Fortina P - Search Results

1

Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.

Danjou F, Anni F, Perseu L, Satta S, Dessì C, Lai ME, Fortina P, Devoto M, Galanello R. Danjou F, et al. Among authors: fortina p. Haematologica. 2012 Jul;97(7):989-93. doi: 10.3324/haematol.2011.053504. Epub 2012 Jan 22. Haematologica. 2012. PMID: 22271886 Free PMC article.

2

Association of a polymorphic variant of the adiponectin gene with insulin resistance in african americans.

Specchia C, Scott K, Fortina P, Devoto M, Falkner B. Specchia C, et al. Among authors: fortina p. Clin Transl Sci. 2008 Dec;1(3):194-9. doi: 10.1111/j.1752-8062.2008.00055.x. Clin Transl Sci. 2008. PMID: 20443850 Free PMC article.

3

Seventy-five genetic loci influencing the human red blood cell.

van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X, Radhakrishnan A, Tan ST, Voss K, Weichenberger CX, Albers CA, Al-Hussani A, Asselbergs FW, Ciullo M, Danjou F, Dina C, Esko T, Evans DM, Franke L, Gögele M, Hartiala J, Hersch M, Holm H, Hottenga JJ, Kanoni S, Kleber ME, Lagou V, Langenberg C, Lopez LM, Lyytikäinen LP, Melander O, Murgia F, Nolte IM, O'Reilly PF, Padmanabhan S, Parsa A, Pirastu N, Porcu E, Portas L, Prokopenko I, Ried JS, Shin SY, Tang CS, Teumer A, Traglia M, Ulivi S, Westra HJ, Yang J, Zhao JH, Anni F, Abdellaoui A, Attwood A, Balkau B, Bandinelli S, Bastardot F, Benyamin B, Boehm BO, Cookson WO, Das D, de Bakker PI, de Boer RA, de Geus EJ, de Moor MH, Dimitriou M, Domingues FS, Döring A, Engström G, Eyjolfsson GI, Ferrucci L, Fischer K, Galanello R, Garner SF, Genser B, Gibson QD, Girotto G, Gudbjartsson DF, Harris SE, Hartikainen AL, Hastie CE, Hedblad B, Illig T, Jolley J, Kähönen M, Kema IP, Kemp JP, Liang L, Lloyd-Jones H, Loos RJ, Meacham S, Medland SE, Meisinger C, Memari Y, Mihailov E, Miller K, Moffatt MF, Nauck M, Novatchkova M, Nutile T, Olafsson I, Onundarson PT, Parracciani D, Penninx BW, Perse… See abstract for full author list ➔ van der Harst P, et al. Among authors: fortina p. Nature. 2012 Dec 20;492(7429):369-75. doi: 10.1038/nature11677. Epub 2012 Dec 5. Nature. 2012. PMID: 23222517 Free PMC article.

4

Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis. On behalf of the GISC.

Forabosco P, Collins A, Latiano A, Annese V, Clementi M, Andriulli A, Fortina P, Devoto M, Morton NE. Forabosco P, et al. Among authors: fortina p. Eur J Hum Genet. 2000 Nov;8(11):846-52. doi: 10.1038/sj.ejhg.5200542. Eur J Hum Genet. 2000. PMID: 11093274

5

Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.

Paul DS, Albers CA, Rendon A, Voss K, Stephens J; HaemGen Consortium; van der Harst P, Chambers JC, Soranzo N, Ouwehand WH, Deloukas P. Paul DS, et al. Genome Res. 2013 Jul;23(7):1130-41. doi: 10.1101/gr.155127.113. Epub 2013 Apr 9. Genome Res. 2013. PMID: 23570689 Free PMC article.

6

Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family.

Feldman GJ, Parvizi J, Levenstien M, Scott K, Erickson JA, Fortina P, Devoto M, Peters CL. Feldman GJ, et al. Among authors: fortina p. J Bone Miner Res. 2013 Dec;28(12):2540-9. doi: 10.1002/jbmr.1999. J Bone Miner Res. 2013. PMID: 23716478 Free article.

7

The Otto Aufranc Award: Identification of a 4 Mb region on chromosome 17q21 linked to developmental dysplasia of the hip in one 18-member, multigeneration family.

Feldman G, Dalsey C, Fertala K, Azimi D, Fortina P, Devoto M, Pacifici M, Parvizi J. Feldman G, et al. Among authors: fortina p. Clin Orthop Relat Res. 2010 Feb;468(2):337-44. doi: 10.1007/s11999-009-1073-6. Epub 2009 Sep 11. Clin Orthop Relat Res. 2010. PMID: 19756907 Free PMC article.

8

Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study.

Annese V, Latiano A, Bovio P, Forabosco P, Piepoli A, Lombardi G, Andreoli A, Astegiano M, Gionchetti P, Riegler G, Sturniolo GC, Clementi M, Rappaport E, Fortina P, Devoto M, Gasparini P, Andriulli A. Annese V, et al. Among authors: fortina p. Eur J Hum Genet. 1999 Jul;7(5):567-73. doi: 10.1038/sj.ejhg.5200328. Eur J Hum Genet. 1999. PMID: 10439963

9

CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencing.

Palmieri O, Toth S, Ferraris A, Andriulli A, Latiano A, Annese V, Dallapiccola B, Vecchi M, Devoto M, Surrey S, Fortina P. Palmieri O, et al. Among authors: fortina p. Clin Chem. 2003 Oct;49(10):1675-9. doi: 10.1373/49.10.1675. Clin Chem. 2003. PMID: 14500598 No abstract available.

10

Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia.

Camaschella C, Kattamis AC, Petroni D, Roetto A, Sivera P, Sbaiz L, Cohen A, Ohene-Frempong K, Trifillis P, Surrey S, Fortina P. Camaschella C, et al. Among authors: fortina p. Am J Hematol. 1997 Jun;55(2):83-8. doi: 10.1002/(sici)1096-8652(199706)55:2<83::aid-ajh6>3.0.co;2-z. Am J Hematol. 1997. PMID: 9209003 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

216 results

Search Page

Filters