Heli Nevanlinna

Helsinki, Finland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 245 publications

Updated ENIGMA recommendations for reporting germline variants in cancer susceptibility genes and their translation into twenty languages.

Updated ENIGMA recommendations for reporting germline variants in cancer susceptibility genes and their translation into twenty languages.

Journal: Journal of medical genetics

Published: January 13, 2026

Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.

Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.

Journal: Nature communications

Published: September 09, 2025

Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction.

Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction.

Journal: Breast cancer research : BCR

Published: August 12, 2024

Lessons learned from a candidate gene study investigating aromatase inhibitor treatment outcome in breast cancer.

Lessons learned from a candidate gene study investigating aromatase inhibitor treatment outcome in breast cancer.

Journal: NPJ breast cancer

Published: July 24, 2024

Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Journal: Nature genetics

Published: July 09, 2024

Rare Germline Variants in DNA Repair Genes Detected in BRCA-Negative Finnish Patients with Early-Onset Breast Cancer.

Rare Germline Variants in DNA Repair Genes Detected in BRCA-Negative Finnish Patients with Early-Onset Breast Cancer.

Journal: Cancers

Published: June 24, 2024

Homozygous FANCM Variant c.5101C>T p.(Gln1701*) in a Patient With Early Onset Breast Cancer, Chemotherapy Toxicity, and Chromosome Fragility: A Case Report.

Homozygous FANCM Variant c.5101C>T p.(Gln1701*) in a Patient With Early Onset Breast Cancer, Chemotherapy Toxicity, and Chromosome Fragility: A Case Report.

Journal: Cancer reports (Hoboken, N.J.)

Published: April 19, 2024

Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction.

Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction.

Journal: medRxiv : the preprint server for health sciences

Published: February 27, 2024

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Journal: medRxiv : the preprint server for health sciences

Published: July 28, 2023

NTHL1 is a recessive cancer susceptibility gene.

NTHL1 is a recessive cancer susceptibility gene.

Journal: Scientific reports

Published: July 06, 2023

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Journal: Nature genetics

Published: June 12, 2023

Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.

Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.

Journal: Research square

Published: February 24, 2023

Showing 1-12 of 245

Last Updated: 09/26/2026