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Imen Chakchouk

Affiliation : Baylor College of Medicine

• 6Publications (affiliation in Tunisia)
• 29Total publications
• 699Citations
• 17h-index

ORCIDOpenAlex

Research profile

Imen Chakchouk has 6 indexed publications (2015–2021). Their work appears mainly in “Journal of Biomolecular Structure and Dynamics”, “Human Genetics” and “Human Mutation”. Their most cited article, “A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia ” (2015), has been cited 91 times. Their work is co-authored with at least 12 researchers, including institutions in United States, China.

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Research areas

• Hearing, Cochlea, Tinnitus, Genetics
• Congenital Ear and Nasal Anomalies
• Reproductive Biology and Fertility
• Genetic Syndromes and Imprinting
• Epigenetics and DNA Methylation

Publications (6)

• Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment
  2021 · Journal of Biomolecular Structure and Dynamics · cited 3 times
• A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
  2016 · Human Genetics · cited 40 times
• MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform
  2016 · Human Mutation · cited 38 times
• A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation
  2015 · Human Molecular Genetics · cited 91 times
• Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53
  2015 · Molecular Genetics and Genomics · cited 28 times
• NADf Chip, a Two-Color Microarray for Simultaneous Screening of Multigene Mutations Associated with Hearing Impairment in North African Mediterranean Countries
  2015 · Journal of Molecular Diagnostics · cited 22 times

Publication venues

• Journal of Biomolecular Structure and Dynamics × 1
• Human Genetics × 1
• Human Mutation × 1
• Human Molecular Genetics × 1
• Molecular Genetics and Genomics × 1
• Journal of Molecular Diagnostics × 1

Publications per year

• 20211
• 20162
• 20153

Collaborations

Partner institutions : University of Sfax · Centre of Biotechnology of Sfax · University of Miami · Hopital Universitaire Habib Bourguiba · Dr. John T. Macdonald Foundation

Co-authors’ countries : United States · China

Co-authors

• Saber Masmoudi
• Mariem Ben Saïd
• Abdelmonem Ghorbel
• Amine Chakroun
• Fida Jbeli
• Riadh Benmarzoug
• Hassen Hadj-Kacem
• B. Hammami
• Aissette Baanannou
• Ibtihel Smeti
• Salma Loukil
• Mounira Hmani‐Aifa

Bibliographic data from OpenAlex (open database).