| Genetic Variability and Trajectories of DNA Methylation May Support a Role for HAMP in Patient Outcomes After Aneurysmal Subarachnoid Hemorrhage LW Heinsberg, AI Arockiaraj, EA Crago, D Ren, JR Shaffer, PR Sherwood, ... Neurocritical care 32, 550-563, 2020 | 16 | 2020 |
| Decreased DNA Methylation of RGMA is Associated with Intracranial Hypertension After Severe Traumatic Brain Injury: An Exploratory Epigenome-Wide … D Liu, BE Zusman, JR Shaffer, Y Li, AI Arockiaraj, S Liu, DE Weeks, ... Neurocritical care 37 (1), 26-37, 2022 | 10 | 2022 |
| Methylation data processing protocol and comparison of blood and cerebral spinal fluid following aneurysmal subarachnoid hemorrhage AI Arockiaraj, D Liu, JR Shaffer, TA Koleck, EA Crago, DE Weeks, ... Frontiers in Genetics 11, 671, 2020 | 10 | 2020 |
| CRISPRa-induced upregulation of human LAMA1 compensates for LAMA2-deficiency in Merosin-deficient congenital muscular dystrophy AI Arockiaraj, MA Johnson, A Munir, P Ekambaram, PC Lucas, ... bioRxiv, 2023 | 4 | 2023 |
| ANGPT1 methylation and delayed cerebral ischemia in aneurysmal subarachnoid hemorrhage patients D Liu, AI Arockiaraj, JR Shaffer, SM Poloyac, PR Sherwood, ... Epigenetics communications 1, 1-12, 2021 | 3 | 2021 |
| CRISPRa-induced upregulation of humanLAMA1compensates forLAMA2-deficiency in Merosin-deficient congenital muscular dystrophy AI Arockiaraj, MA Johnson, A Munir, P Ekambaram, PC Lucas, ... | | 2023 |
| Development of a mutation-independent approach to treat merosin-deficient congenital muscular dystrophy type 1A (MDC1A) AI Arockiaraj University of Pittsburgh, 2023 | | 2023 |
| MOLECULAR AND BEHAVIORAL CHARACTERIZATION OF A NOVEL MOUSE MODEL OF SNYDER-ROBINSON SYNDROME: A PATH TOWARDS THERAPEUTIC DEVELOPMENT O Akinyele, A Munir, M Johnson, JQC Zhang, A Arockiaraj, G Yuan, ... MOLECULAR GENETICS AND METABOLISM 135 (4), 253-253, 2022 | | 2022 |
| From mouse-to patient-relevant models: Using CRISPR activation to upregulate a compensatory disease-modifying gene in LAMA2-CMD D Kemaladewi, A Arockiaraj, JQ Cheng-Zhang, S Daghlas, C Kim NEUROMUSCULAR DISORDERS 30, S167-S167, 2020 | | 2020 |
| LATE BREAKING NEWS E-POSTER PRESENTATION: LBP 1 From mouse-to patient-relevant models: Using CRISPR activation to upregulate a compensatory disease-modifying gene in LAMA2-CMD D Kemaladewi, A Arockiaraj, JQ Cheng-Zhang, S Daghlas, C Kim Neuromuscular Disorders 30, S167, 2020 | | 2020 |
