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Laura Cross

4PUBLICATIONS

20CO-AUTHORS

Infant and child healthNeurogeneticsMolecular targetsEpidemiological modelling

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Publications (4)

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|May 15, 2023

Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.

Monica H Wojcik, Siddharth Srivastava, Pankaj B Agrawal

|Oct 27, 2022

Recurrent FOXP4 nonsense variant in two unrelated patients: Association with neurodevelopmental disease and congenital diaphragmatic hernia.

Florencia Del Viso, Dihong Zhou, Isabelle Thiffault

|Oct 08, 2022

PPP2R1A neurodevelopmental disorder is associated with congenital heart defects.

Elizabeth K Baker, Beulah Solivio, Ben Pode-Shakked

|Feb 06, 2021

Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine.

Víctor Faundes, Martin D Jennings, Siobhan Crilly

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Frequent Collaborators

1 joint publications

Víctor Faundes

1 joint publications

Martin D Jennings

1 joint publications

Siobhan Crilly

1 joint publications

William G Newman

1 joint publications

Miranda Splitt

1 joint publications

Bonnie R Sullivan

1 joint publications

Christopher T Gordon

1 joint publications

Graham D Pavitt

1 joint publications

Siddharth Banka

1 joint publications

Elizabeth K Baker

Frequent Collaborators

1 joint publications

Víctor Faundes

1 joint publications

Martin D Jennings

1 joint publications

Siobhan Crilly

1 joint publications

William G Newman

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