Concepedia

Imen Chakchouk

IC

Statistics

Publications

15

Citations

589

H-Index

15

Active since

2015

Affiliations

Baylor College of Medicine(Current)

University of Washington

Baylor Genetics

Quaid-i-Azam University

Centre of Biotechnology of Sfax

Imen Chakchouk is an author at Baylor College of Medicine specializing in genetics, molecular genetics, and life sciences.

ORCID

Publications per year

2015–2019

15

Publications

15

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

M’hamed Grati, Imen Chakchouk, Qi Ma et al. · Human Molecular Genetics · 2015 · 97 citations · Full text

, , +17

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 · 86 citations

, , +13

Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability

Valeed Khan, Falak Sher Khan, Zaib-Un-Nisa Mughal et al. · Human Genetics · 2018 · 59 citations · Full text

, , +16

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

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FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice

Isabelle Schrauwen, Arnaud P. J. Giese, Abdul Aziz et al. · Journal of Bone and Mineral Research · 2018 · 42 citations · Full text

, , +16

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