Search Results - "Long, Jessica M"
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Research participants’ experiences with return of genetic research results and preferences for web‐based alternatives
Published in Molecular genetics & genomic medicine (01-09-2019)“…Background While there is increasing interest in sharing genetic research results with participants, how best to communicate the risks, benefits and…”
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The role of endoscopy in the management of hereditary diffuse gastric cancer syndrome
Published in World journal of gastroenterology : WJG (21-06-2019)“…Hereditary diffuse gastric cancer (HDGC) syndrome is an inherited cancer risk syndrome associated with pathogenic germline variants. Given the high risk for…”
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Upper Endoscopic Surveillance in Lynch Syndrome Detects Gastric and Duodenal Adenocarcinomas
Published in Cancer prevention research (Philadelphia, Pa.) (01-12-2020)“…Lynch syndrome is a prevalent hereditary cancer predisposition syndrome. While colorectal cancer is the most common gastrointestinal (GI) cancer in Lynch…”
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Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer
Published in Genetics in medicine (01-08-2015)“…Purpose: Clinical testing for germ-line variation in multiple cancer susceptibility genes is available using massively parallel sequencing. Limited information…”
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Endoscopic Ultrasound Has Limited Utility in Diagnosis of Gastric Cancer in Carriers of CDH1 Mutations
Published in Clinical gastroenterology and hepatology (01-02-2020)“…A total of 1%–3% of gastric cancers are related to hereditary syndromes, including hereditary diffuse gastric cancer syndrome (HDGC), which is characterized by…”
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Prevalence of Germline TP53 Mutations in a Prospective Series of Unselected Patients with Adrenocortical Carcinoma
Published in The journal of clinical endocrinology and metabolism (01-01-2013)“…Purpose: Adrenocortical carcinoma (ACC) is a hallmark cancer in families with Li Fraumeni syndrome (LFS) caused by mutations in the TP53 gene. The prevalence…”
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Looking closely at overgrowth: Constitutional mosaicism in PTEN hamartoma tumor syndrome
Published in Clinical genetics (01-12-2022)Get full text
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Evaluation of Classic, Attenuated, and Oligopolyposis of the Colon
Published in Gastrointestinal endoscopy clinics of North America (01-01-2022)“…The goal of this review is to provide an overview of evaluating patients with adenomatous polyposis of the colon, including elements such as generating a…”
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Upper Gastrointestinal Cancer Risk and Surveillance Outcomes in Li-Fraumeni Syndrome
Published in The American journal of gastroenterology (01-12-2020)“…To assess the upper gastrointestinal (UGI) cancer risk and surveillance outcomes in Li-Fraumeni syndrome (LFS). Analysis of the International Agency for…”
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Uptake of Genetic Research Results and Patient-Reported Outcomes With Return of Results Incorporating Web-Based Predisclosure Education
Published in Journal of clinical oncology (01-11-2023)“…We developed a web-based education intervention as an alternative to predisclosure education with a genetic counselor (GC) to reduce participant burden and…”
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Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results
Published in JNCI : Journal of the National Cancer Institute (01-09-2018)“…Germline genetic testing is standard practice in oncology. Outcomes of telephone disclosure of a wide range of cancer genetic test results, including multigene…”
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Earlier Colorectal Cancer Screening May Be Necessary In Patients With Li-Fraumeni Syndrome
Published in Gastroenterology (New York, N.Y. 1943) (01-01-2019)Get full text
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Impact of integrating genomic data into the electronic health record on genetics care delivery
Published in Genetics in medicine (01-11-2022)“…Integrating genomic data into the electronic health record (EHR) is key for optimally delivering genomic medicine. The PennChart Genomics Initiative (PGI) at…”
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Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing
Published in Genetics in medicine (01-01-2016)“…The risks, benefits, and utilities of multiplex panels for breast cancer susceptibility are unknown, and new counseling and informed consent models are needed…”
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Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer
Published in Familial cancer (01-10-2023)“…Transgender and gender diverse (TGD) populations with hereditary cancer syndromes face unique obstacles to identifying and obtaining appropriate cancer…”
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Longitudinal outcomes with cancer multigene panel testing in previously tested BRCA1/2 negative patients
Published in Clinical genetics (01-04-2020)“…Although multigene panel testing (MGPT) is increasingly utilized in clinical practice, there remain limited data on patient‐reported outcomes. BRCA 1/2…”
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Assessment of the Psychosocial Impact of Pancreatic Cancer Surveillance in High-Risk Individuals
Published in Cancers (23-12-2023)“…Pancreatic cancer (PC) surveillance of high-risk individuals (HRIs) downstages PC and improves survival. However, it remains less clear whether PC surveillance…”
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EUS-based Pancreatic Cancer Surveillance in BRCA1/BRCA2/PALB2/ATM Carriers Without a Family History of Pancreatic Cancer
Published in Cancer prevention research (Philadelphia, Pa.) (01-11-2021)“…Carriers of a pathogenic/likely pathogenic (P/LP) variant are at increased risk of pancreatic ductal adenocarcinoma (PDAC), yet current guidelines recommend…”
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Uptake and outcomes of small intestinal and urinary tract cancer surveillance in Lynch syndrome
Published in World journal of clinical oncology (24-11-2021)“…Lynch syndrome (LS) is a hereditary cancer predisposition syndrome associated with increased risk of multiple cancers. While colorectal cancer surveillance…”
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Longitudinal follow-up after telephone disclosure in the randomized COGENT study
Published in Genetics in medicine (01-08-2020)“…Purpose To better understand the longitudinal risks and benefits of telephone disclosure of genetic test results in the era of multigene panel testing. Methods…”
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