47 Publications (Page 2 of 2)
2010
Strategic plan for lung vascular research: An NHLBI-ORDR Workshop Report.Erzurum, Serpil C⋅Polgar, Peter⋅Rounds, Sharon⋅Stevens, Troy⋅Aldred, Micheala⋅Aliotta, Jason⋅Archer, Stephen L⋅Asosingh, Kewal⋅Balaban, Robert⋅Bauer, Natalie⋅Bhattacharya, Jahar⋅Bogaard, Harm⋅Choudhary, Gaurav⋅Dorn, Gerald W⋅Dweik, Raed A⋅Fagan, Karen A⋅Fallon, Michael⋅Finkel, Toren⋅Geraci, Mark W⋅Gladwin, Mark T⋅Hassoun, Paul M⋅Humbert, Marc⋅Kaminski, Naftali⋅Kawut, Steven⋅Loscalzo, Joseph⋅Mc Donald, Donald M⋅Mc Murtry, Ivan⋅Newman, John H⋅Nicolls, Mark R⋅Rabinovitch, Marlene⋅Shizuru, Judy⋅Oka, Masahiko⋅Polgar, Peter⋅Rodman, David⋅Schumacker, Paul T⋅Stenmark, Kurt⋅Tuder, Rubin M⋅Voelkel, Norbert F⋅Sullivan, Eugene⋅Weinshilboum, Richard⋅Yoder, Mervin C⋅Zhao, Yingming⋅Gail, Dorothy and Moore, Timothy MAmerican journal of respiratory and critical care medicine, vol. 182, (no. 12), pp. 1554-62, 2010/Dec/15.
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2008
Circulating angiogenic precursors in idiopathic pulmonary arterial hypertension.Asosingh, Kewal⋅Asosingh, Kewal⋅Aldred, Micheala⋅Aldred, Micheala⋅Vasanji, Amit⋅Vasanji, Amit⋅Drazba, Judith⋅Drazba, Judith⋅Sharp, Jacqueline⋅Sharp, Jacqueline⋅Farver, Carol⋅Farver, Carol⋅Comhair, Suzy⋅Comhair, Suzy A⋅Xu, Weiling⋅Xu, Weiling⋅Licina, Lauren⋅Licina, Lauren⋅Huang, Lan⋅Huang, Lan⋅Anand-Apte, Bela⋅Anand-Apte, Bela⋅Yoder, Mervin C⋅Yoder, Mervin⋅Tuder, Rubin⋅Tuder, Rubin M⋅Erzurum, Serpil C and Erzurum, SerpilThe American journal of pathology, vol. 172, (no. 3), pp. 615-27, 2008/Mar.
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2007
Characterization of the BMPR2 5'-Untranslated Region and a Novel Mutation in Pulmonary HypertensionAldred, Micheala⋅Aldred, Micheala⋅Machado, RD⋅Machado, Rajiv⋅James, V.⋅James, Victoria⋅Morrell, Nicholas⋅Morrell, Nicholas⋅Trembath, Richard and Trembath, R CAmerican Journal of Respiratory and Critical Care Medicine, vol. 176, (no. 8), pp. 819-824, 2007.
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Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation.Mac Conaill, Laura⋅Aldred, Micheala⋅Lu, Xincheng and La Framboise, ThomasBMC genomics, vol. 8, pp. 211, 2007.
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2006
BMPR2 gene rearrangements account for a significant proportion of mutations in familial and idiopathic pulmonary arterial hypertension.Aldred, Micheala A⋅Aldred, Micheala⋅Vijayakrishnan, Jairam⋅Vijayakrishnan, Jairam⋅James, Victoria⋅James, Victoria⋅Soubrier, Florent⋅Soubrier, Florent⋅Gomez‐Sanchez, Miguel A⋅Gomez-Sanchez, Miguel A⋅Martensson, Gunnar⋅Martensson, Gunnar⋅Galie, Nazzareno⋅Galie, Nazzareno⋅Manes, Alessandra⋅Manes, Alessandra⋅Corris, Paul⋅Corris, Paul⋅Simonneau, Gerald⋅Simonneau, Gerald⋅Humbert, Marc⋅Humbert, Marc⋅Morrell, Nicholas W⋅Morrell, Nicholas⋅Trembath, Richard C and Trembath, R CHuman mutation, vol. 27, (no. 2), pp. 212-3, 2006/Feb.
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Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension.Machado, Rajiv D⋅Machado, Rajiv⋅Aldred, Micheala⋅Aldred, Micheala⋅James, Victoria⋅James, Victoria⋅Harrison, Rachel E⋅Harrison, Rachel⋅Patel, Bhakti⋅Patel, Bhakti⋅Schwalbe, Edward⋅Schwalbe, Edward C⋅Gruenig, Ekkehard⋅Gruenig, Ekkehard⋅Janssen, Bart⋅Janssen, Bart⋅Koehler, Rolf⋅Koehler, Rolf⋅Seeger, Werner⋅Seeger, Werner⋅Eickelberg, Oliver⋅Eickelberg, Oliver⋅Olschewski, Horst⋅Olschewski, Horst⋅Elliott, C.⋅Elliott, C G⋅Glissmeyer, Eric⋅Glissmeyer, Eric⋅Carlquist, John⋅Kim, Miryoung⋅Torbicki, Adam⋅Fijalkowska, Anna⋅Szewczyk, Grzegorz⋅Parma, Jasmine⋅Abramowicz, Marc J⋅Galie, Nazzareno⋅Morisaki, Hiroko⋅Kyotani, Shingo⋅Nakanishi, Norifumi⋅Morisaki, Takayuki⋅Humbert, Marc⋅Simonneau, Gerald⋅Sitbon, Olivier⋅Soubrier, Florent⋅Coulet, Florence⋅Morrell, Nicholas and Trembath, R CHuman mutation, vol. 27, (no. 2), pp. 121-32, 2006/Feb.
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2005
Genetic Classification of Benign and Malignant Thyroid Follicular Neoplasia Based on a Three-Gene CombinationWeber, Frank⋅Weber, Frank⋅Shen, Lei⋅Shen, Lei⋅Aldred, Micheala A⋅Aldred, Micheala⋅Morrison, Carl D⋅Morrison, Carl⋅Frilling, Andrea⋅Frilling, Andrea⋅Saji, Motoyasu⋅Saji, Motoyasu⋅Schuppert, Frank⋅Schuppert, Frank⋅Broelsch, Christoph E⋅Broelsch, Christoph E⋅Ringel, Matthew D⋅Ringel, Matthew D⋅Eng, Charis and Eng, CharisJournal of Clinical Endocrinology and Metabolism, vol. 90, (no. 5), pp. 2512-2521, 2005.
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Investigation of Second Genetic Hits at the BMPR2 Locus as a Modulator of Disease Progression in Familial Pulmonary Arterial HypertensionMachado, Rajiv⋅Machado, Rajiv D⋅James, Victoria⋅James, Victoria⋅Southwood, Mark⋅Southwood, Mark⋅Harrison, Rachel E⋅Harrison, Rachel⋅Atkinson, Carl⋅Atkinson, Carl⋅Stewart, Susan⋅Stewart, Susan⋅Morrell, Nicholas⋅Morrell, Nicholas⋅Trembath, Richard⋅Trembath, R C⋅Aldred, Micheala and Aldred, MichealaCirculation, vol. 111, (no. 5), pp. 607-613, 2005.
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Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testingAldred, MA⋅Baumber, L⋅Hill, A⋅Schwalbe, EC⋅Goh, K⋅Karwatowski, W and Trembath, RcAmerican Journal of Ophthalmology, vol. 139, (no. 2), pp. 398-399, Feb 2005.
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Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood.Harrison, Rachel E⋅Harrison, Rachel⋅Berger, Rolf⋅Berger, Rolf⋅Haworth, Sheila⋅Haworth, Sheila G⋅Tulloh, Robert⋅Tulloh, Robert⋅Mache, Christoph⋅Mache, Christoph J⋅Morrell, Nicholas⋅Morrell, Nicholas⋅Aldred, Micheala⋅Aldred, Micheala⋅Trembath, Richard and Trembath, R CCirculation, vol. 111, (no. 4), pp. 435-41, 2005/Feb/1.
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2004
Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing.Aldred, Micheala⋅Aldred, Micheala⋅Baumber, Laura⋅Baumber, Laura⋅Hill, Alison⋅Hill, Alison⋅Schwalbe, Edward C⋅Schwalbe, Edward⋅Goh, Kai⋅Goh, Kai⋅Karwatowski, Wojciech⋅Karwatowski, Wojciech⋅Trembath, Richard and Trembath, R CHuman genetics, vol. 115, (no. 5), pp. 428-31, 2004/Oct.
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Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes.
Aldred, Micheala⋅Sanford, R O⋅Thomas, N S⋅Barrow, M A⋅Wilson, L C⋅Brueton, L A⋅Bonaglia, M C⋅Hennekam, R C⋅Eng, C⋅Dennis, 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, Micheala⋅Aldred, Micheala⋅Huang, Ying⋅Huang, Ying⋅Liyanarachchi, Sandya⋅Liyanarachchi, Sandya⋅Pellegata, Natalia⋅Pellegata, Natalia S⋅Gimm, Oliver⋅Gimm, Oliver⋅Jhiang, Sissy M⋅Jhiang, Sissy⋅Davuluri, Ramana V⋅Davuluri, Ramana⋅La Chapelle, Albert⋅De La Chapelle, Albert⋅Eng, Charis and Eng, CharisJournal of clinical oncology : official journal of the American Society of Clinical Oncology, vol. 22, (no. 17), pp. 3531-9, 2004/Sep/1.
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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 CarcinogenesisAldred, Micheala⋅Ginn-Pease, ME⋅Morrison, Carl⋅Popkie, AP⋅Gimm, O.⋅Hoang-Vu, Cuong⋅Krause, U.⋅Dralle, H.⋅Jhiang, Sissy M⋅Plass, Christoph and Eng, CharisCancer Research, vol. 63, (no. 11), pp. 2864-2871, 2003.
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Peroxisome proliferator-activated receptor gamma is frequently downregulated in a diversity of sporadic nonmedullary thyroid carcinomasAldred, Micheala⋅Morrison, Carl⋅Gimm, O.⋅Hoang-Vu, C.⋅Krause, U.⋅Dralle, H.⋅Jhiang, Sissy M and Eng, CharisOncogene, vol. 22, (no. 22), pp. 3412-3416, 2003.
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2002
Constitutional Deletion of Chromosome 20q in Two Patients Affected With Albright Hereditary OsteodystrophyAldred, Micheala⋅Aldred, Micheala A⋅Aftimos, S.⋅Aftimos, Salim⋅Hall, C.⋅Hall, Christine⋅Waters, KS⋅Waters, Katie S⋅Thakker, RV⋅Thakker, Rajesh V⋅Trembath, R C⋅Trembath, Richard C⋅Brueton, L. and Brueton, LouiseAmerican Journal of Medical Genetics, vol. 113, (no. 2), pp. 167-172, 2002.
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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 P⋅Woodford-Richens, K⋅Lehtonen, R⋅Kurose, K⋅Aldred, Micheala⋅Hampel, Heather L⋅Launonen, Virpi⋅Virta, S⋅Pilarski, Robert⋅Salovaara, R⋅Bodmer, W F⋅Conrad, B A⋅Dunlop, M⋅Hodgson, S V⋅Iwama, T⋅Järvinen, H⋅Kellokumpu, I⋅Kim, J C⋅Leggett, B⋅Markie, David⋅Mecklin, J P⋅Neale, K⋅Phillips, R⋅Piris, J⋅Rozen, P⋅Houlston, Richard S⋅Aaltonen, Lauri⋅Tomlinson, Ian and Eng, Charis EAmerican journal of human genetics, vol. 69, (no. 4), pp. 704-11, 2001/Oct.
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2000
Activating and inactivating mutations in the human GNAS1 gene.Aldred, Micheala and Trembath, R CHuman mutation, vol. 16, (no. 3), pp. 183-9, 2000/Sep.
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A Physical and Transcript Map Based upon Refinement of the Critical Interval for PPH1, a Gene for Familial Primary Pulmonary HypertensionMachado, Rajiv D⋅Machado, Rajiv D⋅Pauciulo, Michael W⋅Pauciulo, Michael W⋅Fretwell, Neale⋅Fretwell, Neale⋅Veal, Colin⋅Veal, Colin⋅Thomson, Jennifer R⋅Thomson, Jennifer R⋅Vilariño Güell, Carles⋅Vilariño Güell, Carles⋅Aldred, Micheala⋅Aldred, Micheala⋅Brannon, Christopher A⋅Brannon, Christopher A⋅Trembath, Richard C⋅Trembath, Richard C⋅Nichols, William C and Nichols, William CGenomics, vol. 68, (no. 2), pp. 228, 2000-09-01.
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Germline mosaicism for a GNAS1 mutation and Albright hereditary osteodystrophy.Aldred, Micheala A⋅Aldred, Micheala⋅BAGSHAW, R JANE⋅Bagshaw, R J⋅MACDERMOT, KAY⋅Macdermot, K⋅CASSON, DAVID⋅Casson, D⋅Murch, S H⋅MURCH, SIMON H⋅Walker-Smith, J A⋅WALKER-SMITH, J A⋅TREMBATH, RICHARD C and Trembath, R CJournal of medical genetics, vol. 37, (no. 11), pp. E35, 2000/Nov.
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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 RegionBench, A J⋅Bench, Anthony J⋅Aldred, Micheala A⋅Aldred, M A⋅Humphray, Sean J⋅Humphray, S J⋅Champion, K M⋅Champion, Kim M⋅Gilbert, James G.R⋅Gilbert, J G⋅Asimakopoulos, Fotis⋅Asimakopoulos, Fotios A⋅Deloukas, Panos⋅Deloukas, P⋅Gwilliam, R⋅Gwilliam, Rhian⋅Bentley, D R⋅Bentley, David R⋅Green, Anthony R and Green, A RGenomics, vol. 49, (no. 3), pp. 362, 1998.
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