Andrew R. Findlay - Concepedia

Author

Andrew R. Findlay

Washington University in St. Louis ORCID

Also Known As

A Findlay, A. Findlay, A.R. Findlay, Andrew Findlay, Andrew R. Findlay

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Washington University in St. Louis Nationwide Children's Hospital The Ohio State University University of Utah Stanford University

About

Andrew R. Findlay is an author at Washington University in St. Louis specializing in medicine, molecular biology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	447
2	Cell Biology	4	4	205
3	Natural Sciences	2	2	57
4	Geriatrics	2	2	265
5	Health Sciences	1	1	10

Andrew R. Findlay

Publications

820

Citations

H-Index

Page 1

	Year	Citations
Clinical Practice Guideline on management of older patients with chronic kidney disease stage 3b or higher (eGFR<45 mL/min/1.73 m2): a summary document from the European Renal Best Practice Group Ken Farrington, Adrian Covic, Ionuţ Nistor, Nephrology Dialysis Transplantation Ckd Stage 3BGlomerulonephritisRenal FunctionChronic Kidney DiseaseOlder Patients	2017	134
Clinical Practice Guideline on management of older patients with chronic kidney disease stage 3b or higher (eGFR <45 mL/min/1.73 m<sup>2</sup>) Ken Farrington, Adrian Covic, Naomi Clyne, Nephrology Dialysis Transplantation GlomerulonephritisHemodialysisUrologyRenal DiseaseRenal Function	2016	131
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice Nicolas Wein, Adeline Vulin, Maria Sofia Falzarano, Nature Medicine PhysiologyIres ResultsDegenerative DiseaseDmd Exon 5Cell Biology	2014	118
Clinical phenotypes as predictors of the outcome of skipping around <scp><i>DMD</i></scp> exon 45 Andrew R. Findlay, Nicolas Wein, Yuuki Kaminoh, Annals of Neurology	2015	50
Dominant inheritance of Scheuermann's juvenile kyphosis. Andrew R. Findlay, A. N. Conner, J M Connor Journal of Medical Genetics	1989	43
Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy Julien Couthouis, Alya R. Raphael, Carly E. Siskind, Neuromuscular Disorders Mendelian DisorderDnajb6 MutationGenetic DisorderGeneticsMolecular Biology	2014	39
Efficient Skipping of Single Exon Duplications in <i>DMD</i> Patient-Derived Cell Lines Using an Antisense Oligonucleotide Approach Nicolas Wein, Adeline Vulin, Andrew R. Findlay, Journal of Neuromuscular Diseases	2017	35
Clinical utility of anti‐cytosolic 5’‐nucleotidase 1A antibody in idiopathic inflammatory myopathies Chiseko Ikenaga, Andrew R. Findlay, Namita Goyal, Annals of Clinical and Translational Neurology ImmunodeficienciesImmunologyPathologyCommon Neurological DisordersAntibody Seropositivity	2021	31
The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development Adeline Vulin, Nicolas Wein, Tabatha R. Simmons, Neuromuscular Disorders Knockout MouseDevelopmental BiologyMendelian DisorderSkeletal MuscleDuchenne Muscular Dystrophy	2015	30
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure Conrad C. Weihl, Ana Töpf, Rocío Bengoechea, Acta Neuropathologica Genome InstabilityEarly Respiratory FailureGenetic DisorderGeneticsMolecular Biology	2022	30

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