Articles with public access mandates - Pouya KhankhanianLearn more
Available somewhere: 34
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
SE Baranzini, J Mudge, JC Van Velkinburgh, P Khankhanian, ...
Nature 464 (7293), 1351-1356, 2010
Mandates: US National Institutes of Health
Systematic integration of biomedical knowledge prioritizes drugs for repurposing
DS Himmelstein, A Lizee, C Hessler, L Brueggeman, SL Chen, D Hadley, ...
Elife 6, e26726, 2017
Mandates: US National Science Foundation, US National Institutes of Health
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
Mandates: US National Institutes of Health, UK Medical Research Council, National …
HLA Diversity in the 1000 Genomes Dataset
PA Gourraud, P Khankhanian, N Cereb, SY Yang, M Feolo, M Maiers, ...
PloS one 9 (7), e97282, 2014
Mandates: US National Institutes of Health
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls
SE Baranzini, P Khankhanian, NA Patsopoulos, M Li, J Stankovich, ...
The American Journal of Human Genetics 92 (6), 854-865, 2013
Mandates: US National Institutes of Health, Research Foundation (Flanders), Wellcome Trust
Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis
SE Baranzini, R Srinivasan, P Khankhanian, DT Okuda, SJ Nelson, ...
Brain 133 (9), 2603-2611, 2010
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health, German Research Foundation
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
Mandates: US National Institutes of Health, National Institute for Health Research, UK …
Genetic risk variants in African Americans with multiple sclerosis
N Isobe, PA Gourraud, HF Harbo, SJ Caillier, A Santaniello, ...
Neurology 81 (3), 219-227, 2013
Mandates: US National Institutes of Health
A genome-wide association study of brain lesion distribution in multiple sclerosis
PA Gourraud, M Sdika, P Khankhanian, RG Henry, A Beheshtian, ...
Brain 136 (4), 1012-1024, 2013
Mandates: US National Institutes of Health
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects
LM Niestroj, E Perez-Palma, DP Howrigan, Y Zhou, F Cheng, ...
Brain 143 (7), 2106-2118, 2020
Mandates: US National Institutes of Health, Academy of Finland, UK Medical Research …
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, 1-11, 2012
Mandates: US National Institutes of Health, German Research Foundation
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
Mandates: US National Institutes of Health, National Health and Medical Research …
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
Mandates: US National Science Foundation, US National Institutes of Health, UK Medical …
A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation
S Ganesan, PD Galer, KL Helbig, SE McKeown, M O’Brien, AK Gonzalez, ...
Genetics in Medicine 22 (12), 2060-2070, 2020
Mandates: US National Institutes of Health
Monitoring the burden of seizures and highly epileptiform patterns in critical care with a novel machine learning method
B Kamousi, S Karunakaran, K Gururangan, M Markert, B Decker, ...
Neurocritical care 34, 908-917, 2021
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health
Harnessing electronic medical records to advance research on multiple sclerosis
V Damotte, A Lizée, M Tremblay, A Agrawal, P Khankhanian, ...
Multiple Sclerosis Journal 25 (3), 408-418, 2019
Mandates: National Institute of Health and Medical Research, France, Patient-Centered …
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, 1-8, 2013
Mandates: US National Institutes of Health
Haplotype-based approach to known MS-associated regions increases the amount of explained risk
P Khankhanian, PA Gourraud, A Lizee, DS Goodin
Journal of medical genetics 52 (9), 587-594, 2015
Mandates: Wellcome Trust
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