Niklas Krumm
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 4
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- Congenital heart defects research 2
- Biomedical Text Mining and Ontologies 2
- Co-authors
- Evan E. Eichler (8 shared papers)Brian J. O’Roak (3 shared papers)Bradley P. Coe (5 shared papers)Jay Shendure (1 shared paper)Deborah A. Nickerson (3 shared papers)Sébastien Jacquemont (2 shared papers)Tychele N. Turner (3 shared papers)Maika Malig (1 shared paper)
- Journals
- American Journal of Clinical Pathology (3 papers)The American Journal of Human Genetics (3 papers)JCO Precision Oncology (2 papers)Journal of Molecular Diagnostics (1 paper)Epigenetics & Chromatin (1 paper)
- Partner nations
- United StatesSwitzerlandIreland
In The Last Decade
Niklas Krumm
22 papers receiving 2.0k citations
Niklas Krumm's Hit Papers
Peers
Comparison fields: 5 of 109
- Genetics 1.2k
- Cognitive Neuroscience 645
- Molecular Biology 752
- Cancer Research 143
- Developmental Neuroscience 30
Countries citing papers authored by Niklas Krumm
This map shows the geographic impact of Niklas Krumm'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 Krumm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Niklas Krumm more than expected).
Fields of papers citing papers by Niklas Krumm
This network shows the impact of papers produced by Niklas Krumm. 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 Krumm. The network helps show where Niklas Krumm may publish in the future.
Co-authors
The 25 scholars most cited alongside Niklas Krumm, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 415 | |
| 2 | A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders Hit paper breakdown → | 2014 | 380 |
| 3 | Excess of rare, inherited truncating mutations in autism Hit paper breakdown → | 2015 | 348 |
| 4 | 2014 | 319 | |
| 5 | 2016 | 121 | |
| 6 | 2019 | 113 | |
| 7 | 2014 | 108 | |
| 8 | 2013 | 83 | |
| 9 | 2013 | 68 | |
| 10 | 2020 | 30 | |
| 11 | 2013 | 28 | |
| 12 | 2020 | 20 | |
| 13 | 2011 | 9 | |
| 14 | 2019 | 9 | |
| 15 | 2023 | 4 | |
| 16 | 2021 | 4 | |
| 17 | 2019 | 3 | |
| 18 | 2019 | 3 | |
| 19 | 2025 | 2 | |
| 20 | 2019 | 2 |
About Niklas Krumm
Niklas Krumm is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cancer Research and Surgery, having authored 24 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers), Autism Spectrum Disorder Research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Cancer Genomics and Diagnostics (4 papers), Blood groups and transfusion (2 papers), Congenital heart defects research (2 papers) and Biomedical Text Mining and Ontologies (2 papers). The work is most often cited by research in Genetics (1.2k citations), Cognitive Neuroscience (645 citations), Molecular Biology (752 citations), Cancer Research (143 citations) and Developmental Neuroscience (30 citations). Niklas Krumm has collaborated with scholars based in United States, Switzerland and Ireland. Frequent co-authors include Evan E. Eichler, Brian J. O’Roak, Bradley P. Coe, Jay Shendure, Deborah A. Nickerson, Sébastien Jacquemont, Tychele N. Turner, Maika Malig, J. Beckmann and Arthur Ko. Their work appears in journals such as American Journal of Clinical Pathology, The American Journal of Human Genetics, JCO Precision Oncology, Journal of Molecular Diagnostics and Epigenetics & Chromatin.
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.