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Liz M. Nouel-Saied
Liz M. Nouel-Saied
Columbia University
Biology
Genetics
Gene
Exome sequencing
Sanger sequencing
4
Papers
4
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0
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2024
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Exome Sequencing Identifies a Novel FBN1 Variant in a Pakistani Family with Marfan Syndrome that Includes Left Ventricle Diastolic Dysfunction
2021
Genes
Nadia Farooqi
Louise A. Metherell
Isabelle Schrauwen
Anushree Acharya
Qayum Khan
Liz M. Nouel-Saied
Yasir Ali
Hamed A. El-Serehy
Fazal Jalil
Suzanne M. Leal
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Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment.
2021
Journal of Human Genetics
Samuel Mawuli Adadey
Isabelle Schrauwen
Elvis Twumasi Aboagye
Thashi Bharadwaj
Kevin K. Esoh
Sulman Basit
Anushree Acharya
Liz M. Nouel-Saied
Khurram Liaqat
Edmond Wonkam Tingang
Shaheen Mowla
Gordon A. Awandare
Wasim Ahmad
Suzanne M. Leal
Ambroise Wonkam
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Citations (1)
A novel variant in DXML2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family
2021
Experimental Biology and Medicine
Edmond Wonkam Tingang
Isabelle Schrauwen
Kevin K. Esoh
Thashi Bharadwaj
Liz M. Nouel-Saied
Anushree Acharya
Abdul Nasir
Suzanne M. Leal
Ambroise Wonkam
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Citations (3)
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family
2021
Genes
Noluthando Manyisa
Isabelle Schrauwen
Leonardo Alves de Souza Rios
Shaheen Mowla
Cedrik Tekendo-Ngongang
Kalinka Popel
Kevin K. Esoh
Thashi Bharadwaj
Liz M. Nouel-Saied
Anushree Acharya
Abdul Nasir
Edmond Wonkam Tingang
Carmen de Kock
Collet Dandara
Suzanne M. Leal
Ambroise Wonkam
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