Chris F Inglehearn

19PUBLICATIONS
250CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Craniofacial biologySensory systemsEpigenetics (incl. genome methylation and epigenomics)Dental materials and equipment
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Publications (19)

|Jul 20, 2026
Diagnostic discovery of structural variants causing foveal hypoplasia using SVRare and long-read nanopore sequencing.

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

Lu Liu, Cheuk Wang Au, Ummey Hany

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Oct 23, 2025
RP9 revisited; RP9 p.(H137L) remains a likely cause of dominant splicing factor-Retinitis Pigmentosa.

Leon Chang, James A Poulter, Andrew R Webster

|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

|Jul 28, 2025
Long-Range PCR and Nanopore Sequencing Enables High-Throughput Detection of TCF4 Trinucleotide Repeat Expansions in Fuchs Endothelial Corneal Dystrophy.

Bushra Alayed, Salina Siddiqui, Seema Anand

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Frequent Collaborators

8 joint publications

Christopher M Watson

6 joint publications

Claire E L Smith

6 joint publications

Manir Ali

4 joint publications

Carmel Toomes