Ichrak Drissi

9PUBLICATIONS
26CO-AUTHORS
Sensory systemsEpigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseGene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)
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Publications (9)

|Apr 28, 2025
Sensory neuron sodium channels as pain targets; from cocaine to Journavx (VX-548, suzetrigine).

John N Wood, Nieng Yan, Jian Huang

|Apr 06, 2021
Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly.

Ichrak Drissi, Emily Fletcher, Ranad Shaheen

|May 21, 2020
De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features.

Julien Buratti, Lei Ji, Boris Keren

|Oct 06, 2018
PEHO syndrome: the endpoint of different genetic epilepsies.

Manali Chitre, Michael S Nahorski, Kaitlin Stouffer

|Jul 14, 2018
Before progressing from "exomes" to "genomes"… don't forget splicing variants.

Samiha S Shaikh, Michael S Nahorski, Harjeet Rai

|Jun 28, 2018
Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.

C Moss, S M Srinivas, N Sarveswaran

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Frequent Collaborators

2 joint publications

Fowzan S Alkuraya

2 joint publications

Alberto Fernández-Jaén

2 joint publications

Steve Lisgo

1 joint publications

Pavithra L Chavali