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Items: 1 to 50 of 95

1.

The PILRA G78R Variant Correlates with Higher HSV-1-Specific IgG Titers in Alzheimer's Disease.

Agostini S, Costa AS, Mancuso R, Guerini FR, Nemni R, Clerici M.

Cell Mol Neurobiol. 2019 Jul 11. doi: 10.1007/s10571-019-00712-5. [Epub ahead of print]

PMID:
31297637
2.

The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease.

Guerini FR, Ripamonti E, Costa AS, Zanzottera M, Agliardi C, Bolognesi E, Clerici M, Racca V.

Medicine (Baltimore). 2019 Jun;98(24):e15846. doi: 10.1097/MD.0000000000015846.

3.

SNARE Complex Polymorphisms Associate with Alterations of Visual Selective Attention in Alzheimer's Disease.

Costa AS, Guerini FR, Arosio B, Galimberti D, Zanzottera M, Bianchi A, Nemni R, Clerici M.

J Alzheimers Dis. 2019;69(1):179-188. doi: 10.3233/JAD-190147.

PMID:
30958380
4.

Correction: BDNF rs6265 polymorphism methylation in Multiple Sclerosis: A possible marker of disease progression.

Nociti V, Santoro M, Quaranta D, Losavio FA, De Fino C, Giordano R, Palomba NP, Rossini PM, Guerini FR, Clerici M, Caputo D, Mirabella M.

PLoS One. 2019 Feb 21;14(2):e0212906. doi: 10.1371/journal.pone.0212906. eCollection 2019.

5.

HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication study.

Guerini FR, Bolognesi E, Sotgiu S, Carta A, Clerici C, Chiappedi M, Ghezzo A, Zanette M, Mensi MM, Canevini MP, Zanzottera M, Agliardi C, Costa AS, Balottin U, Clerici M.

Brain Behav Immun. 2019 Jul;79:314-318. doi: 10.1016/j.bbi.2019.02.003. Epub 2019 Feb 11.

PMID:
30763769
6.

SNAP-25 in Serum Is Carried by Exosomes of Neuronal Origin and Is a Potential Biomarker of Alzheimer's Disease.

Agliardi C, Guerini FR, Zanzottera M, Bianchi A, Nemni R, Clerici M.

Mol Neurobiol. 2019 Aug;56(8):5792-5798. doi: 10.1007/s12035-019-1501-x. Epub 2019 Jan 24.

PMID:
30680692
7.

Association between Hippocampal Shape, Neuroinflammation, and Cognitive Decline in Alzheimer's Disease.

Cabinio M, Saresella M, Piancone F, LaRosa F, Marventano I, Guerini FR, Nemni R, Baglio F, Clerici M.

J Alzheimers Dis. 2018;66(3):1131-1144. doi: 10.3233/JAD-180250.

PMID:
30400090
8.

Reader response: Pregnancy decision-making in women with multiple sclerosis treated with natalizumab: I: Fetal risks.

Sotgiu S, Eusebi A, Begliuomini C, Guerini FR, Carta A.

Neurology. 2018 Oct 30;91(18):850. doi: 10.1212/WNL.0000000000006429. No abstract available.

PMID:
30373925
9.

BDNF rs6265 polymorphism methylation in Multiple Sclerosis: A possible marker of disease progression.

Nociti V, Santoro M, Quaranta D, Losavio FA, De Fino C, Giordano R, Palomba NP, Rossini PM, Guerini FR, Clerici M, Caputo D, Mirabella M.

PLoS One. 2018 Oct 23;13(10):e0206140. doi: 10.1371/journal.pone.0206140. eCollection 2018. Erratum in: PLoS One. 2019 Feb 21;14(2):e0212906.

10.

SNAP25 Gene Polymorphisms Protect Against Parkinson's Disease and Modulate Disease Severity in Patients.

Agliardi C, Guerini FR, Zanzottera M, Riboldazzi G, Zangaglia R, Sturchio A, Casali C, Di Lorenzo C, Minafra B, Nemni R, Clerici M.

Mol Neurobiol. 2019 Jun;56(6):4455-4463. doi: 10.1007/s12035-018-1386-0. Epub 2018 Oct 17.

PMID:
30334187
11.

Empathy and behavior in children affected by Autism Spectrum Disorders.

Mensi MM, Gasparini L, Chiappedi M, Guerini FR, Orlandi M, Rogantini C, Balottin U.

Minerva Pediatr. 2018 Jul 2. doi: 10.23736/S0026-4946.18.05228-3. [Epub ahead of print]

PMID:
29968451
12.

HLA alleles modulate EBV viral load in multiple sclerosis.

Agostini S, Mancuso R, Guerini FR, D'Alfonso S, Agliardi C, Hernis A, Zanzottera M, Barizzone N, Leone MA, Caputo D, Rovaris M, Clerici M.

J Transl Med. 2018 Mar 27;16(1):80. doi: 10.1186/s12967-018-1450-6.

13.

TNF-α -308 G/A and -238 G/A promoter polymorphisms and sporadic Parkinson's disease in an Italian cohort.

Agliardi C, Guerini FR, Zanzottera M, Riboldazzi G, Zangaglia R, Bono G, Casali C, Di Lorenzo C, Pacchetti C, Nemni R, Clerici M.

J Neurol Sci. 2018 Feb 15;385:45-48. doi: 10.1016/j.jns.2017.12.011. Epub 2017 Dec 11.

PMID:
29406912
14.

Modulation of Immune Responses to Herpes Simplex Virus Type 1 by IFNL3 and IRF7 Polymorphisms: A Study in Alzheimer's Disease.

Costa AS, Agostini S, Guerini FR, Mancuso R, Zanzottera M, Ripamonti E, Racca V, Nemni R, Clerici M.

J Alzheimers Dis. 2017;60(3):1055-1063. doi: 10.3233/JAD-170520.

PMID:
28984602
15.

Intermediate and low abundant protein analysis of vitamin D deficient obese and non-obese subjects by MALDI-profiling.

Al-Daghri NM, Torretta E, Capitanio D, Fania C, Guerini FR, Sabico SB, Clerici M, Gelfi C.

Sci Rep. 2017 Oct 3;7(1):12633. doi: 10.1038/s41598-017-13020-z.

16.

HLA-G coding region polymorphism is skewed in autistic spectrum disorders.

Guerini FR, Bolognesi E, Chiappedi M, Ripamonti E, Ghezzo A, Zanette M, Sotgiu S, Mensi MM, Carta A, Canevini MP, Zanzottera M, Agliardi C, Costa AS, Balottin U, Clerici M.

Brain Behav Immun. 2018 Jan;67:308-313. doi: 10.1016/j.bbi.2017.09.007. Epub 2017 Sep 18.

PMID:
28923404
17.

REST, a master regulator of neurogenesis, evolved under strong positive selection in humans and in non human primates.

Mozzi A, Guerini FR, Forni D, Costa AS, Nemni R, Baglio F, Cabinio M, Riva S, Pontremoli C, Clerici M, Sironi M, Cagliani R.

Sci Rep. 2017 Aug 25;7(1):9530. doi: 10.1038/s41598-017-10245-w.

18.

HLA-G∗14bp Insertion and the KIR2DS1-HLAC2 Complex Impact on Behavioral Impairment in Children with Autism Spectrum Disorders.

Guerini FR, Bolognesi E, Chiappedi M, Ghezzo A, Manca S, Zanette M, Sotgiu S, Mensi MM, Zanzottera M, Agliardi C, Costa AS, Balottin U, Clerici M.

Neuroscience. 2018 Feb 1;370:163-169. doi: 10.1016/j.neuroscience.2017.06.012. Epub 2017 Jun 13.

PMID:
28627421
19.

Indoleamine-2,3-dioxygenase(IDO)2 polymorphisms are not associated with multiple sclerosis in Italians.

Agliardi C, Guerini FR, Zanzottera M, Rovaris M, Caputo D, Clerici M.

J Neurol Sci. 2017 Jun 15;377:31-34. doi: 10.1016/j.jns.2017.03.048. Epub 2017 Mar 29.

PMID:
28477703
20.

Overexpression of the Cytokine BAFF and Autoimmunity Risk.

Steri M, Orrù V, Idda ML, Pitzalis M, Pala M, Zara I, Sidore C, Faà V, Floris M, Deiana M, Asunis I, Porcu E, Mulas A, Piras MG, Lobina M, Lai S, Marongiu M, Serra V, Marongiu M, Sole G, Busonero F, Maschio A, Cusano R, Cuccuru G, Deidda F, Poddie F, Farina G, Dei M, Virdis F, Olla S, Satta MA, Pani M, Delitala A, Cocco E, Frau J, Coghe G, Lorefice L, Fenu G, Ferrigno P, Ban M, Barizzone N, Leone M, Guerini FR, Piga M, Firinu D, Kockum I, Lima Bomfim I, Olsson T, Alfredsson L, Suarez A, Carreira PE, Castillo-Palma MJ, Marcus JH, Congia M, Angius A, Melis M, Gonzalez A, Alarcón Riquelme ME, da Silva BM, Marchini M, Danieli MG, Del Giacco S, Mathieu A, Pani A, Montgomery SB, Rosati G, Hillert J, Sawcer S, D'Alfonso S, Todd JA, Novembre J, Abecasis GR, Whalen MB, Marrosu MG, Meloni A, Sanna S, Gorospe M, Schlessinger D, Fiorillo E, Zoledziewska M, Cucca F.

N Engl J Med. 2017 Apr 27;376(17):1615-1626. doi: 10.1056/NEJMoa1610528.

21.

A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples.

Mozzi A, Riva V, Forni D, Sironi M, Marino C, Molteni M, Riva S, Guerini FR, Clerici M, Cagliani R, Mascheretti S.

Am J Med Genet B Neuropsychiatr Genet. 2017 Jul;174(5):578-586. doi: 10.1002/ajmg.b.32546. Epub 2017 Apr 24.

PMID:
28436202
22.

Vitamin D-binding protein gene polymorphisms are not associated with MS risk in an Italian cohort.

Agliardi C, Guerini FR, Zanzottera M, Bolognesi E, Costa AS, Clerici M.

J Neuroimmunol. 2017 Apr 15;305:92-95. doi: 10.1016/j.jneuroim.2017.02.009. Epub 2017 Feb 8.

PMID:
28284354
23.

ApoE and SNAP-25 Polymorphisms Predict the Outcome of Multidimensional Stimulation Therapy Rehabilitation in Alzheimer's Disease.

Guerini FR, Farina E, Costa AS, Baglio F, Saibene FL, Margaritella N, Calabrese E, Zanzottera M, Bolognesi E, Nemni R, Clerici M.

Neurorehabil Neural Repair. 2016 Oct;30(9):883-93. doi: 10.1177/1545968316642523. Epub 2016 Apr 13.

PMID:
27075583
24.

Impact of vitamin D receptor polymorphisms in centenarians.

Gussago C, Arosio B, Guerini FR, Ferri E, Costa AS, Casati M, Bollini EM, Ronchetti F, Colombo E, Bernardelli G, Clerici M, Mari D.

Endocrine. 2016 Aug;53(2):558-64. doi: 10.1007/s12020-016-0908-7. Epub 2016 Mar 8.

PMID:
26956844
25.

The evolutionary history of genes involved in spoken and written language: beyond FOXP2.

Mozzi A, Forni D, Clerici M, Pozzoli U, Mascheretti S, Guerini FR, Riva S, Bresolin N, Cagliani R, Sironi M.

Sci Rep. 2016 Feb 25;6:22157. doi: 10.1038/srep22157.

26.

Synaptosomal Protein of 25 kDa (Snap25) Polymorphisms Associated with Glycemic Parameters in Type 2 Diabetes Patients.

Al-Daghri NM, Costa AS, Alokail MS, Zanzottera M, Alenad AM, Mohammed AK, Clerici M, Guerini FR.

J Diabetes Res. 2016;2016:8943092. doi: 10.1155/2016/8943092. Epub 2015 Dec 8.

27.

Lack of evidence for a role of HHV-6 in the pathogenesis of Alzheimer's disease.

Agostini S, Mancuso R, Baglio F, Cabinio M, Hernis A, Guerini FR, Calabrese E, Nemni R, Clerici M.

J Alzheimers Dis. 2016;49(1):229-35. doi: 10.3233/JAD-150464.

PMID:
26444787
28.

The burden of multiple sclerosis variants in continental Italians and Sardinians.

Barizzone N, Zara I, Sorosina M, Lupoli S, Porcu E, Pitzalis M, Zoledziewska M, Esposito F, Leone M, Mulas A, Cocco E, Ferrigno P, Guerini FR, Brambilla P, Farina G, Murru R, Deidda F, Sanna S, Loi A, Barlassina C, Vecchio D, Zauli A, Clarelli F, Braga D, Poddie F, Cantello R, Martinelli V, Comi G, Frau J, Lorefice L, Pugliatti M, Rosati G; PROGEMUS (PROgnostic GEnetic factors in MUltiple Sclerosis) Consortium PROGRESSO (Italian network of Primary Progressive Multiple Sclerosis) Consortium, Melis M, Marrosu MG, Cusi D, Cucca F, Martinelli Boneschi F, Sanna S, D'Alfonso S.

Mult Scler. 2015 Oct;21(11):1385-95. doi: 10.1177/1352458515596599.

PMID:
26438306
29.

Epstein-Barr virus genetic variants are associated with multiple sclerosis.

Mechelli R, Manzari C, Policano C, Annese A, Picardi E, Umeton R, Fornasiero A, D'Erchia AM, Buscarinu MC, Agliardi C, Annibali V, Serafini B, Rosicarelli B, Romano S, Angelini DF, Ricigliano VA, Buttari F, Battistini L, Centonze D, Guerini FR, D'Alfonso S, Pesole G, Salvetti M, Ristori G.

Neurology. 2015 Mar 31;84(13):1362-8. doi: 10.1212/WNL.0000000000001420. Epub 2015 Mar 4.

30.

Association between SNAP-25 gene polymorphisms and cognition in autism: functional consequences and potential therapeutic strategies.

Braida D, Guerini FR, Ponzoni L, Corradini I, De Astis S, Pattini L, Bolognesi E, Benfante R, Fornasari D, Chiappedi M, Ghezzo A, Clerici M, Matteoli M, Sala M.

Transl Psychiatry. 2015 Jan 27;5:e500. doi: 10.1038/tp.2014.136.

31.

An HLA-G(∗)14bp insertion/deletion polymorphism associates with the development of autistic spectrum disorders.

Guerini FR, Bolognesi E, Chiappedi M, Ghezzo A, Canevini MP, Mensi MM, Vignoli A, Agliardi C, Zanette M, Clerici M.

Brain Behav Immun. 2015 Feb;44:207-12. doi: 10.1016/j.bbi.2014.10.002. Epub 2014 Oct 18.

PMID:
25451607
32.

Relationship between herpes simplex virus-1-specific antibody titers and cortical brain damage in Alzheimer's disease and amnestic mild cognitive impairment.

Mancuso R, Baglio F, Agostini S, Cabinio M, Laganà MM, Hernis A, Margaritella N, Guerini FR, Zanzottera M, Nemni R, Clerici M.

Front Aging Neurosci. 2014 Oct 15;6:285. doi: 10.3389/fnagi.2014.00285. eCollection 2014.

33.

Genetic adaptation of the human circadian clock to day-length latitudinal variations and relevance for affective disorders.

Forni D, Pozzoli U, Cagliani R, Tresoldi C, Menozzi G, Riva S, Guerini FR, Comi GP, Bolognesi E, Bresolin N, Clerici M, Sironi M.

Genome Biol. 2014;15(10):499.

34.

Possible association between SNAP-25 single nucleotide polymorphisms and alterations of categorical fluency and functional MRI parameters in Alzheimer's disease.

Guerini FR, Agliardi C, Sironi M, Arosio B, Calabrese E, Zanzottera M, Bolognesi E, Ricci C, Costa AS, Galimberti D, Griffanti L, Bianchi A, Savazzi F, Mari D, Scarpini E, Baglio F, Nemni R, Clerici M.

J Alzheimers Dis. 2014;42(3):1015-28. doi: 10.3233/JAD-140057.

PMID:
25024311
35.

Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.

Al-Daghri NM, Guerini FR, Al-Attas OS, Alokail MS, Alkharfy KM, Draz HM, Agliardi C, Costa AS, Saulle I, Mohammed AK, Biasin M, Clerici M.

PLoS One. 2014 Jul 14;9(7):e102141. doi: 10.1371/journal.pone.0102141. eCollection 2014.

36.

No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosis.

Guerini FR, Clerici M, Cagliani R, Malhotra S, Montalban X, Forni D, Agliardi C, Riva S, Caputo D, Galimberti D, Asselta R, Fenoglio C, Scarpini E, Comi GP, Bresolin N, Comabella M, Sironi M.

J Neuroimmunol. 2014 Jun 15;271(1-2):49-52. doi: 10.1016/j.jneuroim.2014.04.006. Epub 2014 Apr 16.

PMID:
24794504
37.

Ancient and recent selective pressures shaped genetic diversity at AIM2-like nucleic acid sensors.

Cagliani R, Forni D, Biasin M, Comabella M, Guerini FR, Riva S, Pozzoli U, Agliardi C, Caputo D, Malhotra S, Montalban X, Bresolin N, Clerici M, Sironi M.

Genome Biol Evol. 2014 Apr;6(4):830-45. doi: 10.1093/gbe/evu066.

38.

Genetic burden of common variants in progressive and bout-onset multiple sclerosis.

Sorosina M, Brambilla P, Clarelli F, Barizzone N, Lupoli S, Guaschino C, Osiceanu AM, Moiola L, Ghezzi A, Coniglio G, Patti F, Mancardi G, Manunta P, Glorioso N, Guerini FR, Bergamaschi R, Perla F; PROGRESSO; PROGEMUS, Martinelli V, Cusi D, Leone M, Comi G, D'Alfonso S, Martinelli-Boneschi F.

Mult Scler. 2014 Jun;20(7):802-11. doi: 10.1177/1352458513512707. Epub 2013 Nov 25.

PMID:
24277324
39.

Activating KIR molecules and their cognate ligands prevail in children with a diagnosis of ASD and in their mothers.

Guerini FR, Bolognesi E, Chiappedi M, Manca S, Ghezzo A, Agliardi C, Zanette M, Littera R, Carcassi C, Sotgiu S, Clerici M.

Brain Behav Immun. 2014 Feb;36:54-60. doi: 10.1016/j.bbi.2013.10.006. Epub 2013 Oct 11.

PMID:
24120931
40.

Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients.

Leone MA, Barizzone N, Esposito F, Lucenti A, Harbo HF, Goris A, Kockum I, Oturai AB, Celius EG, Mero IL, Dubois B, Olsson T, Søndergaard HB, Cusi D, Lupoli S, Andreassen BK; International Multiple Sclerosis Genetics Consortium; Wellcome Trust Case Control Consortium 2, Myhr KM, Guerini FR; PROGEMUS Group; PROGRESSO Group, Comi G, Martinelli-Boneschi F, D'Alfonso S.

PLoS One. 2013 Jun 13;8(6):e64408. doi: 10.1371/journal.pone.0064408. Print 2013.

41.

No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis.

Barizzone N, Pauwels I, Luciano B, Franckaert D, Guerini FR, Cosemans L, Hilven K, Salviati A, Dooley J, Danso-Abeam D, di Sapio A, Cavalla P, Decallonne B, Mathieu C, Liston A, Leone M, Dubois B, D'Alfonso S, Goris A.

Ann Neurol. 2013 Mar;73(3):433-7. doi: 10.1002/ana.23834. Epub 2013 Mar 11.

PMID:
23483640
42.

Long-standing balancing selection in the THBS4 gene: influence on sex-specific brain expression and gray matter volumes in Alzheimer disease.

Cagliani R, Guerini FR, Rubio-Acero R, Baglio F, Forni D, Agliardi C, Griffanti L, Fumagalli M, Pozzoli U, Riva S, Calabrese E, Sikora M, Casals F, Comi GP, Bresolin N, Cáceres M, Clerici M, Sironi M.

Hum Mutat. 2013 May;34(5):743-53. doi: 10.1002/humu.22301. Epub 2013 Apr 2.

PMID:
23420636
43.

NK cells in human disease: an evolving story.

Guerini FR, Clerici M.

Clin Immunol. 2012 Jun;143(3):203-6. doi: 10.1016/j.clim.2012.03.003. Epub 2012 Mar 28. No abstract available.

PMID:
22525888
44.

Activating KIR/HLA complexes in classic Kaposi's Sarcoma.

Guerini FR, Mancuso R, Agostini S, Agliardi C, Zanzottera M, Hernis A, Tourlaki A, Calvo MG, Bellinvia M, Brambilla L, Clerici M.

Infect Agent Cancer. 2012 Apr 2;7:9. doi: 10.1186/1750-9378-7-9.

45.

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.

Cagliani R, Guerini FR, Fumagalli M, Riva S, Agliardi C, Galimberti D, Pozzoli U, Goris A, Dubois B, Fenoglio C, Forni D, Sanna S, Zara I, Pitzalis M, Zoledziewska M, Cucca F, Marini F, Comi GP, Scarpini E, Bresolin N, Clerici M, Sironi M.

Mol Biol Evol. 2012 Jun;29(6):1599-613. doi: 10.1093/molbev/mss002. Epub 2012 Jan 6.

PMID:
22319148
46.

A functional variant in ERAP1 predisposes to multiple sclerosis.

Guerini FR, Cagliani R, Forni D, Agliardi C, Caputo D, Cassinotti A, Galimberti D, Fenoglio C, Biasin M, Asselta R, Scarpini E, Comi GP, Bresolin N, Clerici M, Sironi M.

PLoS One. 2012;7(1):e29931. doi: 10.1371/journal.pone.0029931. Epub 2012 Jan 12.

47.

Vitamin D receptor gene polymorphisms and HLA DRB1*04 cosegregation in Saudi type 2 diabetes patients.

Al-Daghri NM, Al-Attas O, Alokail MS, Alkharfy KM, Draz HM, Agliardi C, Mohammed AK, Guerini FR, Clerici M.

J Immunol. 2012 Feb 1;188(3):1325-32. doi: 10.4049/jimmunol.1101954. Epub 2012 Jan 4.

48.

KIR-HLA genotypes in HIV-infected patients lacking immunological recovery despite effective antiretroviral therapy.

Soria A, Guerini FR, Bandera A, Bolognesi E, Uglietti A, Fusco C, Zucchi P, Maserati R, Rizzardini G, Clerici M, Gori A.

PLoS One. 2011;6(11):e27349. doi: 10.1371/journal.pone.0027349. Epub 2011 Nov 3.

49.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

International Multiple Sclerosis Genetics Consortium; Wellcome Trust Case Control Consortium 2, Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, Potter SC, Goris A, Band G, Oturai AB, Strange A, Saarela J, Bellenguez C, Fontaine B, Gillman M, Hemmer B, Gwilliam R, Zipp F, Jayakumar A, Martin R, Leslie S, Hawkins S, Giannoulatou E, D'alfonso S, Blackburn H, Martinelli Boneschi F, Liddle J, Harbo HF, Perez ML, Spurkland A, Waller MJ, Mycko MP, Ricketts M, Comabella M, Hammond N, Kockum I, McCann OT, Ban M, Whittaker P, Kemppinen A, Weston P, Hawkins C, Widaa S, Zajicek J, Dronov S, Robertson N, Bumpstead SJ, Barcellos LF, Ravindrarajah R, Abraham R, Alfredsson L, Ardlie K, Aubin C, Baker A, Baker K, Baranzini SE, Bergamaschi L, Bergamaschi R, Bernstein A, Berthele A, Boggild M, Bradfield JP, Brassat D, Broadley SA, Buck D, Butzkueven H, Capra R, Carroll WM, Cavalla P, Celius EG, Cepok S, Chiavacci R, Clerget-Darpoux F, Clysters K, Comi G, Cossburn M, Cournu-Rebeix I, Cox MB, Cozen W, Cree BA, Cross AH, Cusi D, Daly MJ, Davis E, de Bakker PI, Debouverie M, D'hooghe MB, Dixon K, Dobosi R, Dubois B, Ellinghaus D, Elovaara I, Esposito F, Fontenille C, Foote S, Franke A, Galimberti D, Ghezzi A, Glessner J, Gomez R, Gout O, Graham C, Grant SF, Guerini FR, Hakonarson H, Hall P, Hamsten A, Hartung HP, Heard RN, Heath S, Hobart J, Hoshi M, Infante-Duarte C, Ingram G, Ingram W, Islam T, Jagodic M, Kabesch M, Kermode AG, Kilpatrick TJ, Kim C, Klopp N, Koivisto K, Larsson M, Lathrop M, Lechner-Scott JS, Leone MA, Leppä V, Liljedahl U, Bomfim IL, Lincoln RR, Link J, Liu J, Lorentzen AR, Lupoli S, Macciardi F, Mack T, Marriott M, Martinelli V, Mason D, McCauley JL, Mentch F, Mero IL, Mihalova T, Montalban X, Mottershead J, Myhr KM, Naldi P, Ollier W, Page A, Palotie A, Pelletier J, Piccio L, Pickersgill T, Piehl F, Pobywajlo S, Quach HL, Ramsay PP, Reunanen M, Reynolds R, Rioux JD, Rodegher M, Roesner S, Rubio JP, Rückert IM, Salvetti M, Salvi E, Santaniello A, Schaefer CA, Schreiber S, Schulze C, Scott RJ, Sellebjerg F, Selmaj KW, Sexton D, Shen L, Simms-Acuna B, Skidmore S, Sleiman PM, Smestad C, Sørensen PS, Søndergaard HB, Stankovich J, Strange RC, Sulonen AM, Sundqvist E, Syvänen AC, Taddeo F, Taylor B, Blackwell JM, Tienari P, Bramon E, Tourbah A, Brown MA, Tronczynska E, Casas JP, Tubridy N, Corvin A, Vickery J, Jankowski J, Villoslada P, Markus HS, Wang K, Mathew CG, Wason J, Palmer CN, Wichmann HE, Plomin R, Willoughby E, Rautanen A, Winkelmann J, Wittig M, Trembath RC, Yaouanq J, Viswanathan AC, Zhang H, Wood NW, Zuvich R, Deloukas P, Langford C, Duncanson A, Oksenberg JR, Pericak-Vance MA, Haines JL, Olsson T, Hillert J, Ivinson AJ, De Jager PL, Peltonen L, Stewart GJ, Hafler DA, Hauser SL, McVean G, Donnelly P, Compston A.

Nature. 2011 Aug 10;476(7359):214-9. doi: 10.1038/nature10251.

50.

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

Cagliani R, Fumagalli M, Guerini FR, Riva S, Galimberti D, Comi GP, Agliardi C, Scarpini E, Pozzoli U, Forni D, Caputo D, Asselta R, Biasin M, Paraboschi EM, Bresolin N, Clerici M, Sironi M.

Hum Genet. 2012 Jan;131(1):87-97. doi: 10.1007/s00439-011-1053-2. Epub 2011 Jul 7.

PMID:
21735172

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