Publications by authors named "Ute Hamann"

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Genetic landscape of Pakistani familial breast cancer patients using multigene panel testing.
Muhammad Usman Rashid, Noor Muhammad, Shumaila Arif, Humaira Naeemi, Ute Hamann

Int J Cancer· November 2025

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Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women.
Peh Joo Ho, Christine Kim Yan Loo, Ryan Jak Yang Lim, Meng Huang Goh, Mustapha Abubakar, Ute Hamann

Cancers (Basel)· November 2025

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Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer.
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, Goska Leslie, Manjeet K Bolla, Ute Hamann

NPJ Genom Med· November 2025

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Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer.
Amandine Billaud, Gisella Figlioli, Clémence Mooser, Irene Casamassima, Violette Azzoni, Ute Hamann

Breast· October 2025

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Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
Kate Lawrenson, Siddhartha Kar, Karen McCue, Karoline Kuchenbaeker, Kyriaki Michailidou, Ute Hamann

Nat Commun· September 2025

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Predicting the likelihood of carrying BRCA1 or BRCA2 pathogenic variants in high-risk Pakistani breast cancer patients.
Shumaila Arif, Noor Muhammad, Boon Hong Ang, Humaira Naeemi, Waqas Sami, Ute Hamann

Breast Cancer Res Treat· July 2025

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Establishing the First Genetic Variant Registry for Breast and Ovarian Cancer in Colombia: Insights and Implications.
Robert de Deugd, Julián Camilo Riano, Esther de Vries, Andrés F Cardona, July Rodriguez, Ute Hamann

Diseases· July 2025

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Anticipation effect in Pakistani breast cancer families with or without BRCA1/2 pathogenic variants.
Noor Muhammad, Humaira Naeemi, Shumaila Arif, Ute Hamann, Muhammad Usman Rashid

Cancer Epidemiol· June 2025

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Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification.
Maria Zanti, Denise G O'Mahony, Michael T Parsons, Leila Dorling, Joe Dennis, Ute Hamann

Nat Commun· May 2025

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Overlap of high-risk individuals across family history, genetic & non-genetic breast cancer risk models: Analysis of 180,398 women from European & Asian ancestries.
Peh Joo Ho, Christine Kim Yan Loo, Meng Huang Goh, Mustapha Abubakar, Thomas U Ahearn, Ute Hamann

medRxiv· March 2025

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Lessons learned from a candidate gene study investigating aromatase inhibitor treatment outcome in breast cancer.
Reiner Hoppe, Stefan Winter, Wing-Yee Lo, Kyriaki Michailidou, Manjeet K Bolla, Ute Hamann

NPJ Breast Cancer· February 2025

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Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction.
Kristia Yiangou, Nasim Mavaddat, Joe Dennis, Maria Zanti, Qin Wang, Ute Hamann

Breast Cancer Res· December 2024

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Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset.
Aimee L Davidson, Kyriaki Michailidou, Michael T Parsons, Cristina Fortuno, Manjeet K Bolla, Ute Hamann

Am J Hum Genet· September 2024

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Analysis of more than 400,000 women provides case-control evidence for and variant classification.
Maria Zanti, Denise G O'Mahony, Michael T Parsons, Leila Dorling, Joe Dennis, Ute Hamann

medRxiv· September 2024

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Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Ute Hamann

Nat Genet· August 2024

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Marginal Contribution of Pathogenic Germline Variants to Pakistani Early-Onset and Familial Breast/Ovarian Cancer Patients.
Noor Muhammad, Muhammad Sohail Afzal, Ute Hamann, Muhammad Usman Rashid

J Cancer Allied Spec· August 2024

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Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Ute Hamann

Nat Genet· July 2024

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Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk.
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, Goska Leslie, Manjeet K Bolla, Ute Hamann

medRxiv· March 2024

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Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction.
Kristia Yiangou, Nasim Mavaddat, Joe Dennis, Maria Zanti, Qin Wang, Ute Hamann

medRxiv· February 2024

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Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel.
Hagai Levi, Shai Carmi, Saharon Rosset, Rinat Yerushalmi, Aviad Zick, Ute Hamann

J Med Genet· November 2023

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Contribution of constitutional BRCA1 promoter methylation to early-onset and familial breast cancer patients from Pakistan.
Noor Muhammad, Ayesha Azeem, Muhammad Abu Bakar, Karolina Prajzendanc, Asif Loya, Ute Hamann

Breast Cancer Res Treat· November 2023

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Native American ancestry and breast cancer risk in Colombian and Mexican women: ruling out potential confounding through ancestry-informative markers.
Linda Zollner, Diana Torres, Ignacio Briceno, Michael Gilbert, Gabriela Torres-Mejía, Ute Hamann

Breast Cancer Res· October 2023

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Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer.
Katharina Wichert, Reiner Hoppe, Katja Ickstadt, Thomas Behrens, Stefan Winter, Ute Hamann

Eur J Epidemiol· October 2023

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A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry.
Pooja Middha, Xiaoliang Wang, Sabine Behrens, Manjeet K Bolla, Qin Wang, Ute Hamann

Breast Cancer Res· August 2023

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Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson M de Oliveira, Ute Hamann

medRxiv· June 2023

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