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Chakchouk, Imen
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1

Comparison of Four Protocols for In Vitro Differentiation o..:

Anvar, Zahra ; Chakchouk, Imen ; Sharif, Momal...
Reproductive Sciences.  31 (2023)  1 - p. 173-189 , 2023
Link: https://doi.org/10.1007/..
 
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2

Loss of the Maternal Effect Gene Nlrp2 Alters the Transcrip..:

Anvar, Zahra ; Chakchouk, Imen ; Sharif, Momal...
Reproductive Sciences.  30 (2023)  9 - p. 2780-2793 , 2023
Link: https://doi.org/10.1007/..
 
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3

Overview and recent developments in cell‐based noninvasive ..:

Vossaert, Liesbeth ; Chakchouk, Imen ; Zemet, Roni.
Prenatal Diagnosis.  41 (2021)  10 - p. 1202-1214 , 2021
Link: https://doi.org/10.1002/..
 
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4

DNA Methylation Dynamics in the Female Germline and Materna..:

Anvar, Zahra ; Chakchouk, Imen ; Demond, Hannah...
Genes.  12 (2021)  8 - p. 1214 , 2021
Link: https://doi.org/10.3390/..
 
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5

Molecular insights into MYO3A kinase domain variants explai..:

Souissi, Amal ; Abdelmalek Driss, Dorra ; Chakchouk, Imen...
Journal of Biomolecular Structure and Dynamics.  40 (2021)  21 - p. 10940-10951 , 2021
Link: https://doi.org/10.1080/..
 
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6

Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not I..:

Arian, Sara ; Rubin, Jessica ; Chakchouk, Imen...
Reproductive Sciences.  28 (2020)  7 - p. 1850-1865 , 2020
Link: https://doi.org/10.1007/..
 
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7

Disparities in discovery of pathogenic variants for autosom..:

Chakchouk, Imen ; Zhang, Di ; Zhang, Zhihui...
European Journal of Human Genetics.  27 (2019)  9 - p. 1456-1465 , 2019
Link: https://doi.org/10.1038/..
 
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8

Hearing impairment locus heterogeneity and identification o..:

Schrauwen, Isabelle ; Melegh, Béla I. ; Chakchouk, Imen...
European Journal of Human Genetics.  27 (2019)  6 - p. 869-878 , 2019
Link: https://doi.org/10.1038/..
 
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9

Variants in KIAA0825 underlie autosomal recessive postaxial..:

Ullah, Irfan ; Kakar, Naseebullah ; Schrauwen, Isabelle...
Human Genetics.  138 (2019)  6 - p. 593-600 , 2019
Link: https://doi.org/10.1007/..
 
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10

A variant in LMX1A causes autosomal recessive severe-to-pro..:

Schrauwen, Isabelle ; Chakchouk, Imen ; Liaqat, Khurram...
Human Genetics.  137 (2018)  6-7 - p. 471-478 , 2018
Link: https://doi.org/10.1007/..
 
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11

Novel digenic inheritance of PCDH15 and USH1G underlies pro..:

University of Washington Center for Mendelian Genomics ; Schrauwen, Isabelle ; Chakchouk, Imen...
BMC Medical Genetics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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12

Novel missense and 3′-UTR splice site variants in LHFPL5 ca..:

Liaqat, Khurram ; Chiu, Ilene ; Lee, Kwanghyuk...
Journal of Human Genetics.  63 (2018)  11 - p. 1099-1107 , 2018
Link: https://doi.org/10.1038/..
 
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13

Confirmation of the Role ofDHX38in the Etiology of Early-On..:

Latif, Zahid ; Chakchouk, Imen ; Schrauwen, Isabelle...
Investigative Opthalmology & Visual Science.  59 (2018)  11 - p. 4552 , 2018
Link: https://doi.org/10.1167/..
 
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14

Identification of CACNA1D variants associated with sinoatri..:

University of Washington Center for Mendelian Genomics ; Liaqat, Khurram ; Schrauwen, Isabelle...
Journal of Human Genetics.  64 (2018)  2 - p. 153-160 , 2018
Link: https://doi.org/10.1038/..
 
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15

FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Huma..:

Schrauwen, Isabelle ; Giese, Arnaud PJ ; Aziz, Abdul...
Journal of Bone and Mineral Research.  34 (2018)  2 - p. 375-386 , 2018
Link: https://doi.org/10.1002/..
 
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