Niklas Dahl

15.0k citations

245 papers · 9.8k indexed · 2 hit papers · h-index 50

Impact in

Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Blood disorders and treatments
Molecular Biology top 1%
- RNA modifications and cancer
- Cancer-related gene regulation
- Epigenetics and DNA Methylation
- RNA and protein synthesis mechanisms

Papers in

Genetics 92
- Genetics and Neurodevelopmental Disorders 44
- Genomic variations and chromosomal abnormalities 21
Sensory Systems 11

Co-authors: Joakim Klar Jens Schuster Birgit Carlsson Jean‐Louis Mandel Peter Gustavsson Jocelyn Laporte U. Pettersson Christine Kretz
Journals: European Journal of Human Genetics (15 papers)Human Molecular Genetics (11 papers)Human Genetics (11 papers)Stem Cell Research (8 papers)The American Journal of Human Genetics (8 papers)
Partner nations: Sweden United States France

In The Last Decade

Niklas Dahl

239 papers receiving 9.6k citations

Hit Papers

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The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia 1999 · 594 citations

Peers

Countries citing papers authored by Niklas Dahl

Since Specialization

Citations

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

Fields of papers citing papers by Niklas Dahl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Niklas Dahl, 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 Niklas Dahl Line = papers co-authored together Niklas Dahl 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	Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment Human Molecular Genetics ·Huanting Lu, Pingping Qu, Shining Ma, Ling Lin, María Sofía Iglesias Gómez, Niklas Dahl, Giuseppe Plazzi, Fabio Pizza, Ruth O’Hara, Wing Hung Wong, Joachim Hallmayer, Emmanuel Mignot, Xianglong Zhang, Alexander E. Urban	2023	5
3	GATA-1 Defects in Diamond–Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease Genes ·منال بنت طارق القصبی القصبی, Sima Kheradmand Kia, Niklas Dahl, Odile Fenneteau, Roos J. Leguit, Edward E. S. Nieuwenhuis, Wouter W. van Solinge, Richard van Wijk, Lydie Da Costa, Marije Bartels	2022	12
4	Cohort profile: the Swedish study of SUDden cardiac Death in the Young (SUDDY) 2000–2010: a complete nationwide cohort of SCDs BMJ Open ·Eva‐Lena Stattin, Emil Hagström, Niklas Dahl, Anneli Strömsöe, A M Delgado-Vega, Joakim Klar, Bodil Svennblad, Mats Börjesson, Aase Wisten	2022	5
5	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
6	Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing Human Mutation ·Ida Höijer, Yu‐Chih Tsai, Tyson A. Clark, Jean Allister, Niklas Dahl, Eva‐Lena Stattin, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur	2018	58
7	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
8	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
9	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
10	Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutation European Journal of Human Genetics ·Tahir Naeem Khan, Joakim Klar, Muhammad Tariq, Huang Mao-Sheng, Naveed Altaf Malik, Benno Bartsch, Shahid Mahmood Baig, Niklas Dahl	2014	35
11	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
12	Marrow Failure Hematology ·Alan D. D’Andrea, Niklas Dahl, Eva C. Guinan, Akiko Shimamura	2002	16
13	Characterization of the Myotubularin Dual Specificity Phosphatase Gene Family from Yeast to Human Human Molecular Genetics ·Jocelyn Laporte, F Blondeau, Wilson Thadeu V. Machado, Dmitri Tentler, Christine Kretz, Niklas Dahl, Jean‐Louis Mandel	1998	97
14	Identification of a second locus for progressive intrahepatic familial cholestasis on chromosome 2q24. Hepatology ·Chenyu Han, Étienne Sokal, 孙其新, Ertuğrul Çam, Rahul Verma, Zeʾev Anner, 順子紺野, Taciana Fisac, Hiromu Hasegawa, Niklas Dahl, Henrik Arnell, Fuentes Beta	1997	1
15	PRENATAL DIAGNOSIS OF X-LINKED MYOTUBULAR MYOPATHY: STRATEGIES USING NEW AND TIGHTLY LINKED DNA MARKERS Prenatal Diagnosis ·Ling‐Jia Hu, Jocelyn Laporte, Wolfram Kreß, Niklas Dahl	1996	8
16	X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markers Human Genetics ·Ling‐Jia Hu, Jocelyn Laporte, Petra Kioschis, Timothy F. Little, Christine Kretz, Annemarie Poustka, Jean‐Louis Mandel, Niklas Dahl	1996	25
17	X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21. HAL (Le Centre pour la Communication Scientifique Directe) ·Fadia M Nasser-Abu Alhija, André Hanauer, Niklas Dahl, M Mathieu, О.О. Тоцький, Valérie Biancalana, Timothy F. Little, V. Strunski	1995	20
18	Autosomal dominant cerebellar ataxia deafness and narcolepsy Journal of the Neurological Sciences ·Atle Melberg, Jerker Hetta, Niklas Dahl, Inger Nennesmo, Mats Bengtsson, Rolf Wibom, C. A. Grant, A.M. Ballesteros-Gomez, P. O. Lundberg	1995	24
19	Linkage mapping of a severe X-linked mental retardation syndrome. PubMed ·H Malmgren, Mats Sundvall, Niklas Dahl, K. H. Gustavson, Göran Annerén, Claes Wadelius, James Hardymon, U. Pettersson	1993	26
20	DNA linkage analysis of X-linked retinoschisis Human Genetics ·Niklas Dahl, P. Goonewardena, Jayanti Chotai, Maria Anvret, U. Pettersson	1988	24

About Niklas Dahl

Niklas Dahl is a scholar working on Genetics, Sensory Systems, Molecular Biology, Cell Biology and Urology, having authored 245 papers that have together received 9.8k indexed citations. Recurring topics across this work include RNA modifications and cancer (46 papers), Genetics and Neurodevelopmental Disorders (44 papers), Cancer-related gene regulation (28 papers), Epigenetics and DNA Methylation (23 papers), Genomic variations and chromosomal abnormalities (21 papers), Skin and Cellular Biology Research (19 papers), RNA and protein synthesis mechanisms (11 papers) and Autism Spectrum Disorder Research (11 papers). The work is most often cited by research in Genetics (2.9k citations), Molecular Biology (5.9k citations), Cell Biology (1.3k citations), Urology (373 citations) and Sensory Systems (231 citations). Niklas Dahl has collaborated with scholars based in Sweden, United States and France. Frequent co-authors include Joakim Klar, Jens Schuster, Birgit Carlsson, Jean‐Louis Mandel, Peter Gustavsson, Jocelyn Laporte, U. Pettersson, Christine Kretz, Irma Dianzani and Sarah E. Ball. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, Human Genetics, Stem Cell Research and The American Journal of Human Genetics.

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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