Connection

IMEN CHAKCHOUK to Male

This is a "connection" page, showing publications IMEN CHAKCHOUK has written about Male.
Connection Strength

0.129
  1. Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53. Mol Genet Genomics. 2015 Aug; 290(4):1327-34.
    View in: PubMed
    Score: 0.020
  2. 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.
    View in: PubMed
    Score: 0.020
  3. Maternal loss of mouse Nlrp2 alters the transcriptome and DNA methylome in GV oocytes and impairs zygotic genome activation in embryos. Clin Epigenetics. 2025 Jun 03; 17(1):92.
    View in: PubMed
    Score: 0.010
  4. Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly. Hum Genet. 2019 Jun; 138(6):593-600.
    View in: PubMed
    Score: 0.007
  5. 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.
    View in: PubMed
    Score: 0.007
  6. 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.
    View in: PubMed
    Score: 0.006
  7. Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss. Hum Mutat. 2019 01; 40(1):53-72.
    View in: PubMed
    Score: 0.006
  8. 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.
    View in: PubMed
    Score: 0.006
  9. 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.
    View in: PubMed
    Score: 0.006
  10. 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.
    View in: PubMed
    Score: 0.006
  11. Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability. Hum Genet. 2018 Sep; 137(9):735-752.
    View in: PubMed
    Score: 0.006
  12. Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment. BMC Med Genet. 2018 07 20; 19(1):122.
    View in: PubMed
    Score: 0.006
  13. A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment. Hum Genet. 2018 Jul; 137(6-7):471-478.
    View in: PubMed
    Score: 0.006
  14. 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.
    View in: PubMed
    Score: 0.005
  15. MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform. Hum Mutat. 2016 May; 37(5):481-7.
    View in: PubMed
    Score: 0.005
  16. 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.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.