Farah Kanani

ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 5

Top Venues

American journal of medical genetics. Part A

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Emily Woods, Imogen Marson, Emanuele Coci, Michael Spiller, Ajith Kumar, Angela Brady, Tessa Homfray, Richard Fisher, Peter Turnpenny, Julia Rankin, Farah Kanani, Konrad Platzer, Athina Ververi, Eleftheria Emmanouilidou, Nourxan Bourboun, George Giannakoulas, Meena Balasubramanian
Expanding the phenotype of TAB2 variants and literature review. American journal of medical genetics. Part A 188 (11) (2022)
Jessica A Radley, Melissa Connolly, Ataf Hussain Sabir, Farah Kanani, Helena Carley, Rachel L Jones, Zerin Hyder, Lianne Gompertz, Willie Reardon, Ruth Richardson, Louise McClelland, Eamonn R Maher
Isolated- and Beckwith-Wiedemann syndrome related- lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals. Clinical genetics 100 (3) (2021)
Eva Z Jacobs, Kathleen Brown, Melissa C Byler, Erika D'haenens, Annelies Dheedene, Lindsay B Henderson, Jennifer B Humberson, Richard H van Jaarsveld, Farah Kanani, Robert Roger Lebel, Francisca Millan, Renske Oegema, Ann Oostra, Michael J Parker, Lindsay Rhodes, Margarita Saenz, Laurie H Seaver, Yue Si, Arnaud Vanlander, Sarah Vergult, Bert Callewaert
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants. Clinical genetics 99 (2) (2020)
Farah Kanani, Hannah Titheradge, Nicola Cooper, Frances Elmslie, Melissa M Lees, Jane Juusola, Laura Pisani, Carolyn McKenna, Cyril Mignot, Stephanie Valence, Boris Keren, Katherine Lachlan, null null, Meena Balasubramanian
Expanding the genotype-phenotype correlation of de novo heterozygous missense variants in YWHAG as a cause of developmental and epileptic encephalopathy. American journal of medical genetics. Part A 182 (4) (2020)
Farah Kanani, Michael J Parker, Christine P Burren, Julia Rankin, Meena Balasubramanian
Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype. American journal of medical genetics. Part A 179 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Farah Kanani