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Medicine

D-Index
98
Citations
41012
World Ranking
8843
National Ranking
179

Overview

Kamila Czene is affiliated with the Karolinska Institute in Sweden. Their research focuses primarily on the fields of biochemistry, genetics, and molecular biology, with significant contributions to medicine. The scientist's work spans several key subfields, including genetics, oncology, cancer research, molecular biology, and pulmonary and respiratory medicine.

The main topics of their research include:

  • BRCA gene mutations in cancer
  • Breast cancer treatment studies
  • Global cancer incidence and screening
  • Genetic associations and epidemiology
  • Cancer risks and factors
  • Digital radiography and breast imaging
  • Nutrition, genetics, and disease

Kamila Czene has frequently published in the following venues:

  • UNC Libraries
  • bioRxiv (Cold Spring Harbor Laboratory)
  • International Journal of Cancer
  • Breast Cancer Research
  • JNCI Journal of the National Cancer Institute

Their notable recent papers include:

  • "Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women," 2021, New England Journal of Medicine
  • "Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses," 2020, Nature Genetics
  • "Genetic insights into biological mechanisms governing human ovarian ageing," 2021, Nature
  • "Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes," 2020, Nature Genetics
  • "Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes," 2022, JAMA Oncology

Kamila Czene collaborates frequently with several researchers, including:

  • Per Hall
  • Mikael Eriksson
  • Manjeet K. Bolla
  • Joe Dennis
  • Stig E. Bojesen

Best Publications

  • Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev

  • Association analysis identifies 65 new breast cancer risk loci

    Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley

  • Large-scale genotyping identifies 41 new loci associated with breast cancer risk

    Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini

  • RAD51B in Familial Breast Cancer

    Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski

  • Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

    Nasim Mavaddat;Kyriaki Michailidou;Kyriaki Michailidou;Joe Dennis;Michael Lush

  • Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies

    Xiaohong R. Yang;Jenny Chang-Claude;Ellen L. Goode;Fergus J. Couch

  • Familial Risk and Heritability of Cancer Among Twins in Nordic Countries.

    Lorelei A Mucci;Lorelei A Mucci;Jacob B Hjelmborg;Jennifer R Harris;Kamila Czene

  • Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women

    Leila Dorling;Sara Carvalho;Jamie Allen

  • Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish Family-Cancer Database

    Kamila Czene;Paul Lichtenstein;Kari Hemminki

  • Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

    John R.B. Perry;Felix Day;Cathy E. Elks;Patrick Sulem

  • Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

    Kyriaki Michailidou;Jonathan Beesley;Sara Lindstrom;Sander Canisius

  • Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

    Stig E. Bojesen;Stig E. Bojesen;Karen A. Pooley;Sharon E. Johnatty;Jonathan Beesley

  • Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

    Nasim Mavaddat;Paul D.P. Pharoah;Kyriaki Michailidou;Jonathan Tyrer

  • Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

    Felix R. Day;Deborah J. Thompson;Hannes Helgason;Hannes Helgason;Daniel I. Chasman

  • MicroRNA related polymorphisms and breast cancer risk

    Sofia Khan;Dario Greco;Dario Greco;Kyriaki Michailidou;Roger L. Milne;Roger L. Milne

  • Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

    Shahana Ahmed;Gilles Thomas;Maya Ghoussaini;Catherine S. Healey

  • Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

    Felix R. Day;Katherine S. Ruth;Deborah J Thompson;Kathryn L. Lunetta

  • Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics

    Montserrat Garcia-Closas;Per Hall;Heli Nevanlinna;Karen Pooley

  • Genome-wide association studies identify four ER negative-specific breast cancer risk loci

    Montserrat Garcia-Closas;Fergus J. Couch;Sara Lindstrom;Kyriaki Michailidou

  • Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

    Day Fr;Thompson Dj;elgason H;Chasman Di

Frequent Co-Authors

Per Hall
Per Hall Karolinska Institute
Graham G. Giles
Graham G. Giles University of Melbourne
Hiltrud Brauch
Hiltrud Brauch German Cancer Research Center
Roger L. Milne
Roger L. Milne Cancer Council Victoria
Jenny Chang-Claude
Jenny Chang-Claude German Cancer Research Center
Melissa C. Southey
Melissa C. Southey Monash University
Douglas F. Easton
Douglas F. Easton University of Cambridge
Stig E. Bojesen
Stig E. Bojesen University of Copenhagen
Irene L. Andrulis
Irene L. Andrulis University of Toronto
John L. Hopper
John L. Hopper University of Melbourne

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