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Pouya Khankhanian
Pouya Khankhanian
Email verificata su uphs.upenn.edu
Titolo
Citata da
Citata da
Anno
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
5692010
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
4752017
Pathway and network-based analysis of genome-wide association studies in multiple sclerosis
SE Baranzini, NW Galwey, J Wang, P Khankhanian, R Lindberg, ...
Human molecular genetics 18 (11), 2078-2090, 2009
4732009
Differential micro RNA expression in PBMC from multiple sclerosis patients
D Otaegui, SE Baranzini, R Armaanzas, B Calvo, M Muoz-Culla, ...
PloS one 4 (7), e6309, 2009
3102009
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
2462019
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
2032014
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
1662013
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
1552010
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
962013
An ImmunoChip study of multiple sclerosis risk in African Americans
N Isobe, L Madireddy, P Khankhanian, T Matsushita, SJ Caillier, JM Mor, ...
Brain 138 (6), 1518-1530, 2015
802015
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
762013
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
732013
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
562020
The nature of genetic and environmental susceptibility to multiple sclerosis
DS Goodin, P Khankhanian, PA Gourraud, N Vince
PLoS One 16 (3), e0246157, 2021
452021
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
412012
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
392019
iCTNet: a Cytoscape plugin to produce and analyze integrative complex traits networks
L Wang, P Khankhanian, SE Baranzini, P Mousavi
BMC bioinformatics 12, 1-7, 2011
352011
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
322016
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
302020
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
302015
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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