| Year |
Citation |
Score |
| 2023 |
Ebrhim RS, Furman AE, Watanabe Y, Bruellman RJ, Abdullah MA, Dumitrescu AM, Refetoff S, Bertolini A, Borsò M, Saba A, Zucchi R, Weiss RE. Congenital Hypothyroidism in Two Sudanese Families harboring a novel Iodotyrosine deiodinase mutation (IYD R279C). Thyroid : Official Journal of the American Thyroid Association. PMID 36633921 DOI: 10.1089/thy.2022.0492 |
0.349 |
|
| 2021 |
Furman AE, Hannoush Z, Barrera Echegoyen FX, Dumitrescu AM, Refetoff S, Weiss RE. Novel DIO1 gene mutation acting as phenotype modifier for novel compound heterozygous TPO gene mutations causing congenital hypothyroidism. Thyroid : Official Journal of the American Thyroid Association. PMID 34128397 DOI: 10.1089/thy.2021.0210 |
0.306 |
|
| 2020 |
Furman AE, Dumitrescu AM, Refetoff S, Weiss RE. Early diagnosis and treatment of an infant with a novel THRA gene (pC380SfsX9) mutation. Thyroid : Official Journal of the American Thyroid Association. PMID 33198587 DOI: 10.1089/thy.2020.0695 |
0.328 |
|
| 2020 |
Refetoff S, Pappa T, Williams MK, Matheus MG, Liao XH, Hansen K, Nicol L, Pierce M, Blasco PA, Wiebers Jensen M, Bernal J, Weiss RE, Dumitrescu AM, LaFranchi SH. Prenatal treatment of thyroid hormone cell membrane transport defect caused by MCT8 gene mutation. Thyroid : Official Journal of the American Thyroid Association. PMID 32746752 DOI: 10.1089/Thy.2020.0306 |
0.442 |
|
| 2020 |
Fu J, Korwutthikulrangsri M, Gönç EN, Sillers L, Liao XH, Alikaşifoğlu A, Kandemir N, Menucci MB, Burman KD, Weiss RE, Dumitrescu AM. Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations. The Journal of Clinical Endocrinology and Metabolism. 105. PMID 32084277 DOI: 10.1210/Clinem/Dgz169 |
0.44 |
|
| 2020 |
Ebrhim RS, Bruellman RJ, Watanabe Y, Creech MK, Abdullah MA, Dumitrescu AM, Refetoff S, Weiss RE. Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ. Hormone Research in Paediatrics. 1-5. PMID 31914441 DOI: 10.1159/000504981 |
0.489 |
|
| 2019 |
Bruellman RJ, Watanabe Y, Ebrhim RS, Abdullah MA, Dumitrescu AM, Strauss BS, Refetoff S, Weiss RE. Insertion of an Alu element in the thyroglobulin gene as a novel cause of congenital hypothyroidism. Thyroid : Official Journal of the American Thyroid Association. PMID 31868128 DOI: 10.1089/Thy.2019.0636 |
0.385 |
|
| 2019 |
Fu J, Korwutthikulrangsri M, Ramos-Platt L, Pierson TM, Liao XH, Refetoff S, Weiss RE, Dumitrescu AM. Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 variants. Thyroid : Official Journal of the American Thyroid Association. PMID 31856685 DOI: 10.1089/Thy.2018.0703 |
0.466 |
|
| 2018 |
Watanabe Y, Bruellman RJ, Ebrhim RS, Abdullah MA, Dumitrescu AM, Refetoff S, Weiss RE. Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families. Thyroid : Official Journal of the American Thyroid Association. PMID 30375286 DOI: 10.1089/Thy.2018.0295 |
0.373 |
|
| 2018 |
Watanabe Y, Ebrhim RS, Abdullah MA, Weiss RE. A Novel Missense Mutation in SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism. Thyroid : Official Journal of the American Thyroid Association. PMID 29759035 DOI: 10.1089/Thy.2018.0137 |
0.42 |
|
| 2018 |
Watanabe Y, Sharwood E, Goodwin B, Creech MK, Hassan HY, Netea MG, Jaeger M, Dumitrescu A, Refetoff S, Huynh T, Weiss RE. A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report. Bmc Medical Genetics. 19: 69. PMID 29720101 DOI: 10.1186/S12881-018-0588-7 |
0.434 |
|
| 2017 |
Pappa T, Anselmo J, Mamanasiri S, Dumitrescu AM, Weiss RE, Refetoff S. Prenatal diagnosis of resistance to thyroid hormone and its clinical implications. The Journal of Clinical Endocrinology and Metabolism. PMID 28938413 DOI: 10.1210/Jc.2017-01251 |
0.499 |
|
| 2017 |
Leitch VD, Di Cosmo C, Liao XH, O'Boy S, Galliford TM, Evans H, Croucher PI, Boyde A, Dumitrescu A, Weiss RE, Refetoff S, Williams GR, Bassett JHD. An essential physiological role for MCT8 in bone in male mice. Endocrinology. PMID 28637283 DOI: 10.1210/En.2017-00399 |
0.414 |
|
| 2017 |
Srichomkwun P, Anselmo J, Liao XH, Hönes GS, Moeller LC, Alonso-Sampedro M, Weiss RE, Dumitrescu AM, Refetoff S. Fetal exposure to high maternal thyroid hormone (TH) levels causes central resistance to TH in adult humans and mice. The Journal of Clinical Endocrinology and Metabolism. PMID 28586435 DOI: 10.1210/Jc.2017-00019 |
0.512 |
|
| 2017 |
Berger HR, Creech MK, Hannoush Z, Watanabe Y, Kargi A, Weiss RE. A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE. Aace Clinical Case Reports. 3: e134-e139. PMID 28553659 DOI: 10.4158/Ep161421.Cr |
0.449 |
|
| 2017 |
Hannoush ZC, Weiss RE. Defects of Thyroid Hormone Synthesis and Action. Endocrinology and Metabolism Clinics of North America. 46: 375-388. PMID 28476227 DOI: 10.1016/J.Ecl.2017.01.005 |
0.428 |
|
| 2016 |
Iwayama H, Liao XH, Braun L, Bárez-López S, Kaspar B, Weiss R, Dumitrescu AM, Guadaño-Ferraz A, Refetoff S. Adeno associated virus 9-based gene therapy delivers a functional monocarboxylate transporter 8 (MCT8) which improves thyroid hormone availability to brain of Mct8 deficient mice. Thyroid : Official Journal of the American Thyroid Association. PMID 27432638 DOI: 10.1089/Thy.2016.0060 |
0.448 |
|
| 2016 |
Hannoush ZC, Weiss RE. Thyroid Hormone Replacement in Patients Following Thyroidectomy for Thyroid Cancer. Rambam Maimonides Medical Journal. 7. PMID 26886951 DOI: 10.5041/Rmmj.10229 |
0.468 |
|
| 2015 |
Ferrara AM, Liao XH, Ye H, Weiss RE, Dumitrescu AM, Refetoff S. The thyroid hormone analogue DITPA ameliorates metabolic parameters of male mice with Mct8 deficiency. Endocrinology. en20151234. PMID 26322373 DOI: 10.1210/En.2015-1234 |
0.506 |
|
| 2015 |
Ferrara AM, Pappa T, Fu J, Brown CD, Peterson A, Moeller LC, Wyne K, White KP, Pluzhnikov A, Trubetskoy V, Nobrega M, Weiss RE, Dumitrescu AM, Refetoff S. A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer. The Journal of Clinical Endocrinology and Metabolism. 100: E173-81. PMID 25361180 DOI: 10.1210/Jc.2014-3490 |
0.461 |
|
| 2014 |
Larsen CC, Karaviti LP, Seghers V, Weiss RE, Refetoff S, Dumitrescu AM. A new family with an activating mutation (G431S) in the TSH receptor gene: a phenotype discussion and review of the literature. International Journal of Pediatric Endocrinology. 2014: 23. PMID 25873976 DOI: 10.1186/1687-9856-2014-23 |
0.452 |
|
| 2014 |
Ferrara AM, Liao XH, Gil-Ibáñez P, Bernal J, Weiss RE, Dumitrescu AM, Refetoff S. Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient mice. Endocrinology. 155: 4088-93. PMID 25051435 DOI: 10.1210/En.2014-1085 |
0.486 |
|
| 2014 |
Refetoff S, Bassett JH, Beck-Peccoz P, Bernal J, Brent G, Chatterjee K, De Groot LJ, Dumitrescu AM, Jameson JL, Kopp PA, Murata Y, Persani L, Samarut J, Weiss RE, Williams GR, et al. Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism. European Thyroid Journal. 3: 7-9. PMID 24847459 DOI: 10.1159/000358180 |
0.552 |
|
| 2014 |
Refetoff S, Bassett JH, Beck-Peccoz P, Bernal J, Brent G, Chatterjee K, De Groot LJ, Dumitrescu AM, Jameson JL, Kopp PA, Murata Y, Persani L, Samarut J, Weiss RE, Williams GR, et al. Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism. The Journal of Clinical Endocrinology and Metabolism. 99: 768-70. PMID 24823702 DOI: 10.1210/Jc.2013-3393 |
0.552 |
|
| 2014 |
Refetoff S, Bassett JH, Beck-Peccoz P, Bernal J, Brent G, Chatterjee K, De Groot LJ, Dumitrescu AM, Jameson JL, Kopp PA, Murata Y, Persani L, Samarut J, Weiss RE, Williams GR, et al. Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism. Thyroid : Official Journal of the American Thyroid Association. 24: 407-9. PMID 24588711 DOI: 10.1089/Thy.2013.3393.Nomen |
0.551 |
|
| 2014 |
Greenberg SM, Ferrara AM, Nicholas ES, Dumitrescu AM, Cody V, Weiss RE, Refetoff S. A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction. Thyroid : Official Journal of the American Thyroid Association. 24: 945-50. PMID 24494774 DOI: 10.1089/Thy.2013.0540 |
0.4 |
|
| 2014 |
Bianco AC, Anderson G, Forrest D, Galton VA, Gereben B, Kim BW, Kopp PA, Liao XH, Obregon MJ, Peeters RP, Refetoff S, Sharlin DS, Simonides WS, Weiss RE, Williams GR, et al. American Thyroid Association Guide to investigating thyroid hormone economy and action in rodent and cell models. Thyroid : Official Journal of the American Thyroid Association. 24: 88-168. PMID 24001133 DOI: 10.1089/Thy.2013.0109 |
0.477 |
|
| 2013 |
Grogan RH, Kaplan SP, Cao H, Weiss RE, Degroot LJ, Simon CA, Embia OM, Angelos P, Kaplan EL, Schechter RB. A study of recurrence and death from papillary thyroid cancer with 27 years of median follow-up. Surgery. 154: 1436-46; discussion . PMID 24075674 DOI: 10.1016/J.Surg.2013.07.008 |
0.345 |
|
| 2013 |
Di Cosmo C, Liao XH, Ye H, Ferrara AM, Weiss RE, Refetoff S, Dumitrescu AM. Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels. Endocrinology. 154: 4885-95. PMID 24029243 DOI: 10.1210/En.2013-1150 |
0.397 |
|
| 2013 |
Larsen CC, Dumitrescu A, Guerra-Argüero LM, Gállego-Suárez C, Vazquez-Mellado A, Vinogradova M, Fletterick R, Refetoff S, Weiss RE. Incidental identification of a thyroid hormone receptor beta (THRB) gene variant in a family with autoimmune thyroid disease Thyroid. 23: 1638-1643. PMID 23806029 DOI: 10.1089/Thy.2013.0174 |
0.533 |
|
| 2013 |
Ferrara AM, Liao XH, Gil-Ibáñez P, Marcinkowski T, Bernal J, Weiss RE, Dumitrescu AM, Refetoff S. Changes in thyroid status during perinatal development of MCT8-deficient male mice. Endocrinology. 154: 2533-41. PMID 23696569 DOI: 10.1210/En.2012-2031 |
0.487 |
|
| 2013 |
Monk JA, Sims NA, Dziegielewska KM, Weiss RE, Ramsay RG, Richardson SJ. Delayed development of specific thyroid hormone-regulated events in transthyretin null mice American Journal of Physiology - Endocrinology and Metabolism. 304: E23-E31. PMID 23092911 DOI: 10.1152/Ajpendo.00216.2012 |
0.401 |
|
| 2012 |
Verge CF, Konrad D, Cohen M, Di Cosmo C, Dumitrescu AM, Marcinkowski T, Hameed S, Hamilton J, Weiss RE, Refetoff S. Diiodothyropropionic acid (DITPA) in the treatment of MCT8 deficiency. The Journal of Clinical Endocrinology and Metabolism. 97: 4515-23. PMID 22993035 DOI: 10.1210/Jc.2012-2556 |
0.504 |
|
| 2012 |
Ferrara AM, Onigata K, Ercan O, Woodhead H, Weiss RE, Refetoff S. Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature. The Journal of Clinical Endocrinology and Metabolism. 97: 1328-36. PMID 22319036 DOI: 10.1210/Jc.2011-2642 |
0.503 |
|
| 2011 |
Barca-Mayo O, Liao XH, DiCosmo C, Dumitrescu A, Moreno-Vinasco L, Wade MS, Sammani S, Mirzapoiazova T, Garcia JG, Refetoff S, Weiss RE. Role of type 2 deiodinase in response to acute lung injury (ALI) in mice. Proceedings of the National Academy of Sciences of the United States of America. 108: E1321-9. PMID 22065740 DOI: 10.1073/Pnas.1109926108 |
0.34 |
|
| 2011 |
Müller K, Führer D, Mittag J, Klöting N, Blüher M, Weiss RE, Many MC, Schmid KW, Krohn K. TSH compensates thyroid-specific IGF-I receptor knockout and causes papillary thyroid hyperplasia. Molecular Endocrinology (Baltimore, Md.). 25: 1867-79. PMID 21980075 DOI: 10.1210/Me.2011-0065 |
0.515 |
|
| 2011 |
Barca-Mayo O, Liao XH, Alonso M, Di Cosmo C, Hernandez A, Refetoff S, Weiss RE. Thyroid hormone receptor α and regulation of type 3 deiodinase. Molecular Endocrinology (Baltimore, Md.). 25: 575-83. PMID 21292823 DOI: 10.1210/Jcem.96.3.Zeg873 |
0.437 |
|
| 2011 |
Liao XH, Di Cosmo C, Dumitrescu AM, Hernandez A, Van Sande J, St Germain DL, Weiss RE, Galton VA, Refetoff S. Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes. Endocrinology. 152: 1180-91. PMID 21285310 DOI: 10.1210/En.2010-0900 |
0.439 |
|
| 2011 |
Astapova I, Vella KR, Ramadoss P, Holtz KA, Rodwin BA, Liao XH, Weiss RE, Rosenberg MA, Rosenzweig A, Hollenberg AN. The nuclear receptor corepressor (NCoR) controls thyroid hormone sensitivity and the set point of the hypothalamic-pituitary-thyroid axis. Molecular Endocrinology (Baltimore, Md.). 25: 212-24. PMID 21239618 DOI: 10.1210/Edrv.32.1.Zef153A |
0.54 |
|
| 2010 |
Di Cosmo C, Liao XH, Dumitrescu AM, Philp NJ, Weiss RE, Refetoff S. Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion. The Journal of Clinical Investigation. 120: 3377-88. PMID 20679730 DOI: 10.1172/Jci42113 |
0.522 |
|
| 2010 |
Weiss RE, Dumitrescu A, Refetoff S. Approach to the patient with resistance to thyroid hormone and pregnancy. The Journal of Clinical Endocrinology and Metabolism. 95: 3094-102. PMID 20610605 DOI: 10.1210/Jc.2010-0409 |
0.492 |
|
| 2010 |
Barkoff MS, Kocherginsky M, Anselmo J, Weiss RE, Refetoff S. Autoimmunity in patients with resistance to thyroid hormone. The Journal of Clinical Endocrinology and Metabolism. 95: 3189-93. PMID 20444926 DOI: 10.1210/Jc.2009-2179 |
0.523 |
|
| 2010 |
You SH, Liao X, Weiss RE, Lazar MA. The interaction between nuclear receptor corepressor and histone deacetylase 3 regulates both positive and negative thyroid hormone action in vivo. Molecular Endocrinology (Baltimore, Md.). 24: 1359-67. PMID 20427468 DOI: 10.1210/Jcem.95.5.9994 |
0.412 |
|
| 2010 |
Wang D, Xia X, Weiss RE, Refetoff S, Yen PM. Distinct and histone-specific modifications mediate positive versus negative transcriptional regulation of TSHalpha promoter. Plos One. 5: e9853. PMID 20352046 DOI: 10.1371/Journal.Pone.0009853 |
0.41 |
|
| 2010 |
Dumitrescu AM, Di Cosmo C, Liao XH, Weiss RE, Refetoff S. The syndrome of inherited partial SBP2 deficiency in humans. Antioxidants & Redox Signaling. 12: 905-20. PMID 19769464 DOI: 10.1089/Ars.2009.2892 |
0.445 |
|
| 2009 |
Di Cosmo C, McLellan N, Liao XH, Khanna KK, Weiss RE, Papp L, Refetoff S. Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X). The Journal of Clinical Endocrinology and Metabolism. 94: 4003-9. PMID 19602558 DOI: 10.1210/Jc.2009-0686 |
0.436 |
|
| 2009 |
Di Cosmo C, Liao XH, Dumitrescu AM, Weiss RE, Refetoff S. A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport. Endocrinology. 150: 4450-8. PMID 19497976 DOI: 10.1210/En.2009-0209 |
0.426 |
|
| 2009 |
Moeller LC, Wardrip C, Niekrasz M, Refetoff S, Weiss RE. Comparison of thyroidectomized calf serum and stripped serum for the study of thyroid hormone action in human skin fibroblasts in vitro. Thyroid : Official Journal of the American Thyroid Association. 19: 639-44. PMID 19445627 DOI: 10.1089/Thy.2008.0293 |
0.424 |
|
| 2009 |
Alonso M, Goodwin C, Liao X, Ortiga-Carvalho T, Machado DS, Wondisford FE, Refetoff S, Weiss RE. In vivo interaction of steroid receptor coactivator (SRC)-1 and the activation function-2 domain of the thyroid hormone receptor (TR) beta in TRbeta E457A knock-in and SRC-1 knockout mice. Endocrinology. 150: 3927-34. PMID 19406944 DOI: 10.1210/En.2009-0093 |
0.431 |
|
| 2009 |
Janssen OE, Bertenshaw R, Takeda K, Weiss R, Refetoff S. Molecular basis of inherited thyroxine-binding globulin defects. Trends in Endocrinology and Metabolism: Tem. 3: 49-53. PMID 18407078 DOI: 10.1016/1043-2760(92)90043-Z |
0.411 |
|
| 2008 |
Weiss RE, Brown RL. Doctor... could it be my thyroid? Archives of Internal Medicine. 168: 568-569. PMID 18362247 DOI: 10.1001/Archinte.168.6.568 |
0.462 |
|
| 2008 |
Weiss RE. "They have ears but do not hear" (Psalms 135:17): Non-thyroid hormone receptor β (non-TRβ) resistance to thyroid hormone Thyroid. 18: 3-5. PMID 18302513 DOI: 10.1089/Thy.2007.0373 |
0.464 |
|
| 2008 |
Bassett JH, Williams AJ, Murphy E, Boyde A, Howell PG, Swinhoe R, Archanco M, Flamant F, Samarut J, Costagliola S, Vassart G, Weiss RE, Refetoff S, Williams GR. A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidism. Molecular Endocrinology (Baltimore, Md.). 22: 501-12. PMID 17932107 DOI: 10.1210/Me.2007-0221 |
0.49 |
|
| 2007 |
Brown RL, Wollman R, Weiss RE. Transformation of a pituitary macroadenoma into to a corticotropin-secreting carcinoma over 16 years. Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. 13: 463-71. PMID 17872347 DOI: 10.4158/Ep.13.5.463 |
0.318 |
|
| 2007 |
Alonso M, Goodwin C, Liao X, Page D, Refetoff S, Weiss RE. Effects of maternal levels of thyroid hormone (TH) on the hypothalamus-pituitary-thyroid set point: studies in TH receptor beta knockout mice. Endocrinology. 148: 5305-12. PMID 17690164 DOI: 10.1210/En.2007-0677 |
0.455 |
|
| 2007 |
Moeller LC, Alonso M, Liao X, Broach V, Dumitrescu A, Van Sande J, Montanelli L, Skjei S, Goodwin C, Grasberger H, Refetoff S, Weiss RE. Pituitary-thyroid setpoint and thyrotropin receptor expression in consomic rats. Endocrinology. 148: 4727-33. PMID 17640981 DOI: 10.1210/En.2007-0236 |
0.356 |
|
| 2007 |
Maier J, van Steeg H, van Oostrom C, Paschke R, Weiss RE, Krohn K. Iodine deficiency activates antioxidant genes and causes DNA damage in the thyroid gland of rats and mice Biochimica Et Biophysica Acta - Molecular Cell Research. 1773: 990-999. PMID 17467074 DOI: 10.1016/J.Bbamcr.2007.03.011 |
0.427 |
|
| 2007 |
Bassett JH, O'Shea PJ, Sriskantharajah S, Rabier B, Boyde A, Howell PG, Weiss RE, Roux JP, Malaval L, Clement-Lacroix P, Samarut J, Chassande O, Williams GR. Thyroid hormone excess rather than thyrotropin deficiency induces osteoporosis in hyperthyroidism. Molecular Endocrinology (Baltimore, Md.). 21: 1095-107. PMID 17327419 DOI: 10.1210/Me.2007-0033 |
0.486 |
|
| 2006 |
Suri D, Alonso M, Weiss RE. A case of ACTH-independent bilateral macronodular adrenal hyperplasia and severe congestive heart failure Journal of Endocrinological Investigation. 29: 940-946. PMID 17185906 DOI: 10.1007/Bf03349201 |
0.342 |
|
| 2006 |
Brown RL, Weiss RE. An approach to the evaluation and treatment of Cushing's disease Expert Review of Anticancer Therapy. 6: S37-S46. PMID 17004856 DOI: 10.1586/14737140.6.9S.S37 |
0.308 |
|
| 2006 |
Wu SY, Weiss RE. Radioiodine imaging in the primary care of thyroid disease. Postgraduate Medicine. 119: 70-7. PMID 16961055 DOI: 10.3810/Pgm.2006.07.1740 |
0.402 |
|
| 2006 |
Mamanasiri S, Yesil S, Dumitrescu AM, Liao XH, Demir T, Weiss RE, Refetoff S. Mosaicism of a thyroid hormone receptor-beta gene mutation in resistance to thyroid hormone. The Journal of Clinical Endocrinology and Metabolism. 91: 3471-7. PMID 16804041 DOI: 10.1210/Jc.2006-0727 |
0.507 |
|
| 2006 |
Dumitrescu AM, Liao XH, Weiss RE, Millen K, Refetoff S. Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice. Endocrinology. 147: 4036-43. PMID 16709608 DOI: 10.1210/En.2006-0390 |
0.458 |
|
| 2006 |
Brown RL, Muzzafar T, Wollman R, Weiss RE. A pituitary carcinoma secreting TSH and prolactin: a non-secreting adenoma gone awry. European Journal of Endocrinology / European Federation of Endocrine Societies. 154: 639-43. PMID 16645009 DOI: 10.1530/Eje.1.02141 |
0.395 |
|
| 2006 |
Ramos HE, Weiss RE. Regulation of nuclear coactivator and corepressor expression in mouse cerebellum by thyroid hormone Thyroid. 16: 211-216. PMID 16571082 DOI: 10.1089/Thy.2006.16.211 |
0.428 |
|
| 2006 |
Wu SY, Cohen RN, Simsek E, Senses DA, Yar NE, Grasberger H, Noel J, Refetoff S, Weiss RE. A novel thyroid hormone receptor-beta mutation that fails to bind nuclear receptor corepressor in a patient as an apparent cause of severe, predominantly pituitary resistance to thyroid hormone. The Journal of Clinical Endocrinology and Metabolism. 91: 1887-95. PMID 16464943 DOI: 10.1210/Jc.2005-2428 |
0.532 |
|
| 2006 |
Ringkananont U, Van Durme J, Montanelli L, Ugrasbul F, Yu YM, Weiss RE, Refetoff S, Grasberger H. Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I). Molecular Endocrinology (Baltimore, Md.). 20: 893-903. PMID 16339276 DOI: 10.1210/Me.2005-0339 |
0.317 |
|
| 2005 |
Dumitrescu AM, Liao XH, Abdullah MS, Lado-Abeal J, Majed FA, Moeller LC, Boran G, Schomburg L, Weiss RE, Refetoff S. Mutations in SECISBP2 result in abnormal thyroid hormone metabolism. Nature Genetics. 37: 1247-52. PMID 16228000 DOI: 10.1038/Ng1654 |
0.477 |
|
| 2005 |
Wu SY, Sadow PM, Refetoff S, Weiss RE. Tissue responses to thyroid hormone in a kindred with resistance to thyroid hormone harboring a commonly occurring mutation in the thyroid hormone receptor beta gene (P453T). The Journal of Laboratory and Clinical Medicine. 146: 85-94. PMID 16099238 DOI: 10.1016/J.Lab.2005.04.005 |
0.681 |
|
| 2005 |
Aksoy DY, Gurlek A, Ringkananont U, Weiss RE, Refetoff S. Resistance to thyroid hormone associated with autoimmune thyroid disease in a Turkish family Journal of Endocrinological Investigation. 28: 379-383. PMID 15966514 DOI: 10.1007/Bf03347207 |
0.556 |
|
| 2005 |
Grasberger H, Mimouni-Bloch A, Vantyghem MC, van Vliet G, Abramowicz M, Metzger DL, Abdullatif H, Rydlewski C, Macchia PE, Scherberg NH, van Sande J, Mimouni M, Weiss RE, Vassart G, Refetoff S. Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate loci. The Journal of Clinical Endocrinology and Metabolism. 90: 4025-34. PMID 15870119 DOI: 10.1210/Jc.2005-0572 |
0.416 |
|
| 2005 |
Marrif H, Schifman A, Stepanyan Z, Gillis MA, Calderone A, Weiss RE, Samarut J, Silva JE. Temperature homeostasis in transgenic mice lacking thyroid hormone receptor-alpha gene products. Endocrinology. 146: 2872-84. PMID 15845618 DOI: 10.1210/En.2004-1544 |
0.401 |
|
| 2005 |
Lado-Abeal J, Dumitrescu AM, Liao XH, Cohen RN, Pohlenz J, Weiss RE, Lebrethon MC, Verloes A, Refetoff S. A de novo mutation in an already mutant nucleotide of the thyroid hormone receptor beta gene perpetuates resistance to thyroid hormone. The Journal of Clinical Endocrinology and Metabolism. 90: 1760-7. PMID 15598685 DOI: 10.1210/Jc.2004-1488 |
0.475 |
|
| 2005 |
Suri D, Weiss RE. Effect of pioglitazone on adrenocorticotropic hormone and cortisol secretion in Cushing's disease Journal of Clinical Endocrinology and Metabolism. 90: 1340-1346. PMID 15585550 DOI: 10.1210/Jc.2004-1746 |
0.319 |
|
| 2005 |
Mohammed IA, Aldasouqi S, Schnute R, Refetoff S, Weiss RE, Iqbal N. The syndrome of resistance to thyroid hormone, misdiagnosed and treated as thyrotoxicosis. Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. 4: 391-5. PMID 15251715 DOI: 10.4158/Ep.4.6.391 |
0.452 |
|
| 2005 |
Weiss RE. An odyssey of hyperprolactinemia in a young woman: Idiopathic hyperprolactinemia, hypothyroidism, and a pituitary microadenoma Endocrinologist. 15: 95-98. DOI: 10.1097/01.Ten.0000157884.15969.B1 |
0.399 |
|
| 2005 |
Anselmo J, Cao D, Karrison T, Weiss RE, Reetoff S. Fetal loss associated with excess thyroid hormone exposure Obstetrical and Gynecological Survey. 60: 82-83. DOI: 10.1097/01.Ogx.0000151639.15130.4D |
0.382 |
|
| 2005 |
Refetoff S, Weiss RE, Anselmo J. Fetal Loss Associated With Excess Thyroid Hormone Exposure—Reply Jama. 293: 160-161. DOI: 10.1001/Jama.293.2.161-A |
0.453 |
|
| 2004 |
Martin NM, Small CJ, Sajedi A, Liao XH, Weiss RE, Gardiner JV, Ghatei MA, Bloom SR. Abnormalities of the hypothalamo-pituitary-thyroid axis in the pro-opiomelanocortin deficient mouse Regulatory Peptides. 122: 169-172. PMID 15491787 DOI: 10.1016/J.Regpep.2004.06.012 |
0.464 |
|
| 2004 |
Anselmo J, Cao D, Karrison T, Weiss RE, Refetoff S. Fetal loss associated with excess thyroid hormone exposure. Jama. 292: 691-5. PMID 15304465 DOI: 10.1001/Jama.292.6.691 |
0.404 |
|
| 2004 |
Mannavola D, Moeller LC, Beck-Peccoz P, Persani L, Weiss RE, Refetoff S. A novel splice variant involving the 5′ untranslated region of thyroid hormone receptor β1 (TRβ1) Journal of Endocrinological Investigation. 27: 318-322. PMID 15233549 DOI: 10.1007/Bf03351055 |
0.453 |
|
| 2004 |
Weiss RE, Ramos HE. Thyroid Hormone Receptor Subtypes and Their Interaction with Steroid Receptor Coactivators Vitamins and Hormones. 68: 185-207. PMID 15193455 DOI: 10.1016/S0083-6729(04)68006-X |
0.456 |
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| 2004 |
Van Cauter E, Latta F, Nedeltcheva A, Spiegel K, Leproult R, Vandenbril C, Weiss R, Mockel J, Legros JJ, Copinschi G. Reciprocal interactions between the GH axis and sleep. Growth Hormone & Igf Research : Official Journal of the Growth Hormone Research Society and the International Igf Research Society. 14: S10-7. PMID 15135771 DOI: 10.1016/J.Ghir.2004.03.006 |
0.311 |
|
| 2003 |
Sadow PM, Chassande O, Koo EK, Gauthier K, Samarut J, Xu J, O'Malley BW, Weiss RE. Regulation of expression of thyroid hormone receptor isoforms and coactivators in liver and heart by thyroid hormone. Molecular and Cellular Endocrinology. 203: 65-75. PMID 12782404 DOI: 10.1016/S0303-7207(03)00122-9 |
0.609 |
|
| 2003 |
Yen PM, Feng X, Flamant F, Chen Y, Walker RL, Weiss RE, Chassande O, Samarut J, Refetoff S, Meltzer PS. Effects of ligand and thyroid hormone receptor isoforms on hepatic gene expression profiles of thyroid hormone receptor knockout mice. Embo Reports. 4: 581-7. PMID 12776178 DOI: 10.1038/Sj.Embor.Embor862 |
0.462 |
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| 2003 |
Matalon ST, Blank M, Levy Y, Carp HJ, Arad A, Burek L, Grunebaum E, Sherer Y, Ornoy A, Refetoff S, Weiss RE, Rose NR, Shoenfeld Y. The pathogenic role of anti-thyroglobulin antibody on pregnancy: evidence from an active immunization model in mice. Human Reproduction (Oxford, England). 18: 1094-9. PMID 12721190 DOI: 10.1093/Humrep/Deg210 |
0.359 |
|
| 2003 |
Sadow PM, Koo E, Chassande O, Gauthier K, Samarut J, Xu J, O'Malley BW, Seo H, Murata Y, Weiss RE. Thyroid hormone receptor-specific interactions with steroid receptor coactivator-1 in the pituitary. Molecular Endocrinology (Baltimore, Md.). 17: 882-94. PMID 12576486 DOI: 10.1210/Me.2002-0174 |
0.612 |
|
| 2003 |
Stein MA, Weiss RE. Thyroid function tests and neurocognitive functioning in children referred for attention deficit/hyperactivity disorder Psychoneuroendocrinology. 28: 304-316. PMID 12573298 DOI: 10.1016/S0306-4530(02)00024-0 |
0.334 |
|
| 2003 |
Sadow PM, Chassande O, Gauthier K, Samarut J, Xu J, O'Malley BW, Weiss RE. Specificity of thyroid hormone receptor subtype and steroid receptor coactivator-1 on thyroid hormone action. American Journal of Physiology. Endocrinology and Metabolism. 284: E36-46. PMID 12388168 DOI: 10.1152/Ajpendo.00226.2002 |
0.67 |
|
| 2002 |
Weiss RE. A serpentine thyroid. Thyroid : Official Journal of the American Thyroid Association. 12: 641. PMID 12193312 DOI: 10.1089/105072502320288537 |
0.463 |
|
| 2002 |
Weiss RE, Korcarz C, Chassande O, Cua K, Sadow PM, Koo E, Samarut J, Lang R. Thyroid hormone and cardiac function in mice deficient in thyroid hormone receptor-alpha or -beta: an echocardiograph study. American Journal of Physiology. Endocrinology and Metabolism. 283: E428-35. PMID 12169435 DOI: 10.1152/Ajpendo.00019.2002 |
0.597 |
|
| 2002 |
Macchia PE, Jiang P, Yuan YD, Chandarardna RA, Weiss RE, Chassande O, Samarut J, Refetoff S, Burant CF. RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor. American Journal of Physiology. Endocrinology and Metabolism. 283: E326-31. PMID 12110538 DOI: 10.1152/Ajpendo.00313.2001 |
0.481 |
|
| 2002 |
AvRuskin TW, Juan CS, Weiss RE. Familial dysalbuminemic hyperthyroxinemia: a rare example of albumin polymorphism and its rapid molecular diagnosis. Journal of Pediatric Endocrinology & Metabolism : Jpem. 15: 801-7. PMID 12099390 DOI: 10.1515/Jpem.2002.15.6.801 |
0.391 |
|
| 2002 |
Weiss RE, Gehin M, Xu J, Sadow PM, O'Malley BW, Chambon P, Refetoff S. Thyroid function in mice with compound heterozygous and homozygous disruptions of SRC-1 and TIF-2 coactivators: evidence for haploinsufficiency. Endocrinology. 143: 1554-7. PMID 11897715 DOI: 10.1210/Endo.143.4.8828 |
0.637 |
|
| 2002 |
Takeuchi Y, Murata Y, Sadow P, Hayashi Y, Seo H, Xu J, O'Malley BW, Weiss RE, Refetoff S. Steroid receptor coactivator-1 deficiency causes variable alterations in the modulation of T(3)-regulated transcription of genes in vivo. Endocrinology. 143: 1346-52. PMID 11897691 DOI: 10.1210/Endo.143.4.8730 |
0.652 |
|
| 2002 |
Pohlenz J, Dumitrescu A, Zundel D, Martiné U, Schönberger W, Koo E, Weiss RE, Cohen RN, Kimura S, Refetoff S. Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice Journal of Clinical Investigation. 109: 469-473. PMID 11854318 DOI: 10.1172/Jci14192 |
0.46 |
|
| 2002 |
Weiss RE, Lado-Abeal J. Thyroid nodules: diagnosis and therapy. Current Opinion in Oncology. 14: 46-52. PMID 11790980 DOI: 10.1097/00001622-200201000-00009 |
0.436 |
|
| 2002 |
Weiss RE, Chassande O, Koo EK, Macchia PE, Cua K, Samarut J, Refetoff S, Refetoff S. Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes. The Journal of Endocrinology. 172: 177-85. PMID 11786385 DOI: 10.1677/Joe.0.1720177 |
0.515 |
|
| 2001 |
Pohlenz J, Sadow PM, Koffler T, Schönberger W, Weiss RE, Refetoff S. Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene. The Journal of Pediatrics. 139: 887-91. PMID 11743520 DOI: 10.1067/Mpd.2001.119594 |
0.641 |
|
| 2001 |
Weiss RE, Refetoff S. Resistance to thyroid hormone. Reviews in Endocrine & Metabolic Disorders. 1: 97-108. PMID 11704998 DOI: 10.1023/A:1010072605757 |
0.466 |
|
| 2001 |
Anselmo J, Kay T, Dennis K, Szmulewitz R, Refetoff S, Weiss RE. Resistance to thyroid hormone does not abrogate the transient thyrotoxicosis associated with gestation: report of a case. The Journal of Clinical Endocrinology and Metabolism. 86: 4273-5. PMID 11549661 DOI: 10.1210/Jcem.86.9.7858 |
0.506 |
|
| 2001 |
Gauthier K, Plateroti M, Harvey CB, Williams GR, Weiss RE, Refetoff S, Willott JF, Sundin V, Roux JP, Malaval L, Hara M, Samarut J, Chassande O. Genetic analysis reveals different functions for the products of the thyroid hormone receptor alpha locus. Molecular and Cellular Biology. 21: 4748-60. PMID 11416150 DOI: 10.1128/Mcb.21.14.4748-4760.2001 |
0.435 |
|
| 2001 |
Macchia PE, Takeuchi Y, Kawai T, Cua K, Gauthier K, Chassande O, Seo H, Hayashi Y, Samarut J, Murata Y, Weiss RE, Refetoff S. Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alpha. Proceedings of the National Academy of Sciences of the United States of America. 98: 349-54. PMID 11120878 DOI: 10.1073/Pnas.011306998 |
0.451 |
|
| 2000 |
Reutrakul S, Sadow PM, Pannain S, Pohlenz J, Carvalho GA, Macchia PE, Weiss RE, Refetoff S. Search for abnormalities of nuclear corepressors, coactivators, and a coregulator in families with resistance to thyroid hormone without mutations in thyroid hormone receptor beta or alpha genes. The Journal of Clinical Endocrinology and Metabolism. 85: 3609-17. PMID 11061510 DOI: 10.1210/Jcem.85.10.6873 |
0.653 |
|
| 2000 |
Pannain S, Feldman M, Eiholzer U, Weiss RE, Scherberg NH, Refetoff S. Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine. The Journal of Clinical Endocrinology and Metabolism. 85: 2786-92. PMID 10946882 DOI: 10.1210/Jcem.85.8.6746 |
0.37 |
|
| 2000 |
Weiss RE. Clear fluid from a thyroid cyst. Thyroid. 10: 195-196. PMID 10718560 DOI: 10.1089/Thy.2000.10.195 |
0.391 |
|
| 2000 |
Pohlenz J, Maqueem A, Cua K, Weiss RE, Van Sande J, Refetoff S. Improved radioimmunoassay for measurement of mouse thyrotropin in serum: strain differences in thyrotropin concentration and thyrotroph sensitivity to thyroid hormone. Thyroid : Official Journal of the American Thyroid Association. 9: 1265-71. PMID 10646670 DOI: 10.1089/Thy.1999.9.1265 |
0.389 |
|
| 2000 |
Refetoff S, Sadow PM, Reutrakul S, Dennis K, Mannavola D, Pohlenz J, Weiss RE. Resistance to Thyroid Hormone in the Absence of Mutations in the Thyroid Hormone Receptor Genes Current Opinion in Endocrinology & Diabetes. 7: 89-107. DOI: 10.1007/978-1-4020-7852-1_6 |
0.689 |
|
| 1999 |
Pohlenz J, Manders L, Sadow PM, Kansal PC, Refetoff S, Weiss RE. A novel point mutation in cluster 3 of the thyroid hormone receptor beta gene (P247L) causing mild resistance to thyroid hormone. Thyroid : Official Journal of the American Thyroid Association. 9: 1195-203. PMID 10646658 DOI: 10.1089/Thy.1999.9.1195 |
0.695 |
|
| 1999 |
Pohlenz J, Weiss RE, Macchia PE, Pannain S, Lau IT, Ho H, Refetoff S. Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene. The Journal of Clinical Endocrinology and Metabolism. 84: 3919-28. PMID 10566629 DOI: 10.1210/Jcem.84.11.6080 |
0.468 |
|
| 1999 |
Tiosano D, Pannain S, Vassart G, Parma J, Gershoni-Baruch R, Mandel H, Lotan R, Zaharan Y, Pery M, Weiss RE, Refetoff S, Hochberg Z. The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor. Thyroid : Official Journal of the American Thyroid Association. 9: 887-94. PMID 10524567 DOI: 10.1089/Thy.1999.9.887 |
0.526 |
|
| 1999 |
Weiss RE, Xu J, Ning G, Pohlenz J, O'Malley BW, Refetoff S. Mice deficient in the steroid receptor co-activator 1 (SRC-1) are resistant to thyroid hormone. The Embo Journal. 18: 1900-4. PMID 10202153 DOI: 10.1093/Emboj/18.7.1900 |
0.491 |
|
| 1999 |
Pannain S, Weiss RE, Jackson CE, Dian D, Beck JC, Sheffield VC, Cox N, Refetoff S. Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping. The Journal of Clinical Endocrinology and Metabolism. 84: 1061-71. PMID 10084596 DOI: 10.1210/Jcem.84.3.5541 |
0.405 |
|
| 1999 |
Weiss RE, Refetoff S. Treatment of resistance to thyroid hormone--primum non nocere. The Journal of Clinical Endocrinology and Metabolism. 84: 401-4. PMID 10022391 DOI: 10.1210/Jcem.84.2.5534 |
0.449 |
|
| 1999 |
Gauthier K, Chassande O, Plateroti M, Roux JP, Legrand C, Pain B, Rousset B, Weiss R, Trouillas J, Samarut J. Different functions for the thyroid hormone receptors TRalpha and TRbeta in the control of thyroid hormone production and post-natal development. The Embo Journal. 18: 623-31. PMID 9927422 DOI: 10.1093/Emboj/18.3.623 |
0.507 |
|
| 1999 |
Weiss RE. Treatment of Resistance to Thyroid Hormone--Primum Non Nocere Journal of Clinical Endocrinology & Metabolism. 84: 401-404. DOI: 10.1210/Jc.84.2.401 |
0.449 |
|
| 1998 |
Weiss RE, Murata Y, Cua K, Hayashi Y, Seo H, Refetoff S. Thyroid Hormone Action on Liver, Heart, and Energy Expenditure in Thyroid Hormone Receptor β-Deficient Mice* * Presented in part at the 69th Annual Meeting of the American Thyroid Association Meeting, November 14-17, 1996, San Diego, California. This study was supported in part by the National Institutes of Health Grant DK-17050 and the Seymour J. Abrams Thyroid Research Center; a grant from the Ministry of Health and Welfare, Japan (to H.S.); and Grant-in-Aid for Scientific Research (09671044) from the Ministry of Education, Science and Culture of Japan. Endocrinology. 139: 4945-4952. PMID 28204239 DOI: 10.1210/Endo.139.12.6412 |
0.479 |
|
| 1998 |
Carvalho GA, Weiss RE, Refetoff S. Complete thyroxine-binding globulin (TBG) deficiency produced by a mutation in acceptor splice site causing frameshift and early termination of translation (TBG-Kankakee). The Journal of Clinical Endocrinology and Metabolism. 83: 3604-8. PMID 9768672 DOI: 10.1210/Jcem.83.10.5208 |
0.34 |
|
| 1998 |
Hayashi Y, Xie J, Weiss RE, Pohlenz J, Refetoff S. Selective pituitary resistance to thyroid hormone produced by expression of a mutant thyroid hormone receptor beta gene in the pituitary gland of transgenic mice. Biochemical and Biophysical Research Communications. 245: 204-10. PMID 9535809 DOI: 10.1006/Bbrc.1998.8396 |
0.533 |
|
| 1998 |
Carvalho GA, Weiss RE, Vladutiu AO, Refetoff S. Complete deficiency of thyroxine-binding globulin (TBG-CD Buffalo) caused by a new nonsense mutation in the thyroxine-binding globulin gene. Thyroid : Official Journal of the American Thyroid Association. 8: 161-5. PMID 9510125 DOI: 10.1089/Thy.1998.8.161 |
0.318 |
|
| 1998 |
Pohlenz J, Rosenthal IM, Weiss RE, Jhiang SM, Burant C, Refetoff S. Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site. The Journal of Clinical Investigation. 101: 1028-35. PMID 9486973 DOI: 10.1172/Jci1504 |
0.402 |
|
| 1998 |
Xie J, Pannain S, Pohlenz J, Weiss RE, Moltz K, Morlot M, Asteria C, Persani L, Beck-Peccoz P, Parma J, Vassart G, Refetoff S. Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSH. The Journal of Clinical Endocrinology and Metabolism. 82: 3933-40. PMID 9398691 DOI: 10.1210/Jcem.82.12.4418 |
0.418 |
|
| 1997 |
Weiss RE, Forrest D, Pohlenz J, Cua K, Curran T, Refetoff S. Thyrotropin Regulation by Thyroid Hormone in Thyroid Hormone Receptor β-Deficient Mice. Endocrinology. 138: 3624-3629. PMID 28200139 DOI: 10.1210/endo.138.9.5412 |
0.405 |
|
| 1997 |
Nagashima T, Yagi H, Nagashima K, Sakurai A, Onigata K, Nomura Y, Morikawa A, Matazow G, Couch RM, Weiss RE, Refetoff S. A novel point mutation of thyroid hormone receptor beta gene in a family with resistance to thyroid hormone. Thyroid : Official Journal of the American Thyroid Association. 7: 771-3. PMID 9349582 DOI: 10.1089/Thy.1997.7.771 |
0.531 |
|
| 1997 |
Weiss RE, Forrest D, Pohlenz J, Cua K, Curran T, Refetoff S. Thyrotropin regulation by thyroid hormone in thyroid hormone receptor beta-deficient mice. Endocrinology. 138: 3624-9. PMID 9275045 DOI: 10.1210/Endo.138.9.5412 |
0.485 |
|
| 1997 |
Weiss RE, Stein MA, Refetoff S. Behavioral effects of liothyronine (L-T3) in children with attention deficit hyperactivity disorder in the presence and absence of resistance to thyroid hormone Thyroid. 7: 389-393. PMID 9226208 DOI: 10.1089/Thy.1997.7.389 |
0.334 |
|
| 1997 |
Weiss RE, Tunca H, Knapple WL, Faas FH, Refetoff S. Phenotype differences of resistance to thyroid hormone in two unrelated families with an identical mutation in the thyroid hormone receptor beta gene (R320C). Thyroid : Official Journal of the American Thyroid Association. 7: 35-8. PMID 9086567 DOI: 10.1089/Thy.1997.7.35 |
0.531 |
|
| 1997 |
Refetoff S, Tunca H, Wilansky DL, Mussey VC, Weiss RE. Mutation in the thyroid hormone receptor (TR) beta gene (M313T) not previously reported in two unrelated families with resistance to thyroid hormone (RTH). Thyroid : Official Journal of the American Thyroid Association. 6: 571-3. PMID 9001191 DOI: 10.1089/Thy.1996.6.571 |
0.44 |
|
| 1997 |
Weiss RE, Refetoff S. Effect of thyroid hormone on growth. Lessons from the syndrome of resistance to thyroid hormone. Endocrinology and Metabolism Clinics of North America. 25: 719-30. PMID 8879995 DOI: 10.1016/S0889-8529(05)70349-2 |
0.457 |
|
| 1996 |
Weiss RE, Hayashi Y, Nagaya T, Petty KJ, Murata Y, Tunca H, Seo H, Refetoff S. Dominant inheritance of resistance to thyroid hormone not linked to defects in the thyroid hormone receptor α or β genes may be due to a defective cofactor Journal of Clinical Endocrinology and Metabolism. 81: 4196-4203. PMID 8954015 DOI: 10.1210/Jcem.81.12.8954015 |
0.544 |
|
| 1996 |
Weiss RE, Tunca H, Gerstein HC, Refetoff S. A new mutation in the thyroid hormone receptor (TR) beta gene (V458A) in a family with resistance to thyroid hormone (RTH). Thyroid : Official Journal of the American Thyroid Association. 6: 311-2. PMID 8875752 DOI: 10.1089/Thy.1996.6.311 |
0.522 |
|
| 1996 |
Refetoff S, Marinov VS, Tunca H, Byrne MM, Sunthornthepvarakul T, Weiss RE. A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study. The Journal of Clinical Endocrinology and Metabolism. 81: 3335-40. PMID 8784093 DOI: 10.1210/Jcem.81.9.8784093 |
0.467 |
|
| 1995 |
Refetoff S, Weiss RE, Wing JR, Sarne D, Chyna B, Hayashi Y. Resistance to thyroid hormone in subjects from two unrelated families is associated with a point mutation in the thyroid hormone receptor beta gene resulting in the replacement of the normal proline 453 with serine. Thyroid : Official Journal of the American Thyroid Association. 4: 249-54. PMID 7833659 DOI: 10.1089/Thy.1994.4.249 |
0.525 |
|
| 1995 |
Weiss RE, Sunthornthepvarakul T, Angkeow P, Marcus-Bagley D, Cox N, Alper CA, Refetoff S. Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred. The Journal of Clinical Endocrinology and Metabolism. 80: 116-21. PMID 7829599 DOI: 10.1210/Jcem.80.1.7829599 |
0.383 |
|
| 1995 |
Hayashi Y, Weiss RE, Sarne DH, Yen PM, Sunthornthepvarakul T, Marcocci C, Chin WW, Refetoff S. Do clinical manifestations of resistance to thyroid hormone correlate with the functional alteration of the corresponding mutant thyroid hormone-beta receptors? The Journal of Clinical Endocrinology and Metabolism. 80: 3246-56. PMID 7593433 DOI: 10.1210/Jcem.80.11.7593433 |
0.437 |
|
| 1994 |
Weiss RE, Stein MA, Duck SC, Chyna B, Phillips W, O'Brien T, Gutermuth L, Refetoff S. Low intelligence but not attention deficit hyperactivity disorder is associated with resistance to thyroid hormone caused by mutation R316H in the thyroid hormone receptor β gene Journal of Clinical Endocrinology and Metabolism. 78: 1525-1528. PMID 8200958 DOI: 10.1210/Jcem.78.6.8200958 |
0.491 |
|
| 1994 |
Weiss RE, Chyna B, Duell PB, Hayashi Y, Sunthornthepvarakul T, Refetoff S. A new point mutation (C446R) in the thyroid hormone receptor-beta gene of a family with resistance to thyroid hormone. The Journal of Clinical Endocrinology and Metabolism. 78: 1253-6. PMID 8175986 DOI: 10.1210/Jcem.78.5.8175986 |
0.514 |
|
| 1994 |
Sunthornthepvarakul T, Angkeow P, Weiss RE, Hayashi Y, Refetoff S. An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families. Biochemical and Biophysical Research Communications. 202: 781-7. PMID 8048949 DOI: 10.1006/Bbrc.1994.1998 |
0.36 |
|
| 1993 |
Weiss RE, Weinberg M, Refetoff S. Identical mutations in unrelated families with generalized resistance to thyroid hormone occur in cytosine-guanine-rich areas of the thyroid hormone receptor beta gene. Analysis of 15 families. The Journal of Clinical Investigation. 91: 2408-15. PMID 8514853 DOI: 10.1172/Jci116474 |
0.47 |
|
| 1993 |
Hayashi Y, Janssen OE, Weiss RE, Murata Y, Seo H, Refetoff S. The relative expression of mutant and normal thyroid hormone receptor genes in patients with generalized resistance to thyroid hormone determined by estimation of their specific messenger ribonucleic acid products. The Journal of Clinical Endocrinology and Metabolism. 76: 64-9. PMID 8421105 DOI: 10.1210/Jcem.76.1.8421105 |
0.492 |
|
| 1993 |
Weiss RE, Marcocci C, Bruno-Bossio G, Refetoff S. Multiple genetic factors in the heterogeneity of thyroid hormone resistance. The Journal of Clinical Endocrinology and Metabolism. 76: 257-9. PMID 8421095 DOI: 10.1210/Jcem.76.1.8421095 |
0.5 |
|
| 1993 |
Weiss RE, Stein MA, Trommer B, Refetoff S. Attention-deficit hyperactivity disorder and thyroid function The Journal of Pediatrics. 123: 539-545. PMID 8410504 DOI: 10.1016/S0022-3476(05)80947-3 |
0.358 |
|
| 1993 |
Refetoff S, Weiss RE, Usala SJ. The syndromes of resistance to thyroid hormone. Endocrine Reviews. 14: 348-99. PMID 8319599 DOI: 10.1210/Edrv-14-3-348 |
0.509 |
|
| 1993 |
Hayashi Y, Mori Y, Janssen OE, Sunthornthepvarakul T, Weiss RE, Takeda K, Weinberg M, Seo H, Bell GI, Refetoff S. Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation. Molecular Endocrinology (Baltimore, Md.). 7: 1049-60. PMID 8232304 DOI: 10.1210/Mend.7.8.8232304 |
0.35 |
|
| 1992 |
Weiss RE, Refetoff S. Thyroid hormone resistance. Annual Review of Medicine. 43: 363-75. PMID 1580595 DOI: 10.1146/Annurev.Me.43.020192.002051 |
0.516 |
|
| 1992 |
Takeda K, Weiss RE, Refetoff S. Rapid localization of mutations in the thyroid hormone receptor-beta gene by denaturing gradient gel electrophoresis in 18 families with thyroid hormone resistance. The Journal of Clinical Endocrinology and Metabolism. 74: 712-9. PMID 1548332 DOI: 10.1210/Jcem.74.4.1548332 |
0.456 |
|
| 1990 |
Weiss RE. Neonatal detection of generalized resistance to thyroid hormone Jama: the Journal of the American Medical Association. 264: 2245-2250. DOI: 10.1001/Jama.1990.03450170093029 |
0.465 |
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