Publications by authors named "Arpit Mehta"

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ASHP Statement on Leadership as a Professional Obligation.
Ashley Mains Espinosa, Arpit Mehta, Tara Behring Vlasimsky

Am J Health Syst Pharm· October 2025

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ASHP Statement on Leadership as a Professional Obligation.
Ashley Mains Espinosa, Arpit Mehta, Tara Behring Vlasimsky

Am J Health Syst Pharm· February 2024

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Timing and factors associated with complementary feeding in India.
Morium B Bably, Sarah B Laditka, Arpit Mehta, Suparna Ghosh-Jerath, Elizabeth F Racine

Health Care Women Int· March 2023

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Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease.
Juan I Young, Sathesh K Sivasankaran, Lily Wang, Aleena Ali, Arpit Mehta

Neurol Genet· August 2019

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Factors Associated With Extended Breastfeeding in India.
Arpit R Mehta, Sigamani Panneer, Suparna Ghosh-Jerath, Elizabeth F Racine

J Hum Lact· February 2017

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Detection of canonical A-to-G editing events at 3' UTRs and microRNA target sites in human lungs using next-generation sequencing.
Ramani Soundararajan, Timothy M Stearns, Anthony L Griswold, Arpit Mehta, Alexander Czachor

Oncotarget· November 2015

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Consequences of zygote injection and germline transfer of mutant human mitochondrial DNA in mice.
Hong Yu, Rajeshwari D Koilkonda, Tsung-Han Chou, Vittorio Porciatti, Arpit Mehta

Proc Natl Acad Sci U S A· October 2015

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Regulation of AKT signaling by Id1 controls t(8;21) leukemia initiation and progression.
Lan Wang, Na Man, Xiao-Jian Sun, Yurong Tan, Marta García-Cao, Arpit Mehta

Blood· July 2015

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Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome.
Chiara Pastori, Veronica J Peschansky, Deborah Barbouth, Arpit Mehta, Jose P Silva

Hum Genet· January 2014

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Next-generation sequencing of mitochondrial targeted AAV transfer of human ND4 in mice.
Hong Yu, Arpit Mehta, Gaofeng Wang, William W Hauswirth, Vince Chiodo

Mol Vis· September 2013

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Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.
Karen Nuytemans, Guney Bademci, Vanessa Inchausti, Amy Dressen, Daniel D Kinnamon, Arpit Mehta

Neurology· March 2013

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Comparison of three targeted enrichment strategies on the SOLiD sequencing platform.
Dale J Hedges, Toumy Guettouche, Shan Yang, Guney Bademci, Ashley Diaz, Arpit Mehta

PLoS One· April 2011

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