Publications by authors named "Mary Velthuizen"

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Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome.
Michael R Sargen, Jung Kim, Thomas P Potjer, Mary E Velthuizen, Arelis E Martir-Negron

JAMA Dermatol· October 2023

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Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing.
Kyra Bokkers, Eveline M A Bleiker, Jacob P Hoogendam, Mary E Velthuizen, Henk W R Schreuder

Hered Cancer Clin Pract· September 2022

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Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer.
Kyra Bokkers, Ronald P Zweemer, Marco J Koudijs, Sanne Stehouwer, Mary E Velthuizen

Fam Cancer· July 2022

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Effect of a health literacy training program for surgical oncologists and specialized nurses on disparities in referral to breast cancer genetic testing.
Jeanine A M van der Giessen, Sandra van Dulmen, Mary E Velthuizen, Maria E T C van den Muijsenbergh, Klaartje van Engelen

Breast· August 2021

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Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries.
Mohammad Sina, Zeinab Ghorbanoghli, Amal Abedrabbo, Fahd Al-Mulla, Rihab Ben Sghaier, Mary E Velthuizen

Fam Cancer· July 2021

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Changes in empowerment and anxiety of patients and parents during genetic counselling for epilepsy.
Danique R M Vlaskamp, Patrick Rump, Petra M C Callenbach, Eva H Brilstra, Mary E Velthuizen

Eur J Paediatr Neurol· May 2021

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Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals.
Jeanine van der Giessen, Mirjam P Fransen, Peter Spreeuwenberg, Mary Velthuizen, Sandra van Dulmen

J Community Genet· January 2021

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Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences.
Mary E Velthuizen, Rob B van der Luijt, Beja J de Vries, Marco J Koudijs, Eveline M A Bleiker

Hered Cancer Clin Pract· January 2021

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Cognitive and affective outcomes of genetic counselling in the Netherlands at group and individual level: a personalized approach seems necessary.
Jan S Voorwinden, Mirjam Plantinga, Margreet Ausems, Nine Knoers, Mary Velthuizen

Eur J Hum Genet· September 2020

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Increased prevalence of Barrett's esophagus in patients with MUTYH-associated polyposis (MAP).
Ceranza G Daans, Zeinab Ghorbanoghli, Mary E Velthuizen, Hans F A Vasen, George J A Offerhaus

Fam Cancer· April 2020

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A validated PROM in genetic counselling: the psychometric properties of the Dutch version of the Genetic Counselling Outcome Scale.
Jan S Voorwinden, Mirjam Plantinga, Wim Krijnen, Margreet Ausems, Nine Knoers, Mary Velthuizen

Eur J Hum Genet· May 2019

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Identifying patients with a history of ovarian cancer for referral for genetic counselling: non-randomised comparison of two case-finding strategies in primary care.
Charles W Helsper, Liesbeth M Van Vliet, Mary E Velthuizen, Niek J de Wit, Roy Ph Beijaert

Br J Gen Pract· November 2018

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Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry.
Hans F A Vasen, Mary E Velthuizen, Jan H Kleibeuker, Fred H Menko, Fokke M Nagengast

Fam Cancer· July 2016

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Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.
Sanne W ten Broeke, Richard M Brohet, Carli M Tops, Heleen M van der Klift, Mary E Velthuizen

J Clin Oncol· February 2015

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Effect of routine assessment of specific psychosocial problems on personalized communication, counselors’ awareness, and distress levels in cancer genetic counseling practice: a randomized controlled trial.
Willem Eijzenga, Neil K Aaronson, Daniela E E Hahn, Grace N Sidharta, Lizet E van der Kolk, Mary E Velthuizen

J Clin Oncol· September 2014

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Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study.
Jae-Gahb Park, Duck-Woo Kim, Chang Won Hong, Byung-Ho Nam, Young-Kyoung Shin, Mary Velthuizen

Clin Cancer Res· June 2006

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