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Genes|December 24, 2021
Exome Sequencing Identifies a Novel FBN1 Variant in a Pakistani Family with Marfan Syndrome That Includes Left Ventricle Diastolic DysfunctionNadia Farooqi, Louise A Metherell, Isabelle Schrauwen, et al.
Scientific Reports|May 16, 2024
Optical genome mapping unveils hidden structural variants in neurodevelopmental disordersIsabelle Schrauwen, Yasmin Rajendran, Anushree Acharya, et al.
Clinical Genetics|May 15, 2025
The Diverse Genetic Landscape of Hearing Impairment in South African FamiliesThashi Bharadwaj, Anushree Acharya, Noluthando Rearabetswe Manyisa, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 29, 2026
Novel Variants Identified in Families With SNX27-Related Neurodevelopmental Disorder, Aiding in Characterizing Its Genotypic and Phenotypic SpectrumTayyaba Shan, Abrar Hussain, Anushree Acharya, et al.
European Journal of Human Genetics : EJHG|March 16, 2019
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian RomaIsabelle Schrauwen, Béla I Melegh, Imen Chakchouk, et al.
BMC Medical Genomics|November 11, 2022
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in GhanaSamuel Mawuli Adadey, Elvis Twumasi Aboagye, Kevin Esoh, et al.
Genes|October 29, 2020
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing ImpairmentEdmond Wonkam-Tingang, Isabelle Schrauwen, Kevin K Esoh, et al.
Pathogens and Global Health|November 11, 2017
Molecular surveillance of chloroquine drug resistance markers (Pfcrt and Pfmdr1) among imported Plasmodium falciparum malaria in QatarAnushree Acharya, Devendra Bansal, Praveen K Bharti, et al.
Plos One|January 4, 2017
Human Papillomavirus (HPV) Infection: Molecular Epidemiology, Genotyping, Seroprevalence and Associated Risk Factors among Arab Women in QatarAsha A Elmi, Devendra Bansal, Anushree Acharya, et al.
European Journal of Human Genetics : EJHG|February 14, 2023
Rare-variant association analysis reveals known and new age-related hearing loss genesDiana M Cornejo-Sanchez, Guangyou Li, Tabassum Fabiha, et al.
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