Karin A W Wadt

Associated Professor

University of Copenhagen

Denmark

Research Interests

Explore related searches

Professors in Medical Science

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Dr. Karin A W Wadt is an Associate Professor at the University of Copenhagen, Denmark. Her research primarily focuses on genetic predisposition to cancer, particularly through studies on germline BRCA testing and somatic mutations in various cancer types. Recent publications highlight advancements in cancer genetics and clinical practices, including the impact of testing on treatment decisions and survival outcomes.

Articles (14)

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Collaborators (6)

Simon Rasmussen

Professor

University of Copenhagen

DENMARK

View details

Inge Søkilde Pedersen

Aalborg University

DENMARK

View details

Kristine Degn

Technical University of Denmark

DENMARK

View details

Kasper Amund Henriksen

Københavns Universitet

DENMARK

View details

Zeynep Tumer

Professor

University of Copenhagen

DENMARK

View details

Anne-Vibeke Lænkholm

Zealand University Hospital

DENMARK

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Karin A W Wadt

Research Interests

Explore related searches

Contact this professor

About

Articles (14)

Timely germline BRCA testing after invasive breast cancer promotes contralateral risk-reducing mastectomy and improves survival: an observational retrospective study

Germline BRCA testing in Denmark following invasive breast cancer: Progress since 2000

The evolutionary impact of childhood cancer on the human gene pool

National Experiences from 30 Years of Provider-Mediated Cascade Testing in Lynch Syndrome Families—The Danish Model

Characterization of somatic mutations in sporadic uveal melanoma and uveal melanoma in patients with germline BAP1 pathogenic variants

Evolutionary evidence precludes ELP1 as a high-penetrance pediatric cancer predisposition syndrome gene

Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors

Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort

Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome

Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants

Molecular reclassification reveals low prevalence of germline predisposition in children with ependymoma

New pathogenic germline variants identified in mesothelioma

RosettaDDGPrediction for high-throughput mutational scans: From stability to binding

TINF2 is a major susceptibility gene in Danish patients with multiple primary melanoma

Collaborators (6)

Simon Rasmussen

Inge Søkilde Pedersen

Kristine Degn

Kasper Amund Henriksen

Zeynep Tumer

Anne-Vibeke Lænkholm

Make your next move.