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Maryam Al Shehhi
Maryam Al Shehhi
Boston Children's Hospital
Biology
Proband
Autism spectrum disorder
Genetics
Population
3
Papers
32
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Towards establishing consistency in triage in a tertiary specialty
2019
European Journal of Human Genetics
Terri P. McVeigh
Deirdre E. Donnelly
Maryam Al Shehhi
Elizabeth A. Jones
Alexandra Murray
Sarah Wedderburn
Mary Porteous
Sally Ann Lynch
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Citations (3)
NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families
2019
European Journal of Medical Genetics
Maryam Al Shehhi
Eva B. Forman
Jacqueline Fitzgerald
Veronica McInerney
Janusz Krawczyk
Sanbing Shen
David R. Betts
Linda Mc Ardle
Kathleen M. Gorman
Mary D. King
Andrew Green
Louise Gallagher
Sally Ann Lynch
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Citations (29)
DECONSTRUCTING THE NEUREXIN1 DELETION PHENOTYPE: A NEUROPSYCHOLOGICAL, NEUROCOGNITIVE AND NEUROIMAGING PERSPECTIVE
2019
European Neuropsychopharmacology
Louise Gallagher
Jacqueline Fitzgerald
Maryam Al Shehhi
Sally Ann Lynch
Sanbing Shen
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