23, 2016
Using large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation.Sami S Amr, Saeed H Al Turki, Matthew Lebo
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Frequent Collaborators
2 joint publications
Ahmad N Abou Tayoun
2 joint publications
Pushkala Jayaraman
1 joint publications
Sami S Amr
1 joint publications
Saeed H Al Turki
1 joint publications
Matthew Lebo
1 joint publications
Heidi L Rehm
1 joint publications
Michael A Gonzalez
1 joint publications
Matthew A Deardorff
1 joint publications
Timothy L Mosbruger
1 joint publications
Amalia Dinou
