Laura M Bryant
5PUBLICATIONS
114CO-AUTHORS
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Publications (5)
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|Nov 17, 2025
Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long-Standing Clinical Utility of FISH.Laura M Bryant, Rose Hokanson, Scott E Hickey
|May 01, 2023
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.Victoria Patterson, Farid Ullah, Laura Bryant
|Mar 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara
|Jun 30, 2022
Brain Abnormalities in Patients with Germline Variants in <i>H3F3</i>: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors.C A P F Alves, O Sherbini, F D'Arco
|Dec 03, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients.Laura Bryant, Dong Li, Samuel G Cox
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Frequent Collaborators
4 joint publications
Elizabeth J Bhoj
2 joint publications
Maureen Mulhern
2 joint publications
Frédéric Tran Mau-Them
2 joint publications
Dong Li
2 joint publications
Antonio Vitobello
2 joint publications
Boris Keren
2 joint publications
Julia Hoefele
2 joint publications
Thomas Klopstock
2 joint publications
Davor Lessel
1 joint publications
Rebecca Burdine
