Jack W Miller (Q94522086)

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Neuroscientist

Jack Miller
Jack W. Miller

Language	Label	Description	Also known as
English	Jack W Miller	Neuroscientist	Jack Miller Jack W. Miller

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King's College London

Clinical neuroscience

1 reference

https://www.researchgate.net/profile/Jack-Miller-16

https://pubmed.ncbi.nlm.nih.gov/28469040/#full-view-affiliation-1

1 September 2024

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

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1 reference

PubMed publication ID

PMC publication ID

10.1126/scitranslmed.aad9157

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function

7

1 reference

PubMed publication ID

PMC publication ID

10.1016/j.neurobiolaging.2018.06.015

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

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PubMed publication ID

PMC publication ID

10.1038/ng.3626

The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosis

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1 reference

PubMed publication ID

PMC publication ID

10.1093/brain/aww028

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

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1 reference

PubMed publication ID

PMC publication ID

10.1126/science.aaa3650

The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients.

5

1 reference

PubMed publication ID

10.1016/j.neurobiolaging.2015.07.014

Autosomal dominant inheritance of rapidly progressive amyotrophic lateral sclerosis due to a truncation mutation in the fused in sarcoma (FUS) gene

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PubMed publication ID

10.3109/21678421.2014.920033

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

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PubMed publication ID

PMC publication ID

10.1016/j.neuron.2014.09.027

Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic

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1 reference

PubMed publication ID

PMC publication ID

10.1016/j.celrep.2013.10.049

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

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PubMed publication ID

PMC publication ID

10.1038/nature11922

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

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PubMed publication ID

PMC publication ID

10.1038/ejhg.2012.98

Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patients

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1 reference

PubMed publication ID

10.1016/j.neurobiolaging.2012.06.003

Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients

2

1 reference

PubMed publication ID

10.1016/j.neurobiolaging.2012.06.023

Identifiers

0000-0002-3835-474X

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