Khurram Liaqat

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss

Élodie M. Richard, Regie Lyn P. Santos‐Cortez, Rabia Faridi et al. · Human Mutation · 2018 · 84 citations

Genetics, Genetic Epidemiology, Consanguineous Pakistani Families +20

Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance

Khurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza et al. · Journal of Human Genetics · 2018 · 46 citations · Full text

Genetic Disorder, Genetics, Clinical Significance +4

Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment

Isabelle Schrauwen, Khurram Liaqat, Isabelle Schatteman et al. · Genes · 2020 · 40 citations · Full text

Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Isabelle Schrauwen, Imen Chakchouk, Anushree Acharya et al. · BMC Medical Genetics · 2018 · 27 citations · Full text

Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly

Irfan Ullah, Naseebullah Kakar, Isabelle Schrauwen et al. · Human Genetics · 2019 · 23 citations

Allelic Variant, Developmental Biology, Genetic Disorder +5