Rizwan Hamid
Faculty Member
Last active: 5/30/2014

  1. SHC2 gene copy number in multiple system atrophy (MSA). Ferguson MC, Garland EM, Hedges L, Womack-Nunley B, Hamid R, Phillips JA, Shibao CA, Raj SR, Biaggioni I, Robertson D (2014) Clin Auton Res 24(1): 25-30
    › Primary publication · 24170347 (PubMed) · PMC3946192 (PubMed Central)
  2. Rescuing the BMPR2 signaling axis in pulmonary arterial hypertension. West J, Austin E, Fessel JP, Loyd J, Hamid R (2014) Drug Discov Today 19(8): 1241-5
    › Primary publication · 24794464 (PubMed) · PMC4396626 (PubMed Central)
  3. Tgif1 regulates quiescence and self-renewal of hematopoietic stem cells. Yan L, Womack B, Wotton D, Guo Y, Shyr Y, Davé U, Li C, Hiebert S, Brandt S, Hamid R (2013) Mol Cell Biol 33(24): 4824-33
    › Primary publication · 24100014 (PubMed) · PMC3889555 (PubMed Central)
  4. Abnormal trafficking of endogenously expressed BMPR2 mutant allelic products in patients with heritable pulmonary arterial hypertension. Frump AL, Lowery JW, Hamid R, Austin ED, de Caestecker M (2013) PLoS One 8(11): e80319
    › Primary publication · 24224048 (PubMed) · PMC3818254 (PubMed Central)
  5. The B55α-containing PP2A holoenzyme dephosphorylates FOXO1 in islet β-cells under oxidative stress. Yan L, Guo S, Brault M, Harmon J, Robertson RP, Hamid R, Stein R, Yang E (2012) Biochem J 444(2): 239-47
    › Primary publication · 22417654 (PubMed) · PMC5006628 (PubMed Central)
  6. Role of BMPR2 alternative splicing in heritable pulmonary arterial hypertension penetrance. Cogan J, Austin E, Hedges L, Womack B, West J, Loyd J, Hamid R (2012) Circulation 126(15): 1907-16
    › Primary publication · 22923426 (PubMed) · PMC4113011 (PubMed Central)
  7. Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats. Stankiewicz P, Kulkarni S, Dharmadhikari AV, Sampath S, Bhatt SS, Shaikh TH, Xia Z, Pursley AN, Cooper ML, Shinawi M, Paciorkowski AR, Grange DK, Noetzel MJ, Saunders S, Simons P, Summar M, Lee B, Scaglia F, Fellmann F, Martinet D, Beckmann JS, Asamoah A, Platky K, Sparks S, Martin AS, Madan-Khetarpal S, Hoover J, Medne L, Bonnemann CG, Moeschler JB, Vallee SE, Parikh S, Irwin P, Dalzell VP, Smith WE, Banks VC, Flannery DB, Lovell CM, Bellus GA, Golden-Grant K, Gorski JL, Kussmann JL, McGregor TL, Hamid R, Pfotenhauer J, Ballif BC, Shaw CA, Kang SH, Bacino CA, Patel A, Rosenfeld JA, Cheung SW, Shaffer LG (2012) Hum Mutat 33(1): 165-79
    › Primary publication · 21948486 (PubMed) · PMC3655525 (PubMed Central)
  8. Pre-implantation genetic testing for hereditary pulmonary arterial hypertension: promise and caution. Hamid R, Loyd J (2012) Eur Respir J 39(6): 1292-3
    › Primary publication · 22654004 (PubMed)
  9. Metabolomic analysis of bone morphogenetic protein receptor type 2 mutations in human pulmonary endothelium reveals widespread metabolic reprogramming. Fessel JP, Hamid R, Wittmann BM, Robinson LJ, Blackwell T, Tada Y, Tanabe N, Tatsumi K, Hemnes AR, West JD (2012) Pulm Circ 2(2): 201-13
    › Primary publication · 22837861 (PubMed) · PMC3401874 (PubMed Central)
  10. Longitudinal analysis casts doubt on the presence of genetic anticipation in heritable pulmonary arterial hypertension. Larkin EK, Newman JH, Austin ED, Hemnes AR, Wheeler L, Robbins IM, West JD, Phillips JA, Hamid R, Loyd JE (2012) Am J Respir Crit Care Med 186(9): 892-6
    › Primary publication · 22923661 (PubMed) · PMC3530218 (PubMed Central)