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Alanna Strong

17PUBLICATIONS
24CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Cancer geneticsKnowledge and information managementCardiology (incl. cardiovascular diseases)
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Journal

Publications (17)

Sort by Publication Date:
|May 26, 2025
Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay.

Alanna Strong, Caoimhe McKenna, Karen Stals

|Apr 01, 2025
A New EP300 -Related Syndrome With Prominent Developmental and Immune Phenotypes.

Devi Priyanka Maripuri, Jessica Gold, Nina Gold

|Jan 31, 2025
Elucidating the Molecular Landscape of Cystic Kidney Disease: Old Friends, New Friends and Some Surprises.

Deborah Watson, Frank Mentch, Jonathan Billings

|Dec 10, 2024
Executive and adaptive function impacts long-term outcomes for adults with maple syrup urine disease.

Jessica I Gold, Alanna Strong, Nina B Gold

|Dec 10, 2023
Patent ductus arteriosus and coarctation of the aorta in association with PRDM6 variants.

Helen M Stanley, Brian R White, Christopher J LaRosa

|May 25, 2023
TOPORS as a novel causal gene for Joubert syndrome.

Alanna Strong, Hui-Qi Qu, Sinéad Cullina

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Frequent Collaborators

7 joint publications

Hakon Hakonarson

2 joint publications

Cara Skraban

2 joint publications

Jennifer M Kalish

1 joint publications

Emma Bedoukian

1 joint publications

Sanmati Cuddapah

1 joint publications

Jacklyn Omorodion

1 joint publications

Nina B Gold

1 joint publications

Catherine Gooch

1 joint publications

Lord Jephthah Joojo Gowans

1 joint publications

Stephen W Scherer

Frequent Collaborators

7 joint publications

Hakon Hakonarson

2 joint publications

Cara Skraban

2 joint publications

Jennifer M Kalish

1 joint publications

Emma Bedoukian

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