Jens Schuster

1.6k citations

49 papers · 1.1k indexed · h-index 19

Impact in

Molecular Biology top 10%
- Cancer-related gene regulation
- RNA modifications and cancer
- Wnt/β-catenin signaling in development and cancer
- Pluripotent Stem Cells Research
- dental development and anomalies
- RNA Research and Splicing
Genetics top 10%
- Genetics and Neurodevelopmental Disorders

Papers in

Molecular Biology 41
- RNA modifications and cancer 9
- CRISPR and Genetic Engineering 8
- Cancer-related gene regulation 8
- Pluripotent Stem Cells Research 8
- Epigenetics and DNA Methylation 7
- RNA and protein synthesis mechanisms 6
Genetics 15
- Genetics and Neurodevelopmental Disorders 8

Co-authors: Niklas Dahl Joakim Klar Jitendra Badhai Maria Sobol Phillip J. Stone J S Brody Kojiro Wasano R M Niles
Journals: Stem Cell Research (8 papers)The American Journal of Human Genetics (3 papers)eLife (2 papers)PLoS ONE (2 papers)Clinical Epigenetics (1 paper)
Partner nations: Sweden Pakistan United States

In The Last Decade

Jens Schuster

49 papers receiving 1.1k citations

Peers

Countries citing papers authored by Jens Schuster

Since Specialization

Citations

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

Fields of papers citing papers by Jens Schuster

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Jens Schuster, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jens Schuster Line = papers co-authored together Jens Schuster links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Abnormalities in the functional activity of neural networks in a human iPSC model of Dravet syndrome Neuroscience Research ·Sunil Phatak, Tanja Hyvärinen, Danielle M. Frey, 雅俊本田, 小林和夫, 刘新燕, Mohammad Shamsul Arefin, Fikret Emre Kapucu, Jens Schuster, Niklas Dahl, Susanna Narkilahti	2025	1
2	ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function Frontiers in Molecular Neuroscience ·Jens Schuster, Joakim Klar, André Luiz da Silva Lira, S. Sterz, Diederik van de Beek Anusha van Samkar, Ambrin Fatima, Roberto Rothermel, Zhe Jin, Sergiy V. Korol, Mikael Huss, Ann Nordgren, Britt Marie Anderlid, Caroline J. Gallant, Bryndis Birnir, Niklas Dahl	2022	1
3	A combined approach for single-cell mRNA and intracellular protein expression analysis Communications Biology ·Johan Reimegård, Marcel Tarbier, Marcus Danielsson, Jens Schuster, Sathishkumar Baskaran, 柱芬郭, Niklas Dahl, Marc R. Friedländer, Caroline J. Gallant	2021	74
4	Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21) Stem Cell Research ·Jens Schuster, Diederik van de Beek Anusha van Samkar, Maria Sobol, Ambrin Fatima, Göran Annerén, Niklas Dahl	2020	1
5	DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors Clinical Epigenetics ·S. Sterz, Joakim Klar, Maria Sobol, Diederik van de Beek Anusha van Samkar, Mansoureh Shahsavani, S Howard, Ambrin Fatima, I Iavicoli, Göran Annerén, Anna Falk, Jens Schuster, Niklas Dahl	2020	22
6	Aberrant splicing due to a novel RPS7 variant causes Diamond-Blackfan Anemia associated with spontaneous remission and meningocele International Journal of Hematology ·R. Toyozawa, Ambrin Fatima, Joakim Klar, Diederik van de Beek Anusha van Samkar, I Iavicoli, Muhammad Tariq, Shahid Mahmood Baig, Jens Schuster, Niklas Dahl	2020	6
7	Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutations Stem Cell Research ·Jens Schuster, Ambrin Fatima, Maria Sobol, G. Basar, S. Sterz, Niklas Dahl	2019	11
8	Generation of human induced pluripotent stem cell (iPSC) lines from three patients with von Hippel-Lindau syndrome carrying distinct VHL gene mutations Stem Cell Research ·Jens Schuster, Ambrin Fatima, César Quintana Sánchez, Joakim Klar, S. Sterz, Niklas Dahl	2019	4
9	Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant Stem Cell Research ·Jens Schuster, Maria Sobol, Ambrin Fatima, André Luiz da Silva Lira, S. Sterz, Britt‐Marie Anderlid, Ann Nordgren, Niklas Dahl	2019	5
10	Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage PLoS Genetics ·Joakim Klar, Jörg Piontek, Susanne Milatz, Muhammad Tariq, Muhammad Jameel, Tilman Breiderhoff, Jens Schuster, Ambrin Fatima, Maria Asif, 徳永尚登, Katrin Mäbert, Anja Fromm, Shahid Mahmood Baig, Dorothee Günzel, Niklas Dahl	2017	51
11	Transcriptome Profiling Reveals Degree of Variability in Induced Pluripotent Stem Cell Lines: Impact for Human Disease Modeling Cellular Reprogramming ·Jens Schuster, Jonatan Halvardson, S Andreea, Adam Ameur, Maria Sobol, Areeba Shaikh, Göran Annerén, Lars Feuk, Niklas Dahl	2015	19
12	Methods of Reprogramming to Induced Pluripotent Stem Cell Associated with Chromosomal Integrity and Delineation of a Chromosome 5q Candidate Region for Growth Advantage Stem Cells and Development ·Maria Sobol, Areeba Shaikh, Lucia Cavelier, André Luiz da Silva Lira, Jens Schuster, Niklas Dahl	2015	20
13	5′UTR Variants of Ribosomal Protein S19 Transcript Determine Translational Efficiency: Implications for Diamond-Blackfan Anemia and Tissue Variability PLoS ONE ·Jitendra Badhai, Jens Schuster, Olof Gidlöf, Niklas Dahl	2011	11
14	Down-regulation of progesterone receptor membrane component 1 (PGRMC1) in peripheral nucleated blood cells associated with premature ovarian failure (POF) and polycystic ovary syndrome (PCOS) Reproductive Biology and Endocrinology ·Jens Schuster, V. C. Bradley, Per‐Olof Karlström, Inger Sundström Poromaa, Niklas Dahl	2010	43
15	A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis The American Journal of Human Genetics ·Johanna Dahlqvist, Joakim Klar, Neha Tiwari, Jens Schuster, Hans Törmä, Jitendra Badhai, Ramón M. Pujol, Maurice A. M. Van Steensel, Tjinta Brinkhuizen, Lieke Gijezen, 金小毛, Gianluca Tadini, 知佳子西田, Niklas Dahl	2010	1
16	Ribosomal protein S19 binds to its own mRNA with reduced affinity in Diamond-Blackfan anemia Blood Cells Molecules and Diseases ·Jens Schuster, Anne-Sophie Fröjmark, Per Nilsson, Jitendra Badhai, Anders Virtanen, Niklas Dahl	2010	8
17	Ribosomal protein S19 and S24 insufficiency cause distinct cell cycle defects in Diamond–Blackfan anemia Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jitendra Badhai, Anne-Sophie Fröjmark, Edward J. Davey, Jens Schuster, Niklas Dahl	2009	35
18	WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome European Journal of Human Genetics ·H. H. B., Joakim Klar, Stina Westerlund, Muhammad Aslam, Muhammad Tariq, Jens Schuster, Shahid Mahmood Baig, Niklas Dahl	2009	52
19	Posttranscriptional down‐regulation of small ribosomal subunit proteins correlates with reduction of 18S rRNA in RPS19 deficiency FEBS Letters ·Jitendra Badhai, Anne-Sophie Fröjmark, Hamid Reza Razzaghian, Edward J. Davey, Jens Schuster, Niklas Dahl	2009	18
20	A Splice Variant of the Human CCA-adding Enzyme with Modified Activity Journal of Molecular Biology ·Esther Lizano, Jens Schuster, Martin Müller, Janet Kelso, Mario Mörl	2006	10

About Jens Schuster

Jens Schuster is a scholar working on Molecular Biology, Genetics, Developmental Biology, Cell Biology and Neurology, having authored 49 papers that have together received 1.1k indexed citations. Recurring topics across this work include RNA modifications and cancer (9 papers), CRISPR and Genetic Engineering (8 papers), Cancer-related gene regulation (8 papers), Pluripotent Stem Cells Research (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Epigenetics and DNA Methylation (7 papers), RNA and protein synthesis mechanisms (6 papers) and Skin and Cellular Biology Research (5 papers). The work is most often cited by research in Molecular Biology (712 citations), Genetics (247 citations), Cell Biology (134 citations), Reproductive Medicine (50 citations) and Oral Surgery (41 citations). Jens Schuster has collaborated with scholars based in Sweden, Pakistan and United States. Frequent co-authors include Niklas Dahl, Joakim Klar, Jitendra Badhai, Maria Sobol, Phillip J. Stone, J S Brody, Kojiro Wasano, R M Niles, Shahid Mahmood Baig and Anne-Sophie Fröjmark. Their work appears in journals such as Stem Cell Research, The American Journal of Human Genetics, eLife, PLoS ONE and Clinical Epigenetics.

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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