Farah Kanani

6PUBLICATIONS
11CO-AUTHORS
Cell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Cellular nervous systemMajor global burdens of diseaseComposite and hybrid materials
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Publications (6)

|Dec 23, 2024
A tandem duplication of exon 42 of the DMD gene is a likely benign variant.

Jesse B G Hayesmoore, Ruth Newbury-Ecob, Sarah Durell

|Aug 16, 2022
Expanding the phenotype of TAB2 variants and literature review.

Emily Woods, Imogen Marson, Emanuele Coci

|May 16, 2021
Isolated- and Beckwith-Wiedemann syndrome related- lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals.

Jessica A Radley, Melissa Connolly, Ataf Sabir

|Nov 01, 2020
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants.

Eva Z Jacobs, Kathleen Brown, Melissa C Byler

|Jan 12, 2020
Expanding the genotype-phenotype correlation of de novo heterozygous missense variants in YWHAG as a cause of developmental and epileptic encephalopathy.

Farah Kanani, Hannah Titheradge, Nicola Cooper

|Dec 18, 2018
Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype.

Farah Kanani, Michael J Parker, Christine P Burren

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Frequent Collaborators

2 joint publications

Meena Balasubramanian

1 joint publications

Eva Z Jacobs

1 joint publications

Sarah Vergult

1 joint publications

Bert Callewaert