Ummey Hany

6PUBLICATIONS
21CO-AUTHORS
Craniofacial biologyDental materials and equipmentGene mappingEpigenetics (incl. genome methylation and epigenomics)Oral implantology
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Journal

Publications (6)

|Apr 11, 2026
ACP4 Variants in Hypoplastic Amelogenesis Imperfecta.

Lu Liu, Cheuk Wang Au, Ummey Hany

|Jul 31, 2025
Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target Loci.

Ummey Hany, Christopher M Watson, Lu Liu

|Jun 26, 2025
AgileMultiIdeogram: Rapid Identification and Visualization of Autozygous Regions Using Illumina Short-Read Sequencing Data.

Christopher M Watson, Carolina Lascelles, Morag Raynor

|Mar 08, 2024
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.

Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany

|Dec 07, 2023
Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes.

U Hany, C M Watson, L Liu

|Nov 18, 2023
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta.

Ummey Hany, Christopher M Watson, Lu Liu

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Frequent Collaborators

6 joint publications

Christopher M Watson

4 joint publications

James A Poulter

3 joint publications

Chris F Inglehearn

3 joint publications

Claire E L Smith