Ashley L. Siniard - Concepedia

Author

Ashley L. Siniard

Translational Genomics Research Institute

Also Known As

A L Siniard, A. L. Siniard, A. Siniard, Ashley L Siniard, Ashley L. Siniard, Ashley L. Siniard (618764), Ashley Siniard, Siniard, Ashley

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Translational Genomics Research Institute Arizona State University University of Southern California University of Antwerp University of Arizona

About

Ashley L. Siniard is an author at Translational Genomics Research Institute specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	582
2	Natural Sciences	2	2	156
3	Public Health	1	1	20
4	Social Sciences	1	1	28
5	Biochemistry	1	1	21

Ashley L. Siniard

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Brain Differences in Infants at Differential Genetic Risk for Late-Onset Alzheimer Disease Douglas Dean, Beth A. Jerskey, Kewei Chen, JAMA Neurology	2013	262
Total Extracellular Small RNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects Ashish Yeri, Amanda Courtright, Rebecca Reiman, Scientific Reports	2017	155
Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease Margarita Giraldo, Francisco Lopera, Ashley L. Siniard, Neurobiology of Aging Alzheimer's DiseaseGeneticsDegenerative DiseaseMyeloid Cells 2Frontotemporal Dementia	2013	144
Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms Elizabeth Hutchins, Glenn J. Markov, Walter L. Eckalbar, PLoS ONE GeneticsFunctional TailGenomic MechanismMolecular GeneticsRepair Mechanisms	2014	135
Transcriptome response of human skeletal muscle to divergent exercise stimuli Jared M. Dickinson, Andrew C. D’Lugos, Marcus Naymik, Journal of Applied Physiology	2018	85
De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy Anna Fassio, Alessandro Esposito, Mitsuhiro Kato, Brain V-type ProtonMilder EpilepsyGenetic DisorderGeneticsMolecular Genetics	2018	85
DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s Disease Adrienne Henderson, Qi Wang, Bessie Meechoovet, Frontiers in Genetics	2021	78
Hippocampal Transcriptomic Profiles: Subfield Vulnerability to Age and Cognitive Impairment Lara Ianov, Matt De Both, Monica K. Chawla, Frontiers in Aging Neuroscience	2017	56
A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome Isabelle Schrauwen, Szabolcs Szelinger, Ashley L. Siniard, PLoS ONE Cav1 Is AssociatedFrame-shift MutationSevere Neonatal ProgeroidGeneticsPathogenesis	2015	51
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish Aleksandra Siekierska, Hannah Stamberger, Tine Deconinck, Nature Communications	2019	50

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