Barry Chioza

11PUBLICATIONS
52CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Central nervous systemCell and nuclear divisionGene mappingEpigenetics (incl. genome methylation and epigenomics)
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Publications (11)

|Jun 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.

Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar

|Sep 27, 2021
A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder.

Zineb Ammous, Lettie E Rawlins, Hannah Jones

|Sep 20, 2019
MNS1 variant associated with situs inversus and male infertility.

Joseph S Leslie, Lettie E Rawlins, Barry A Chioza

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