Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome.

de Smith, A.J.; Walsh, K.M.; Morimoto, L.M.; Francis, S.S.; Hansen, H.M.; Jeon, S.; Gonseth, S.; Chen, M.; Sun, H.; Luna-Fineman, S.; Antillón, F.; Girón, V.; Kang, A.Y.; Smirnov, I.; Shao, X.; Whitehead, T.P.; Barcellos, L.F.; Jolly, K.W.; Healy, J.; Laverdière, C.; Sinnett, D.; Taub, J.W.; Birch, J.M.; Thompson, P.D.; Pombo-de-Oliveira, M.S.; Spector, L.G.; DeWan, A.T.; Mueller, B.A.; Chiang, C.; Metayer, C.; Ma, X.; Wiemels, J.L.

doi:10.1038/s41375-019-0514-9

Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome.

Détails

Télécharger: 31296947_BIB_CD7D0655AE76.pdf (532.30 [Ko])
Etat: Public
Version: Author's accepted manuscript
Licence: CC BY 4.0

ID Serval

serval:BIB_CD7D0655AE76

Type

Article: article d'un périodique ou d'un magazine.

Sous-type

Lettre (letter): communication adressée à l'éditeur.

Collection

Publications

Institution

UNIL/CHUV

Titre

Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome.

Périodique

Leukemia

Auteur⸱e⸱s

de Smith A.J., Walsh K.M., Morimoto L.M., Francis S.S., Hansen H.M., Jeon S., Gonseth S., Chen M., Sun H., Luna-Fineman S., Antillón F., Girón V., Kang A.Y., Smirnov I., Shao X., Whitehead T.P., Barcellos L.F., Jolly K.W., Healy J., Laverdière C., Sinnett D., Taub J.W., Birch J.M., Thompson P.D., Pombo-de-Oliveira M.S., Spector L.G., DeWan A.T., Mueller B.A., Chiang C., Metayer C., Ma X., Wiemels J.L.

ISSN

1476-5551 (Electronic)

ISSN-L

0887-6924

Statut éditorial

Publié

Date de publication

11/2019

Peer-reviewed

Oui

Volume

33

Numéro

11

Pages

2746-2751

Langue

anglais

Notes

Publication types: Letter ; Meta-Analysis ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
Publication Status: ppublish

Mots-clé

Adolescent, California/epidemiology, California/ethnology, Case-Control Studies, Child, Child, Preschool, Chromosomes, Human, Pair 21/genetics, Down Syndrome/complications, Down Syndrome/ethnology, Down Syndrome/genetics, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Guatemala/epidemiology, Guatemala/ethnology, Haplotypes, Hispanic Americans, Humans, Infant, Infant, Newborn, Male, Polymorphism, Single Nucleotide, Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications, Precursor Cell Lymphoblastic Leukemia-Lymphoma/ethnology, Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics, Principal Component Analysis, Risk Factors, Transcriptional Regulator ERG/genetics

URN

urn:nbn:ch:serval-BIB_CD7D0655AE769

OAI-PMH

oai:serval.unil.ch:BIB_CD7D0655AE76

DOI

10.1038/s41375-019-0514-9

Pubmed

31296947

Web of science

000495104300020

Open Access

Oui