Eirini I. Bimpaki - Concepedia

Author

Eirini I. Bimpaki

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Also Known As

E Bimpaki, E. Bimpaki, Eirini Bimpaki, Eirini I Bimpaki, Eirini I. Bimpaki

Publications

688

Citations

H-Index

Concepts

All Affiliations

Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health Harvard University Johns Hopkins University

About

Eirini I. Bimpaki is an author at Eunice Kennedy Shriver National Institute of Child Health and Human Development.

Eirini I. Bimpaki

Publications

362

Citations

H-Index

Page 1

	Year	Citations
MicroRNA Signature of Primary Pigmented Nodular Adrenocortical Disease: Clinical Correlations and Regulation of <i>Wnt</i> Signaling Dimitrios Iliopoulos, Eirini I. Bimpaki, Maria Nesterova, Cancer Research	2009	74
Activation of Cyclic AMP Signaling Leads to Different Pathway Alterations in Lesions of the Adrenal Cortex Caused by Germline PRKAR1A Defects versus Those due to Somatic GNAS Mutations Madson Q. Almeida, Monalisa Ferreira Azevedo, Paraskevi Xekouki, The Journal of Clinical Endocrinology & Metabolism	2012	68
MicroRNA signature in massive macronodular adrenocortical disease and implications for adrenocortical tumourigenesis Eirini I. Bimpaki, Dimitrios Iliopoulos, Andreas Moraitis, Clinical Endocrinology	2009	62
Integrated Genomic Analysis of Nodular Tissue in Macronodular Adrenocortical Hyperplasia: Progression of Tumorigenesis in a Disorder Associated with Multiple Benign Lesions Madson Q. Almeida, Michelle D. Harran, Eirini I. Bimpaki, The Journal of Clinical Endocrinology & Metabolism	2011	49
Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes Eirini I. Bimpaki, Maria Nesterova, Constantine A. Stratakis European Journal of Endocrinology	2009	39
Association of the M1V<i>PRKAR1A</i>Mutation with Primary Pigmented Nodular Adrenocortical Disease in Two Large Families Alberto M. Pereira, Frederik J. Hes, Anélia Horvath, The Journal of Clinical Endocrinology & Metabolism	2009	34
<i>In Vitro</i>Studies of Novel<i>PRKAR1A</i>Mutants that Extend the Predicted RIα Protein Sequence into the 3′-Untranslated Open Reading Frame: Proteasomal Degradation Leads to RIα Haploinsufficiency and Carney Complex Yianna Patronas, Anélia Horvath, Elizabeth Greene, The Journal of Clinical Endocrinology & Metabolism	2011	21
An Intronic Mutation is Associated with Prolactinoma in a Young Boy, Decreased Penetrance in his Large Family, and Variable Effects on<i>MEN1 mRNA</i>and Protein Limor Drori-Herishanu, Anélia Horvath, Maria Nesterova, Hormone and Metabolic Research	2009	15

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