Get started
Author

Alison Homstad

Observed names: Alison K. Homstad, Homstad, Alison
OpenAlex ID: A5088268500
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis
2014 · Andrew F. Malone, Paul J. Phelan, et al. · Kidney International · 238
Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
2014 · Rasheed A. Gbadegesin, Gentzon Hall, et al. · Journal of the American Society of Nephrology · 161
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
2014 · Rasheed A. Gbadegesin, Adebowale Adeyemo, et al. · Journal of the American Society of Nephrology · 144
TRPC6 Enhances Angiotensin II-induced Albuminuria
2011 · Jason Eckel, Peter J. Lavin, et al. · Journal of the American Society of Nephrology · 127
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis
2011 · Rasheed A. Gbadegesin, Peter J. Lavin, et al. · Kidney International · 76
TNXB Mutations Can Cause Vesicoureteral Reflux
2013 · Rasheed A. Gbadegesin, Patrick D. Brophy, et al. · Journal of the American Society of Nephrology · 71
A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
2014 · Gentzon Hall, Rasheed A. Gbadegesin, et al. · Journal of the American Society of Nephrology · 51
Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity
2014 · Gentzon Hall, Janelle Rowell, et al. · American Journal of Physiology-Renal Physiology · 33
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux
2015 · Shan Elahi, Alison Homstad, et al. · Pediatric Nephrology · 14
A New Locus for Familial FSGS on Chromosome 2P
2010 · Rasheed Gbadegesin, Peter Lavin, et al. · Journal of the American Society of Nephrology · 7
Baseline and innate immune response characterization of a Zfp30 knockout mouse strain
2020 · Lucas T. Laudermilk, Adelaide Tovar, et al. · Mammalian Genome · 2
PDF
New Inf2 mutations in a large cohort with sporadic and hereditary FSGS and further evidence for variable
2012 · Rasheed Gbadegesin, Peter Lavin, et al. · Lenus, The Irish Health Repository (Dr Steevens Hospital Library)
Works count: 13
Citation count: 924
H-index: 9
I10-index: 9
Year
Topic
Type