HuGE Literature Finder
Rare Disease
Records 1-7
Genome-wide association study of erythrocyte density in sickle cell disease patients.
Blood cells, molecules & diseases 2017 Jun 65 60-65. Ilboudo Yann, Bartolucci Pablo, Rivera Alicia, Sedzro Josepha-Clara, Beaudoin Mélissa, Trudel Marie, Alper Seth L, Brugnara Carlo, Galactéros Frédéric, Lettre Guillau |
|
Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.
Blood 2017 08 130 (5): 686-688. Chaturvedi Shruti, Bhatnagar Pallav, Bean Christopher J, Steinberg Martin H, Milton Jaqueline N, Casella James F, Barron-Casella Emily, Arking Dan E, DeBaun Michael |
|
The genetics of hemoglobin A2 regulation in sickle cell anemia.
American journal of hematology 2014 Nov 89 (11): 1019-23. Griffin Paula J, Sebastiani Paola, Edward Heather, Baldwin Clinton T, Gladwin Mark T, Gordeuk Victor R, Chui David H K, Steinberg Martin |
|
Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
PloS one 2014 9 (11): e111464. Mtatiro Siana Nkya, Singh Tarjinder, Rooks Helen, Mgaya Josephine, Mariki Harvest, Soka Deogratius, Mmbando Bruno, Msaki Evarist, Kolder Iris, Thein Swee Lay, Menzel Stephan, Cox Sharon E, Makani Julie, Barrett Jeffrey |
|
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
PloS one 2012 7 (4): e34741. Milton Jacqueline N, Sebastiani Paola, Solovieff Nadia, Hartley Stephen W, Bhatnagar Pallav, Arking Dan E, Dworkis Daniel A, Casella James F, Barron-Casella Emily, Bean Christopher J, Hooper W Craig, DeBaun Michael R, Garrett Melanie E, Soldano Karen, Telen Marilyn J, Ashley-Koch Allison, Gladwin Mark T, Baldwin Clinton T, Steinberg Martin H, Klings Elizabeth |
|
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
Blood 2010 Mar 115 (9): 1815-22. Solovieff Nadia, Milton Jacqueline N, Hartley Stephen W, Sherva Richard, Sebastiani Paola, Dworkis Daniel A, Klings Elizabeth S, Farrer Lindsay A, Garrett Melanie E, Ashley-Koch Allison, Telen Marilyn J, Fucharoen Supan, Ha Shau Yin, Li Chi-Kong, Chui David H K, Baldwin Clinton T, Steinberg Martin |
|
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Proceedings of the National Academy of Sciences of the United States of America 2008 Feb 105 (5): 1620-5. Uda Manuela, Galanello Renzo, Sanna Serena, Lettre Guillaume, Sankaran Vijay G, Chen Weimin, Usala Gianluca, Busonero Fabio, Maschio Andrea, Albai Giuseppe, Piras Maria Grazia, Sestu Natascia, Lai Sandra, Dei Mariano, Mulas Antonella, Crisponi Laura, Naitza Silvia, Asunis Isadora, Deiana Manila, Nagaraja Ramaiah, Perseu Lucia, Satta Stefania, Cipollina Maria Dolores, Sollaino Carla, Moi Paolo, Hirschhorn Joel N, Orkin Stuart H, Abecasis Gonçalo R, Schlessinger David, Cao Anton |
- Page last reviewed:Oct 1, 2020
- Page last updated:Mar 05, 2021
- Content source: