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

P. Keagle · SciRah

Researcher profile · Semantic Scholar

P. Keagle

Share profile

P. Keagle — researcher profile on SciRah

h-index: 21
Works: 27
Citations: 4,385

Most-cited papers

Complete genome sequence of Methanobacterium thermoautotrophicum deltaH: functional analysis and comparative genomics
Douglas R. Smith, L. Doucette-Stamm, C. Deloughery, Hong-Mei Lee +21 more
1997Journal of Bacteriology1,105 citations Open access
Semantic Scholar
Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis
Chi-Hong Wu, C. Fallini, N. Ticozzi, P. Keagle +34 more
2012Nature620 citations Open access
Semantic Scholar
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
A. Nicolas, K. Kenna, A. Renton, N. Ticozzi +200 more
2018Neuron409 citations Open access
Semantic Scholar
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS
Bradley Smith, N. Ticozzi, C. Fallini, A. Gkazi +61 more
2014Neuron317 citations Open access
Semantic Scholar
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
K. Kenna, P. V. van Doormaal, Annelot M. Dekker, N. Ticozzi +77 more
2016Nature Genetics281 citations Open access
Semantic Scholar
Genome-Wide Analyses Identify Kif5A As A Novel Als Gene
A. Nicolas, K. Kenna, A. Renton, F. Faghri +23 more
2021244 citations
Semantic Scholar
Angiogenin Variants in Parkinson Disease and Amyotrophic Lateral Sclerosis
M. van Es, H. Schelhaas, P. W. V. van Vught, N. Ticozzi +52 more
2011Annals of Neurology207 citations Open access
Semantic Scholar
Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis
N. Ticozzi, C. Vance, A. L. Leclerc, P. Keagle +8 more
2011American Journal of Medical Genetics Part B: Neuropsychiatric Genetics179 citations
Semantic Scholar
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
N. Ticozzi, V. Silani, A. L. Leclerc, P. Keagle +8 more
2009Neurology163 citations Open access
Semantic Scholar
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
C. Akimoto, A. Volk, M. van Blitterswijk, M. Van den Broeck +39 more
2014Journal of Medical Genetics126 citations Open access
Semantic Scholar
The distinct genetic pattern of ALS in Turkey and novel mutations
Aslıhan Özoğuz, Özgün Uyan, G. Birdal, Ceren Iskender +34 more
2015Neurobiology of Aging108 citations Open access
Semantic Scholar
ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function
Desiree M. Baron, Adam R. Fenton, S. Saez-Atienzar, Anthony Giampetruzzi +16 more
2022Cell Reports86 citations Open access
Semantic Scholar
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
Ramita Dewan, R. Chia, Jinhui Ding, R. Hickman +52 more
2020Neuron82 citations Open access
Semantic Scholar
Paraoxonase Gene Mutations in Amyotrophic Lateral Sclerosis
N. Ticozzi, A. L. Leclerc, P. Keagle, J. Glass +13 more
2010Annals of Neurology79 citations Open access
Semantic Scholar
Mutational Analysis of TARDBP in Neurodegenerative Diseases
N. Ticozzi, A. L. Leclerc, M. van Blitterswijk, P. Keagle +6 more
2009Neurobiology of Aging71 citations Open access
Semantic Scholar
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
Janel O. Johnson, Ruth Chia, Danny E. Miller, Rachel Li +286 more
2021JAMA Neurology70 citations Open access
Semantic Scholar
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease
P. Hop, Dongbing Lai, P. Keagle, Desiree M. Baron +18 more
2024Nature Genetics62 citations Open access
Semantic Scholar
ATXN2 intermediate expansions in amyotrophic lateral sclerosis.
J. Glass, Ramita Dewan, Jinhui Ding, R. Gibbs +7 more
2022Brain : a journal of neurology46 citations Open access
Semantic Scholar
Complete Genome Sequence of Methanobacterium thermoautotrophicum D H: Functional Analysis and Comparative Genomics
Douglas R. Smith, L. Doucette-Stamm, C. Deloughery, Hong-Mei Lee +33 more
199734 citations
Semantic Scholar
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson’s Disease Risk
L. Straniero, V. Rimoldi, E. Monfrini, Salvatore Bonvegna +15 more
2022Movement Disorders31 citations Open access
Semantic Scholar
Characterization of FUS Mutations in Amyotrophic Lateral Sclerosis Using RNA-Seq
M. van Blitterswijk, Eric T. Wang, Brad A. Friedman, P. Keagle +6 more
2013PLoS ONE26 citations Open access
Semantic Scholar
Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients
E. Ramos, P. Keagle, T. Gillis, Patrick P. Lowe +11 more
2012Amyotrophic Lateral Sclerosis21 citations
Semantic Scholar
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia
Salome Funes, Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda +20 more
2024Nature Communications15 citations Open access
Semantic Scholar
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia
Salome Funes, Del Hayden Gadd, Michelle Mosqueda, Jian-hua Zhong +16 more
2023bioRxiv8 citations Open access
Semantic Scholar
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genes
Arianna Manini, Alberto Brusati, M. Grassano, Giulia Scacciatella +23 more
2025Journal of Neurology2 citations
Semantic Scholar
Identification of FUS/TLS gene mutation in a cohort of Italian FALS patients
N. Ticozzi, V. Silani, A. L. Leclerc, P. Keagle +8 more
20090 citations
Semantic Scholar
Sequencage multiplex induit par des transposons
P. August, P. Keagle, Henry Long, Anna Wiencis +2 more
20010 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

J. Landers×23
Invite
J. Landers — researcher profile on SciRah
N. Ticozzi×13
Invite
N. Ticozzi — researcher profile on SciRah
V. Silani×13
Invite
V. Silani — researcher profile on SciRah
A. Ratti×11
Invite
A. Ratti — researcher profile on SciRah

×11

Invite

C. Gellera — researcher profile on SciRah

Robert H. Brown×11

Invite

Robert H. Brown — researcher profile on SciRah

Invite

P. Sapp — researcher profile on SciRah

D. McKenna-Yasek×10

Invite

D. McKenna-Yasek — researcher profile on SciRah

A. L. Leclerc×9

Invite

A. L. Leclerc — researcher profile on SciRah

Invite

J. Veldink — researcher profile on SciRah

Invite

J. Glass — researcher profile on SciRah

M. van Blitterswijk×7

Invite

M. van Blitterswijk — researcher profile on SciRah