Get started
Author

Jennifer A. Fifita

Observed names: Fifita, Jennifer, Fifita, Jennifer A., J. A. Fifita, J.A. Fifita, Jennifer A Fifita, Jennifer A. Solski, Jennifer Fifita, Jennifer A. Fifita
ORCID: 0000-0002-0814-0118
Observed ORCID: 0000-0002-0814-0118
OpenAlex ID: A5083778124
Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene
2018 · Aude Nicolas, Kevin P. Kenna, et al. · Neuron · 679
PDF
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
2016 · PARALS Registry, Wouter van Rheenen, et al. · Nature Genetics · 572
PDF
A yeast functional screen predicts new candidate ALS disease genes
2011 · Julien Couthouis, Michael P. Hart, et al. · Proceedings of the National Academy of Sciences · 389
Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis
2012 · Julien Couthouis, Michael P. Hart, et al. · Human Molecular Genetics · 289
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
2016 · Kelly L. Williams, Simon Topp, et al. · Nature Communications · 207
PDF
UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosis
2012 · Kelly L. Williams, Sadaf T. Warraich, et al. · Neurobiology of Aging · 170
ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19
2013 · Yuji Takahashi, Yoko Fukuda, et al. · The American Journal of Human Genetics · 156
PDF
Exome sequencing to identify de novo mutations in sporadic ALS trios
2013 · Alessandra Chesi, Brett T Staahl, et al. · Nature Neuroscience · 150
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
2017 · Beben Benyamin, Ji He, et al. · Nature Communications · 110
PDF
Pathophysiological insights into ALS with C9ORF72 expansions
2013 · K. L. Williams, J. A. Fifita, et al. · Journal of Neurology Neurosurgery & Psychiatry · 100
Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosis
2015 · Vinod Sundaramoorthy, Adam K. Walker, et al. · Human Molecular Genetics · 99
Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis
2020 · Emily P McCann, Lyndal Henden, et al. · Journal of Medical Genetics · 89
CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis
2020 · Carol Dobson-Stone, Marianne Hallupp, et al. · Brain · 84
The genotype–phenotype landscape of familial amyotrophic lateral sclerosis in Australia
2017 · E.P. McCann, K.L. Williams, et al. · Clinical Genetics · 80
Altered SOD1 maturation and post-translational modification in amyotrophic lateral sclerosis spinal cord
2022 · Benjamin G Trist, Sian Genoud, et al. · Brain · 76
PDF
Co-deposition of SOD1, TDP-43 and p62 proteinopathies in ALS: evidence for multifaceted pathways underlying neurodegeneration
2022 · Benjamin G. Trist, Jennifer A. Fifita, et al. · Acta Neuropathologica Communications · 50
PDF
Expression of ALS/FTD-linked mutant CCNF in zebrafish leads to increased cell death in the spinal cord and an aberrant motor phenotype
2017 · Alison L. Hogan, Emily K. Don, et al. · Human Molecular Genetics · 50
A Simple Differentiation Protocol for Generation of Induced Pluripotent Stem Cell-Derived Basal Forebrain-Like Cholinergic Neurons for Alzheimer’s Disease and Frontotemporal Dementia Disease Modeling
2020 · Sonia Sanz Muñoz, Martin Engel, et al. · Cells · 49
PDF
Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin
2015 · Kelly L. Williams, Emily P. McCann, et al. · Neurobiology of Aging · 41
Cyclin F: A component of an E3 ubiquitin ligase complex with roles in neurodegeneration and cancer
2017 · Jasmin Galper, Stephanie L. Rayner, et al. · The International Journal of Biochemistry & Cell Biology · 36
Mutant Human FUS Is Ubiquitously Mislocalized and Generates Persistent Stress Granules in Primary Cultured Transgenic Zebrafish Cells
2014 · Jamie Rae Acosta, Claire Goldsbury, et al. · PLoS ONE · 36
PDF
Expression of ALS/FTD-linked mutant CCNF in zebrafish leads to increased cell death in the spinal cord and an aberrant motor phenotype
2018 · Alison L Hogan, Emily K Don, et al. · Human Molecular Genetics · 34
Evaluation of Skin Fibroblasts from Amyotrophic Lateral Sclerosis Patients for the Rapid Study of Pathological Features
2015 · Shu Yang, Katharine Y. Zhang, et al. · Neurotoxicity Research · 34
A novel amyotrophic lateral sclerosis mutation in OPTN induces ER stress and Golgi fragmentation in vitro
2016 · Jennifer A. Fifita, Kelly L. Williams, et al. · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 33
Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis
2017 · Jennifer A. Fifita, Katharine Y. Zhang, et al. · Neurodegenerative Diseases · 32
Works count: 56
Citation count: 3,972
H-index: 26
I10-index: 42
Year
Topic
Type