Andrew J Griffith

Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss

K. Honda, Andrew J Griffith, 2021, Human Genetics.

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

Andrew R. Grant, Marina T. DiStefano, I. Krantz, 2021, Genetics in Medicine.

Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss

K. Honda, A. Griffith, Andrew J Griffith, 2021, Human Genetics.

Expert Specification of the ACMG/AMP Variant Interpretation Guidelines for Genetic Hearing Loss

Alex Chapin, Margaret Kenna, Heidi L Rehm, 2018, bioRxiv.

Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria

S. Leal, T. Friedman, R. Yousaf, 2021, European journal of human genetics : EJHG.

Modifier genes of hereditary hearing loss

J. Battey, S. Riazuddin, T. Friedman, 2000, Current Opinion in Neurobiology.

Variants of LRP2, encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

S. Leal, S. Riazuddin, T. Friedman, 2023, Clinical genetics.