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Lavanya Jain
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DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome
LC Schenkel, E Aref-Eshghi, K Rooney, J Kerkhof, MA Levy, H McConkey, ...
Clinical epigenetics 13, 1-17, 2021
362021
Neurofibromatosis type 2 in Phelan-McDermid syndrome: Institutional experience and review of the literature
CA Ziats, L Jain, B McLarney, E Vandenboom, BR DuPont, C Rogers, ...
European Journal of Medical Genetics 63 (11), 104042, 2020
172020
Genetic and metabolic profiling of individuals with Phelan‐McDermid syndrome presenting with seizures
L Jain, LM Oberman, L Beamer, L Cascio, M May, S Srikanth, C Skinner, ...
Clinical Genetics 101 (1), 87-100, 2022
112022
Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome
S Srikanth, L Jain, C Zepeda-Mendoza, L Cascio, K Jones, R Pauly, ...
PLoS One 16 (7), e0253859, 2021
92021
ATN cerebrospinal fluid biomarkers in dementia with Lewy bodies: Initial results from the United States Dementia with Lewy Bodies Consortium
L Jain, M Khrestian, S Formica, ED Tuason, JA Pillai, S Rao, O Oguh, ...
Alzheimer's and Dementia, 2023
12023
AD and ADRD Differences in Luminex and Lumipulse ATN Categories
L Jain, M Khrestian, S Formica, ED Tuason, JA Pillai, SM Rao, ...
Alzheimer's & Dementia 19, e079993, 2023
2023
Blood-Based Biomarkers 1
TB Murphy, LM Bekris, L Jain, JE Mintzer, AJ Lerner
Alzheimer's Association International Conference, 2023
2023
Sleep disturbances in Phelan-McDermid syndrome: Clinical and metabolic profiling of 56 individuals
BA Moffitt, LM Oberman, L Beamer, S Srikanth, L Jain, L Cascio, K Jones, ...
Clinical Genetics, 1-12, 2023
2023
Cerebrospinal fluid glial fibrillary acidic protein (GFAP) and soluble triggering receptor expressed on myeloid cells 2 (sTREM2) in Alzheimer’s Disease and Related Dementias (ADRD)
L Jain, M Khrestian, ED Tuason, JA Pillai, SM Rao, JB Leverenz, ...
Alzheimer's & Dementia 18, e068332, 2022
2022
Neurodegenerative Disease Differences in Luminex and Lumipulse ATN Categories
L Jain, M Khrestian, S Formica, E Tuason, J Pillai, S Rao, J Leverenz, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 24 (10), S132-S132, 2022
2022
Conflict of Interest Statement
L Jain
CLINICAL AND GENETIC PROFILING IN PHELAN-MCDERMID SYNDROME (PMS), 61, 2021
2021
CHAPTER TWO POSITION EFFECTS OF 22q13 REARRANGEMENTS ON CANDIDATE GENES IN
S Srikanth, L Jain, RP Jones, B DuPont, C Rogers, S Sarasua, K Phelan, ...
CLINICAL AND GENETIC PROFILING IN PHELAN-MCDERMID SYNDROME (PMS), 19, 2021
2021
Clinical and Genetic Profiling in Phelan-McDermid Syndrome (PMS)
L Jain
Clemson University, 2021
2021
DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome
K Phelan, L Jain, N Brunetti-Pierri, B DuPont, SM Sarasua, R Pauly, ...
figshare Academic Research System, 2021
2021
Additional file 3 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome
E Aref-Eshghi, MA Levy, L Boccuto, LC Schenkel, J Kerkhof, RC Rogers, ...
figshare Academic Research System, 2021
2021
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