Výsledky vyhledávání - "Kristen Pauley"

Akademický článek

P083: Incidental findings in FH and SDHA genes: Navigating cancer risk assessment and follow-up recommendations

Autor: Wendy Kohlmann, Kristen Pauley, Anne Naumer, Samantha Greenberg, Nicole Stevenson, Kelsey Ellis, Aciana Franco Roberts, Joshua Kawasaki, Taylor Jump, Nykole Sutherland

Publikováno v: Genetics in Medicine Open, Vol 1, Iss 1, Pp 100102- (2023)

Externí odkaz: https://doaj.org/article/cd0df1a57aca4b658f19e099880600ef

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Akademický článek

Considerations for Germline Testing in Melanoma: Updates in Behavioral Change and Pancreatic Surveillance for Carriers of CDKN2A Pathogenic Variants

Autor: Kristen Pauley, Ambreen Khan, Wendy Kohlmann, Joanne Jeter

Publikováno v: Frontiers in Oncology, Vol 12 (2022)

The largest proportion of hereditary melanoma cases are due to pathogenic variants (PVs) in the CDKN2A/p16 gene, which account for 20%-40% of familial melanomas and confer up to a 30%-70% lifetime risk for melanoma in individuals with these variants.

Externí odkaz: https://doaj.org/article/f8a9ecfa77fd4540b1f4bff461b9e9a8

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V05-10 ROBOTIC BILATERAL PARTIAL ADRENALECTOMY FOR TREATMENT OF VON HIPPEL-LINDAU ASSOCIATED BILATERAL PHEOCHROMOCYTOMA

Autor: Kassandra Dindinger-Hill, Kristen Pauley, Benjamin Maughan, Bogdana Schmidt, Brock O'Neil, Christopher Dechet, Alejandro Sanchez

Publikováno v: Journal of Urology. 209

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::96097a539a78e25d2cf6cd445b24c63d
https://doi.org/10.1097/ju.0000000000003263.10

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Considerations for Germline Testing in Melanoma: Updates in Behavioral Change and Pancreatic Surveillance for Carriers of

Autor: Kristen, Pauley, Ambreen, Khan, Wendy, Kohlmann, Joanne, Jeter

Publikováno v: Frontiers in oncology. 12

The largest proportion of hereditary melanoma cases are due to pathogenic variants (PVs) in the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dc9bd8db105b2dcf27b0809692650a33
https://pubmed.ncbi.nlm.nih.gov/35372037

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Case series examining somatic test results for patients with hereditary cancer syndromes associated with gastrointestinal cancer risk

Autor: Ignacio Garrido-Laguna, Jennie Vagher, Christopher Nevala-Plagemann, Samantha Greenberg, Glynn Weldon Gilcrease, Gammon Amanda, Kristen Pauley, Cathryn Koptiuch, Wendy Kohlmann, Whitney Espinel

Publikováno v: Journal of Clinical Oncology. 38:680-680

680 Background: Somatic tumor testing may identify germline pathogenic variants (PV) associated with cancer predisposition syndromes. Labs differ whether they offer somatic only or paired germline analysis. Methods used by somatic testing labs, even

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6905a9dada2825c4c87d3b793de1beff
https://doi.org/10.1200/jco.2020.38.4_suppl.680

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