M. Nolan

发表

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

Robert H. Brown, M. Weale, F. Baas, 2017, Science Translational Medicine.

Diabetes, aging, and the brain: A comparative test of brain amylin in diabetics with late-onset Alzheimer's disease versus non-diabetics with late-onset Alzheimer's disease or early-onset Alzheimer's disease

C. Troakes, S. Al-Sarraj, P. Nelson, 2015, Alzheimer's & Dementia.

Pathogenesis of FUS-associated ALS and FTD: insights from rodent models

K. Talbot, M. Nolan, O. Ansorge, 2016, Acta Neuropathologica Communications.

Quantitative patterns of motor cortex proteinopathy across ALS genotypes

M. Turner, A. Santamaría-Pang, K. Talbot, 2020, Acta Neuropathologica Communications.

Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS–TDP

M. Turner, M. Keogh, P. Chinnery, 2021, Journal of Neurology, Neurosurgery, and Psychiatry.

Mutations in ANXA11 cause familial and sporadic amyotrophic lateral sclerosis

F. Baas, J. Belleroche, A. Al-Chalabi, 2017 .

Title: Mutations in ANXA11 cause familial and sporadic amyotrophic lateral sclerosis

Robert H. Brown, M. Weale, F. Baas, 2016 .

ALS-FUS pathology revisited: singleton FUS mutations and an unusual case with both a FUS and TARDBP mutation

C. Shaw, C. Troakes, S. Al-Sarraj, 2015, Acta Neuropathologica Communications.

Assessment of the degree of asymmetry of pathological features in neurodegenerative diseases. What is the significance for brain banks?

C. Troakes, S. Al-Sarraj, A. King, 2015, Journal of Neural Transmission.

Title: Mutations in ANXA11 cause familial and sporadic amyotrophic lateral sclerosis

Robert H. Brown, M. Weale, F. Baas, 2016 .

Dipeptide repeat protein inclusions are rare in the spinal cord and almost absent from motor neurons in C9ORF72 mutant amyotrophic lateral sclerosis and are unlikely to cause their degeneration

C. Shaw, C. Troakes, S. Al-Sarraj, 2015, Acta Neuropathologica Communications.

Genome‐wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis‐regulation of BORCS7, AS3MT, and NT5C2 in the human brain

R. Murray, C. Troakes, D. Srivastava, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Quantitative patterns of motor cortex proteinopathy across ALS genotypes

M. Turner, A. Santamaría-Pang, K. Talbot, 2020, Acta Neuropathologica Communications.

Fanconi anemia and mTOR pathways functionally interact during stalled replication fork recovery

M. Holz, M. Nolan, I. Chaudhury, 2021, FEBS letters.

Control tissue in brain banking: the importance of thorough neuropathological assessment

C. Troakes, S. Al-Sarraj, A. King, 2015, Journal of Neural Transmission.

Pathogenesis of FUS-associated ALS and FTD: insights from rodent models

K. Talbot, M. Nolan, O. Ansorge, 2016, Acta neuropathologica communications.

Dipeptide repeat protein inclusions are rare in the spinal cord and almost absent from motor neurons in C9ORF72 mutant amyotrophic lateral sclerosis and are unlikely to cause their degeneration

C. Shaw, C. Troakes, S. Al-Sarraj, 2015, Acta neuropathologica communications.