Tuomo Mantere - Concepedia

Author

Tuomo Mantere

Also Known As

Amanda Elliott, Arto Lehisto, Jarmo Harju, Maral Jamshidi, Minna Karjalainen, Reetta Hinttala, Riitta Kaarteenaho, Seppo Vainio, T Mantere, T. Mantere

Publications

6.3K

Citations

H-Index

Concepts

All Affiliations

University of Oulu Radboud University Medical Center Radboud University Nijmegen Radboud Institute for Molecular Life Sciences NordLab

About

Tuomo Mantere is an author at University of Oulu specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	687
2	Health Sciences	3	3	235
3	Engineering	2	2	66
4	Genomic Medicine	2	2	50
5	Cell Biology	1	1	13

Tuomo Mantere

Publications

Citations

H-Index

Page 1

	Year	Citations
Presence of Genetic Variants Among Young Men With Severe COVID-19 Caspar I. van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers, JAMA	2020	822
Optical genome mapping enables constitutional chromosomal aberration detection Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard, The American Journal of Human Genetics ChromatinSpectral KaryotypingOptical Genome MappingGeneticsChromosomal Rearrangement	2021	239
Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping Kornelia Neveling, Tuomo Mantere, Susan Vermeulen, The American Journal of Human Genetics ChromatinNext-generation CytogeneticsSomatic VariantHealth SciencesTumor Heterogeneity	2021	185
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy Jaakko Tyrmi, Tea Kaartokallio, A. Inkeri Lokki, JAMA Cardiology	2023	114
Familial long-read sequencing increases yield of de novo mutations Michelle D. Noyes, William T. Harvey, David Porubský, The American Journal of Human Genetics Long-read SequencingGenetic DisorderGeneticsMolecular GeneticsGenomics	2022	78
Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders Juhani Junttila, Lauri Holmström, Katri Pylkäs, Circulation	2018	55
Optical Genome Mapping: A Promising New Tool to Assess Genomic Complexity in Chronic Lymphocytic Leukemia (CLL) Anna Puiggros, Sílvia Ramos‐Campoy, Joanna Kamaso, Cancers	2022	46
Optical genome mapping identifies a germline retrotransposon insertion in <scp><i>SMARCB1</i></scp> in two siblings with atypical teratoid rhabdoid tumors Mariangela Sabatella, Tuomo Mantere, Esmé Waanders, The Journal of Pathology EngineeringGeneticsPathologyMolecular GeneticsDisease Gene Identification	2021	41
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population Johanna I. Kiiski, Anna Tervasmäki, Liisa M. Pelttari, Breast Cancer Research and Treatment	2017	36
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility Tuomo Mantere, Anna Tervasmäki, Anna Nurmi, Scientific Reports	2017	34

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