2023 - Research.com Medicine in Finland Leader Award
2023 - Research.com Molecular Biology in Finland Leader Award
2022 - Research.com Genetics and Molecular Biology in Finland Leader Award
The scientist’s investigation covers issues in Comparative genomic hybridization, Molecular biology, Pathology, Genetics and Cancer research. His study in Comparative genomic hybridization is interdisciplinary in nature, drawing from both Gene duplication and Carcinogenesis, Cancer. His Molecular biology study integrates concerns from other disciplines, such as Human genome, Gene expression profiling, DNA, Lymphoma and Colorectal cancer.
His Pathology research includes themes of Stomach, Internal medicine, Karyotype and Cytogenetics. Sakari Knuutila interconnects Messenger RNA, Gene expression and Gene isoform in the investigation of issues within Cancer research. His studies in Gene integrate themes in fields like Lung cancer and Adenocarcinoma.
His primary scientific interests are in Molecular biology, Comparative genomic hybridization, Genetics, Pathology and Cancer research. His Molecular biology study incorporates themes from Cell culture, Chromosomal translocation, Amplicon, Mitosis and Antibody. Sakari Knuutila focuses mostly in the field of Comparative genomic hybridization, narrowing it down to topics relating to Cancer and, in certain cases, Oncology.
The various areas that Sakari Knuutila examines in his Pathology study include Leukemia, In situ hybridization and Cytogenetics. His Cytogenetics research is multidisciplinary, relying on both Aneuploidy and Karyotype. His research integrates issues of Carcinoma, Immunology, Bioinformatics and Gene expression profiling in his study of Cancer research.
Sakari Knuutila mainly investigates Cancer research, microRNA, Molecular biology, Pathology and Internal medicine. His Cancer research study combines topics from a wide range of disciplines, such as Immunohistochemistry, Bioinformatics, KRAS, Carcinoma and Gene. His studies deal with areas such as Gene expression profiling, Microarray analysis techniques, Myeloid leukemia, Regulation of gene expression and Bone marrow as well as microRNA.
His Molecular biology study combines topics in areas such as Comparative genomic hybridization, Real-time polymerase chain reaction and Copy-number variation. His Comparative genomic hybridization study is concerned with the larger field of Genetics. His studies examine the connections between Internal medicine and genetics, as well as such issues in Oncology, with regards to Targeted therapy, Young adult, Malignancy and Biomarker.
His main research concerns Cancer research, microRNA, Molecular biology, Cancer and Pathology. The study incorporates disciplines such as Immunohistochemistry, Downregulation and upregulation, Gene and Merkel cell carcinoma, Merkel cell polyomavirus in addition to Cancer research. His microRNA research is multidisciplinary, incorporating perspectives in Bioinformatics, Gene expression profiling, Microarray analysis techniques, Myeloid leukemia and Colorectal cancer.
His Molecular biology research is multidisciplinary, incorporating elements of Anaplastic lymphoma kinase, Comparative genomic hybridization, Fusion gene and Real-time polymerase chain reaction. Sakari Knuutila combines subjects such as CDKN2A and DNA methylation with his study of Comparative genomic hybridization. His research investigates the link between Cancer and topics such as Carcinoma that cross with problems in Chromosome 3, Fluorescence in situ hybridization and Adenocarcinoma.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Prognostic subgroups in B-cell chronic lymphocytic leukemia defined by specific chromosomal abnormalities.
Gunnar Juliusson;David G. Oscier;Margaret Fitchett;Fiona M. Ross.
The New England Journal of Medicine (1990)
DNA copy number amplifications in human neoplasms : Review of comparative genomic hybridization studies
S. Knuutila;A.-M. Björkqvist;K. Autio;M. Tarkkanen.
American Journal of Pathology (1998)
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
A Hemminki;I Tomlinson;D Markie;H Järvinen.
Nature Genetics (1997)
DNA Copy Number Losses in Human Neoplasms
Sakari Knuutila;Yan Aalto;Kirsi Autio;Anna Maria Björkqvist.
American Journal of Pathology (1999)
A novel endothelial cell surface receptor tyrosine kinase with extracellular epidermal growth factor homology domains.
J Partanen;E Armstrong;T P Mäkelä;J Korhonen.
Molecular and Cellular Biology (1992)
CDKN2A, NF2, and JUN are dysregulated among other genes by miRNAs in malignant mesothelioma -A miRNA microarray analysis.
Mohamed Guled;Leo Lahti;Leo Lahti;Pamela M. Lindholm;Kaisa Salmenkivi.
Genes, Chromosomes and Cancer (2009)
Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: evidence for its fusion with MLL in acute myeloid leukemia.
Peter J. Kourlas;Matthew P. Strout;Brian Becknell;Maria Luisa Veronese.
Proceedings of the National Academy of Sciences of the United States of America (2000)
DNA sequence copy number changes in gastrointestinal stromal tumors: tumor progression and prognostic significance.
Wa’el El-Rifai;Maarit Sarlomo-Rikala;Leif C. Andersson;Sakari Knuutila.
Cancer Research (2000)
Rearrangement of ALL1 (MLL) in Acute Myeloid Leukemia with Normal Cytogenetics
Michael A. Caligiuri;Matthew P. Strout;David Lawrence;Diane C. Arthur.
Cancer Research (1998)
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
Katri Heikkinen;Katrin Rapakko;Sanna Maria Karppinen;Hannele Erkko.
Carcinogenesis (2005)
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