47 Publications (Page 2 of 2)
2010
Strategic plan for lung vascular research: An NHLBI-ORDR Workshop Report.
Erzurum, Serpil CPolgar, PeterRounds, SharonStevens, TroyAldred, MichealaAliotta, JasonArcher, Stephen LAsosingh, KewalBalaban, RobertBauer, NatalieBhattacharya, JaharBogaard, HarmChoudhary, GauravDorn, Gerald WDweik, Raed AFagan, Karen AFallon, MichaelFinkel, TorenGeraci, Mark WGladwin, Mark THassoun, Paul MHumbert, MarcKaminski, NaftaliKawut, StevenLoscalzo, JosephMc Donald, Donald MMc Murtry, IvanNewman, John HNicolls, Mark RRabinovitch, MarleneShizuru, JudyOka, MasahikoPolgar, PeterRodman, DavidSchumacker, Paul TStenmark, KurtTuder, Rubin MVoelkel, Norbert FSullivan, EugeneWeinshilboum, RichardYoder, Mervin CZhao, YingmingGail, Dorothy and Moore, Timothy M
American journal of respiratory and critical care medicine, vol. 182, (no. 12), pp. 1554-62, 2010/Dec/15. | Journal Article
2008
Circulating angiogenic precursors in idiopathic pulmonary arterial hypertension.
Asosingh, KewalAsosingh, KewalAldred, MichealaAldred, MichealaVasanji, AmitVasanji, AmitDrazba, JudithDrazba, JudithSharp, JacquelineSharp, JacquelineFarver, CarolFarver, CarolComhair, SuzyComhair, Suzy AXu, WeilingXu, WeilingLicina, LaurenLicina, LaurenHuang, LanHuang, LanAnand-Apte, BelaAnand-Apte, BelaYoder, Mervin CYoder, MervinTuder, RubinTuder, Rubin MErzurum, Serpil C and Erzurum, Serpil
The American journal of pathology, vol. 172, (no. 3), pp. 615-27, 2008/Mar. | Journal Article
2007
Characterization of the BMPR2 5'-Untranslated Region and a Novel Mutation in Pulmonary Hypertension
Aldred, MichealaAldred, MichealaMachado, RDMachado, RajivJames, V.James, VictoriaMorrell, NicholasMorrell, NicholasTrembath, Richard and Trembath, R C
American Journal of Respiratory and Critical Care Medicine, vol. 176, (no. 8), pp. 819-824, 2007. | Journal Article
 
Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation.
Mac Conaill, LauraAldred, MichealaLu, Xincheng and La Framboise, Thomas
BMC genomics, vol. 8, pp. 211, 2007. | Journal Article
2006
BMPR2 gene rearrangements account for a significant proportion of mutations in familial and idiopathic pulmonary arterial hypertension.
Aldred, Micheala AAldred, MichealaVijayakrishnan, JairamVijayakrishnan, JairamJames, VictoriaJames, VictoriaSoubrier, FlorentSoubrier, FlorentGomez‐Sanchez, Miguel AGomez-Sanchez, Miguel AMartensson, GunnarMartensson, GunnarGalie, NazzarenoGalie, NazzarenoManes, AlessandraManes, AlessandraCorris, PaulCorris, PaulSimonneau, GeraldSimonneau, GeraldHumbert, MarcHumbert, MarcMorrell, Nicholas WMorrell, NicholasTrembath, Richard C and Trembath, R C
Human mutation, vol. 27, (no. 2), pp. 212-3, 2006/Feb. | Journal Article
 
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension.
Machado, Rajiv DMachado, RajivAldred, MichealaAldred, MichealaJames, VictoriaJames, VictoriaHarrison, Rachel EHarrison, RachelPatel, BhaktiPatel, BhaktiSchwalbe, EdwardSchwalbe, Edward CGruenig, EkkehardGruenig, EkkehardJanssen, BartJanssen, BartKoehler, RolfKoehler, RolfSeeger, WernerSeeger, WernerEickelberg, OliverEickelberg, OliverOlschewski, HorstOlschewski, HorstElliott, C.Elliott, C GGlissmeyer, EricGlissmeyer, EricCarlquist, JohnKim, MiryoungTorbicki, AdamFijalkowska, AnnaSzewczyk, GrzegorzParma, JasmineAbramowicz, Marc JGalie, NazzarenoMorisaki, HirokoKyotani, ShingoNakanishi, NorifumiMorisaki, TakayukiHumbert, MarcSimonneau, GeraldSitbon, OlivierSoubrier, FlorentCoulet, FlorenceMorrell, Nicholas and Trembath, R C
Human mutation, vol. 27, (no. 2), pp. 121-32, 2006/Feb. | Journal Article
2005
Genetic Classification of Benign and Malignant Thyroid Follicular Neoplasia Based on a Three-Gene Combination
Weber, FrankWeber, FrankShen, LeiShen, LeiAldred, Micheala AAldred, MichealaMorrison, Carl DMorrison, CarlFrilling, AndreaFrilling, AndreaSaji, MotoyasuSaji, MotoyasuSchuppert, FrankSchuppert, FrankBroelsch, Christoph EBroelsch, Christoph ERingel, Matthew DRingel, Matthew DEng, Charis and Eng, Charis
Journal of Clinical Endocrinology and Metabolism, vol. 90, (no. 5), pp. 2512-2521, 2005. | Journal Article
 
Investigation of Second Genetic Hits at the BMPR2 Locus as a Modulator of Disease Progression in Familial Pulmonary Arterial Hypertension
Machado, RajivMachado, Rajiv DJames, VictoriaJames, VictoriaSouthwood, MarkSouthwood, MarkHarrison, Rachel EHarrison, RachelAtkinson, CarlAtkinson, CarlStewart, SusanStewart, SusanMorrell, NicholasMorrell, NicholasTrembath, RichardTrembath, R CAldred, Micheala and Aldred, Micheala
Circulation, vol. 111, (no. 5), pp. 607-613, 2005. | Journal Article
 
Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing
Aldred, MABaumber, LHill, ASchwalbe, ECGoh, KKarwatowski, W and Trembath, Rc
American Journal of Ophthalmology, vol. 139, (no. 2), pp. 398-399, Feb 2005. | Journal Article
 
Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood.
Harrison, Rachel EHarrison, RachelBerger, RolfBerger, RolfHaworth, SheilaHaworth, Sheila GTulloh, RobertTulloh, RobertMache, ChristophMache, Christoph JMorrell, NicholasMorrell, NicholasAldred, MichealaAldred, MichealaTrembath, Richard and Trembath, R C
Circulation, vol. 111, (no. 4), pp. 435-41, 2005/Feb/1. | Journal Article
2004
Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing.
Aldred, MichealaAldred, MichealaBaumber, LauraBaumber, LauraHill, AlisonHill, AlisonSchwalbe, Edward CSchwalbe, EdwardGoh, KaiGoh, KaiKarwatowski, WojciechKarwatowski, WojciechTrembath, Richard and Trembath, R C
Human genetics, vol. 115, (no. 5), pp. 428-31, 2004/Oct. | Journal Article
 
Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes.
Aldred, MichealaSanford, R OThomas, N SBarrow, M AWilson, L CBrueton, L ABonaglia, M CHennekam, R CEng, CDennis, Nicholas R and Trembath, R C
Journal of medical genetics, vol. 41, (no. 6), pp. 433-9, 2004/Jun. | Journal Article
 
Papillary and follicular thyroid carcinomas show distinctly different microarray expression profiles and can be distinguished by a minimum of five genes.
Aldred, MichealaAldred, MichealaHuang, YingHuang, YingLiyanarachchi, SandyaLiyanarachchi, SandyaPellegata, NataliaPellegata, Natalia SGimm, OliverGimm, OliverJhiang, Sissy MJhiang, SissyDavuluri, Ramana VDavuluri, RamanaLa Chapelle, AlbertDe La Chapelle, AlbertEng, Charis and Eng, Charis
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, vol. 22, (no. 17), pp. 3531-9, 2004/Sep/1. | Journal Article
2003
Caveolin-1 and Caveolin-2, Together with Three Bone Morphogenetic Protein-related Genes, May Encode Novel Tumor Suppressors Down-Regulated in Sporadic Follicular Thyroid Carcinogenesis
Aldred, MichealaGinn-Pease, MEMorrison, CarlPopkie, APGimm, O.Hoang-Vu, CuongKrause, U.Dralle, H.Jhiang, Sissy MPlass, Christoph and Eng, Charis
Cancer Research, vol. 63, (no. 11), pp. 2864-2871, 2003. | Journal Article
 
Peroxisome proliferator-activated receptor gamma is frequently downregulated in a diversity of sporadic nonmedullary thyroid carcinomas
Aldred, MichealaMorrison, CarlGimm, O.Hoang-Vu, C.Krause, U.Dralle, H.Jhiang, Sissy M and Eng, Charis
Oncogene, vol. 22, (no. 22), pp. 3412-3416, 2003. | Journal Article
2002
Constitutional Deletion of Chromosome 20q in Two Patients Affected With Albright Hereditary Osteodystrophy
Aldred, MichealaAldred, Micheala AAftimos, S.Aftimos, SalimHall, C.Hall, ChristineWaters, KSWaters, Katie SThakker, RVThakker, Rajesh VTrembath, R CTrembath, Richard CBrueton, L. and Brueton, Louise
American Journal of Medical Genetics, vol. 113, (no. 2), pp. 167-172, 2002. | Journal Article
2001
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.
Zhou, X PWoodford-Richens, KLehtonen, RKurose, KAldred, MichealaHampel, Heather LLaunonen, VirpiVirta, SPilarski, RobertSalovaara, RBodmer, W FConrad, B ADunlop, MHodgson, S VIwama, TJärvinen, HKellokumpu, IKim, J CLeggett, BMarkie, DavidMecklin, J PNeale, KPhillips, RPiris, JRozen, PHoulston, Richard SAaltonen, LauriTomlinson, Ian and Eng, Charis E
American journal of human genetics, vol. 69, (no. 4), pp. 704-11, 2001/Oct. | Journal Article
2000
Activating and inactivating mutations in the human GNAS1 gene.
Aldred, Micheala and Trembath, R C
Human mutation, vol. 16, (no. 3), pp. 183-9, 2000/Sep. | Journal Article
 
A Physical and Transcript Map Based upon Refinement of the Critical Interval for PPH1, a Gene for Familial Primary Pulmonary Hypertension
Machado, Rajiv DMachado, Rajiv DPauciulo, Michael WPauciulo, Michael WFretwell, NealeFretwell, NealeVeal, ColinVeal, ColinThomson, Jennifer RThomson, Jennifer RVilariño Güell, CarlesVilariño Güell, CarlesAldred, MichealaAldred, MichealaBrannon, Christopher ABrannon, Christopher ATrembath, Richard CTrembath, Richard CNichols, William C and Nichols, William C
Genomics, vol. 68, (no. 2), pp. 228, 2000-09-01. | Journal Article
 
Germline mosaicism for a GNAS1 mutation and Albright hereditary osteodystrophy.
Aldred, Micheala AAldred, MichealaBAGSHAW, R JANEBagshaw, R JMACDERMOT, KAYMacdermot, KCASSON, DAVIDCasson, DMurch, S HMURCH, SIMON HWalker-Smith, J AWALKER-SMITH, J ATREMBATH, RICHARD C and Trembath, R C
Journal of medical genetics, vol. 37, (no. 11), pp. E35, 2000/Nov. | Journal Article
1999
New light on retinal gene therapy
Aldred, Micheala A
Molecular Medicine Today, vol. 5, (no. 2), pp. 52, 1999. | Journal Article
1998
A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region
Bench, A JBench, Anthony JAldred, Micheala AAldred, M AHumphray, Sean JHumphray, S JChampion, K MChampion, Kim MGilbert, James G.RGilbert, J GAsimakopoulos, FotisAsimakopoulos, Fotios ADeloukas, PanosDeloukas, PGwilliam, RGwilliam, RhianBentley, D RBentley, David RGreen, Anthony R and Green, A R
Genomics, vol. 49, (no. 3), pp. 362, 1998. | Journal Article