Header Logo

IMEN CHAKCHOUK

TitleInstructor
InstitutionBaylor College of Medicine
DepartmentDepartment of Obstetrics & Gynecology
Address1250 MOURSUND STREET
vCardDownload vCard

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Anvar Z, Jochum MD, Chakchouk I, Sharif M, Demond H, To AK, Kraushaar DC, Wan YW, Andrews S, Kelsey G, Veyver IB. Maternal loss-of-function of Nlrp2 results in failure of epigenetic reprogramming in mouse oocytes. Res Sq. 2024 Jun 04. PMID: 38883732; PMCID: PMC11177987.
      Citations:    
    2. Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Su L, Anikar S, Naini FA, Utama AB, Van den Veyver IB. Comparison of Four Protocols for In Vitro Differentiation of Human Embryonic Stem Cells into Trophoblast Lineages by BMP4 and Dual Inhibition of Activin/Nodal and FGF2 Signaling. Reprod Sci. 2024 01; 31(1):173-189. PMID: 37658178; PMCID: PMC10784360.
      Citations:    Fields:    Translation:HumansCells
    3. Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Nasiotis ET, Su L, Liu Z, Wan YW, Van den Veyver IB. Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B. Reprod Sci. 2023 09; 30(9):2780-2793. PMID: 36976514; PMCID: PMC10524210.
      Citations:    Fields:    Translation:AnimalsCells
    4. Souissi A, Abdelmalek Driss D, Chakchouk I, Ben Said M, Ben Ayed I, Mosrati MA, Elloumi I, Tlili A, Aifa S, Masmoudi S. Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment. J Biomol Struct Dyn. 2022; 40(21):10940-10951. PMID: 34423747.
      Citations:    Fields:    
    5. Anvar Z, Chakchouk I, Demond H, Sharif M, Kelsey G, Van den Veyver IB. DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting. Genes (Basel). 2021 08 06; 12(8). PMID: 34440388; PMCID: PMC8394515.
      Citations: 5     Fields:    Translation:HumansCells
    6. Chakchouk I, Vossaert L, Zemet R, Van den Veyver IB. Overview and recent developments in cell-based noninvasive prenatal testing. Prenat Diagn. 2021 Sep; 41(10):1202-1214. PMID: 33974713; PMCID: PMC9355411.
      Citations:    Fields:    Translation:HumansCells
    7. Arian S, Rubin J, Chakchouk I, Sharif M, Mahadevan SK, Erfani H, Shelly K, Liao L, Lorenzo I, Ramakrishnan R, Van den Veyver IB. Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect. Reprod Sci. 2021 07; 28(7):1850-1865. PMID: 33090377; PMCID: PMC8060370.
      Citations: 1     Fields:    Translation:AnimalsCells
    8. Chakchouk I, Zhang D, Zhang Z, Francioli LC, Santos-Cortez RLP, Schrauwen I, Leal SM. Disparities in discovery of pathogenic variants for autosomal recessive non-syndromic hearing impairment by ancestry. Eur J Hum Genet. 2019 09; 27(9):1456-1465. PMID: 31053783; PMCID: PMC6777454.
      Citations: 13     Fields:    Translation:Humans
    9. Ullah I, Kakar N, Schrauwen I, Hussain S, Chakchouk I, Liaqat K, Acharya A, Wasif N, Santos-Cortez RLP, Khan S, Aziz A, Lee K, Couthouis J, Thiele H, Nickerson DA, Bamshad MJ, Gitler AD, Ahmad J, Ansar M, Borck G, Ahmad W, Leal SM, Horn D, Kragesteen BK, Spielmann M. Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly. Hum Genet. 2019 Jun; 138(6):593-600. PMID: 30982135; PMCID: PMC6724712.
      Citations: 5     Fields:    Translation:HumansAnimals
    10. Schrauwen I, Chakchouk I, Acharya A, Nasir A, Poston A, Cornejo-Sanchez DM, Szabo Z, Bene J, Leal SM, Melegh BI, Karosi T, Melegh B. Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma. Eur J Hum Genet. 2019 06; 27(6):869-878. PMID: 30872814; PMCID: PMC6777543.
      Citations: 3     Fields:    Translation:HumansCTClinical Trials
    11. Liaqat K, Schrauwen I, Raza SI, Lee K, Hussain S, Chakchouk I, Nasir A, Acharya A, Abbe I, Umair M, Ansar M, Ullah I, Shah K, University of Washington Center for Mendelian Genomics, Bamshad MJ, Nickerson DA, Ahmad W, Leal SM. Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance. J Hum Genet. 2019 Feb; 64(2):153-160. PMID: 30498240; PMCID: PMC6561484.
      Citations: 16     Fields:    Translation:Humans
    12. Richard EM, Santos-Cortez RLP, Faridi R, Rehman AU, Lee K, Shahzad M, Acharya A, Khan AA, Imtiaz A, Chakchouk I, Takla C, Abbe I, Rafeeq M, Liaqat K, Chaudhry T, Bamshad MJ, Nickerson DA, University of Washington Center for Mendelian Genomics, Schrauwen I, Khan SN, Morell RJ, Zafar S, Ansar M, Ahmed ZM, Ahmad W, Riazuddin S, Friedman TB, Leal SM, Riazuddin S. Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss. Hum Mutat. 2019 01; 40(1):53-72. PMID: 30303587; PMCID: PMC6296877.
      Citations: 21     Fields:    Translation:Humans
    13. Schrauwen I, Giese AP, Aziz A, Lafont DT, Chakchouk I, Santos-Cortez RLP, Lee K, Acharya A, Khan FS, Ullah A, Nickerson DA, Bamshad MJ, Ali G, Riazuddin S, Ansar M, Ahmad W, Ahmed ZM, Leal SM. FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice. J Bone Miner Res. 2019 02; 34(2):375-386. PMID: 30395363; PMCID: PMC6489482.
      Citations: 5     Fields:    Translation:HumansAnimalsCTClinical Trials
    14. Latif Z, Chakchouk I, Schrauwen I, Lee K, Santos-Cortez RLP, Abbe I, Acharya A, Jarral A, Ali I, Ullah E, Khan MN, Ali G, Tahir TH, Bamshad MJ, Nickerson DA, Ahmad W, Ansar M, Leal SM, University of Washington Center for Mendelian Genomics (UWCMG) Study Group. Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa. Invest Ophthalmol Vis Sci. 2018 09 04; 59(11):4552-4557. PMID: 30208423; PMCID: PMC6133250.
      Citations: 6     Fields:    Translation:Humans
    15. Liaqat K, Chiu I, Lee K, Chakchouk I, Andrade-Elizondo PB, Santos-Cortez RLP, Hussain S, Nawaz S, Ansar M, Khan MN, Basit S, Schrauwen I, Ahmad W, Leal SM. Novel missense and 3'-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. J Hum Genet. 2018 Nov; 63(11):1099-1107. PMID: 30177809; PMCID: PMC6202120.
      Citations: 1     Fields:    Translation:HumansCells
    16. Santos-Cortez RLP, Khan V, Khan FS, Mughal ZU, Chakchouk I, Lee K, Rasheed M, Hamza R, Acharya A, Ullah E, Saqib MAN, Abbe I, Ali G, Hassan MJ, Khan S, Azeem Z, Ullah I, Bamshad MJ, Nickerson DA, Schrauwen I, Ahmad W, Ansar M, Leal SM. Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability. Hum Genet. 2018 Sep; 137(9):735-752. PMID: 30167849; PMCID: PMC6201268.
      Citations: 16     Fields:    Translation:Humans
    17. Schrauwen I, Chakchouk I, Acharya A, Liaqat K, University of Washington Center for Mendelian Genomics, Nickerson DA, Bamshad MJ, Shah K, Ahmad W, Leal SM. Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment. BMC Med Genet. 2018 07 20; 19(1):122. PMID: 30029624; PMCID: PMC6053831.
      Citations: 7     Fields:    Translation:HumansAnimalsCells
    18. Schrauwen I, Chakchouk I, Liaqat K, Jan A, Nasir A, Hussain S, Nickerson DA, Bamshad MJ, Ullah A, Ahmad W, Leal SM. A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment. Hum Genet. 2018 Jul; 137(6-7):471-478. PMID: 29971487; PMCID: PMC6094940.
      Citations: 6     Fields:    Translation:HumansAnimals
    19. Grati M, Ishimoto T, Zou B, Ma Q, Yao Q, Yan D, Mittal R, Nakamichi N, Neng L, Tekin M, Shi XR, Kato Y, Lu Z, Liu X, Ben Said M, Chakchouk I, Hammami B, Ghorbel A, Masmoudi S, Hmani M. A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60. Hum Genet. 2016 May; 135(5):513-524. PMID: 27023905; PMCID: PMC4836961.
      Citations: 15     Fields:    Translation:HumansAnimalsCells
    20. Grati M, Yan D, Raval MH, Walsh T, Ma Q, Chakchouk I, Kannan-Sundhari A, Mittal R, Blanton SH, Tekin M, King MC, Yengo CM, Liu XZ, Masmoudi S. MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform. Hum Mutat. 2016 May; 37(5):481-7. PMID: 26841241; PMCID: PMC4833613.
      Citations: 12     Fields:    Translation:HumansAnimalsCells
    21. Grati M, Bademci G, Bensaid M, Ma Q, Chakroun A, Foster J, Yan D, Duman D, Diaz-Horta O, Ghorbel A, Mittal R, Farooq A, Tekin M, Masmoudi S, Liu XZ, Chakchouk I. Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53. Mol Genet Genomics. 2015 Aug; 290(4):1327-34. PMID: 25633957; PMCID: PMC4707654.
      Citations: 14     Fields:    Translation:HumansCells
    22. Grati M, Ma Q, Desmidt A, Yan D, Mittal R, Blanton S, Farooq A, Lu Z, Liu XZ, Chakchouk I, Bensaid M, Turki N, Baanannou A, Driss N, Masmoudi S. A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. Hum Mol Genet. 2015 May 01; 24(9):2482-91. PMID: 25601850; PMCID: PMC4383862.
      Citations: 44     Fields:    Translation:HumansAnimalsCells
    23. Chakchouk I, Ben Said M, Jbeli F, Benmarzoug R, Loukil S, Smeti I, Chakroun A, Gibriel AA, Ghorbel A, Hadjkacem H, Masmoudi S. NADf chip, a two-color microarray for simultaneous screening of multigene mutations associated with hearing impairment in North African Mediterranean countries. J Mol Diagn. 2015 Mar; 17(2):155-61. PMID: 25560255.
      Citations: 14     Fields:    Translation:Humans
    CHAKCHOUK's Networks
    Click the
    Explore
    buttons for more information and interactive visualizations!
    Concepts (149)
    Explore
    _
    Co-Authors (11)
    Explore
    _
    Similar People (60)
    Explore
    _
    Same Department Expand Description
    Explore
    _