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Evaluating mitochondrial DNA variation in autism spectrum disorders.
Ann Hum Genet. 2013 Jan;77(1):9-21. doi: 10.1111/j.1469-1809.2012.00736.x. Epub 2012 Nov 6.
Ann Hum Genet. 2013.
PMID: 23130936
Free PMC article.
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
International Multiple Sclerosis Genetics Consortium (IMSGC); Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, Cotsapas C, Shah TS, Spencer C, Booth D, Goris A, Oturai A, Saarela J, Fontaine B, Hemmer B, Martin C, Zipp F, D'Alfonso S, Martinelli-Boneschi F, Taylor B, Harbo HF, Kockum I, Hillert J, Olsson T, Ban M, Oksenberg JR, Hintzen R, Barcellos LF; Wellcome Trust Case Control Consortium 2 (WTCCC2); International IBD Genetics Consortium (IIBDGC); Agliardi C, Alfredsson L, Alizadeh M, Anderson C, Andrews R, Søndergaard HB, Baker A, Band G, Baranzini SE, Barizzone N, Barrett J, Bellenguez C, Bergamaschi L, Bernardinelli L, Berthele A, Biberacher V, Binder TM, Blackburn H, Bomfim IL, Brambilla P, Broadley S, Brochet B, Brundin L, Buck D, Butzkueven H, Caillier SJ, Camu W, Carpentier W, Cavalla P, Celius EG, Coman I, Comi G, Corrado L, Cosemans L, Cournu-Rebeix I, Cree BA, Cusi D, Damotte V, Defer G, Delgado SR, Deloukas P, di Sapio A, Dilthey AT, Donnelly P, Dubois B, Duddy M, Edkins S, Elovaara I, Esposito F, Evangelou N, Fiddes B, Field J, Franke A, Freeman C, Frohlich IY, Galimberti D, Gieger C, Gourraud PA, Graetz C, Graham A, Grummel V, Guaschino C, Hadjixenof…
See abstract for full author list ➔
International Multiple Sclerosis Genetics Consortium (IMSGC), et al. Among authors: hadjixenofontos a.
Nat Genet. 2013 Nov;45(11):1353-60. doi: 10.1038/ng.2770. Epub 2013 Sep 29.
Nat Genet. 2013.
PMID: 24076602
Free PMC article.
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Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families.
Fazia T, Marzanati D, Carotenuto AL, Beecham A, Hadjixenofontos A, McCauley JL, Saddi V, Piras M, Bernardinelli L, Gentilini D.
Fazia T, et al. Among authors: hadjixenofontos a.
Curr Issues Mol Biol. 2021 Oct 27;43(3):1778-1793. doi: 10.3390/cimb43030125.
Curr Issues Mol Biol. 2021.
PMID: 34889895
Free PMC article.
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Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci.
Fazia T, Pastorino R, Foco L, Han L, Abney M, Beecham A, Hadjixenofontos A, Guo H, Gentilini D, Papachristou C, Bitti PP, Ticca A, Berzuini C, McCauley JL, Bernardinelli L.
Fazia T, et al. Among authors: hadjixenofontos a.
Mult Scler. 2018 Dec;24(14):1815-1824. doi: 10.1177/1352458517732841. Epub 2017 Sep 21.
Mult Scler. 2018.
PMID: 28933650
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Enrichment for Northern European-derived multiple sclerosis risk alleles in Sardinia.
Hadjixenofontos A, Gourraud PA, Bakthavachalam V, Foco L, Ticca A, Bitti P, Pastorino R, Bernardinelli L, McCauley JL.
Hadjixenofontos A, et al.
Mult Scler. 2015 Oct;21(11):1396-403. doi: 10.1177/1352458515581872. Epub 2015 Apr 28.
Mult Scler. 2015.
PMID: 25921054
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Clinical Expression of Multiple Sclerosis in Hispanic Whites of Primarily Caribbean Ancestry.
Hadjixenofontos A, Beecham AH, Manrique CP, Pericak-Vance MA, Tornes L, Ortega M, Rammohan KW, McCauley JL, Delgado SR.
Hadjixenofontos A, et al.
Neuroepidemiology. 2015;44(4):262-8. doi: 10.1159/000431375. Epub 2015 Jul 11.
Neuroepidemiology. 2015.
PMID: 26184860
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A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility.
Damotte V, Guillot-Noel L, Patsopoulos NA, Madireddy L, El Behi M; International Multiple Sclerosis Genetics Consortium; Wellcome Trust Case Control Consortium 2; De Jager PL, Baranzini SE, Cournu-Rebeix I, Fontaine B.
Damotte V, et al.
Genes Immun. 2014 Mar;15(2):126-32. doi: 10.1038/gene.2013.70. Epub 2014 Jan 16.
Genes Immun. 2014.
PMID: 24430173
Free article.
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