John E Landers

14PUBLICATIONS
217CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cancer diagnosisGene mappingMedical infection agents (incl. prions)Neurology and neuromuscular diseases
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Publications (14)

|Mar 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Paul J Hop, Maarten Kooyman, Brendan J Kenna

|Jul 02, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp

|Jun 10, 2024
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease.

Paul J Hop, Dongbing Lai, Pamela J Keagle

|Mar 21, 2024
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia.

Salome Funes, Jonathan Jung, Del Hayden Gadd

|Aug 16, 2023
Loss of function of the ALS-associated NEK1 kinase disrupts microtubule homeostasis and nuclear import.

Jacob R Mann, Elizabeth D McKenna, Darilang Mawrie

|Nov 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp

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