W. Kohlmann

发表

NCCN CLINICAL PRACTICE GUIDELINES IN ONCOLOGY Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2021

So, B. Karlan, S. Friedman, 2020 .

Parental preferences for CDKN2A/p16 testing of minors

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2010, Genetics in Medicine.

Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis.

Yelena P. Wu, L. Pappas, Cathryn Koptiuch, 2018, Patient education and counseling.

Psychological Aspects of Hereditary Cancer Risk Counseling and Genetic Testing

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2013 .

Barriers to family history collection among Spanish-speaking primary care patients: a BRIDGE qualitative study

R. Bradshaw, S. Buys, Kensaku Kawamoto, 2022, PEC Innovation.

Parent and child perspectives on family interactions related to melanoma risk and prevention after CDKN2A/p16 testing of minor children

L. Aspinwall, P. Cassidy, S. Leachman, 2020, Journal of Community Genetics.

Increasing Skin Cancer Prevention in Young Adults: the Cumulative Impact of Personalized UV Photography and MC1R Genetic Testing

Xue-chen Wang, J. Hamilton, Yelena P. Wu, 2022, Journal of Cancer Education.

‘I had a bigger cancer risk than I thought…’: The experience of receiving personalized risk information as part of a skin cancer prevention intervention in the college setting

J. Hamilton, Yelena P. Wu, J. Hay, 2022, Health expectations : an international journal of public participation in health care and health policy.

Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing Approach

G. Fiol, R. Bradshaw, Kensaku Kawamoto, 2022, JMIR medical informatics.

Selection criteria for genetic assessment of patients with familial melanoma.

A. Halpern, S. Puig, S. Swetter, 2009, Journal of the American Academy of Dermatology.

Discrepancies between tumor genomic profiling and germline genetic testing

S. Greenberg, I. Garrido-Laguna, J. Whisenant, 2022, ESMO open.

Biallelic inactivation of the APC gene is associated with hepatocellular carcinoma in familial adenomatous polyposis coli

E. Abdalla, J. Vauthey, A. Rashid, 2001, Cancer.

Inherited Gene Mutations in Melanoma

S. Leachman, L. Pho, Marjan Champine, 2016 .

Genetic Testing for Melanoma

S. Leachman, W. Kohlmann, 2011 .

Genetic Test Reporting and Counseling for Melanoma Risk in Minors May Improve Sun Protection Without Inducing Distress

L. Aspinwall, P. Cassidy, S. Leachman, 2018, Journal of Genetic Counseling.

CDKN2A/p16 Genetic Test Reporting Improves Early Detection Intentions and Practices in High-Risk Melanoma Families

L. Aspinwall, S. Leachman, Samantha L Leaf, 2008, Cancer Epidemiology Biomarkers & Prevention.

CDKN2A testing and genetic counseling promote reductions in objectively measured sun exposure one year later

Jennifer M. Taber, L. Aspinwall, P. Cassidy, 2019, Genetics in Medicine.

Uptake of genetic counseling and multi‐gene panel testing among women in the Intermountain West with previous negative BRCA1 and BRCA2 results contacted for updated testing

Wendy Kohlmann, K. Kaphingst, Ryan Mooney, 2021, Journal of genetic counseling.

Pediatric Predispositional Genetic Risk Communication: Potential Utility for Prevention and Control of Melanoma Risk as an Exemplar

Yelena P. Wu, D. Mays, K. Tercyak, 2017, Journal of Genetic Counseling.

Genetic Counseling

K. Hamman, Wendy Kohlmann, Sancy L. Leachman, 2019, Melanoma.

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

Wendy Kohlmann, J. Jeter, Kristen Pauley, 2022, Frontiers in Oncology.

Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma–pheochromocytoma syndrome

K. Nathanson, L. Fishbein, Amanda M Schaefer, 2020, Genetics in Medicine.

Paraganglioma and other tumour detection rates in individuals with SDHx pathogenic variants by age of diagnosis and after the age of 50

S. Greenberg, L. Buchmann, A. Naumer, 2021, Clinical endocrinology.

Melanoma Genetic Counseling and Test Reporting Improve Screening Adherence Among Unaffected Carriers 2 Years Later

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2013, Cancer Epidemiology, Biomarkers & Prevention.

Role of genetic testing in hereditary melanoma

S. Leachman, W. Kohlmann, K. Dunn, 2008 .

Genetic test reporting of CDKN2A provides informational and motivational benefits for managing melanoma risk.

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2018, Translational behavioral medicine.

Genetic Counseling and Testing for Hereditary Melanoma: An Updated Guide for Dermatologists

S. Leachman, Marjan Champine, W. Kohlmann, 2012 .

Discussion of photoprotection, screening, and risk behaviors with children and grandchildren after melanoma genetic testing

L. Aspinwall, S. Leachman, Yelena P. Wu, 2015, Journal of Community Genetics.

Unaffected family members report improvements in daily routine sun-protection 2 years following melanoma genetic testing

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2014, Genetics in Medicine.

Perceived Risk Following Melanoma Genetic Testing: A 2-Year Prospective Study Distinguishing Subjective Estimates from Recall

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2014, Journal of Genetic Counseling.

Barriers and Facilitators to Melanoma Prevention and Control Behaviors Among At-Risk Children

L. Aspinwall, S. Leachman, D. Grossman, 2018, Journal of Community Health.

Partner involvement in conduct of skin self-examinations remains low following CDKN2A/p16 genetic test reporting and counseling.

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2013, Journal of the American Academy of Dermatology.

Development of an Educational Program Integrating Concepts of Genetic Risk and Preventive Strategies for Children with a Family History of Melanoma

L. Aspinwall, P. Cassidy, S. Leachman, 2018, Journal of Cancer Education.

Genetic testing for hereditary melanoma and pancreatic cancer: a longitudinal study of psychological outcome

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2011, Psycho-oncology.

Patterns of photoprotection following CDKN2A/p16 genetic test reporting and counseling.

L. Aspinwall, S. Leachman, Wendy Kohlmann, 2009, Journal of the American Academy of Dermatology.

A pilot study of a telehealth family‐focused melanoma preventive intervention for children with a family history of melanoma

D. Bowen, L. Aspinwall, S. Leachman, 2020, Psycho-oncology.

A novel educational intervention targeting melanoma risk and prevention knowledge among children with a familial risk for melanoma.

L. Aspinwall, S. Leachman, D. Grossman, 2017, Patient education and counseling.

Impact of melanoma genetic test reporting on perceived control over melanoma prevention

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2015, Journal of Behavioral Medicine.

Psychological Aspects of Hereditary Cancer Risk Counseling and Genetic Testing: Toward an Expanded and More Equitable View

Jennifer M. Taber, L. Aspinwall, W. Kohlmann, 2022, Psychological Aspects of Cancer.

Discussion of photoprotection, screening, and risk behaviors with children and grandchildren after melanoma genetic testing

L. Aspinwall, S. Leachman, Yelena P. Wu, 2015, Journal of Community Genetics.

Priority of Risk (But Not Perceived Magnitude of Risk) Predicts Improved Sun-Protection Behavior Following Genetic Counseling for Familial Melanoma.

Jennifer M. Taber, L. Aspinwall, P. Cassidy, 2020, Annals of behavioral medicine : a publication of the Society of Behavioral Medicine.

Genetic test reporting enhances understanding of risk information and acceptance of prevention recommendations compared to family history-based counseling alone

Jennifer M. Taber, L. Aspinwall, S. Leachman, 2015, Journal of Behavioral Medicine.

Correction: Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing Approach

G. Fiol, R. Bradshaw, Kensaku Kawamoto, 2022, JMIR Medical Informatics.

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version

K. Offit, S. Buys, Rashmi Kumar, 2014 .

Development of an Educational Program Integrating Concepts of Genetic Risk and Preventive Strategies for Children with a Family History of Melanoma

L. Aspinwall, P. Cassidy, S. Leachman, 2016, Journal of Cancer Education.

Predictors of Women's Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members

K. Kaphingst, Ryan Mooney, Ashley Elrick, 2023, Public Health Genomics.

Investigating Patient Interactions with an Automated Conversational Agent Delivering Pre-test Genetics Education: A Descriptive Study (Preprint)

R. Bradshaw, G. Del Fiol, R. Hess, 2021 .