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Tyler Mark Pierson

10PUBLICATIONS

32CO-AUTHORS

Medical infection agents (incl. prions)Central nervous systemAdolescent healthCancer geneticsNeurogenetics

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Publications (10)

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|May 03, 2025

Compound Heterozygous MRPS14 Variants Associated With Leigh Syndrome.

Maria Gabriela Otero, Christina Freeman, Ruchi Shah

|Feb 14, 2024

Cellular Modeling of CLN6 with IPSC-derived Neurons and Glia.

Maria Gabriela Otero, Jaemin Kim, Yogesh Kumar Kushwaha

|Nov 08, 2022

A neurodevelopmental disorder associated with an activating de novo missense variant in ARF1.

Morié Ishida, María G Otero, Christina Freeman

|Jul 09, 2021

International retrospective natural history study of <i>LMNA</i>-related congenital muscular dystrophy.

Rabah Ben Yaou, Pomi Yun, Ivana Dabaj

|May 10, 2021

Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.

Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni

|Feb 01, 2020

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.

Holger Hengel, Célia Bosso-Lefèvre, George Grady

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Frequent Collaborators

1 joint publications

Philip J Ostrowski

1 joint publications

Alison Foster

1 joint publications

Dragana Josifova

1 joint publications

Ivana Dabaj

1 joint publications

Hui Xiong

1 joint publications

Luisa Politano

1 joint publications

Gisèle Bonne

1 joint publications

Maria G Otero

1 joint publications

Holger Hengel

1 joint publications

Élise Lebigot

Frequent Collaborators

1 joint publications

Philip J Ostrowski

1 joint publications

Alison Foster

1 joint publications

Dragana Josifova

1 joint publications

Ivana Dabaj

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