M
Maria A Yialamas
Researcher at Brigham and Women's Hospital
Publications - 41
Citations - 3130
Maria A Yialamas is an academic researcher from Brigham and Women's Hospital. The author has contributed to research in topics: Insulin resistance & Insulin. The author has an hindex of 14, co-authored 39 publications receiving 2520 citations. Previous affiliations of Maria A Yialamas include Harvard University & Boston Children's Hospital.
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Journal ArticleDOI
Testosterone Therapy in Men With Hypogonadism: An Endocrine Society Clinical Practice Guideline
Shalender Bhasin,Juan P. Brito,Glenn R. Cunningham,Frances J. Hayes,Howard N. Hodis,Alvin M. Matsumoto,Peter J. Snyder,Ronald S. Swerdloff,Frederick C. W. Wu,Maria A Yialamas +9 more
TL;DR: It is suggested that when clinicians institute T therapy, they aim at achieving T concentrations in the mid-normal range during treatment with any of the approved formulations, taking into consideration patient preference, pharmacokinetics, formulation-specific adverse effects, treatment burden, and cost.
Journal ArticleDOI
Increasing insulin resistance is associated with a decrease in Leydig cell testosterone secretion in men.
Nelly Pitteloud,Megan Hardin,Andrew A. Dwyer,Elena Valassi,Maria A Yialamas,Dariush Elahi,Dariush Elahi,Frances J. Hayes +7 more
TL;DR: It is concluded that insulin resistance is associated with a decrease in Leydig cell T secretion in men with a spectrum of insulin sensitivity.
Journal ArticleDOI
Relationship Between Testosterone Levels, Insulin Sensitivity, and Mitochondrial Function in Men
Nelly Pitteloud,Vamsi K. Mootha,Andrew A. Dwyer,Megan Hardin,Hang Lee,Karl-Fredrik Eriksson,Devjit Tripathy,Maria A Yialamas,Leif Groop,Dariush Elahi,Frances J. Hayes +10 more
TL;DR: These data indicate that low serum testosterone levels are associated with an adverse metabolic profile and suggest a novel unifying mechanism for the previously independent observations that low testosterone levels and impaired mitochondrial function promote insulin resistance in men.
Journal ArticleDOI
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
Hichem Miraoui,Andrew A. Dwyer,Andrew A. Dwyer,Gerasimos P. Sykiotis,Gerasimos P. Sykiotis,Lacey Plummer,Wilson C. J. Chung,Bihua Feng,Andrew Beenken,Jeffrey A Clarke,Tune H. Pers,Tune H. Pers,Tune H. Pers,Piotr Dworzynski,Kimberley Keefe,Marek Niedziela,Taneli Raivio,William F. Crowley,Stephanie B. Seminara,Richard Quinton,Virginia A. Hughes,Virginia A. Hughes,Philip Kumanov,Jacques Young,Maria A Yialamas,Janet E. Hall,Guy Van Vliet,Jean-Pierre Chanoine,John L.R. Rubenstein,Moosa Mohammadi,Pei-San Tsai,Yisrael Sidis,Yisrael Sidis,Kasper Lage,Nelly Pitteloud,Nelly Pitteloud +35 more
TL;DR: It is hypothesized that mutations in genes encoding a broader range of modulators of the FGFR1 pathway might contribute to the genetics of CHH as causal or modifier mutations and validate the ability of a bioinformatics algorithm on the basis of protein-protein interactome data (interactome-based affiliation scoring [IBAS]) to identify high-quality candidate genes.
Journal ArticleDOI
Mutations in Fibroblast Growth Factor Receptor 1 Cause Both Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism
Nelly Pitteloud,James S. Acierno,Astrid U. Meysing,Anna V. Eliseenkova,Jinghong Ma,Omar A. Ibrahimi,Daniel Metzger,Frances J. Hayes,Andrew A. Dwyer,Virginia A. Hughes,Maria A Yialamas,Janet E. Hall,Ellen Grant,Moosa Mohammadi,William F. Crowley +14 more
TL;DR: It is concluded that loss-of-function mutations in FGFR1 cause nIHH with normal MRI of the olfactory system and also account for some of the mixed pedigrees, thus challenging the current idea that KS and nI HH are distinct entities.