Items per page
Sort by

Send to:

Choose Destination

Search results

Items: 1 to 20 of 23


Meta-analysis of genome-wide association studies reveals genetic overlap between Hodgkin lymphoma and multiple sclerosis.

Khankhanian P, Cozen W, Himmelstein DS, Madireddy L, Din L, van den Berg A, Matsushita T, Glaser SL, Moré JM, Smedby KE, Baranzini SE, Mack TM, Lizée A, de Sanjosé S, Gourraud PA, Nieters A, Hauser SL, Cocco P, Maynadié M, Foretová L, Staines A, Delahaye-Sourdeix M, Li D, Bhatia S, Melbye M, Onel K, Jarrett R, McKay JD, Oksenberg JR, Hjalgrim H.

Int J Epidemiol. 2016 Mar 12. pii: dyv364. [Epub ahead of print]


Genetic contribution to multiple sclerosis risk among Ashkenazi Jews.

Khankhanian P, Matsushita T, Madireddy L, Lizée A, Din L, Moré JM, Gourraud PA, Hauser SL, Baranzini SE, Oksenberg JR.

BMC Med Genet. 2015 Jul 28;16:55. doi: 10.1186/s12881-015-0201-2.


Haplotype-based approach to known MS-associated regions increases the amount of explained risk.

Khankhanian P, Gourraud PA, Lizee A, Goodin DS.

J Med Genet. 2015 Sep;52(9):587-94. doi: 10.1136/jmedgenet-2015-103071. Epub 2015 Jul 16.


An ImmunoChip study of multiple sclerosis risk in African Americans.

Isobe N, Madireddy L, Khankhanian P, Matsushita T, Caillier SJ, Moré JM, Gourraud PA, McCauley JL, Beecham AH; International Multiple Sclerosis Genetics Consortium, Piccio L, Herbert J, Khan O, Cohen J, Stone L, Santaniello A, Cree BA, Onengut-Gumuscu S, Rich SS, Hauser SL, Sawcer S, Oksenberg JR.

Brain. 2015 Jun;138(Pt 6):1518-30. doi: 10.1093/brain/awv078. Epub 2015 Mar 28.


Pseudo-Pelger-Huët anomaly and granulocytic dysplasia associated with human granulocytic anaplasmosis.

Lee S, Khankhanian P, Salama C, Brown M, Lieber J.

Int J Hematol. 2015 Jul;102(1):129-33. doi: 10.1007/s12185-015-1769-1. Epub 2015 Mar 7.


SNP imputation bias reduces effect size determination.

Khankhanian P, Din L, Caillier SJ, Gourraud PA, Baranzini SE.

Front Genet. 2015 Feb 9;6:30. doi: 10.3389/fgene.2015.00030. eCollection 2015.


Genetic associations with brain cortical thickness in multiple sclerosis.

Matsushita T, Madireddy L, Sprenger T, Khankhanian P, Magon S, Naegelin Y, Caverzasi E, Lindberg RL, Kappos L, Hauser SL, Oksenberg JR, Henry R, Pelletier D, Baranzini SE.

Genes Brain Behav. 2015 Feb;14(2):217-27. doi: 10.1111/gbb.12190. Epub 2015 Mar 5.


Corticosteroid-induced morphological changes in cells of the myeloid lineage.

Lee S, Khankhanian P, Mascarenhas JO.

Am J Hematol. 2015 Jul;90(7):679-80. doi: 10.1002/ajh.23943. Epub 2015 Feb 17. No abstract available.


HLA diversity in the 1000 genomes dataset.

Gourraud PA, Khankhanian P, Cereb N, Yang SY, Feolo M, Maiers M, Rioux JD, Hauser S, Oksenberg J.

PLoS One. 2014 Jul 2;9(7):e97282. doi: 10.1371/journal.pone.0097282. eCollection 2014.


Single nucleotide polymorphism (SNP)-strings: an alternative method for assessing genetic associations.

Goodin DS, Khankhanian P.

PLoS One. 2014 Apr 11;9(4):e90034. doi: 10.1371/journal.pone.0090034. eCollection 2014.


Patients recovering from abdominal surgery who walked with volunteers had improved postoperative recovery profiles during their hospitalization.

Le H, Khankhanian P, Joshi N, Maa J, Crevensten H.

World J Surg. 2014 Aug;38(8):1961-5. doi: 10.1007/s00268-014-2491-5.


Sequencing of the IL6 gene in a case-control study of cerebral palsy in children.

Khankhanian P, Baranzini SE, Johnson BA, Madireddy L, Nickles D, Croen LA, Wu YW.

BMC Med Genet. 2013 Dec 7;14:126. doi: 10.1186/1471-2350-14-126.


Genetic risk variants in African Americans with multiple sclerosis.

Isobe N, Gourraud PA, Harbo HF, Caillier SJ, Santaniello A, Khankhanian P, Maiers M, Spellman S, Cereb N, Yang S, Pando MJ, Piccio L, Cross AH, De Jager PL, Cree BA, Hauser SL, Oksenberg JR.

Neurology. 2013 Jul 16;81(3):219-27. doi: 10.1212/WNL.0b013e31829bfe2f. Epub 2013 Jun 14.


Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls.

Nickles D, Chen HP, Li MM, Khankhanian P, Madireddy L, Caillier SJ, Santaniello A, Cree BA, Pelletier D, Hauser SL, Oksenberg JR, Baranzini SE.

Hum Mol Genet. 2013 Oct 15;22(20):4194-205. doi: 10.1093/hmg/ddt267. Epub 2013 Jun 6.


A genome-wide association study of brain lesion distribution in multiple sclerosis.

Gourraud PA, Sdika M, Khankhanian P, Henry RG, Beheshtian A, Matthews PM, Hauser SL, Oksenberg JR, Pelletier D, Baranzini SE.

Brain. 2013 Apr;136(Pt 4):1012-24. doi: 10.1093/brain/aws363. Epub 2013 Feb 13.


Transcriptional expression patterns triggered by chemically distinct neuroprotective molecules.

Pappas DJ, Gabatto PA, Oksenberg D, Khankhanian P, Baranzini SE, Gan L, Oksenberg JR.

Neuroscience. 2012 Dec 13;226:10-20. doi: 10.1016/j.neuroscience.2012.09.007. Epub 2012 Sep 15.


In depth comparison of an individual's DNA and its lymphoblastoid cell line using whole genome sequencing.

Nickles D, Madireddy L, Yang S, Khankhanian P, Lincoln S, Hauser SL, Oksenberg JR, Baranzini SE.

BMC Genomics. 2012 Sep 14;13:477. doi: 10.1186/1471-2164-13-477.


iCTNet: a Cytoscape plugin to produce and analyze integrative complex traits networks.

Wang L, Khankhanian P, Baranzini SE, Mousavi P.

BMC Bioinformatics. 2011 Sep 26;12:380. doi: 10.1186/1471-2105-12-380.


Genetic variation in the odorant receptors family 13 and the mhc loci influence mate selection in a multiple sclerosis dataset.

Khankhanian P, Gourraud PA, Caillier SJ, Santaniello A, Hauser SL, Baranzini SE, Oksenberg JR.

BMC Genomics. 2010 Nov 10;11:626. doi: 10.1186/1471-2164-11-626.


Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.

Baranzini SE, Srinivasan R, Khankhanian P, Okuda DT, Nelson SJ, Matthews PM, Hauser SL, Oksenberg JR, Pelletier D.

Brain. 2010 Sep;133(9):2603-11. doi: 10.1093/brain/awq192.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk