Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Bojana, Pencheva"'
Autor:
Kristen Murphey, Paul E. George, Bojana Pencheva, Christopher C. Porter, Stephanie Burns Wechsler, Michael J. Gambello, Hong Li
Publikováno v:
American Journal of Medical Genetics Part A. 188:2707-2711
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b230bfc9b7d3c23b9fefb4623ea39f3b
https://doi.org/10.1002/ajmg.a.62891
https://doi.org/10.1002/ajmg.a.62891
Autor:
Sarah Mitchell, Santiago Arconada Alvarez, Bojana Pencheva, Eleanor Westfall, Comfort Mwalija, Maren Parsell, Morgan Greenleaf, Christopher C Porter, Wilbur Lam, Robert Mannino G
Background: At least 5-10% of malignancies occur secondary to an underlying cancer predisposition syndrome (CPS). For patients with a CPS, cancer surveillance is recommended with the goal of identifying malignancy earlier, in a presumably more curabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a66eb97581558ec926be751eb0705d8
https://doi.org/10.22541/au.167446805.56326115/v1
https://doi.org/10.22541/au.167446805.56326115/v1
Autor:
Ryan J. Summers, Sharon M. Castellino, Christopher C. Porter, Tobey J. MacDonald, Gargi D. Basu, Szabolcs Szelinger, Manoj K. Bhasin, Thomas Cash, Alexis B. Carter, Robert Craig Castellino, Jason R. Fangusaro, Sarah G. Mitchell, Melinda G. Pauly, Bojana Pencheva, Daniel S. Wechsler, Douglas K. Graham, Kelly C. Goldsmith
Publikováno v:
JCO Precision Oncology.
PURPOSE Profiling of pediatric cancers through deep sequencing of large gene panels and whole exomes is rapidly being adopted in many clinical settings. However, the most impactful approach to genomic profiling of pediatric cancers remains to be defi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0567d9235f069d2875288cfb40bba246
https://doi.org/10.1200/po.21.00451
https://doi.org/10.1200/po.21.00451
Autor:
Joyce Turner, Kami Wolfe Schneider, Christopher C. Porter, Cecelia Bellcross, Olivia A Juarez, Bojana Pencheva
Publikováno v:
Journal of Genetic Counseling. 30:710-719
Previous surveys of adults with cancer have revealed increased levels of genetic knowledge, varying levels of worry, and high satisfaction with cancer genetic counseling. We sought to determine the impact of cancer genetic counseling on parental leve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45f605caf936d0fe4c9535ae3e1c2b9a
https://doi.org/10.1002/jgc4.1357
https://doi.org/10.1002/jgc4.1357
Autor:
Glaivy Batsuli, Sanyukta K. Janardan, Heidi Karpen, Anthony Ross, Bojana Pencheva, Heather Rytting
Publikováno v:
Pediatrics.
Severe combined immunodeficiency (SCID) consists of a group of disorders defined by abnormal B and T cell development that typically results in death within the first year of life if undiagnosed or untreated. Reticular dysgenesis (RD) is a rare but e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f48843ffc5f15a6d97326089b584497
https://pubmed.ncbi.nlm.nih.gov/34814161
https://pubmed.ncbi.nlm.nih.gov/34814161
Publikováno v:
Clinics in perinatology. 48(1)
Pediatric cancer is rare, and malignancy during the neonatal period even rarer. However, several malignancies can present in infancy, most commonly in the form of solid tumors. Specific cancer types, bilateral or multifocal disease, associated congen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a2db504afe695e8e64fac6c3dfba946
https://pubmed.ncbi.nlm.nih.gov/33583498
https://pubmed.ncbi.nlm.nih.gov/33583498
Autor:
Kristen Ferriero, Michael J. Gambello, Christopher C. Porter, Hong Li, Bojana Pencheva, Paul George
Publikováno v:
Molecular Genetics and Metabolism. 132:S18-S19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d60f0f7a816d4e6ab05dbee46eac6a83
https://doi.org/10.1016/s1096-7192(21)00113-x
https://doi.org/10.1016/s1096-7192(21)00113-x
Publikováno v:
Current oncology reports. 21(10)
Germline genetic variants contribute to a substantial proportion of cases of cancer in childhood. The purpose of this review is to describe two emerging pediatric cancer predisposition syndromes, including published surveillance protocols, as well as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93773de5f3a87fc35256b89dde28eba
https://pubmed.ncbi.nlm.nih.gov/31414239
https://pubmed.ncbi.nlm.nih.gov/31414239