Ultra-rare variants in <i>LAMA2</i> are risk factors for frontotemporal dementia and motor neuron disease

Hiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp, Sophie Matis, Ramon Landin-Romero, Boris Guennewig, Hamish Mundell, Anthony S Don, Jennifer Fifita, Emily P McCann, Sandrine Chan Moi Fat, Ian P Blair, Karen A Mather, Anbupalam Thalamuthu, Wei Wen, Perminder S Sachdev, William S Brooks, Olivier Piguet, Glenda M Halliday, Woojin S Kim, John B Kwok

Open source

DOI: 10.1093/hmg/ddag034
Published: 2026
Container: Human Molecular Genetics
Publisher: Oxford University Press (OUP)
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1093/hmg/ddag034,
  title = {Ultra-rare variants in
                    <i>LAMA2</i>
                    are risk factors for frontotemporal dementia and motor neuron disease},
  author = {Hiu Chuen Lok and Carol Dobson-Stone and Marianne Hallupp and Sophie Matis and Ramon Landin-Romero and Boris Guennewig and Hamish Mundell and Anthony S Don and Jennifer Fifita and Emily P McCann and Sandrine Chan Moi Fat and Ian P Blair and Karen A Mather and Anbupalam Thalamuthu and Wei Wen and Perminder S Sachdev and William S Brooks and Olivier Piguet and Glenda M Halliday and Woojin S Kim and John B Kwok},
  year = {2026},
  journal = {Human Molecular Genetics},
  doi = {10.1093/hmg/ddag034},
  url = {https://doi.org/10.1093/hmg/ddag034}
}

RIS

TY  - JOUR
TI  - Ultra-rare variants in
                    <i>LAMA2</i>
                    are risk factors for frontotemporal dementia and motor neuron disease
AU  - Hiu Chuen Lok
AU  - Carol Dobson-Stone
AU  - Marianne Hallupp
AU  - Sophie Matis
AU  - Ramon Landin-Romero
AU  - Boris Guennewig
AU  - Hamish Mundell
AU  - Anthony S Don
AU  - Jennifer Fifita
AU  - Emily P McCann
AU  - Sandrine Chan Moi Fat
AU  - Ian P Blair
AU  - Karen A Mather
AU  - Anbupalam Thalamuthu
AU  - Wei Wen
AU  - Perminder S Sachdev
AU  - William S Brooks
AU  - Olivier Piguet
AU  - Glenda M Halliday
AU  - Woojin S Kim
AU  - John B Kwok
PY  - 2026
JO  - Human Molecular Genetics
DO  - 10.1093/hmg/ddag034
UR  - https://doi.org/10.1093/hmg/ddag034
ER  -

APA

Lok, H. C., Dobson-Stone, C., Hallupp, M., Matis, S., Landin-Romero, R., Guennewig, B., Mundell, H., Don, A. S., Fifita, J., McCann, E. P., Fat, S. C. M., Blair, I. P., Mather, K. A., Thalamuthu, A., Wen, W., Sachdev, P. S., Brooks, W. S., Piguet, O., Halliday, G. M., Kim, W. S., & Kwok, J. B. (2026). Ultra-rare variants in <i>LAMA2</i> are risk factors for frontotemporal dementia and motor neuron disease. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddag034

Source records

crossref · retrieved 2026-09-25T02:11:22.771Z