Shehla Mohammed
14PUBLICATIONS
87CO-AUTHORS
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Publications (14)
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|Apr 09, 2026
ACAN-related disorder, antenatal presentation and phenotypic variability: a case series.Nikhil Pattani, Anna Page, Joy L Barber
|Apr 18, 2025
Phenotypic heterogeneity in DYNC2H1-related short-rib thoracic dysplasia: antenatal indicators and postnatal outcomes.Nikhil Pattani, Nour Elkhateeb, Aakash Joshi
|Jul 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition.Jiarna R Zerella, Claire C Homan, Peer Arts
|Apr 27, 2024
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function.Murat Alpaslan, Elodie Fastré, Sandrine Mestre
|Apr 08, 2022
Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B.Stefanie Brock, Annie Laquerriere, Florent Marguet
|Dec 17, 2021
Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts.Sahar Mansour, Katherine S Josephs, Pia Ostergaard
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Frequent Collaborators
6 joint publications
Pia Ostergaard
4 joint publications
Kristiana Gordon
3 joint publications
Silvia Martin-Almedina
2 joint publications
Alexandra Robinson
2 joint publications
Kazim Ogmen
2 joint publications
Ege Sackey
2 joint publications
Dionysios Grigoriadis
2 joint publications
Christina Karapouliou
2 joint publications
Jenny Lord
2 joint publications
Rhiannon Mellis
