Johanna Sandgren

2.2k total citations
21 papers, 818 citations indexed

About

Johanna Sandgren is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Johanna Sandgren has authored 21 papers receiving a total of 818 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Cancer Research and 6 papers in Genetics. Recurrent topics in Johanna Sandgren's work include Genomic variations and chromosomal abnormalities (5 papers), Glioma Diagnosis and Treatment (4 papers) and Cancer Genomics and Diagnostics (4 papers). Johanna Sandgren is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Glioma Diagnosis and Treatment (4 papers) and Cancer Genomics and Diagnostics (4 papers). Johanna Sandgren collaborates with scholars based in Sweden, United States and Poland. Johanna Sandgren's co-authors include Teresita Díaz de Ståhl, Jan P. Dumanski, Jan Komorowski, Uwe Menzel, Robin Andersson, Carl E.G. Bruder, Arkadiusz Piotrowski, Ammar Zaghlool, Joannah Score and Vilmantas Giedraitis and has published in prestigious journals such as Nature Genetics, Bioinformatics and International Journal of Cancer.

In The Last Decade

Johanna Sandgren

20 papers receiving 809 citations

Peers

Countries citing papers authored by Johanna Sandgren

Since Specialization

Citations

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

Fields of papers citing papers by Johanna Sandgren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Johanna Sandgren

This figure shows the co-authorship network connecting the top 25 collaborators of Johanna Sandgren. A scholar is included among the top collaborators of Johanna Sandgren 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 Johanna Sandgren. Johanna Sandgren 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	Pediatric brain tumor classification using digital pathology and deep learning: Evaluation of SOTA methods on a multi‐center Swedish cohort 2025 ·Brain Pathology ·(unknown), Per Olof Nyman, (unknown), Ida Blystad, Alia Shamikh, (unknown), Teresita Díaz de Ståhl, Johanna Sandgren, Peter Lundberg, Neda Haj‐Hosseini	0
2	The potential of liquid biopsy for detection of the KIAA1549-BRAF fusion in circulating tumor DNA from children with pilocytic astrocytoma 2024 ·Neuro-Oncology Advances ·(unknown), Teresita Díaz de Ståhl, (unknown), (unknown), G Giraud, Per Olof Nyman, (unknown), Johanna Sandgren, Emma Tham, Ulrika Sandvik	6
3	Simultaneous Ultra-Sensitive Detection of Structural and Single Nucleotide Variants Using Multiplex Droplet Digital PCR in Liquid Biopsies from Children with Medulloblastoma 2023 ·Cancers ·(unknown), (unknown), Teresita Díaz de Ståhl, Alia Shamikh, Johanna Sandgren, Richard Rosenquist, Magnus Nordenskjöld, Arja Harila‐Saari, Gisela Barbany, Ulrika Sandvik, Emma Tham	11
4	Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma: A potential treatment target in rare cases? 2021 ·Genes Chromosomes and Cancer ·Shamik Mitra, (unknown), Linda Magnusson, Paul Piccinelli, (unknown), Ingrid Øra, Gustaf Ljungman, Johanna Sandgren, David Gisselsson, Fredrik Mertens	2
5	Identification of Mutations, Expression Alterations and Fusion Transcripts by Next Generation RNAseq in Castration-Resistant Prostate Cancer Cell lines with Possible Clinical Relevance 2017 ·Yuanjun Ma, Yali Miao, (unknown), Johanna Sandgren, Teresita Díaz de Ståhl, Lena Lennartsson, Sten Nilsson, Chunde Li	2
6	Identification of mutations, gene expression changes and fusion transcripts by whole transcriptome RNAseq in docetaxel resistant prostate cancer cells 2016 ·SpringerPlus ·Yuanjun Ma, Yali Miao, (unknown), Johanna Sandgren, Teresita Díaz de Ståhl, Mikael Huss, Lena Lennartsson, Yanling Liu, Monica Nistér, Sten Nilsson, Chunde Li	16
7	Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context ofSMARCB1Deficiency 2015 ·BioMed Research International ·Johanna Sandgren, Stefan Holm, (unknown), (unknown), Pernilla Grillner, Monica Nistér, Teresita Díaz de Ståhl	7
8	Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer 2014 ·Nature Genetics ·Lars A. Forsberg, Chiara Rasi, (unknown), Hanna Davies, (unknown), (unknown), Johanna Sandgren, Teresita Díaz de Ståhl, Ammar Zaghlool, Vilmantas Giedraitis, Lars Lannfelt, Joannah Score, Nicholas C.P. Cross, Devin Absher, Eva Tiensuu Janson, Cecilia M. Lindgren, Andrew P. Morris, Erik Ingelsson, Lars Lind, Jan P. Dumanski	287
9	Age dependence of tumor genetics in unfavorable neuroblastoma: arrayCGH profiles of 34 consecutive cases, using a Swedish 25-year neuroblastoma cohort for validation 2013 ·BMC Cancer ·Cihan Cetinkaya, Tommy Martinsson, Johanna Sandgren, Catarina Träger, Per Kogner, Jan P. Dumanski, Teresita Díaz de Ståhl, Fredrik Hedborg	10
10	Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling 2011 ·Journal of Neuro-Oncology ·Helena Nord, Susan Pfeifer, Pelle Nilsson, Johanna Sandgren, Svetlana N. Popova, Bo Strömberg, Irina Alafuzoff, Monica Nistér, Teresita Díaz de Ståhl	2
11	MicroRNA profiling of benign and malignant pheochromocytomas identifies novel diagnostic and therapeutic targets 2010 ·Endocrine Related Cancer ·Goswin Y. Meyer‐Rochow, Nicole Jackson, John V. Conaglen, (unknown), Muthusamy Kunnimalaiyaan, Herbert Chen, Gunnar Westin, Johanna Sandgren, Peter Stålberg, Elham Khanafshar, Daniel Shibru, Quan‐Yang Duh, Orlo H. Clark, Electron Kebebew, Anthony J. Gill, Roderick Clifton‐Bligh, Bruce G. Robinson, Diana E. Benn, Stan B. Sidhu	68
12	Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis 2010 ·Endocrine Related Cancer ·Johanna Sandgren, Teresita Díaz de Ståhl, Robin Andersson, Uwe Menzel, Arkadiusz Piotrowski, Helena Nord, Martin Bäckdahl, Nimrod Kiss, Michael Brauckhoff, Jan Komorowski, Henning Dralle, Ola Hessman, Catharina Larsson, Göran Åkerström, Carl E.G. Bruder, Jan P. Dumanski, Gunnar Westin	24
13	Integrative epigenomic and genomic analysis of malignant pheochromocytoma 2010 ·Experimental & Molecular Medicine ·Johanna Sandgren, Robin Andersson, Álvaro Rada-Iglesias, Stefan Enroth, Göran Åkerström, Jan P. Dumanski, Jan Komorowski, Gunnar Westin, Claes Wadelius	24
14	Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma 2009 ·International Journal of Cancer ·Helena Nord, Ulrika Segersten, Johanna Sandgren, Kenneth Wester, Christer Busch, Uwe Menzel, Jan Komorowski, Jan P. Dumanski, Per‐Uno Malmström, Teresita Díaz de Ståhl	55
15	Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array 2009 ·Neuro-Oncology ·Helena Nord, Christian Hartmann, Robin Andersson, Uwe Menzel, Susan Pfeifer, Arkadiusz Piotrowski, (unknown), Wojciech Kloc, Johanna Sandgren, Tommie Olofsson, Göran Hesselager, Erik Blomquist, Jan Komorowski, Andreas von Deimling, Carl E.G. Bruder, Jan P. Dumanski, Teresita Díaz de Ståhl	42
16	Somatic mosaicism for copy number variation in differentiated human tissues 2008 ·Human Mutation ·Arkadiusz Piotrowski, Carl E.G. Bruder, Robin Andersson, Teresita Díaz de Ståhl, Uwe Menzel, Johanna Sandgren, Andrzej Poplawski, Désirée von Tell, Chiquito Crasto, (unknown), Rafał Bartoszewski, Zsuzsa Bebők, Maciej Krzyżanowski, Zbigniew Jankowski, E. Christopher Partridge, Jan Komorowski, Jan P. Dumanski	150
17	Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array 2007 ·Human Mutation ·Teresita Díaz de Ståhl, Johanna Sandgren, Arkadiusz Piotrowski, Helena Nord, Robin Andersson, Uwe Menzel, (unknown), Ann‐Charlotte Thuresson, Andrzej Poplawski, Désirée von Tell, (unknown), (unknown), Gehad ElGhazali, Stephan Imreh, Magnus Nordenskjöld, Meena Upadhyaya, Jan Komorowski, Carl E.G. Bruder, Jan P. Dumanski	35
18	Arachidonic acid is a physiological activator of the ryanodine receptor in pancreatic β-cells 2006 ·Cell Calcium ·Orison O. Woolcott, (unknown), Mensur Džabić, Cristina Pierro, (unknown), Johanna Sandgren, (unknown), Khanh Nguyen, Marta Bianchi, Marija Rakonjac, Olof Rådmark, Claes‐Göran Östenson, Md. Shahidul Islam	20
19	Cytokines affect PDX-1 expression, insulin and proinsulin secretion from iNOS deficient murine islets 2005 ·Molecular and Cellular Endocrinology ·Annika Andersson, (unknown), Johanna Sandgren, Stellan Sandler	24
20	High prevalence of overweight and metabolic syndrome among 60 year old women and men in Stockholm, Sweden 2000 ·Atherosclerosis ·M.-L. Hellénius, Magdalena Rosell, Johanna Sandgren, Ulf dé Fairé	4

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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