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1. Sripichai O, Munkongdee T, Kumkhaek C, Svasti S, Winichagoon P, Fucharoen S. Coinheritance of the different copy numbers of -globin gene modifies severity of -thalassemia/Hb E disease. Ann Hematol 2008; 87: 375-79.
2. Sripichai O, Fucharoen S. Genetic polymorphisms and implications for human diseases. J Med Assoc Thai. 2007;90:394-8.
3. Ma Q, Abel K, Sripichai O, Whitacre J, Angkachatchai V, Makarasara W, Winichagoon P, Fucharoen S, Braun A, Farrer LA. Beta-globin gene clusterpolymorphisms are strongly associated with severity of Hb E/b0-thalassemia.  Clin Genet. 2007;72:497-505.
4. Sripichai O, Munkongdee T, Khumkhaek C, Svasti S, Winichagoon P, Fucharoen S. Coinheritance of the different copy number of a-globin gene modifies severity of        b-thalassemia/Hb E disease. Ann Hematol. 2008;87:375-9.
5. Pandit R, Svasti S, Sripichai O, Munkongdee T, Triwitayakorn K, Winichagoon P, Fucharoen S, Preerapittayamongkol C. Association of SNP in exon 1 of HBS1L with hemoglobin F level in β0-thalassemia/hemoglobin E. Int J hematol. 2008;88:357-361.
6. Sripichai O, Makarasara W, Munkongdee T, Kumkhaek C, Nuchprayoon I, Chuansumrit A, Chuncharunee S, Chantrakoon N, Boonmongkol P, Winichagoon P, Fucharoen S. A scoring system for the classification of beta-thalassemia/Hb E disease severity. Am J Hematol. 2008;83:482-4.
7. Rund D and Fucharoen S. Genetic modifiers in hemoglobinopathies. Current Molecular Medicine 2008; 8: 600-608.
8. Wannatung T, Lithanatudom P, Leecharoenkiat A, Svasti S, Fucharoen S and Smith DR. Increased erythropoiesis of b-thalassaemia/Hb E proerythroblasts is mediated by high basal levels of ERK1/2 activation. Br J Haematol 2009; 146: 557-568.
9. Lithanatudom P, Leecharoenkiat A, Wannatung T, Svasti S, Fucharoen S and Smith DR. A mechanism of ineffective erythropoiesis in b-thalassemia/HbE disease. Haematologica doi: 10.3324/ haematol.2009.015701
10. Nuinoon M, Makarasara W, Mushiroda T, Setianingih I, Wahidiyat P.A, Sripichai O, Kumasaka N, Takahashi A, Svasti S, Munkongdee T, Mahasirimongkol S, Peerapittayamongkol C, Viprakasit V, Kamatani N, Winichagoon P, Kubo M, Nakamura Y, Fucharoen S. A genome-wide association identified the common genetic variants influences disease severity in b0-thalassemia/hemoglobin E. Hum Genet 2010; 127: 303-314.
11. Sherva R, Ma Q, Abel K, Sripichai O, Whitacre J, Angkachatchai V, Makarasara W, Chui D, Winichagoon P, Fucharoen S, Braun A, Farrer LA. Genetic modifiers of HbE/b0thalassemia identified by a two-stage genome-wide association study. BMC Medical Genetics. 2010. (In press)