Grethe I.G. Alnæs

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk”.

Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

Scientific Reports(2020)10.1038/s41598-020-65665-y

N/A

0DataRank · unranked

6 citations

Wendy J.C. Prager ‐ van der Smissen, J. Margriet Collée, Manjeet K. Bolla, Qin Wang, Kyriaki Michailidou +95 more

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

British Journal of Cancer(2021)10.1038/s41416-021-01432-8

N/A

0DataRank · unranked

24 citations

Sonja Neumeyer, Kyriaki Michailidou, Manjeet K. Bolla, Qin Wang, Joe Dennis +94 more

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

Breast Cancer Research(2021)10.1186/s13058-021-01450-7

N/A

0DataRank · unranked

23 citations

Maria Escala-Garcia, Jonathan Beesley, Renske Keeman, Sander Canisius, Thomas U. Ahearn +94 more

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Breast Cancer Research(2022)10.1186/s13058-021-01484-x

N/A

0DataRank · unranked

32 citations

Haoyu Zhang, Kyriaki Michailidou, Roger L. Milne, Manjeet K. Bolla, Joe Dennis +94 more

Rare germline copy number variants (CNVs) and breast cancer risk

Communications Biology(2022)10.1038/s42003-021-02990-6

N/A

0DataRank · unranked

15 citations

Jonathan P. Tyrer, Logan C. Walker, Kyriaki Michailidou, Leila Dorling, Manjeet K. Bolla +94 more

The impact of coding germline variants on contralateral breast cancer risk and survival

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.02.003

N/A

0DataRank · unranked

27 citations

Nasim Mavaddat, Taru Muranen, Thomas U. Ahearn, Jamie Allen, Irene L. Andrulis +94 more

Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

Genome Medicine(2023)10.1186/s13073-022-01152-5

N/A

0DataRank · unranked

15 citations

Alvina G. Lai, Maria Valkovskaya, Kyriaki Michailidou, Manjeet K. Bolla, Qin Wang +95 more

FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

European Journal of Human Genetics(2023)10.1038/s41431-022-01257-w

N/A

0DataRank · unranked

14 citations

Amandine Billaud, Thomas U. Ahearn, Natalia Antonenkova, Heiko Becher, Matthias W. Beckmann +95 more

Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.004

N/A

0DataRank · unranked

8 citations

Kyriaki Michailidou, Michael T. Parsons, Cristina Fortuño, Manjeet K. Bolla, Qin Wang +95 more

Germline polygenic risk scores are associated with immune gene expression signature and immune cell infiltration in breast cancer

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.08.009

N/A

0DataRank · unranked

3 citations

Cheng Peng, Ina Skaara Brorson, Denise G O'Mahony, Rebecca L. Kelly, Yujing J. Heng +10 more