Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

N. Parkinson · SciRah

Researcher profile · Semantic Scholar

N. Parkinson

Share profile

N. Parkinson — researcher profile on SciRah

h-index: 17
Works: 33
Citations: 2,810

Most-cited papers

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
G. Skibinski, N. Parkinson, Jeremy Brown, L. Chakrabarti +15 more
2005Nature Genetics858 citations
Semantic Scholar
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
N. Parkinson, Paul G. Ince, M. O. Smith, Robin Highley +8 more
2006Neurology434 citations Open access
Semantic Scholar
Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy.
Lyndsay M. Murray, L. Comley, D. Thomson, N. Parkinson +2 more
2008Human Molecular Genetics402 citations Open access
Semantic Scholar
Alternative Splicing Events Are a Late Feature of Pathology in a Mouse Model of Spinal Muscular Atrophy
Dirk Bäumer, Sheena Lee, G. Nicholson, Joanna L. Davies +6 more
2009PLoS Genetics251 citations Open access
Semantic Scholar
Mutant β-spectrin 4 causes auditory and motor neuropathies in quivering mice
N. Parkinson, C. Olsson, J. Hallows, J. McKee-Johnson +4 more
2001Nature Genetics123 citations
Semantic Scholar
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice.
S. Ghazi-Noori, K. Froud, S. Mizielinska, C. Powell +10 more
2012Brain : a journal of neurology115 citations
Semantic Scholar
Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media
N. Parkinson, Rachel E Hardisty-Hughes, Hilda Tateossian, Hsun-Tien Tsai +14 more
2006PLoS Genetics98 citations Open access
Semantic Scholar
A postmortem study of the mediodorsal nucleus of the thalamus in schizophrenia.
T. Cullen, M. Walker, N. Parkinson, R. Craven +3 more
2003Schizophrenia Research84 citations
Semantic Scholar
Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.
B. J. Turner, N. Parkinson, K. Davies, K. Talbot
2009Neurobiology of Disease77 citations Open access
Semantic Scholar
Preparation of high-quality next-generation sequencing libraries from picogram quantities of target DNA.
N. Parkinson, Siarhei Maslau, Ben Ferneyhough, Gang Zhang +5 more
2012Genome Research74 citations Open access
Semantic Scholar
TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy
B. J. Turner, Dirk Bäumer, N. Parkinson, Jakub Scaber +2 more
2008BMC Neuroscience70 citations Open access
Semantic Scholar
Mutant beta-spectrin 4 causes auditory and motor neuropathies in quivering mice.
N. Parkinson, C. Olsson, J. Hallows, J. McKee-Johnson +4 more
2001Nature Genetics67 citations
Semantic Scholar
Studies of the lethargic (lh/lh) mouse model of absence seizures: regulatory mechanisms and identification of the lh gene.
David A. Hosford, F. Lin, Y. Wang, S. Caddick +8 more
1999Advances in neurology40 citations
Semantic Scholar
The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon
Charlotte R. Rhodes, N. Parkinson, H. Tsai, D. Brooker +5 more
2003Journal of Neurocytology33 citations
Semantic Scholar
Behavioural and other phenotypes in a cytoplasmic dynein light intermediate chain 1 mutant mouse
G. Banks, Matilda Haas, Samantha J. Line, H. Shepherd +17 more
2011Journal of Neuroscience31 citations Open access
Semantic Scholar
Catheter‐associated venous air embolism in hospitalized horses: 32 cases
N. Parkinson, H. McKenzie, M. Barton, Jennifer L. Davis +3 more
2018Journal of Veterinary Internal Medicine23 citations Open access
Semantic Scholar
Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss
F. Mackenzie, A. Parker, N. Parkinson, Peter L. Oliver +6 more
2009Genes, Brain and Behavior18 citations Open access
Semantic Scholar
Characterization of basal and lipopolysaccharide-induced microRNA expression in equine peripheral blood mononuclear cells using Next-Generation Sequencing
N. Parkinson, V. Buechner-Maxwell, S. Witonsky, R. Pleasant +2 more
2017PLoS ONE9 citations Open access
Semantic Scholar
Violation of the 12/23 rule of genomic V(D)J recombination is common in lymphocytes
N. Parkinson, M. Roddis, Ben Ferneyhough, Gang Zhang +10 more
2015Genome Research2 citations Open access
Semantic Scholar
th UK spinal muscular atrophy ( SMA ) researchers network meeting
N. Parkinson
20081 citations
Semantic Scholar
An inverse PCR strategy for the recovery of end fragments from the pRML YAC vector
N. Parkinson, J. Barclay, M. Gardiner, Michele Rees
19971 citations Open access
Semantic Scholar
307 Managing health and safety in the healthcare setting – an e-learning training programme
N. Parkinson
20180 citations Open access
Semantic Scholar
Explorer Alternative Splicing Events Are a Late Feature of Pathology in a Mouse Model of Spinal Muscular Atrophy
Dirk Bäumer, Sheena Lee, G. Nicholson, Joanna L. Davies +6 more
20170 citations
Semantic Scholar
Venous Air Embolism Associated With Intravenous Catheter Disconnection In Horses: A Multicentre Retrospective Study
N. Jocelyn, C. Wylie, A. Barrelet, M. Lean +5 more
20170 citations Open access
Semantic Scholar
Endotoxin-induced microRNA expression in equine peripheral blood mononuclear cells
N. Parkinson
20160 citations
Semantic Scholar
Progressive Neuronal Inclusion Formation and Neurodegenerative Changes in CHMP2B mutant transgenic mice
S. Ghazi-Noori, K. Froud, S. Mizielinska, N. Parkinson +5 more
20120 citations
Semantic Scholar
TARDBP IN AMYOTROPHIC LATERAL SCLEROSIS: MUTATION SCREENING AND GENETIC COPY NUMBER ANALYSIS IN A CLINIC COHORT
Dirk Bäumer, N. Parkinson, K. Talbot
20090 citations
Semantic Scholar
GENETIC SCREEN AND FUNCTIONAL ANALYSIS OF TARDBP MUTATIONS
Dirk Bäumer, N. Parkinson, K. Talbot
20090 citations
Semantic Scholar
Reduction in SMN gene dosage leads to reduced survival in the G93A SOD1 mouse model of amyotrophic lateral sclerosis
K. Talbot, B. J. Turner, N. Parkinson, K. Davies
20080 citations
Semantic Scholar
A mutation in the endosomal gene CHMP2B in frontotemporal dementia.
A. Isaacs, G. Skibinski, N. Parkinson, Julia Brown +9 more
20060 citations
Semantic Scholar
A mutation in CHMP2B is the likely cause of frontotemporal dementia in a large Danish kindred.
A. Isaacs, G. Skibinski, N. Parkinson, Julia Brown +9 more
20060 citations
Semantic Scholar
Positional cloning of the lh absence disease gene
M. Rees, N. Parkinson, J. Barclay, R. D. Cox +6 more
19990 citations
Semantic Scholar
Genetic and physical mapping around the mouse epilepsy locus, lethargic ( lh )
N. Parkinson, J. Barclay, M. Gardiner, Michele Rees
19980 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

K. Talbot×8
Invite
K. Talbot — researcher profile on SciRah
J. Collinge×6
Invite
J. Collinge — researcher profile on SciRah
Dirk Bäumer×5
Invite
Dirk Bäumer — researcher profile on SciRah
G. Skibinski×4
Invite
G. Skibinski — researcher profile on SciRah

×4

Invite

S. Brandner — researcher profile on SciRah

Invite

E. Fisher — researcher profile on SciRah

Invite

K. Davies — researcher profile on SciRah

Invite

A. Isaacs — researcher profile on SciRah

Invite

J. Barclay — researcher profile on SciRah

Invite

J. Nielsen — researcher profile on SciRah

T. Thusgaard×3

Invite

T. Thusgaard — researcher profile on SciRah

Invite

A. Brun — researcher profile on SciRah