Lohith Madireddy
Lohith Madireddy
Janssen Research & Development, LLC
Verified email at its.jnj.com
Cited by
Cited by
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
Astrocyte-encoded positional cues maintain sensorimotor circuit integrity
AV Molofsky, KW Kelley, HH Tsai, SA Redmond, SM Chang, L Madireddy, ...
Nature 509 (7499), 189-194, 2014
The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility
NA Patsopoulos, SE Baranzini, A Santaniello, P Shoostari, C Cotsapas, ...
BioRxiv, 143933, 2017
In vivo Phosphoproteome of Human Skeletal Muscle Revealed by Phosphopeptide Enrichment and HPLC−ESI−MS/MS
K Hřjlund, BP Bowen, H Hwang, CR Flynn, L Madireddy, T Geetha, ...
Journal of proteome research 8 (11), 4954-4965, 2009
Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls
D Nickles, HP Chen, MM Li, P Khankhanian, L Madireddy, SJ Caillier, ...
Human molecular genetics 22 (20), 4194-4205, 2013
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1
AM Slavotinek, SE Baranzini, D Schanze, C Labelle-Dumais, KM Short, ...
Journal of medical genetics 48 (6), 375-382, 2011
Exome sequencing in 32 patients with anophthalmia/microphthalmia and developmental eye defects
AM Slavotinek, ST Garcia, G Chandratillake, T Bardakjian, E Ullah, D Wu, ...
Clinical genetics 88 (5), 468-473, 2015
An ImmunoChip study of multiple sclerosis risk in African Americans
N Isobe, L Madireddy, P Khankhanian, T Matsushita, SJ Caillier, JM Moré, ...
Brain 138 (6), 1518-1530, 2015
Expression profiling of Aldh1l1‐precursors in the developing spinal cord reveals glial lineage‐specific genes and direct Sox9‐Nfe2l1 interactions
AV Molofsky, SM Glasgow, LS Chaboub, HH Tsai, AT Murnen, KW Kelley, ...
Glia 61 (9), 1518-1532, 2013
In depth comparison of an individual’s DNA and its lymphoblastoid cell line using whole genome sequencing
D Nickles, L Madireddy, S Yang, P Khankhanian, S Lincoln, SL Hauser, ...
BMC genomics 13 (1), 1-11, 2012
PINBPA: cytoscape app for network analysis of GWAS data
L Wang, T Matsushita, L Madireddy, P Mousavi, SE Baranzini
Bioinformatics 31 (2), 262-264, 2015
A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis
International Multiple Sclerosis Genetics Consortium
Nature communications 10, 2019
Genetic associations with brain cortical thickness in multiple sclerosis
T Matsushita, L Madireddy, T Sprenger, P Khankhanian, S Magon, ...
Genes, Brain and Behavior 14 (2), 217-227, 2015
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility
V Damotte, L Guillot-Noel, NA Patsopoulos, L Madireddy, M El Behi, ...
Genes & Immunity 15 (2), 126-132, 2014
Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis
X Jia, L Madireddy, S Caillier, A Santaniello, F Esposito, G Comi, O Stuve, ...
Annals of neurology 84 (1), 51-63, 2018
Sequencing of the IL6 gene in a case–control study of cerebral palsy in children
P Khankhanian, SE Baranzini, BA Johnson, L Madireddy, D Nickles, ...
BMC medical genetics 14 (1), 1-8, 2013
Meta-analysis of genome-wide association studies reveals genetic overlap between Hodgkin lymphoma and multiple sclerosis
P Khankhanian, W Cozen, DS Himmelstein, L Madireddy, L Din, ...
International journal of epidemiology 45 (3), 728-740, 2016
Prognostic biomarkers of IFNb therapy in multiple sclerosis patients
SE Baranzini, LR Madireddy, A Cromer, M D’Antonio, L Lehr, M Beelke, ...
Multiple Sclerosis Journal 21 (7), 894-904, 2015
Genetic overlap between autoimmune diseases and non‐Hodgkin lymphoma subtypes
L Din, M Sheikh, N Kosaraju, KE Smedby, S Bernatsky, SI Berndt, ...
Genetic epidemiology 43 (7), 844-863, 2019
Genetic contribution to multiple sclerosis risk among Ashkenazi Jews
P Khankhanian, T Matsushita, L Madireddy, A Lizée, L Din, JM Moré, ...
BMC medical genetics 16 (1), 1-10, 2015
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