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I. Andrulis · SciRah

Researcher profile · Semantic Scholar

I. Andrulis

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I. Andrulis — researcher profile on SciRah

h-index: 109
Works: 647
Citations: 46K

Most-cited papers

Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women
L. Dorling, S. Carvalho, Jamie Allen, A. González-Neira +193 more
2021New England Journal of Medicine894 citations Open access
Semantic Scholar
Genetic insights into biological mechanisms governing human ovarian ageing
K. Ruth, F. Day, Jazib Hussain, Ana Martínez-Marchal +264 more
2021Nature341 citations Open access
Semantic Scholar
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants
Shuai Li, Valentina Silvestri, Goska Leslie, T. Rebbeck +98 more
2022Journal of Clinical Oncology239 citations Open access
Semantic Scholar
Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes
N. Mavaddat, L. Dorling, S. Carvalho, Jamie Allen +90 more
2022JAMA Oncology134 citations Open access
Semantic Scholar
Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&I)
Jennifer D. Brooks, H. Nabi, I. Andrulis, A. Antoniou +25 more
2021Journal of Personalized Medicine94 citations Open access
Semantic Scholar
Physical activity, sedentary time and breast cancer risk: A Mendelian randomization study
S. Dixon-Suen, S. Lewis, Richard M. Martin, D. English +154 more
2022British Journal of Sports Medicine66 citations Open access
Semantic Scholar
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
E. Dareng, J. Tyrer, D. Barnes, Michelle R. Jones +263 more
2022European Journal of Human Genetics57 citations Open access
Semantic Scholar
Lineage-defined leiomyosarcoma subtypes emerge years before diagnosis and determine patient survival
Nathaniel D. Anderson, Y. Babichev, F. Fuligni, Federico Comitani +27 more
2021Nature Communications56 citations Open access
Semantic Scholar
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
L. Dorling, S. Carvalho, Jamie Allen, M. Parsons +102 more
2021medRxiv54 citations Open access
Semantic Scholar
Immuno-transcriptomic profiling of extracranial pediatric solid malignancies
A. Brohl, Sivasish Sindiri, Jun S. Wei, D. Milewski +33 more
2021Cell Reports50 citations Open access
Semantic Scholar
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
K. Kentistou, L. R. Kaisinger, S. Stankovic, Marc Vaudel +217 more
2024Nature Genetics40 citations Open access
Semantic Scholar
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M. M. Lakeman, A. J. van den Broek, J. A. Vos, D. Barnes +210 more
2021Genetics in Medicine37 citations Open access
Semantic Scholar
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard, M. Lush, J. Beesley, T. O'Mara +388 more
2021Nature Communications37 citations Open access
Semantic Scholar
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores
D. Barnes, Valentina Silvestri, Goska Leslie, L. McGuffog +160 more
2021Journal of the National Cancer Institute36 citations Open access
Semantic Scholar
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
Hong-Yan Li, C. Engel, M. de la Hoya, P. Peterlongo +57 more
2021Genetics in Medicine31 citations Open access
Semantic Scholar
Association of Risk-Reducing Salpingo-Oophorectomy With Breast Cancer Risk in Women With BRCA1 and BRCA2 Pathogenic Variants.
Yun-Hee Choi, M. Terry, M. Daly, R. MacInnis +7 more
2021JAMA Oncology27 citations Open access
Semantic Scholar
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
K. Kentistou, L. R. Kaisinger, S. Stankovic, M. Vaudel +216 more
2023medRxiv26 citations Open access
Semantic Scholar
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
T. Ahearn, Hao-Yu Zhang, K. Michailidou, R. Milne +155 more
2022Breast Cancer Research26 citations Open access
Semantic Scholar
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
Hong-Jie Chen, Shao-Qi Fan, J. Stone, D. Thompson +52 more
2022Breast Cancer Research26 citations Open access
Semantic Scholar
Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival
J. L. Lopes Cardozo, I. Andrulis, S. Bojesen, T. Dörk +11 more
2023Journal of Clinical Oncology25 citations Open access
Semantic Scholar
The impact of coding germline variants on contralateral breast cancer risk and survival
A. Morra, N. Mavaddat, T. Muranen, T. Ahearn +76 more
2023American Journal of Human Genetics25 citations Open access
Semantic Scholar
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects
Na Li, Magnus Zethoven, S. McInerny, L. Devereux +29 more
2021npj Breast Cancer23 citations Open access
Semantic Scholar
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2
Denise G. O'Mahony, S. Ramus, M. Southey, N. Meagher +83 more
2023British Journal of Cancer20 citations Open access
Semantic Scholar
Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Isabelle Grootes, R. Keeman, F. Blows, R. Milne +99 more
2022European Journal of Cancer19 citations Open access
Semantic Scholar
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
C. Hakkaart, J. Pearson, L. Marquart, J. Dennis +157 more
2022Communications Biology18 citations Open access
Semantic Scholar
Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Hanla A. Park, Sonja Neumeyer, K. Michailidou, M. Bolla +146 more
2021British Journal of Cancer18 citations Open access
Semantic Scholar
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
A. Morra, M. Escala-Garcia, J. Beesley, R. Keeman +146 more
2021Breast Cancer Research16 citations Open access
Semantic Scholar
Detection and utility of cell-free and circulating tumour DNA in bone and soft-tissue sarcomas
Kim M. Tsoi, N. Gokgoz, Paige Darville-O'Quinn, Patrick Prochazka +5 more
2021Bone & Joint Research16 citations Open access
Semantic Scholar
Rare germline copy number variants (CNVs) and breast cancer risk
J. Dennis, J. Tyrer, L. Walker, K. Michailidou +116 more
2022Communications Biology15 citations Open access
Semantic Scholar
Hormonal Contraception and Breast Cancer Risk for Carriers of Germline Mutations in BRCA1 and BRCA2
K. Phillips, J. Kotsopoulos, S. Domchek, M. Terry +25 more
2024Journal of Clinical Oncology14 citations Open access
Semantic Scholar
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Stefanie H. Müller, A. Lai, M. Valkovskaya, K. Michailidou +203 more
2023Genome Medicine14 citations Open access
Semantic Scholar
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
Pooja Middha, Xiaoliang Wang, S. Behrens, M. Bolla +128 more
2023Breast Cancer Research13 citations Open access
Semantic Scholar
Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction
Kristia Yiangou, N. Mavaddat, J. Dennis, Maria Zanti +123 more
2024Breast Cancer Research12 citations Open access
Semantic Scholar
Diet Quality and All-Cause Mortality in Women with Breast Cancer from the Breast Cancer Family Registry
Danielle E. Haslam, E. M. John, J. Knight, Zhongyu Li +6 more
2022Cancer Epidemiology, Biomarkers and Prevention12 citations Open access
Semantic Scholar
Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification
Maria Zanti, Denise G. O'Mahony, M. Parsons, L. Dorling +100 more
2024medRxiv11 citations Open access
Semantic Scholar
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women
G. Figlioli, A. Billaud, T. Ahearn, N. Antonenkova +90 more
2023European Journal of Human Genetics11 citations Open access
Semantic Scholar
Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
K. Kast, E. John, J. Hopper, N. Andrieu +49 more
2023Breast Cancer Research11 citations Open access
Semantic Scholar
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival
Anna Morra, M. Schreurs, I. Andrulis, H. Anton-Culver +113 more
2023Cancer Medicine9 citations Open access
Semantic Scholar
Investigating the Potential of Isolating and Expanding Tumour-Infiltrating Lymphocytes from Adult Sarcoma
A. Ko, Victoria S Coward, N. Gokgoz, B. Dickson +3 more
2022Cancers9 citations Open access
Semantic Scholar
CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers
N. Johnson, S. Maguire, A. Morra, P. Kapoor +144 more
2021British Journal of Cancer9 citations Open access
Semantic Scholar
Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?
JooYong Park, Ji-Yeob Choi, Jaesung Choi, Seokang Chung +87 more
2021Cancers8 citations Open access
Semantic Scholar
Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction
Kristia Yiangou, N. Mavaddat, J. Dennis, Maria Zanti +123 more
2024medRxiv7 citations Open access
Semantic Scholar
Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset.
Aimee L. Davidson, K. Michailidou, M. Parsons, Cristina Fortuno +88 more
2024American Journal of Human Genetics7 citations Open access
Semantic Scholar
Pregnancy-Related Factors and Breast Cancer Risk for Women Across a Range of Familial Risk
J. McDonald, Yu-Yan Liao, J. Knight, Esther M. John +13 more
2024JAMA Network Open7 citations Open access
Semantic Scholar
Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer
K. Wichert, Reiner Hoppe, Katja Ickstadt, T. Behrens +44 more
2023European Journal of Epidemiology7 citations Open access
Semantic Scholar
Weight is more informative than body mass index for predicting post-menopausal breast cancer risk: Prospective Family Study Cohort (ProF-SC)
Zhou-Feng Ye, Shuai Li, G. Dite, T. Nguyen +17 more
2021Cancer Prevention Research7 citations Open access
Semantic Scholar
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
J. Baxter, N. Johnson, K. Tomczyk, Andrea Gillespie +179 more
2021American Journal of Human Genetics7 citations Open access
Semantic Scholar
Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification
Maria Zanti, Denise G. O'Mahony, M. Parsons, L. Dorling +100 more
2025Nature Communications6 citations Open access
Semantic Scholar
Mother and Daughter Perspectives on Genetic Counseling and Testing of Adolescents for Hereditary Breast Cancer Risk.
Catherine Jennings, J. Wynn, Cecilia Miguel, Elana Levinson +13 more
2022Jornal de Pediatria6 citations Open access
Semantic Scholar
The Terry Fox Research Institute Marathon of Hope Cancer Centres Network: A pan-Canadian precision oncology initiative.
Tess Aalto, M. Abacan, S. Abadi, F. Aghababazadeh +496 more
2025Cancer Cell5 citations
Semantic Scholar

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