Tuomo Mantere

6.4k total citations
22 papers, 605 citations indexed

About

Tuomo Mantere is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Tuomo Mantere has authored 22 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Pathology and Forensic Medicine. Recurrent topics in Tuomo Mantere's work include DNA Repair Mechanisms (8 papers), Cancer Genomics and Diagnostics (7 papers) and BRCA gene mutations in cancer (5 papers). Tuomo Mantere is often cited by papers focused on DNA Repair Mechanisms (8 papers), Cancer Genomics and Diagnostics (7 papers) and BRCA gene mutations in cancer (5 papers). Tuomo Mantere collaborates with scholars based in Finland, Netherlands and United States. Tuomo Mantere's co-authors include Alexander Hoischen, Simone Kersten, Katri Pylkäs, Kornelia Neveling, Marian Stevens‐Kroef, Daniël Olde Weghuis, Marc Pauper, Michiel Oorsprong, Ronald van Beek and Ellen Kater‐Baats and has published in prestigious journals such as Circulation, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Tuomo Mantere

20 papers receiving 600 citations

Peers

Countries citing papers authored by Tuomo Mantere

Since Specialization

Citations

This map shows the geographic impact of Tuomo Mantere'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 Tuomo Mantere with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tuomo Mantere more than expected).

Fields of papers citing papers by Tuomo Mantere

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tuomo Mantere. 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 Tuomo Mantere. The network helps show where Tuomo Mantere may publish in the future.

Co-authorship network of co-authors of Tuomo Mantere

This figure shows the co-authorship network connecting the top 25 collaborators of Tuomo Mantere. A scholar is included among the top collaborators of Tuomo Mantere 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 Tuomo Mantere. Tuomo Mantere is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Population-based study of recurrent DNA damage response gene variants in breast cancer cases 2025 ·Breast Cancer Research and Treatment ·(unknown), (unknown), Mervi Grip, (unknown), (unknown), Robert Winqvist, Tuomo Mantere, Katri Pylkäs	0
2	Structural Variant Analysis of Complex Karyotype Myelodysplastic Neoplasia Through Optical Genome Mapping 2025 ·Genes Chromosomes and Cancer ·(unknown), (unknown), (unknown), (unknown), Eeva‐Riitta Savolainen, Katri Pylkäs, Tuomo Mantere	3
3	Optical Genome Mapping Identifies a Second Xq27.1 Rearrangement Associated With Charcot–Marie–Tooth Neuropathy CMTX3 2024 ·Molecular Genetics & Genomic Medicine ·Elisa Rahikkala, (unknown), (unknown), (unknown), Maria Suo‐Palosaari, Päivi Vieira, (unknown), Johanna Uusimaa, Katri Pylkäs, Tuomo Mantere	0
4	A framework for the clinical implementation of optical genome mapping in hematologic malignancies 2024 ·American Journal of Hematology ·Brynn Levy, Rashmi Kanagal‐Shamanna, Nikhil Sahajpal, Kornelia Neveling, Katrina Rack, Barbara Dewaele, Daniël Olde Weghuis, Marian Stevens‐Kroef, Anna Puiggros, Mar Mallo, Ben Clifford, Tuomo Mantere, Alexander Hoischen, Blanca Espinet, Ravindra Kolhe, Françesc Solé, Gordana Raca, Adam C. Smith	19
5	A complex structural variant near SOX3 causes X-linked split-hand/foot malformation 2023 ·Human Genetics and Genomics Advances ·Elke de Boer, Carlo Marcelis, Kornelia Neveling, Ellen van Beusekom, Alexander Hoischen, Willemijn M. Klein, Nicole de Leeuw, Tuomo Mantere, Uirá Souto Melo, Jeroen van Reeuwijk, Dominique Smeets, Malte Spielmann, Tjitske Kleefstra, Hans van Bokhoven, Lisenka E.L.M. Vissers	1
6	Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predisposition 2023 ·Familial Cancer ·(unknown), (unknown), (unknown), (unknown), Jukka S. Moilanen, Robert Winqvist, Tuomo Mantere, Outi Kuismin, Katri Pylkäs	3
7	Optical Genome Mapping as an Alternative to FISH-Based Cytogenetic Assessment in Chronic Lymphocytic Leukemia 2023 ·Cancers ·(unknown), (unknown), (unknown), (unknown), Eeva‐Riitta Savolainen, Katri Pylkäs, Tuomo Mantere	20
8	Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility 2022 ·Familial Cancer ·(unknown), (unknown), Tiina M. Mattila, (unknown), (unknown), Outi Kuismin, Robert Winqvist, Jukka S. Moilanen, Tuomo Mantere, Katri Pylkäs	1
9	Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors 2021 ·The Journal of Pathology ·Mariangela Sabatella, Tuomo Mantere, Esmé Waanders, Kornelia Neveling, Arjen R. Mensenkamp, Freerk van Dijk, Jayne Y. Hehir‐Kwa, (unknown), Michael Kwint, (unknown), (unknown), Corrie Gidding, Maarten H. Lequin, Benno Küsters, Pieter Wesseling, Marcel Nelen, (unknown), Alexander Hoischen, Marjolijn C.J. Jongmans, Roland P. Kuiper	28
10	Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping 2021 ·The American Journal of Human Genetics ·Kornelia Neveling, Tuomo Mantere, (unknown), Michiel Oorsprong, Ronald van Beek, Ellen Kater‐Baats, Marc Pauper, (unknown), Dominique Smeets, Daniël Olde Weghuis, Marian Stevens‐Kroef, Alexander Hoischen	110
11	Long-read technologies identify a hidden inverted duplication in a family with choroideremia 2021 ·SHILAP Revista de lepidopterología ·(unknown), Kornelia Neveling, Tuomo Mantere, Ronny Derks, Lonneke Haer‐Wigman, (unknown), Michael Kwint, (unknown), (unknown), Carel B. Hoyng, Christian Gilissen, Lisenka E.L.M. Vissers, Marcel Nelen, Frans P.M. Cremers, Alexander Hoischen, Susanne Roosing	13
12	Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition 2020 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), Tuomo Mantere, (unknown), Laura Huilaja, Kaisa Tasanen, Robert Winqvist, Richarda M. de Voer, Katri Pylkäs	2
13	Long-Read Sequencing Emerging in Medical Genetics 2019 ·Frontiers in Genetics ·Tuomo Mantere, Simone Kersten, Alexander Hoischen	256
14	Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly 2019 ·International Journal of Cancer ·(unknown), Tuomo Mantere, Leila Eshraghi, (unknown), (unknown), Veli‐Pekka Ronkainen, (unknown), (unknown), Hellevi Peltoketo, Katri Pylkäs	9
15	Mutation of TP53, translocation analysis and immunohistochemical expression of MYC, BCL-2 and BCL-6 in patients with DLBCL treated with R-CHOP 2018 ·Scientific Reports ·(unknown), Mette Ølgod Pedersen, Tuomo Mantere, Peter Nørgaard, (unknown), Kirsi‐Maria Haapasaari, Jan Böhm, Esa Jantunen, Taina Turpeenniemi‐Hujanen, Katrin Rapakko, Peeter Karihtala, Ylermi Soini, Kaija Vasala, Outi Kuittinen	23
16	Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders 2018 ·Circulation ·Juhani Junttila, Lauri Holmström, Katri Pylkäs, Tuomo Mantere, Kari Kaikkonen, Katja Porvari, (unknown), Lasse Pakanen, Risto Kerkelä, Robert J. Myerburg, (unknown)	39
17	Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer 2018 ·International Journal of Cancer ·(unknown), Tuomo Mantere, Jaana M. Hartikainen, Saila Kauppila, (unknown), (unknown), Mervi Grip, Peeter Karihtala, Arja Jukkola‐Vuorinen, (unknown), Robert Winqvist, Katri Pylkäs	13
18	FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population 2017 ·Breast Cancer Research and Treatment ·Johanna I. Kiiski, (unknown), Liisa M. Pelttari, Sofia Khan, Tuomo Mantere, Katri Pylkäs, (unknown), Maria Tengström, Anders Kvist, Åke Borg, Veli‐Matti Kosma, Anne Kallioniemi, Johanna Schleutker, Ralf Bützow, Carl Blomqvist, Kristiina Aittomäki, Robert Winqvist, Heli Nevanlinna	22
19	FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome 2016 ·International Journal of Cancer ·Johanna I. Kiiski, Rainer Fagerholm, (unknown), Liisa M. Pelttari, Sofia Khan, (unknown), Tuomo Mantere, Katri Pylkäs, Jiří Bártek, Jiřina Bártková, (unknown), Maria Tengström, Veli‐Matti Kosma, Robert Winqvist, Anne Kallioniemi, Kristiina Aittomäki, Carl Blomqvist, Heli Nevanlinna	9
20	Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility 2016 ·PLoS Genetics ·Tuomo Mantere, Robert Winqvist, Saila Kauppila, Mervi Grip, Arja Jukkola‐Vuorinen, (unknown), Katrin Rapakko, Katri Pylkäs	18

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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