Lotte N. Krogh

Odense, Denmark

Last Updated: 09/26/2026

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Found 14 publications

Genomic profiling and expanded use of targeted anticancer drugs in solid cancers with exhausted evidence-based treatment options (PRECODE): study protocol of a prospective, non-randomized, cohort study.

Genomic profiling and expanded use of targeted anticancer drugs in solid cancers with exhausted evidence-based treatment options (PRECODE): study protocol of a prospective, non-randomized, cohort study.

Journal: BMC medical genomics

Published: October 09, 2024

Reclassification of Two MLH1 Variants of Uncertain Significance Utilizing Clinical and Functional Data.

Reclassification of Two MLH1 Variants of Uncertain Significance Utilizing Clinical and Functional Data.

Journal: Molecular genetics & genomic medicine

Published: June 17, 2024

Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer.

Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer.

Journal: Human genetics

Published: May 06, 2022

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness.

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness.

Journal: Cancer research

Published: July 01, 2019

Exploring the hereditary background of renal cancer in Denmark.

Exploring the hereditary background of renal cancer in Denmark.

Journal: PloS one

Published: August 29, 2018

Is MED13L-related intellectual disability a recognizable syndrome?

Is MED13L-related intellectual disability a recognizable syndrome?

Journal: European journal of medical genetics

Published: February 24, 2018

Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes.

Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes.

Journal: American journal of human genetics

Published: February 02, 2018

Novel Somatic RET Mutation Questioning the Causality of the RET I852M Germline Sequence Variant in Multiple Endocrine Neoplasia 2A.

Novel Somatic RET Mutation Questioning the Causality of the RET I852M Germline Sequence Variant in Multiple Endocrine Neoplasia 2A.

Journal: Thyroid : official journal of the American Thyroid Association

Published: June 06, 2017

Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores.

Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Published: April 28, 2017

Management of Gene Variants of Unknown Significance: Analysis Method and Risk Assessment of the VHL Mutation p.P81S (c.241C>T).

Management of Gene Variants of Unknown Significance: Analysis Method and Risk Assessment of the VHL Mutation p.P81S (c.241C>T).

Journal: Current genomics

Published: April 10, 2016

No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families.

No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families.

Journal: Familial cancer

Published: March 09, 2016

Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.

Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.

Journal: PloS one

Published: November 26, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026