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GSTM1 and Liver Iron Content in Children with Sickle Cell Anemia and Iron Overload.
Published in:
Journal of Clinical Medicine, 2019, v. 8, n. 11, p. 1878, doi. 10.3390/jcm8111878
By:
- Puri, Latika;
- Flanagan, Jonathan M.;
- Kang, Guolian;
- Ding, Juan;
- Bi, Wenjian;
- McCarville, Beth M.;
- Loeffler, Ralf B.;
- Tipirneni-Sajja, Aaryani;
- Villavicencio, Martha;
- Crews, Kristine R.;
- Hillenbrand, Claudia M.;
- Hankins, Jane S.
Publication type:
Article
Genome‐wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci.
Published in:
British Journal of Haematology, 2023, v. 201, n. 2, p. 343, doi. 10.1111/bjh.18637
By:
- Earley, Eric Jay;
- Kelly, Shannon;
- Fang, Fang;
- Alencar, Cecília Salete;
- Rodrigues, Daniela de Oliveira Werneck;
- Soares Cruz, Dahra Teles;
- Flanagan, Jonathan M.;
- Ware, Russell E.;
- Zhang, Xu;
- Gordeuk, Victor;
- Gladwin, Mark;
- Zhang, Yingze;
- Nouraie, Mehdi;
- Nekhai, Sergei;
- Sabino, Ester;
- Custer, Brian;
- Dinardo, Carla;
- Page, Grier P.
Publication type:
Article
Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia.
Published in:
PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110740
By:
- Sheehan, Vivien A.;
- Crosby, Jacy R.;
- Sabo, Aniko;
- Mortier, Nicole A.;
- Howard, Thad A.;
- Muzny, Donna M.;
- Dugan-Perez, Shannon;
- Aygun, Banu;
- Nottage, Kerri A.;
- Boerwinkle, Eric;
- Gibbs, Richard A.;
- Ware, Russell E.;
- Flanagan, Jonathan M.
Publication type:
Article
The fatty acid amide hydrolase 385 A/A (P129T) variant: haplotype analysis of an ancient missense mutation and validation of risk for drug addiction.
Published in:
Human Genetics, 2006, v. 120, n. 4, p. 581, doi. 10.1007/s00439-006-0250-x
By:
- Flanagan, Jonathan M.;
- Gerber, Alexandra L.;
- Cadet, Jean Lud;
- Beutler, Ernest;
- Sipe, Jack C.
Publication type:
Article
Refractory autoimmune cytopenias in pediatric Evans syndrome with underlying systemic immune dysregulation.
Published in:
European Journal of Haematology, 2021, v. 106, n. 6, p. 783, doi. 10.1111/ejh.13600
By:
- Grimes, Amanda B.;
- Kim, Taylor O.;
- Kirk, Susan E.;
- Flanagan, Jonathan;
- Lambert, Michele P.;
- Grace, Rachael F.;
- Despotovic, Jenny M.
Publication type:
Article
Tripartite collaboration of blood‐derived endothelial cells, next generation RNA sequencing and bioengineered vessel‐chip may distinguish vasculopathy and thrombosis among sickle cell disease patients.
Published in:
Bioengineering & Translational Medicine, 2021, v. 6, n. 3, p. 1, doi. 10.1002/btm2.10211
By:
- Mathur, Tanmay;
- Flanagan, Jonathan M.;
- Jain, Abhishek
Publication type:
Article
Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia.
Published in:
PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164364
By:
- Schaefer, Beverly A.;
- Flanagan, Jonathan M.;
- Alvarez, Ofelia A.;
- Nelson, Stephen C.;
- Aygun, Banu;
- Nottage, Kerri A.;
- George, Alex;
- Roberts, Carla W.;
- Piccone, Connie M.;
- Howard, Thad A.;
- Davis, Barry R.;
- Ware, Russell E.
Publication type:
Article
Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition.
Published in:
2018
By:
- Mwesigwa, Savannah;
- Moulds, Joann M.;
- Chen, Alice;
- Flanagan, Jonathan;
- Sheehan, Vivien A.;
- George, Alex;
- Hanchard, Neil A.
Publication type:
journal article
Genetic variants in toll-like receptor 4 are associated with lack of steroid-responsiveness in pediatric ITP patients.
Published in:
American Journal of Hematology, 2020, v. 95, n. 4, p. 395, doi. 10.1002/ajh.25716
By:
- Olmsted Kim, Taylor;
- Flanagan, Jonathan M.;
- Habibi, Ali;
- Arulselvan, Abinaya;
- Lambert, Michele P.;
- Grace, Rachael F.;
- Despotovic, Jenny M.
Publication type:
Article
Pain and other non-neurological adverse events in children with sickle cell anemia and previous stroke who received hydroxyurea and phlebotomy or chronic transfusions and chelation: Results from the SWiTCH clinical trial.
Published in:
American Journal of Hematology, 2013, v. 88, n. 11, p. 932, doi. 10.1002/ajh.23547
By:
- Alvarez, Ofelia;
- Yovetich, Nancy A.;
- Scott, J. Paul;
- Owen, William;
- Miller, Scott T.;
- Schultz, William;
- Lockhart, Alexandre;
- Aygun, Banu;
- Flanagan, Jonathan;
- Bonner, Melanie;
- Mueller, Brigitta U.;
- Ware, Russell E.
Publication type:
Article
Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
Published in:
American Journal of Hematology, 2013, v. 88, n. 7, p. 571, doi. 10.1002/ajh.23457
By:
- Sheehan, Vivien A.;
- Luo, Zhaoyu;
- Flanagan, Jonathan M.;
- Howard, Thad A.;
- Thompson, Bruce W.;
- Wang, Winfred C.;
- Kutlar, Abdullah;
- Ware, Russell E.
Publication type:
Article
Microarray analysis of liver gene expression in iron overloaded patients with sickle cell anemia and beta-thalassemia.
Published in:
American Journal of Hematology, 2009, v. 84, n. 6, p. 328, doi. 10.1002/ajh.21407
By:
- Flanagan, Jonathan M.;
- Steward, Shirley;
- Hankins, Jane S.;
- Howard, Thad M.;
- Neale, Geoffrey;
- Ware, Russell E.
Publication type:
Article
Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia.
Published in:
British Journal of Haematology, 2012, v. 157, n. 2, p. 240, doi. 10.1111/j.1365-2141.2012.09061.x
By:
- Flanagan, Jonathan M.;
- Steward, Shirley;
- Howard, Thad A.;
- Mortier, Nicole A.;
- Kimble, Amy C.;
- Aygun, Banu;
- Hankins, Jane S.;
- Neale, Geoffrey A.;
- Ware, Russell E.
Publication type:
Article
Chromosome damage and repair in children with sickle cell anaemia and long-term hydroxycarbamide exposure.
Published in:
British Journal of Haematology, 2011, v. 154, n. 1, p. 134, doi. 10.1111/j.1365-2141.2011.08698.x
By:
- McGann, Patrick T.;
- Howard, Thad A.;
- Flanagan, Jonathan M.;
- Lahti, Jill M.;
- Ware, Russell E.
Publication type:
Article
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA.
Published in:
British Journal of Haematology, 2006, v. 134, n. 2, p. 233, doi. 10.1111/j.1365-2141.2006.06143.x
By:
- Flanagan, Jonathan M.;
- Rhodes, Melissa;
- Wilson, Meredith;
- Beutler, Ernest
Publication type:
Article
Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: Results from the BABY-HUG phase III clinical trial.
Published in:
Pediatric Blood & Cancer, 2012, v. 59, n. 2, p. 254, doi. 10.1002/pbc.23365
By:
- McGann, Patrick T.;
- Flanagan, Jonathan M.;
- Howard, Thad A.;
- Dertinger, Stephen D.;
- He, Jin;
- Kulharya, Anita S.;
- Thompson, Bruce W.;
- Ware, Russell E.
Publication type:
Article
Massive accidental overdose of hydroxyurea in a young child with sickle cell anemia.
Published in:
Pediatric Blood & Cancer, 2012, v. 59, n. 1, p. 170, doi. 10.1002/pbc.23244
By:
- Miller, Scott T.;
- Rey, Kathy;
- He, Jin;
- Flanagan, Jonathan;
- Fish, Billie J.;
- Rogers, Zora R.;
- Wang, Winfred C.;
- Ware, Russell E.
Publication type:
Article
Vascular Transcriptomics: Investigating Endothelial Activation and Vascular Dysfunction Using Blood Outgrowth Endothelial Cells, Organ‐Chips, and RNA Sequencing.
Published in:
Current Protocols, 2022, v. 2, n. 10, p. 1, doi. 10.1002/cpz1.582
By:
- Mathur, Tanmay;
- Kumar, Ankit;
- Flanagan, Jonathan M.;
- Jain, Abhishek
Publication type:
Article
Soluble Transferrin Receptor-1 Levels in Mice Do Not Affect Iron Absorption.
Published in:
Acta Haematologica, 2006, v. 116, n. 4, p. 249, doi. 10.1159/000095875
By:
- Flanagan, Jonathan M.;
- Hongfan Peng;
- Lei Wang;
- Gelbart, Terri;
- Lee, Pauline;
- Sasu, Barbra Johnson;
- Beutler, Ernest
Publication type:
Article

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