Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Vanessa, Marcell"'
Autor:
Robert C. Kurtz, Kenneth Offit, Peter J. Allen, Zsofia K. Stadler, Vanessa Marcell, Erin Salo-Mullen, Marguerite L. Samson, Xiaolin Liang, Pamela Nunes, Sara H. Olson, Amethyst Saldia
Supplemental Table 2. Secondary analysis findings among high-risk BRCA1/2 individuals with IPMNs who have >1 affected relative with pancreas cancer but no affected first-degree relatives (n=7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cb4b3f090401ab2d4face9913e24f0e
https://doi.org/10.1158/1940-6207.22533349.v1
https://doi.org/10.1158/1940-6207.22533349.v1
Autor:
Robert C. Kurtz, Kenneth Offit, Peter J. Allen, Zsofia K. Stadler, Vanessa Marcell, Erin Salo-Mullen, Marguerite L. Samson, Xiaolin Liang, Pamela Nunes, Sara H. Olson, Amethyst Saldia
Germline mutations in BRCA1/2 are risk factors for pancreatic ductal adenocarcinoma (PDAC). The aim of this study was to evaluate whether results of surveillance for PDAC in high risk individuals (HRI) differ between those with and without a pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81d5b5bf2265ebdaa00b2fbab59030e
https://doi.org/10.1158/1940-6207.c.6547036
https://doi.org/10.1158/1940-6207.c.6547036
Autor:
Robert C. Kurtz, Kenneth Offit, Peter J. Allen, Zsofia K. Stadler, Vanessa Marcell, Erin Salo-Mullen, Marguerite L. Samson, Xiaolin Liang, Pamela Nunes, Sara H. Olson, Amethyst Saldia
Supplemental Table 1. Main analysis findings among high-risk individuals with IPMNs who have at least one affected first-degree relative with pancreas cancer (n=27)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bde2acc9017fc70432f6283781f6518
https://doi.org/10.1158/1940-6207.22533352
https://doi.org/10.1158/1940-6207.22533352
Autor:
David B. Solit, Angela G. Arnold, Mark E. Robson, Diana Mandelker, Michael F. Berger, Shweta S. Chavan, Maksym Misyura, Michael Walsh, Anna Maio, Sarah R. Kane, Karen Cadoo, Yelena Kemel, Preethi Srinivasan, Ying Liu, Jinru Shia, Kenneth Offit, Kelsey Breen, Jennifer Kennedy, Margaret Sheehan, Semanti Mukherjee, Caitlin Bourque, Chaitanya Bandlamudi, Zalak Patel, Maria I. Carlo, Zsofia K. Stadler, Amanda Catchings, Erin E. Salo-Mullen, Arnold J. Markowitz, Barry S. Taylor, Prince Rainier Tejada, Rosalba Sacca, Vanessa Marcell, Alicia Latham, Ozge Ceyhan-Birsoy, Mark T.A. Donoghue, Kimberly Amoroso, Megha Ranganathan
Publikováno v:
JCO Precision Oncology. :455-465
PURPOSE NTHL1 and MSH3 have been implicated as autosomal recessive cancer predisposition genes. Although individuals with biallelic NTHL1 and MSH3 pathogenic variants (PVs) have increased cancer and polyposis risk, risks for monoallelic carriers are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba859253338af25f8aa87589967d494
https://doi.org/10.1200/po.20.00443
https://doi.org/10.1200/po.20.00443
Autor:
Kelly M. Morgan, Jada G. Hamilton, Heather Symecko, Daniella Kamara, Colby Jenkins, Jenny Lester, Kelsey Spielman, Lydia E. Pace, Camila Gabriel, Jeffrey D. Levin, Prince Rainier Tejada, Anthony Braswell, Vanessa Marcell, Temima Wildman, Bryan Devolder, Robin Camhi Baum, Jeremy N. Block, Yuri Fesko, Kylin Boehler, Victoria Howell, Jacob Heitler, Mark E. Robson, Katherine L. Nathanson, Nadine Tung, Beth Y. Karlan, Susan M. Domchek, Judy E. Garber, Kenneth Offit
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics, vol 24, iss 3
Genet Med
Genet Med
PurposeThis study aimed to evaluate uptake and follow-up using internet-assisted population genetic testing (GT) for BRCA1/2 Ashkenazi Jewish founder pathogenic variants (AJPVs).MethodsAcross 4 cities in the United States, from December 2017 to March
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3283c07b2c89d138d0c553ef9e9ede4
https://escholarship.org/uc/item/3g27c893
https://escholarship.org/uc/item/3g27c893
Autor:
Kelsey E. Breen, Bryson W. Katona, Amanda Catchings, Megha Ranganathan, Vanessa Marcell, Alicia Latham, Matthew B. Yurgelun, Zsofia K. Stadler
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(12)
With the recent guideline change for individuals at average risk for colorectal cancer (CRC) to initiate colonoscopy at the age of 45 years, there is a need to provide an updated counseling framework for individuals with variants in moderate-penetran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fb48956878ed2766da254f638c4b26f
https://pubmed.ncbi.nlm.nih.gov/36222830
https://pubmed.ncbi.nlm.nih.gov/36222830
Autor:
Liying Zhang, Erin E. Salo-Mullen, Vanessa Marcell, Zarina Yelskaya, Vivian E. Strong, Laura H. Tang, Angela G. Arnold, Zsofia K. Stadler
Publikováno v:
Eur J Hum Genet
Hereditary Diffuse Gastric Cancer (HDGC) syndrome is associated with CDH1 germline likely pathogenic/pathogenic variants. Carriers of CDH1 germline likely pathogenic/pathogenic variants are predisposed to diffuse gastric cancer and lobular breast can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7192e7ade52ee8621a3e3ea11891db57
https://europepmc.org/articles/PMC8298625/
https://europepmc.org/articles/PMC8298625/
Autor:
Erin E, Salo-Mullen, Anna, Maio, Semanti, Mukherjee, Chaitanya, Bandlamudi, Jinru, Shia, Yelena, Kemel, Karen A, Cadoo, Ying, Liu, Maria, Carlo, Megha, Ranganathan, Sarah, Kane, Preethi, Srinivasan, Shweta S, Chavan, Mark T A, Donoghue, Caitlin, Bourque, Margaret, Sheehan, Prince Rainier, Tejada, Zalak, Patel, Angela G, Arnold, Jennifer A, Kennedy, Kimberly, Amoroso, Kelsey, Breen, Amanda, Catchings, Rosalba, Sacca, Vanessa, Marcell, Arnold J, Markowitz, Alicia, Latham, Michael, Walsh, Maksym, Misyura, Ozge, Ceyhan-Birsoy, David B, Solit, Michael F, Berger, Mark E, Robson, Barry S, Taylor, Kenneth, Offit, Diana, Mandelker, Zsofia K, Stadler
Publikováno v:
JCO Precis Oncol
NTHL1 and MSH3 have been implicated as autosomal recessive cancer predisposition genes. Although individuals with biallelic NTHL1 and MSH3 pathogenic variants (PVs) have increased cancer and polyposis risk, risks for monoallelic carriers are uncertai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::570d76aa04006e2cfd20804e33478a42
https://pubmed.ncbi.nlm.nih.gov/34250384
https://pubmed.ncbi.nlm.nih.gov/34250384
Autor:
Pamela Nunes, Vanessa Marcell, Peter J. Allen, Robert C. Kurtz, Marguerite Samson, Xiaolin Liang, Zsofia K. Stadler, Sara H. Olson, Erin E. Salo-Mullen, Amethyst Saldia, Kenneth Offit
Germline mutations in BRCA1/2 are risk factors for pancreatic ductal adenocarcinoma (PDAC). The aim of this study was to evaluate whether results of surveillance for PDAC in high risk individuals (HRI) differ between those with and without a pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::873a03ce339a88784411f3a45249476f
https://europepmc.org/articles/PMC6726560/
https://europepmc.org/articles/PMC6726560/
Autor:
Vivian E. Strong, Angela G. Arnold, Zarina Yelskaya, Laura H. Tang, Vanessa Marcell, Zsofia K. Stadler, Liying Zhang, Erin E. Salo-Mullen
Publikováno v:
Eur J Hum Genet
Hereditary Diffuse Gastric Cancer (HDGC) syndrome is associated with CDH1 germline likely pathogenic/pathogenic variants. Carriers of CDH1 germline likely pathogenic/pathogenic variants are predisposed to diffuse gastric cancer and lobular breast can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c71b1bed35bc04a807e865819e5bf74
https://doi.org/10.1038/s41431-021-00895-w
https://doi.org/10.1038/s41431-021-00895-w