Sosipatros A. Boikos

Author

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

Also Known As

Boikos, Sosipatros, S A Boikos, S Boikos, S. Boikos, Sosipatros A Boikos, Sosipatros A. Boikos, Sosipatros Alexandros Boikos, Sosipatros Boikos

216

Publications

5.1K

Citations

H-Index

Concepts

All Affiliations

Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health Virginia Commonwealth University National Cancer Institute Massachusetts General Hospital

About

Sosipatros A. Boikos is an author at Eunice Kennedy Shriver National Institute of Child Health and Human Development specializing in medicine, pathology, and tumor biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	14	1.3K
2	Health Sciences	3	3	122
3	Engineering	1	1	13
4	Social Sciences	1	1	116
5	Biochemistry	1	1	116

Sosipatros A. Boikos

Publications

4.1K

Citations

H-Index

Page 1

	Year	Citations
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
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
Molecular Subtypes of<i>KIT/PDGFRA</i>Wild-Type Gastrointestinal Stromal Tumors Sosipatros A. Boikos, Alberto S. Pappo, J. Keith Killian, JAMA Oncology	2016	383
A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia Anélia Horvath, Sosipatros A. Boikos, Christoforos Giatzakis, Nature Genetics Adrenal GlandEndocrine DiseaseGenetic DisorderGeneticsAdrenal Health	2006	342
The role of germline <i>AIP</i>, <i>MEN1, PRKAR1A</i>, <i>CDKN1B</i> and <i>CDKN2C</i> mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes MA Tichomirowa, Sosipatros A. Boikos, MF Azevedo, Clinical Genetics	2010	207
Recurrent epimutation of<i>SDHC</i>in gastrointestinal stromal tumors Jonathan Keith Killian, Markku Miettinen, Robert L. Walker, Science Translational Medicine	2014	191
Clinical and Genetic Heterogeneity, Overlap with Other Tumor Syndromes, and Atypical Glucocorticoid Hormone Secretion in Adrenocorticotropin-Independent Macronodular Adrenal Hyperplasia Compared with Other Adrenocortical Tumors Hui‐Pin Hsiao, Lawrence S. Kirschner, Isabelle Bourdeau, The Journal of Clinical Endocrinology & Metabolism	2009	176
Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors Ludmila Matyakhina, Thalia Bei, Sarah R. McWhinney, The Journal of Clinical Endocrinology & Metabolism	2007	150
<i>MYCN</i> -Amplified Neuroblastoma Is Addicted to Iron and Vulnerable to Inhibition of the System Xc-/Glutathione Axis Konstantinos V. Floros, Jinyang Cai, Sheeba Jacob, Cancer Research	2021	143
Venetoclax Is Effective in Small-Cell Lung Cancers with High BCL-2 Expression Timothy L. Lochmann, Konstantinos V. Floros, Mitra Naseri, Clinical Cancer Research	2017	127

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