Publications by authors named "Neeme Tonisson"

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Use of Estonian Biobank data and participant recall to improve Wilson's disease management.
Miriam Nurm, Anu Reigo, Tarmo Annilo, Toomas Toomsoo, Margit Nõukas

Eur J Hum Genet· November 2025

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Clinical Implementation Study of Genetic Risk-Based Breast Cancer Screening.
Madli Tamm, Peeter Padrik, Kristiina Ojamaa, Anette Paas, Anni Lepland

Clin Breast Cancer· September 2025

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The Estonian Biobank's journey from biobanking to personalized medicine.
Lili Milani, Maris Alver, Sven Laur, Sulev Reisberg, Toomas Haller

Nat Commun· April 2025

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Guidance for the Clinical Use of the Breast Cancer Polygenic Risk Scores.
Peeter Padrik, Neeme Tõnisson, Tone Hovda, Kristine Kleivi Sahlberg, Eivind Hovig

Cancers (Basel)· March 2025

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Implementation of Risk-Stratified Breast Cancer Prevention With a Polygenic Risk Score Test in Clinical Practice.
Peeter Padrik, Mikk Puustusmaa, Neeme Tõnisson, Berit Kolk, Regina Saar

Breast Cancer (Auckl)· October 2023

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Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank.
Liis Leitsalu, Anu Reigo, Marili Palover, Tiit Nikopensius, Kristi Läll

Eur J Hum Genet· September 2023

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The Prevalence and Molecular Landscape of Lynch Syndrome in the Affected and General Population.
Laura Roht, Piret Laidre, Mikk Tooming, Neeme Tõnisson, Margit Nõukas

Cancers (Basel)· July 2023

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Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia.
Miriam Nurm, Anu Reigo, Margit Nõukas, Liis Leitsalu, Tiit Nikopensius

Front Genet· July 2022

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Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting.
Hannes Jürgens, Laura Roht, Liis Leitsalu, Margit Nõukas, Marili Palover

Front Genet· July 2022

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Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review.
Kristine Pavlovica, Arvids Irmejs, Margit Noukas, Marili Palover, Mart Kals, Neeme Tonisson

Eur J Med Genet· May 2022

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Prenatal diagnosis of a 46,XY karyotype female fetus with an SRY-associated gonadal dysgenesis, conceived through an intracytoplasmic sperm injection: a case report.
Lidiia Zhytnik, Maire Peters, Kadi Tilk, Tiia Reimand, Piret Ilisson

BMC Pregnancy Childbirth· February 2022

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Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients.
Tiit Nikopensius, Priit Niibo, Toomas Haller, Triin Jagomägi, Ülle Voog-Oras

Clin Rheumatol· October 2021

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From late fatherhood to prenatal screening of monogenic disorders: evidence and ethical concerns.
Lidiia Zhytnik, Maire Peters, Kadi Tilk, Kadri Simm, Neeme Tõnisson

Hum Reprod Update· October 2021

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Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants.
Liis Leitsalu, Marili Palover, Timo Tõnis Sikka, Anu Reigo, Mart Kals

Eur J Hum Genet· March 2021

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[Not Available].
Olga Žilina, Kadri Rekker, Lauris Kaplinski, Martin Sauk, Priit Paluoja

Prenat Diagn· December 2019

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Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics.
Jesse Fest, Lisanne S Vijfhuizen, Jelle J Goeman, Olga Veth, Anni Joensuu, Neeme Tonisson

Endocrinology· July 2019

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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification.
Kristi Läll, Maarja Lepamets, Marili Palover, Tõnu Esko, Andres Metspalu

BMC Cancer· June 2019

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Detection of a balanced translocation carrier through trophectoderm biopsy analysis: a case report.
Olga Tšuiko, Tuuli Dmitrijeva, Katrin Kask, Pille Tammur, Neeme Tõnisson

Mol Cytogenet· June 2019

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Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia.
Maris Alver, Marili Palover, Aet Saar, Kristi Läll, Seyedeh Maryam Zekavat

Genet Med· May 2019

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Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.
Tomas Tanskanen, Linda van den Berg, Niko Välimäki, Mervi Aavikko, Eivind Ness-Jensen

Int J Cancer· February 2018

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The target landscape of clinical kinase drugs.
Susan Klaeger, Stephanie Heinzlmeir, Mathias Wilhelm, Harald Polzer, Binje Vick

Science· December 2017

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Correction: Methylation Markers of Early-Stage Non-Small Cell Lung Cancer.
Kaie Lokk, Tõnu Vooder, Raivo Kolde, Kristjan Välk, Urmo Võsa

PLoS One· January 2017

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Erratum to: DNA methylome profiling of human tissues identifies global and tissue-specific methylation patterns.
Kaie Lokk, Vijayachitra Modhukur, Balaji Rajashekar, Kaspar Märtens, Reedik Mägi

Genome Biol· November 2016

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Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.
Olga Žilina, Marina Koltšina, Raivo Raid, Ants Kurg, Neeme Tõnisson

BMC Genomics· September 2015

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DNA methylome profiling of human tissues identifies global and tissue-specific methylation patterns.
Kaie Lokk, Vijayachitra Modhukur, Balaji Rajashekar, Kaspar Märtens, Reedik Mägi

Genome Biol· April 2014

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