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Uptake of Cancer Genetic Services for Chatbot vs Standard-of-Care Delivery Models: The BRIDGE Randomized Clinical Trial. JAMA Netw Open. 2024 Sep 03; 7(9):e2432143.
Kaphingst KA, Kohlmann WK, Lorenz Chambers R, Bather JR, Goodman MS, Bradshaw RL, Chavez-Yenter D, Colonna SV, Espinel WF, Everett JN, Flynn M, Gammon A, Harris A, Hess R, Kaiser-Jackson L, Lee S, Monahan R, Schiffman JD, Volkmar M, Wetter DW, Zhong L, Mann DM, Ginsburg O, Sigireddi M, Kawamoto K, Del Fiol G, Buys SS. PMID: 39250153; PMCID: PMC11385050.
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PubMed Mentions: Fields:
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The role of family history in predicting germline pathogenic variant carriers who develop pancreatic cancer: Results of a multicenter collaboration. Cancer. 2024 Oct 01; 130(19):3297-3304.
Karloski E, Dudley B, Diergaarde B, Blanco A, Everett JN, Levinson E, Rangarajan T, Stanich PP, Childers K, Brown S, Drogan C, Cavestro GM, Gordon K, Singh A, Simeone DM, Reich H, Kastrinos F, Zakalik D, Hampel H, Pearlman R, Gordon OK, Kupfer SS, Puzzono M, Zuppardo RA, Brand RE. PMID: 38809542; PMCID: PMC11371512.
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Humans
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The Pancreatic Cancer Early Detection (PRECEDE) Study is a Global Effort to Drive Early Detection: Baseline Imaging Findings in High-Risk Individuals. J Natl Compr Canc Netw. 2024 04; 22(3):158-166.
Zogopoulos G, Haimi I, Sanoba SA, Everett JN, Wang Y, Katona BW, Farrell JJ, Grossberg AJ, Paiella S, Klute KA, Bi Y, Wallace MB, Kwon RS, Stoffel EM, Wadlow RC, Sussman DA, Merchant NB, Permuth JB, Golan T, Raitses-Gurevich M, Lowy AM, Liau J, Jeter JM, Lindberg JM, Chung DC, Earl J, Brentnall TA, Schrader KA, Kaul V, Huang C, Chandarana H, Smerdon C, Graff JJ, Kastrinos F, Kupfer SS, Lucas AL, Sears RC, Brand RE, Parmigiani G, Simeone DM, PRECEDE Consortium. PMID: 38626807.
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1 Fields:
Translation:
Humans
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Racial, Ethnic, and Sex-based Disparities among High-risk Individuals Undergoing Pancreatic Cancer Surveillance. Cancer Prev Res (Phila). 2023 06 01; 16(6):343-352.
Katona BW, Klute K, Brand RE, Everett JN, Farrell JJ, Hawthorne K, Kaul V, Kupfer SS, Paiella S, Simeone DM, Sussman DA, Zogopoulos G, Lucas AL, Kastrinos F, PRECEDE Consortium. PMID: 37259800.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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Impact of comprehensive family history and genetic analysis in the multidisciplinary pancreatic tumor clinic setting. Cancer Med. 2023 02; 12(3):2345-2355.
Everett JN, Sanoba SA, Jing X, Stender C, Schmitter M, Baptiste A, Chun J, Kawaler EA, Khanna LG, Gross SA, Gonda TA, Beri N, Oberstein PE, Simeone DM. PMID: 35906821; PMCID: PMC9939217.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Standardization of MRI Screening and Reporting in Individuals With Elevated Risk of Pancreatic Ductal Adenocarcinoma: Consensus Statement of the PRECEDE Consortium. AJR Am J Roentgenol. 2022 12; 219(6):903-914.
Huang C, Simeone DM, Luk L, Hecht EM, Khatri G, Kambadakone A, Chandarana H, Ream JM, Everett JN, Guimaraes A, Liau J, Dasyam AK, Harmath C, Megibow AJ, PRECEDE Consortium. PMID: 35856454.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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Recommendations for a More Organized and Effective Approach to the Early Detection of Pancreatic Cancer From the PRECEDE (Pancreatic Cancer Early Detection) Consortium. Gastroenterology. 2021 12; 161(6):1751-1757.
Gonda TA, Everett JN, Wallace M, Simeone DM, PRECEDE Consortium. PMID: 34454916.
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7 Fields:
Translation:
Humans
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Impact of changing guidelines on genetic testing and surveillance recommendations in a contemporary cohort of breast cancer survivors with family history of pancreatic cancer. Sci Rep. 2021 06 14; 11(1):12491.
Wang A, Everett JN, Chun J, Cen C, Simeone DM, Schnabel F. PMID: 34127761; PMCID: PMC8203798.
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2 Fields:
Translation:
Humans
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Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomized controlled trial. BMC Health Serv Res. 2021 Jun 02; 21(1):542.
Kaphingst KA, Kohlmann W, Chambers RL, Goodman MS, Bradshaw R, Chan PA, Chavez-Yenter D, Colonna SV, Espinel WF, Everett JN, Gammon A, Goldberg ER, Gonzalez J, Hagerty KJ, Hess R, Kehoe K, Kessler C, Kimball KE, Loomis S, Martinez TR, Monahan R, Schiffman JD, Temares D, Tobik K, Wetter DW, Mann DM, Kawamoto K, Del Fiol G, Buys SS, Ginsburg O, BRIDGE research team. PMID: 34078380; PMCID: PMC8170651.
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PubMed Mentions:
9 Fields:
Translation:
Humans
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Cancer surveillance awareness and practice among families at increased risk for pancreatic adenocarcinoma. Cancer. 2021 07 01; 127(13):2271-2278.
Everett JN, Burgos G, Chun J, Baptiste A, Khanna LG, Oberstein PE, Simeone DM. PMID: 33721345.
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PubMed Mentions:
1 Fields:
Translation:
Humans
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Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019 May; 21(5):1261-1262.
Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, Ghazani AA, Gilmore MJ, Goddard KAB, Jarvik GP, Johnston JJ, Kauffman TL, Kelley WV, Krier JB, Lewis KL, McGuire AL, McMullen C, Ou J, Plon SE, Rehm HL, Richards CS, Romasko EJ, Sagardia AM, Spinner NB, Thompson ML, Turbitt E, Vassy JL, Wilfond BS, Veenstra DL, Berg JS, Green RC, Biesecker LG, Hindorff LA. PMID: 30670880.
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Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019 05; 21(5):1100-1110.
Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, Ghazani AA, Gilmore MJ, Goddard KAB, Jarvik GP, Johnston JJ, Kauffman TL, Kelley WV, Krier JB, Lewis KL, McGuire AL, McMullen C, Ou J, Plon SE, Rehm HL, Richards CS, Romasko EJ, Miren Sagardia A, Spinner NB, Thompson ML, Turbitt E, Vassy JL, Wilfond BS, Veenstra DL, Berg JS, Green RC, Biesecker LG, Hindorff LA. PMID: 30287922; PMCID: PMC6450774.
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PubMed Mentions:
73 Fields:
Translation:
Humans
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Physician Experiences and Understanding of Genomic Sequencing in Oncology. J Genet Couns. 2018 02; 27(1):187-196.
Weipert CM, Ryan KA, Everett JN, Yashar BM, Chinnaiyan AM, Scott Roberts J, De Vries R, Zikmund-Fisher BJ, Raymond VM. PMID: 28840409; PMCID: PMC5810555.
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PubMed Mentions:
13 Fields:
Translation:
Humans
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Incorporating genetic counseling into clinical care for children and adolescents with cancer. Future Oncol. 2016 Apr; 12(7):883-6.
Everett JN, Mody RJ, Stoffel EM, Chinnaiyan AM. PMID: 26888175; PMCID: PMC4820829.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals. Fam Cancer. 2015 Mar; 14(1):167-74.
Gustafson SL, Raymond VM, Marvin ML, Else T, Koeppe E, Stoffel EM, Everett JN. PMID: 25245322.
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1 Fields:
Translation:
Humans
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Screening for germline mismatch repair mutations following diagnosis of sebaceous neoplasm. JAMA Dermatol. 2014 Dec; 150(12):1315-21.
Everett JN, Raymond VM, Dandapani M, Marvin M, Kohlmann W, Chittenden A, Koeppe E, Gustafson SL, Else T, Fullen DR, Johnson TM, Syngal S, Gruber SB, Stoffel EM. PMID: 25006859; PMCID: PMC4977578.
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PubMed Mentions:
27 Fields:
Translation:
HumansCells
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The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). J Clin Endocrinol Metab. 2014 Aug; 99(8):E1482-6.
Else T, Marvin ML, Everett JN, Gruber SB, Arts HA, Stoffel EM, Auchus RJ, Raymond VM. PMID: 24758179; PMCID: PMC4121019.
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PubMed Mentions:
24 Fields:
Translation:
Humans
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Traditional roles in a non-traditional setting: genetic counseling in precision oncology. J Genet Couns. 2014 Aug; 23(4):655-60.
Everett JN, Gustafson SL, Raymond VM. PMID: 24578120; PMCID: PMC4096055.
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16 Fields:
Translation:
Humans
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An oncocytic adrenal tumour in a patient with Birt-Hogg-Dubé syndrome. Clin Endocrinol (Oxf). 2014 Jun; 80(6):925-7.
Raymond VM, Long JM, Everett JN, Caoili EM, Gruber SB, Stoffel EM, Giordano TJ, Hammer GD, Else T. PMID: 23848572; PMCID: PMC3893308.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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Adrenocortical carcinoma is a lynch syndrome-associated cancer. J Clin Oncol. 2013 Aug 20; 31(24):3012-8.
Raymond VM, Everett JN, Furtado LV, Gustafson SL, Jungbluth CR, Gruber SB, Hammer GD, Stoffel EM, Greenson JK, Giordano TJ, Else T. PMID: 23752102; PMCID: PMC3739861.
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PubMed Mentions:
76 Fields:
Translation:
Humans
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Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma. J Clin Endocrinol Metab. 2013 Jan; 98(1):E119-25.
Raymond VM, Else T, Everett JN, Long JM, Gruber SB, Hammer GD. PMID: 23175693; PMCID: PMC3537086.
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PubMed Mentions:
38 Fields:
Translation:
Humans
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Disclosing individual CDKN2A research results to melanoma survivors: interest, impact, and demands on researchers. Cancer Epidemiol Biomarkers Prev. 2011 Mar; 20(3):522-9.
Christensen KD, Roberts JS, Shalowitz DI, Everett JN, Kim SY, Raskin L, Gruber SB. PMID: 21307304; PMCID: PMC3833711.
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PubMed Mentions:
30 Fields:
Translation:
Humans
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Returning individual research results: development of a cancer genetics education and risk communication protocol. J Empir Res Hum Res Ethics. 2010 Sep; 5(3):17-30.
Roberts JS, Shalowitz DI, Christensen KD, Everett JN, Kim SY, Raskin L, Gruber SB. PMID: 20831418; PMCID: PMC3159194.
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18 Fields:
Translation:
Humans
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Genetic counselling and genetic testing in hereditary gastrointestinal cancer syndromes. Best Pract Res Clin Gastroenterol. 2009; 23(2):275-83.
Raymond VM, Everett JN. PMID: 19414152.
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PubMed Mentions:
4 Fields:
Translation:
Humans
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Differences in physician referral practices and attitudes regarding hereditary breast cancer by clinical practice location. Genet Med. 2003 Sep-Oct; 5(5):364-9.
Koil CE, Everett JN, Hoechstetter L, Ricer RE, Huelsman KM. PMID: 14501831.
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22 Fields:
Translation:
Humans
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Breast cancer genetics education for college women: an evaluation of approaches. J Cancer Educ. 2002; 17(2):74-7.
Howell KA, Huelsman KM, Everett JN, Hopkin RJ. PMID: 12092856.
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PubMed Mentions:
1 Fields:
Translation:
Humans