Schaida Schirwani

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 6

Top Topics

Intellectual Disability

Tyrosine Kinase

Top Venues

American journal of medical genetics. Part A

Clinical and experimental dermatology

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

Publications

Schaida Schirwani, Bea Suarez, Matthew Sommerlad, Emma Corden, Geeta Belgi, Diana Eccles, Adam Fityan
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. Clinical and experimental dermatology 49 (6) (2024)
Schaida Schirwani, Bea Suarez, Matthew Sommerlad, Emma Corden, Geeta Belgi, Diana Eccles, Adam Fityan
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. Clinical and experimental dermatology 49 (6) (2024)
Schaida Schirwani, Bea Suarez, Matthew Sommerlad, Emma Corden, Geeta Belgi, Diana Eccles, Adam Fityan
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 gene. Clinical and experimental dermatology (2023)
Schaida Schirwani, Emily Woods, David A Koolen, Charlotte W Ockeloen, Sally Ann Lynch, Karl Kavanagh, John M Graham, Katheryn Grand, Tyler Mark Pierson, Jeffrey M Chung, Meena Balasubramanian
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype. American journal of medical genetics. Part A (2022)
Schaida Schirwani, Shadi Albaba, Deanna Alexis Carere, Maria J Guillen Sacoto, Francisca Milan Zamora, Yue Si, Rachel Rabin, John Pappas, Deborah L Renaud, Natalie S Hauser, Evan Reid, Patricia Blanchet, Nichola Foulds, Abhijit Dixit, Richard Fisher, Ruth Armstrong, Bertrand Isidor, Benjamin Cogne, Samantha A Schrier Vergano, Serwet Demirdas, Natalie Dykzeul, Julie S Cohen, Katheryn Grand, Dayna Morel, Anne Slavotinek, Hessa F Albassam, Swati Naik, John Dean, Nicola Ragge, Costa Cinzia, Maria Giovanna Tedesco, Rachel E Harrison, Arjan Bouman, Emily Palen, Thomas D Challman, Marjolein H Willemsen, Julie Vogt, Christopher M Cunniff, Katherine L Bergstrom, Jagdeep S Walia, Ange-Line Bruel, Usha Kini, Fowzan Sami Alkuraya, Valerie Slegesky, Naomi Meeks, Paula Girotto, Diana Johnson, null null, Ruth Newbury-Ecob, Charlotte W Ockeloen, Paolo Prontera, Sally Ann Lynch, Dong Li, John M Graham, Meena Balasubramanian
Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3. American journal of medical genetics. Part A 185 (11) (2021)
Schaida Schirwani, Emma Wakeling, Kath Smith, null null, Meena Balasubramanian
Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability. American journal of medical genetics. Part A 176 (5) (2019)