Liz M Nouel-Saied
5PUBLICATIONS
18CO-AUTHORS
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Publications (5)
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|Feb 12, 2022
Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant.Thashi Bharadwaj, Isabelle Schrauwen, Anushree Acharya
|Dec 24, 2021
Exome Sequencing Identifies a Novel FBN1 Variant in a Pakistani Family with Marfan Syndrome That Includes Left Ventricle Diastolic Dysfunction.Nadia Farooqi, Louise A Metherell, Isabelle Schrauwen
|Nov 27, 2021
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family.Noluthando Manyisa, Isabelle Schrauwen, Leonardo Alves de Souza Rios
|Mar 15, 2021
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family.Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin K Esoh
|Oct 29, 2020
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment.Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin K Esoh
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Frequent Collaborators
3 joint publications
Isabelle Schrauwen
3 joint publications
Kevin K Esoh
3 joint publications
Thashi Bharadwaj
3 joint publications
Abdul Nasir
3 joint publications
Ambroise Wonkam
2 joint publications
Shaheen Mowla
1 joint publications
Louise A Metherell
1 joint publications
Yasir Ali
1 joint publications
Hamed A El-Serehy
1 joint publications
Fazal Jalil
