Constantine A. Stratakis

Author

Eunice Kennedy Shriver National Institute of Child Health and Human Development ORCID

Also Known As

A Boyce, A. Stratakis, Constantine, C A Stratakis, C A. Stratakis, C STRATAKIS, C Stratakis, C. A Stratakis, C. A. STRATAKIS, C. A. Stratakis, C. Stratakis

1.9K

Publications

48.2K

Citations

110

H-Index

314

Concepts

All Affiliations

Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health National Cancer Institute National Institutes of Health Clinical Center Inserm

About

Constantine A. Stratakis is an author at Eunice Kennedy Shriver National Institute of Child Health and Human Development specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	58	186	13.4K
2	Health Sciences	13	17	480
3	Natural Sciences	9	9	599
4	Engineering	4	4	514
5	Education	3	3	95

Constantine A. Stratakis

415

Publications

31.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex Lawrence S. Kirschner, J. Aidan Carney, Svetlana Pack, Nature Genetics Transcriptional RegulationSignal TransductionMolecular PhysiologySignaling PathwayMolecular Regulation	2000	1.1K
Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking <i>KIT</i> and <i>PDGFRA</i> mutations Katherine A. Janeway, Su Young Kim, Maya Lodish, Proceedings of the National Academy of Sciences Complex Ii ActivitySuccinate DehydrogenaseSomatic VariantAlcohol DehydrogenasesBiochemistry	2010	603
An inherited <i>p53</i> mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma Raul C. Ribeiro, Fabiano Sandrini, Bonald C. Figueiredo, Proceedings of the National Academy of Sciences	2001	530
Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD Barbara Pasini, Sarah R. McWhinney, Thalia Bei, European Journal of Human Genetics Genetic DisorderMedicineGeneticsInherited Metabolic DiseaseMolecular Biology	2007	482
Bone Mineral Density in Women with Depression David Michelson, Constantine A. Stratakis, Lauren Hill, New England Journal of Medicine	1996	469
Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2. Constantine A. Stratakis, J A Carney, Jing‐Ping Lin, Journal of Clinical Investigation Short ArmBlood SamplesMendelian DisorderFamily MembersGenetic Disorder	1996	457
Mutations in Regulatory Subunit Type 1A of Cyclic Adenosine 5′-Monophosphate-Dependent Protein Kinase (<i>PRKAR1A</i>): Phenotype Analysis in 353 Patients and 80 Different Genotypes Jérôme Bertherat, Anélia Horvath, Lionel Groussin, The Journal of Clinical Endocrinology & Metabolism	2009	432
Constitutive Activation of PKA Catalytic Subunit in Adrenal Cushing's Syndrome Felix Beuschlein, Guillaume Assié, Davide Calebiro, New England Journal of Medicine	2014	423
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes Rainer Ruf, Pin‐Xian Xu, Derek Silvius, Proceedings of the National Academy of Sciences	2004	417
Chronic insomnia and activity of the stress system Alexandros N. Vgontzas, Constantine Tsigos, Edward O. Bixler, Journal of Psychosomatic Research Sleep DisordersSleepSleep DisorderPsychiatryPsychology	1998	398

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