Ilari Scheinin

1.2k total citations
14 papers, 712 citations indexed

About

Ilari Scheinin is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ilari Scheinin has authored 14 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Ilari Scheinin's work include Genomic variations and chromosomal abnormalities (5 papers), Glioma Diagnosis and Treatment (3 papers) and Cancer-related molecular mechanisms research (3 papers). Ilari Scheinin is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Glioma Diagnosis and Treatment (3 papers) and Cancer-related molecular mechanisms research (3 papers). Ilari Scheinin collaborates with scholars based in Netherlands, Finland and United States. Ilari Scheinin's co-authors include Jarno Tuimala, Massimiliano Gentile, Taavi Hupponen, Petri Klemelä, Eija Korpelainen, Bauke Ylstra, Jaap C. Reijneveld, Pieter Wesseling, Hinke F. van Thuijl and Hendrik F. van Essen and has published in prestigious journals such as Nucleic Acids Research, Cancer Research and Clinical Cancer Research.

In The Last Decade

Ilari Scheinin

14 papers receiving 702 citations

Peers

Countries citing papers authored by Ilari Scheinin

Since Specialization

Citations

This map shows the geographic impact of Ilari Scheinin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ilari Scheinin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ilari Scheinin more than expected).

Fields of papers citing papers by Ilari Scheinin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ilari Scheinin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ilari Scheinin. The network helps show where Ilari Scheinin may publish in the future.

Co-authorship network of co-authors of Ilari Scheinin

This figure shows the co-authorship network connecting the top 25 collaborators of Ilari Scheinin. A scholar is included among the top collaborators of Ilari Scheinin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ilari Scheinin. Ilari Scheinin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Abstract 52: QDNAseq: A bioinformatics pipeline for DNA copy number analysis from shallow whole genome sequencing with noise levels near the probabilistic lower limit imposed by read counting 2016 ·Clinical Cancer Research ·Daoud Sie, Ilari Scheinin, Stef van Lieshout, Martijn Cordes, Daniel Pinkel, Donna G. Albertson, Mark A. van de Wiel, Bauke Ylstra	1
2	Driver Gene and Novel Mutations in Asbestos-Exposed Lung Adenocarcinoma and Malignant Mesothelioma Detected by Exome Sequencing 2015 ·Lung ·(unknown), Virinder Kaur Sarhadi, Aija Knuuttila, Ilari Scheinin, Pekka Ellonen, Sonja Lagström, Mikko Rönty, Eeva Kettunen, Kirsti Husgafvel‐Pursiainen, Henrik Wolff, Sakari Knuutila	32
3	Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours 2015 ·Neuropathology and Applied Neurobiology ·Avanita S. Prabowo, Hinke F. van Thuijl, Ilari Scheinin, Daoud Sie, Hendrik F. van Essen, Anand M. Iyer, Wim G.M. Spliet, Cyrille H. Ferrier, Peter C. van Rijen, Tim J. Veersema, Maria Thom, (unknown), Jaap C. Reijneveld, Bauke Ylstra, Pieter Wesseling, Eleonora Aronica	25
4	DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly 2014 ·Genome Research ·Ilari Scheinin, Daoud Sie, Henrik Bengtsson, Mark A. van de Wiel, Adam B. Olshen, Hinke F. van Thuijl, Hendrik F. van Essen, Paul P. Eijk, François Rustenburg, Gerrit A. Meijer, Jaap C. Reijneveld, Pieter Wesseling, Daniel Pinkel, Donna G. Albertson, Bauke Ylstra	265
5	Abstract 3426: A novel approach to copy number assessment by whole genome sequencing reveals extensive spatial heterogeneity in diffuse low-grade glioma 2014 ·Cancer Research ·Ilari Scheinin, Hinke F. van Thuijl, Daoud Sie, Hendrik F. van Essen, Paul P. Eijk, François Rustenburg, Ahmed Idbaïh, Agustí Alentorn, Gerrit A. Meijer, (unknown), Henrik Bengtsson, Adam B. Olshen, Eleonora Aronica, J.J. Heimans, Jaap C. Reijneveld, Pieter Wesseling, Donna G. Albertson, Dan Pinkel, Bauke Ylstra	1
6	Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations 2013 ·Genomics ·Virinder Kaur Sarhadi, Leo Lahti, Ilari Scheinin, (unknown), Suvi Savola, (unknown), Riikka Räty, Erkki Elonen, Pekka Ellonen, Ulla M. Saarinen‐Pihkala, Sakari Knuutila	13
7	Clinical value of chromosome arms 19q and 11p losses in low-grade gliomas 2013 ·Neuro-Oncology ·Agustí Alentorn, Hinke F. van Thuijl, Yannick Marie, (unknown), Alain Carpentier, Blandine Boisselier, Florence Laigle–Donadey, Karima Mokhtari, Ilari Scheinin, Pieter Wesseling, Bauke Ylstra, Laurent Capelle, Khê Hoang‐Xuan, Marc Sanson, Jean‐Yves Delattre, Jaap C. Reijneveld, Ahmed Idbaïh	11
8	Biologist-friendly analysis software for NGS data 2013 ·EMBnet journal ·Aleksi Kallio, Taavi Hupponen, Massimiliano Gentile, Jarno Tuimala, Kimmo Mattila, Ari-Matti Sarén, Petri Klemelä, Ilari Scheinin, Eija Korpelainen	1
9	Homozygous deletions of cadherin genes in chondrosarcoma—an array comparative genomic hybridization study 2012 ·Cancer Genetics ·Tarja Niini, Ilari Scheinin, Leo Lahti, Suvi Savola, Fredrik Mertens, Jaakko Hollmén, Tom Böhling, Aarne Kivioja, Karolin H. Nord, Sakari Knuutila	1
10	miRNA expression profiles in myelodysplastic syndromes reveal Epstein–Barr virus miR-BART13 dysregulation 2011 ·Leukemia & lymphoma ·Ioana Borze, Ilari Scheinin, Sanna Siitonen, Erkki Elonen, Eeva Juvonen, Sakari Knuutila	20
11	Chipster: user-friendly analysis software for microarray and other high-throughput data 2011 ·BMC Genomics ·(unknown), Jarno Tuimala, Taavi Hupponen, Petri Klemelä, Massimiliano Gentile, Ilari Scheinin, (unknown), (unknown), Eija Korpelainen	259
12	CGHpower: exploring sample size calculations for chromosomal copy number experiments 2010 ·BMC Bioinformatics ·Ilari Scheinin, José A. Ferreira, Sakari Knuutila, Gerrit A. Meijer, Mark A. van de Wiel, Bauke Ylstra	5
13	Integrated gene copy number and expression microarray analysis of gastric cancer highlights potential target genes 2008 ·International Journal of Cancer ·Samuel Myllykangas, Siina Junnila, Arto Kokkola, Reija Autio, Ilari Scheinin, Tuula Kiviluoto, Marja‐Liisa Karjalainen‐Lindsberg, Jaakko Hollmén, Sakari Knuutila, Pauli Puolakkainen, Outi Monni	54
14	CanGEM: mining gene copy number changes in cancer 2007 ·Nucleic Acids Research ·Ilari Scheinin, Samuel Myllykangas, Ioana Borze, Tom Böhling, Sakari Knuutila, Juha Saharinen	24

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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