Senno Verhoef

Leiden, ZH 2333ZA, Netherlands

Last Updated: 09/26/2026

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Found 36 publications

Low-level constitutional mosaicism of BRCA1 in two women with young onset ovarian cancer.

Low-level constitutional mosaicism of BRCA1 in two women with young onset ovarian cancer.

Journal: Hereditary cancer in clinical practice

Published: March 08, 2022

A randomized experimental study to test the effects of discussing uncertainty during cancer genetic counseling: different strategies, different outcomes?

A randomized experimental study to test the effects of discussing uncertainty during cancer genetic counseling: different strategies, different outcomes?

Journal: European journal of human genetics : EJHG

Published: July 22, 2020

Three-step site-directed mutagenesis screen identifies pathogenic MLH1 variants associated with Lynch syndrome.

Three-step site-directed mutagenesis screen identifies pathogenic MLH1 variants associated with Lynch syndrome.

Journal: Journal of medical genetics

Published: August 22, 2019

A head-to-head comparison of conjugation methods for VHHs: Random maleimide-thiol coupling versus controlled click chemistry.

A head-to-head comparison of conjugation methods for VHHs: Random maleimide-thiol coupling versus controlled click chemistry.

Journal: International journal of pharmaceutics: X

Published: April 17, 2019

'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations.

'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations.

Journal: Familial cancer

Published: March 16, 2019

Rapid genetic counseling and testing in newly diagnosed breast cancer: Patients' and health professionals' attitudes, experiences, and evaluation of effects on treatment decision making.

Rapid genetic counseling and testing in newly diagnosed breast cancer: Patients' and health professionals' attitudes, experiences, and evaluation of effects on treatment decision making.

Journal: Journal of surgical oncology

Published: April 07, 2017

Risk algorithms that include pathology adjustment for HER2 amplification need to make further downward adjustments in likelihood scores.

Risk algorithms that include pathology adjustment for HER2 amplification need to make further downward adjustments in likelihood scores.

Journal: Familial cancer

Published: November 01, 2016

Do BRCA1/2 mutation carriers have an earlier onset of natural menopause?

Do BRCA1/2 mutation carriers have an earlier onset of natural menopause?

Journal: Menopause (New York, N.Y.)

Published: June 22, 2016

Recurrent HOXB13 mutations in the Dutch population do not associate with increased breast cancer risk.

Recurrent HOXB13 mutations in the Dutch population do not associate with increased breast cancer risk.

Journal: Scientific reports

Published: April 07, 2016

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

Journal: Journal of medical genetics

Published: March 29, 2016

Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.

Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 09, 2016

Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.

Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.

Journal: Human mutation

Published: February 19, 2016

Showing 1-12 of 36

Last Updated: 09/26/2026