Andrew H Crosby

5PUBLICATIONS
30CO-AUTHORS
NeurogeneticsCellular nervous systemGene mappingEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Mar 04, 2024
TECPR2-related hereditary sensory and autonomic neuropathy in two siblings from Palestine.

Reham Khalaf-Nazzal, Imad Dweikat, Nishanka Ubeyratna

|Jul 17, 2023
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission.

James Fasham, Antje K Huebner, Lutz Liebmann

|Jul 12, 2023
Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes.

Maria O Levitin, Lettie E Rawlins, Gabriela Sanchez-Andrade

|Mar 17, 2022
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice.

Lettie E Rawlins, Hashem Almousa, Shazia Khan

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

Zineb Ammous, Lettie E Rawlins, Hannah Jones

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