Schaida Schirwani

5PUBLICATIONS
13CO-AUTHORS
Cancer geneticsAnthropological geneticsGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)
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Publications (5)

|Sep 03, 2025
Multiple early onset atypical cutaneous fibrous histiocytomas in multilocus inherited neoplasia allele syndrome involving TP53 and FLCN genes.

Schaida Schirwani, Sylvia Ghattas, Nicholas Wilson

|Dec 19, 2023
Coexistence of multiple self-healing squamous epithelioma and features of Loeys-Dietz syndrome caused by a pathogenic missense variant in the kinase domain of TGFBR1.

Schaida Schirwani, Bea Suarez, Matthew Sommerlad

|Sep 30, 2022
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype.

Schaida Schirwani, Emily Woods, David A Koolen

|Aug 26, 2021
Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3.

Schaida Schirwani, Shadi Albaba, Deanna Alexis Carere

|Apr 23, 2018
Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability.

Schaida Schirwani, Emma Wakeling, Kath Smith

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Frequent Collaborators

2 joint publications

Meena Balasubramanian

2 joint publications

John M Graham

1 joint publications

Rachel Rabin

1 joint publications

Natalie Hauser