Ursula

Ursula Kaiser, M.D.

Professor of Medicine
617-525-8867
Harvard Catalyst Profile
Harvard Title

Professor of Medicine

Address

Brigham and Women's Hospital
Endocrine RFB 296
221 Longwood Ave
Boston MA 02115

Publications View
Editorial: The Rise of the Asterisk: One Step to Facilitate Team Science.
Authors: Goldberg MA, Kaiser UB.
Mol Endocrinol
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Cushing's disease: towards precision medicine.
Authors: Kaiser UB.
Cell Res
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Substance p regulates puberty onset and fertility in the female mouse.
Authors: Simavli S, Thompson IR, Maguire CA, Gill JC, Carroll RS, Wolfe A, Kaiser UB, Navarro VM.
Endocrinology
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A new pathway in the control of the initiation of puberty: the MKRN3 gene.
Authors: Abreu AP, Macedo DB, Brito VN, Kaiser UB, Latronico AC.
J Mol Endocrinol
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Systemic high-dose corticosteroid treatment does not improve the outcome of ipilimumab-related hypophysitis: a retrospective cohort study.
Authors: Min L, Hodi FS, Giobbie-Hurder A, Ott PA, Luke JJ, Donahue H, Davis M, Carroll RS, Kaiser UB.
Clin Cancer Res
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The integrated hypothalamic tachykinin-kisspeptin system as a central coordinator for reproduction.
Authors: Navarro VM, Bosch MA, León S, Simavli S, True C, Pinilla L, Carroll RS, Seminara SB, Tena-Sempere M, Rønnekleiv OK, Kaiser UB.
Endocrinology
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KISS1R signals independently of Gaq/11 and triggers LH secretion via the ß-arrestin pathway in the male mouse.
Authors: Ahow M, Min L, Pampillo M, Nash C, Wen J, Soltis K, Carroll RS, Glidewell-Kenney CA, Mellon PL, Bhattacharya M, Tobet SA, Kaiser UB, Babwah AV.
Endocrinology
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Editorial: advances in neuroscience: the BRAIN initiative and implications for neuroendocrinology.
Authors: Kaiser UB.
Mol Endocrinol
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Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay.
Authors: Beneduzzi D, Trarbach EB, Min L, Jorge AA, Garmes HM, Renk AC, Fichna M, Fichna P, Arantes KA, Costa EM, Zhang A, Adeola O, Wen J, Carroll RS, Mendonça BB, Kaiser UB, Latronico AC, Silveira LF.
Fertil Steril
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Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.
Authors: Macedo DB, Abreu AP, Reis AC, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LF, Teles MG, Carroll RS, Junior GG, Filho GG, Gucev Z, Arnhold IJ, de Castro M, Moreira AC, Martinelli CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC.
J Clin Endocrinol Metab
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