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Changing predictor measurement procedures affected the performance of prediction models in clinical examples

Journal of clinical epidemiology, 2020-03, Vol.119, p.7-18

2020

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MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome

Cancers, 2023-01, Vol.15 (2), p.391

2023

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Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population

Genetics in medicine, 2023-11, Vol.25 (11), p.100923, Article 100923

2023

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Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access

Genetics in medicine, 2022-06, Vol.24 (6), p.1196-1205

2022

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Development and validation of the PREMMplus clinical prediction model for multigene hereditary cancer risk assessment

Journal of clinical oncology, 2020-05, Vol.38 (15_suppl), p.1579-1579

2020

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Implementation of systematic genetic counseling (GC) and multigene germline testing (MGT) for pancreatic cancer (PC) patients (pts)

Journal of clinical oncology, 2020-02, Vol.38 (4_suppl), p.678-678

2020

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Clinical factors associated with urinary tract cancers (UTCs) among Lynch syndrome (LS) patients (Pts)

Journal of clinical oncology, 2018-05, Vol.36 (15_suppl), p.1517-1517

2018

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Improving cascade genetic testing for families with inherited pancreatic cancer (PDAC) risk: The GENetic Education, Risk Assessment and TEsting (GENERATE) study

Journal of clinical oncology, 2020-02, Vol.38 (4_suppl), p.TPS779-TPS779

2020

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Identification of Lynch syndrome (LS) in patients (pts) without prior LS-associated cancer

Journal of clinical oncology, 2016-05, Vol.34 (15_suppl), p.1521-1521

2016

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Implementing universal genetic counseling (GC) and multigene germline testing (MGT) for pancreatic cancer (PC) patients (pts)

Journal of clinical oncology, 2018-05, Vol.36 (15_suppl), p.1512-1512

2018

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Prevalence of germline cancer susceptibility gene mutations in a consecutive series of 799 colorectal cancer (CRC) patients (pts)

Journal of clinical oncology, 2016-05, Vol.34 (15_suppl), p.1501-1501

2016

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Abstract 4272: Mutations in RABL3 alter RAS prenylation and are associated with hereditary pancreatic cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.4272-4272

2017

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Therapy-associated polyposis – a novel form of acquired gastrointestinal polyposis

Clinical gastroenterology and hepatology, 2013-12, Vol.12 (6), p.1046-1050

2013

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Cancer risks and mutation spectrum of mismatch repair genes in African American families with Lynch syndrome

Journal of clinical oncology, 2013-05, Vol.31 (15_suppl), p.1530-1530

2013

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Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome

Journal of clinical oncology, 2017-07, Vol.35 (19), p.2165-2172

2017

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Mutational signature profiling classifies subtypes of clinically different mismatch-repair-deficient tumours with a differential immunogenic response potential

British journal of cancer, 2022-06, Vol.126 (11), p.1595-1603

2022

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Clinical Factors Associated With Gastric Cancer in Individuals With Lynch Syndrome

Clinical gastroenterology and hepatology, 2020-04, Vol.18 (4), p.830-837.e1

2020

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Tu1018 A MIXED METHODS APPROACH TO ASSESSING BARRIERS AND FACILITATORS TO CANCER GENETICS CARE IN BLACK AND LATINO/A/X INDIVIDUALS AFFECTED BY PANCREATIC CANCER: THE RACIAL/ETHNIC GENETIC EDUATION, RISK ASSESSMENT, AND TESTING (REGENERATE) STUDY

Gastroenterology (New York, N.Y. 1943), 2024-05, Vol.166 (5), p.S-1221-S-1222

2024

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Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment

Journal of clinical oncology, 2022-12, Vol.40 (35), p.4083-4094

2022

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Implementing systematized patient-facing Lynch syndrome (LS) risk assessment in oncology using the electronic health record (EHR) system

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.10503-10503

2022

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Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing

Journal of clinical oncology, 2020-12, Vol.38 (34), p.4086-4094

2020

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Prevalence of unexpected actionable germline pathogenic variants identified on broad-based multi-gene panel testing in a cohort of cancer patients

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.10523-10523

2023

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Mo1020 RACIAL/ETHNIC EQUITY IN GENETIC EDUCATION, RISK ASSESSMENT, AND TESTING (REGENERATE) AMONG BLACK AND LATINO/A/X COMMUNITIES AT-RISK FOR PANCREATIC CANCER – PRELIMINARY FINDINGS FROM ONLINE FOCUS GROUPS

Gastroenterology (New York, N.Y. 1943), 2023-05, Vol.164 (6), p.S-733-S-734

2023

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Tu1212 RELEVANT HETEROGENEITY IN MISMATCH REPAIR DEFICIENT TUMORS

Gastroenterology (New York, N.Y. 1943), 2020-05, Vol.158 (6), p.S-1020-S-1020

2020

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Clinical factors associated with skin neoplasms in individuals with Lynch syndrome in a longitudinal observational cohort

Journal of the American Academy of Dermatology, 2023-06, Vol.88 (6), p.1282-1290

2023

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Changing predictor measurement procedures affected the performance of prediction models in clinical examples

MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome

Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population

Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access

Development and validation of the PREMMplus clinical prediction model for multigene hereditary cancer risk assessment

Implementation of systematic genetic counseling (GC) and multigene germline testing (MGT) for pancreatic cancer (PC) patients (pts)

Clinical factors associated with urinary tract cancers (UTCs) among Lynch syndrome (LS) patients (Pts)

Improving cascade genetic testing for families with inherited pancreatic cancer (PDAC) risk: The GENetic Education, Risk Assessment and TEsting (GENERATE) study

Identification of Lynch syndrome (LS) in patients (pts) without prior LS-associated cancer

Implementing universal genetic counseling (GC) and multigene germline testing (MGT) for pancreatic cancer (PC) patients (pts)

Prevalence of germline cancer susceptibility gene mutations in a consecutive series of 799 colorectal cancer (CRC) patients (pts)

Abstract 4272: Mutations in RABL3 alter RAS prenylation and are associated with hereditary pancreatic cancer

Therapy-associated polyposis – a novel form of acquired gastrointestinal polyposis

Cancer risks and mutation spectrum of mismatch repair genes in African American families with Lynch syndrome

Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome

Mutational signature profiling classifies subtypes of clinically different mismatch-repair-deficient tumours with a differential immunogenic response potential

Clinical Factors Associated With Gastric Cancer in Individuals With Lynch Syndrome

Tu1018 A MIXED METHODS APPROACH TO ASSESSING BARRIERS AND FACILITATORS TO CANCER GENETICS CARE IN BLACK AND LATINO/A/X INDIVIDUALS AFFECTED BY PANCREATIC CANCER: THE RACIAL/ETHNIC GENETIC EDUATION, RISK ASSESSMENT, AND TESTING (REGENERATE) STUDY

Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment

Implementing systematized patient-facing Lynch syndrome (LS) risk assessment in oncology using the electronic health record (EHR) system

Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing

Prevalence of unexpected actionable germline pathogenic variants identified on broad-based multi-gene panel testing in a cohort of cancer patients

Mo1020 RACIAL/ETHNIC EQUITY IN GENETIC EDUCATION, RISK ASSESSMENT, AND TESTING (REGENERATE) AMONG BLACK AND LATINO/A/X COMMUNITIES AT-RISK FOR PANCREATIC CANCER – PRELIMINARY FINDINGS FROM ONLINE FOCUS GROUPS

Tu1212 RELEVANT HETEROGENEITY IN MISMATCH REPAIR DEFICIENT TUMORS

Clinical factors associated with skin neoplasms in individuals with Lynch syndrome in a longitudinal observational cohort

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