|
Sickle Cell Disease |
4548 |
A pilot project to demonstrate the utility of the TOPMed genome graph and population gene annotation to improve the mapping of structural and other variants associated with red blood cell traits and hemoglobin disorders |
ross@bx.psu.edu |
|
Sickle Cell Disease |
4500 |
Assessment of blood group genetic variation and blood group-related alloimmunization risk in the REDS-III Brazil SCD and OMG SCD cohorts |
Brian Custer |
|
Sickle Cell Disease |
6952 |
Assessment of blood group genetic variation and blood group-related alloimmunization risk in the REDS-III Brazil SCD and OMG SCD cohorts |
carlaluana@usp.br |
|
Sickle Cell Disease |
4250 |
Assessment of RH, GYPA, GYPB and GYPE genetic variation in the REDS-III Brazil and OMG SCD cohorts |
Brian Custer |
|
Sickle Cell Disease |
5105 |
Association study of iron overload in sickle cell disease population |
Fayuan Wen |
|
Sickle Cell Disease |
2745 |
Effects of variant and null KEL, XK, ET3, and EDNRB alleles on cardiovascular phenotypes in African-Americans with Sickle Cell Disease |
Marilyn Telen |
|
Sickle Cell Disease |
6316 |
Genetic factors and the mediation of hemolytic rate in cardiopulmonary dysfunction in SCD |
Xu Zhang |
|
Sickle Cell Disease |
15041 |
Genetics of alloimmunization of blood transfusion recipients among sickle cell patients |
Yun Li |
|
Sickle Cell Disease |
10071 |
Measured Soluble Urokinase Plasminogen Activator Receptor (suPAR) and African CKD susceptibility variants in the Jackson Heart Study |
Alex Reiner |
|
Sickle Cell Disease |
11032 |
Whole genome analysis to identify risk-association of rs3176891G and rs10748643G with venous thromboembolism events (VTE) in subject with African descent |
Seyed Mehdi Nouraie |
