A new panel of SNPs to assess thyroid carcinoma risk: a pilot study in a Brazilian admixture population.
Bmc Medical Genetics
Dos Santos, Isabelle C C ICC; Genre, Julieta J; Marques, Diego D; da Silva, Ananília M G AMG; Dos Santos, Jéssica C JC; de Araújo, Jéssica N G JNG; Duarte, Victor H R VHR; Carracedo, Angel A; Torres-Español, Maria M; Bastos, Gisele G; de Oliveira Ramos, Carlos C CC; Luchessi, André D AD; Silbiger, Vivian N VN
The Effects of Sequence Variation on Genome-wide NRF2 Binding--New Target Genes and Regulatory SNPs.
Nucleic Acids Research
Kuosmanen, Suvi M SM; Viitala, Sari S; Laitinen, Tuomo T; Peräkylä, Mikael M; Pölönen, Petri P; Kansanen, Emilia E; Leinonen, Hanna H; Raju, Suresh S; Wienecke-Baldacchino, Anke A; Närvänen, Ale A; Poso, Antti A; Heinäniemi, Merja M; Heikkinen, Sami S; Levonen, Anna-Liisa AL
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability.
American Journal Of Human Genetics
Emison, Eileen Sproat ES; Garcia-Barcelo, Merce M; Grice, Elizabeth A EA; Lantieri, Francesca F; Amiel, Jeanne J; Burzynski, Grzegorz G; Fernandez, Raquel M RM; Hao, Li L; Kashuk, Carl C; West, Kristen K; Miao, Xiaoping X; Tam, Paul K H PK; Griseri, Paola P; Ceccherini, Isabella I; Pelet, Anna A; Jannot, Anne-Sophie AS; de Pontual, Loic L; Henrion-Caude, Alexandra A; Lyonnet, Stanislas S; Verheij, Joke B G M JB; Hofstra, Robert M W RM; Antiñolo, Guillermo G; Borrego, Salud S; McCallion, Andrew S AS; Chakravarti, Aravinda A