P. Andrade

Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

S. Leal, S. Riazuddin, Z. Ahmed, 2011, Human Genetics.

Topical Fixed-Dose Combinations: Current in vitro methodologies for pre-clinical development.

C. Vitorino, P. Andrade, R. Videira, 2022, International journal of pharmaceutics.

Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB90 Maps to 7p22.1-p15.3

S. Leal, S. Basit, W. Ahmad, 2011, Human Heredity.

DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2

S. Leal, S. Basit, W. Ahmad, 2011, Human Genetics.

Diabetes-associated mitochondrial DNA mutation A3243G impairs cellular metabolic pathways necessary for beta cell function

J. Maassen, F. Frigerio, P. Andrade, 2006, Diabetologia.

Novel CLDN14 mutations in Pakistani families with autosomal recessive non‐syndromic hearing loss

S. Leal, W. Ahmad, R. Santos-Cortez, 2012, American journal of medical genetics. Part A.

Novel TMPRSS3 variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment

W. Ahmad, R. Santos-Cortez, M. Ansar, 2012, Clinical genetics.

A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13

S. Leal, S. Basit, W. Ahmad, 2011, Journal of Human Genetics.

Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment.

E. Sartorato, F. Alexandrino, P. Andrade, 2009, Biochemical and biophysical research communications.