Imen Chakchouk

693 total citations
20 papers, 354 citations indexed

About

Imen Chakchouk is a scholar working on Molecular Biology, Sensory Systems and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Imen Chakchouk has authored 20 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Sensory Systems and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Imen Chakchouk's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Prenatal Screening and Diagnostics (4 papers) and RNA and protein synthesis mechanisms (4 papers). Imen Chakchouk is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Prenatal Screening and Diagnostics (4 papers) and RNA and protein synthesis mechanisms (4 papers). Imen Chakchouk collaborates with scholars based in United States, Tunisia and Pakistan. Imen Chakchouk's co-authors include Ignatia B. Van den Veyver, Saber Masmoudi, Isabelle Schrauwen, Suzanne M. Leal, Qi Ma, M’hamed Grati, Rahul Mittal, Denise Yan, Mariem Ben Saïd and Zahra Anvar and has published in prestigious journals such as Human Molecular Genetics, Journal of Bone and Mineral Research and Investigative Ophthalmology & Visual Science.

In The Last Decade

Imen Chakchouk

19 papers receiving 352 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Imen Chakchouk United States	13	203	134	84	50	33	20	354
Janice C. Palumbos United States	8	245 1.2×	32 0.2×	161 1.9×	56 1.1×	13 0.4×	13	391
Noah R. Druckenbrod United States	11	200 1.0×	92 0.7×	77 0.9×	10 0.2×	32 1.0×	12	615
W. J. Kimberling United States	8	126 0.6×	167 1.2×	94 1.1×	52 1.0×	80 2.4×	19	374
Ahmet Karagüzel Türkiye	11	236 1.2×	222 1.7×	95 1.1×	62 1.2×	104 3.2×	24	458
Ali Muhammad Waryah Pakistan	12	191 0.9×	150 1.1×	77 0.9×	21 0.4×	69 2.1×	39	412
Alisha Wilkens United States	13	239 1.2×	61 0.5×	255 3.0×	104 2.1×	25 0.8×	20	438
Tiia Reimand Estonia	13	229 1.1×	23 0.2×	291 3.5×	97 1.9×	15 0.5×	41	488
Joon Suk Lee South Korea	10	123 0.6×	80 0.6×	67 0.8×	13 0.3×	32 1.0×	14	284
Wie‐Yen Young China	16	500 2.5×	272 2.0×	39 0.5×	9 0.2×	82 2.5×	19	624
Dean Phelan Australia	11	188 0.9×	51 0.4×	180 2.1×	19 0.4×	23 0.7×	15	398

Countries citing papers authored by Imen Chakchouk

Since Specialization

Citations

This map shows the geographic impact of Imen Chakchouk's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Imen Chakchouk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Imen Chakchouk more than expected).

Fields of papers citing papers by Imen Chakchouk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Imen Chakchouk. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Imen Chakchouk. The network helps show where Imen Chakchouk may publish in the future.

Co-authorship network of co-authors of Imen Chakchouk

This figure shows the co-authorship network connecting the top 25 collaborators of Imen Chakchouk. A scholar is included among the top collaborators of Imen Chakchouk based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Imen Chakchouk. Imen Chakchouk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Anvar, Zahra, Michael D. Jochum, Imen Chakchouk, et al.. (2025). Maternal loss of mouse Nlrp2 alters the transcriptome and DNA methylome in GV oocytes and impairs zygotic genome activation in embryos. Clinical Epigenetics. 17(1). 92–92. 1 indexed citations

Anvar, Zahra, et al.. (2023). 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. Reproductive Sciences. 31(1). 173–189. 2 indexed citations

Anvar, Zahra, Imen Chakchouk, Sangeetha Mahadevan, et al.. (2023). Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B. Reproductive Sciences. 30(9). 2780–2793. 3 indexed citations

Souissi, Amal, Baha Eddine Abdelmalek, Imen Chakchouk, et al.. (2021). Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment. Journal of Biomolecular Structure and Dynamics. 40(21). 10940–10951.

Anvar, Zahra, et al.. (2021). DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting. Genes. 12(8). 1214–1214. 37 indexed citations

Vossaert, Liesbeth, Imen Chakchouk, Roni Zemet, & Ignatia B. Van den Veyver. (2021). Overview and recent developments in cell‐based noninvasive prenatal testing. Prenatal Diagnosis. 41(10). 1202–1214. 20 indexed citations

Arian, Sara E., Imen Chakchouk, Sangeetha Mahadevan, et al.. (2020). Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect. Reproductive Sciences. 28(7). 1850–1865. 5 indexed citations

Schrauwen, Isabelle, Béla Melegh, Imen Chakchouk, et al.. (2019). Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma. European Journal of Human Genetics. 27(6). 869–878. 10 indexed citations

Chakchouk, Imen, Di Zhang, Laurent C. Francioli, et al.. (2019). Disparities in discovery of pathogenic variants for autosomal recessive non-syndromic hearing impairment by ancestry. European Journal of Human Genetics. 27(9). 1456–1465. 16 indexed citations

10.

Schrauwen, Isabelle, Syed Irfan Raza, Kwanghyuk Lee, et al.. (2018). Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance. Journal of Human Genetics. 64(2). 153–160. 28 indexed citations

11.

Lee, Kwanghyuk, Imen Chakchouk, Regie Lyn P. Santos‐Cortez, et al.. (2018). Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. Journal of Human Genetics. 63(11). 1099–1107. 2 indexed citations

12.

Schrauwen, Isabelle, Imen Chakchouk, Anushree Acharya, et al.. (2018). Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment. BMC Medical Genetics. 19(1). 122–122. 16 indexed citations

13.

Schrauwen, Isabelle, Imen Chakchouk, Abdul Nasır, et al.. (2018). A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment. Human Genetics. 137(6-7). 471–478. 16 indexed citations

14.

Schrauwen, Isabelle, Arnaud P. J. Giese, Abdul Aziz, et al.. (2018). FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice. Journal of Bone and Mineral Research. 34(2). 375–386. 25 indexed citations

15.

Chakchouk, Imen, Isabelle Schrauwen, Kwanghyuk Lee, et al.. (2018). Confirmation of the Role ofDHX38in the Etiology of Early-Onset Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 59(11). 4552–4552. 12 indexed citations

16.

Saïd, Mariem Ben, M’hamed Grati, Takahiro Ishimoto, et al.. (2016). A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60. Human Genetics. 135(5). 513–524. 26 indexed citations

17.

Grati, M’hamed, Denise Yan, Tom Walsh, et al.. (2016). MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform. Human Mutation. 37(5). 481–487. 25 indexed citations

18.

Chakchouk, Imen, Mariem Ben Saïd, Ibtihel Smeti, et al.. (2015). NADf Chip, a Two-Color Microarray for Simultaneous Screening of Multigene Mutations Associated with Hearing Impairment in North African Mediterranean Countries. Journal of Molecular Diagnostics. 17(2). 155–161. 18 indexed citations

19.

Grati, M’hamed, Imen Chakchouk, Qi Ma, et al.. (2015). A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. Human Molecular Genetics. 24(9). 2482–2491. 75 indexed citations

20.

Chakchouk, Imen, M’hamed Grati, Güney Bademci, et al.. (2015). Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53. Molecular Genetics and Genomics. 290(4). 1327–1334. 17 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact