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 12
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 4
- 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)Sven Bergmann (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)JCO Precision Oncology (2 papers)American Journal of Clinical Pathology (2 papers)Clinical Infectious Diseases (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesSwitzerlandSlovakia
In The Last Decade
Niklas Krumm
22 papers receiving 2.0k citations
Niklas Krumm's Hit Papers
Peers
Comparison fields: 5 of 116
- Genetics 1.3k
- Cognitive Neuroscience 705
- Cancer Research 193
- Molecular Biology 871
- Developmental Neuroscience 35
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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 411 | |
| 2 | A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders Hit paper breakdown → | 2014 | 375 |
| 3 | Excess of rare, inherited truncating mutations in autism Hit paper breakdown → | 2015 | 345 |
| 4 | 2014 | 317 | |
| 5 | 2016 | 120 | |
| 6 | 2019 | 113 | |
| 7 | 2014 | 107 | |
| 8 | 2013 | 83 | |
| 9 | 2013 | 65 | |
| 10 | 2020 | 29 | |
| 11 | 2013 | 28 | |
| 12 | 2020 | 18 | |
| 13 | 2019 | 9 | |
| 14 | 2011 | 8 | |
| 15 | 2019 | 3 | |
| 16 | 2023 | 3 | |
| 17 | 2021 | 3 | |
| 18 | 2019 | 3 | |
| 19 | 2025 | 2 | |
| 20 | 2019 | 2 |
About Niklas Krumm
Niklas Krumm is a scholar working on Genetics, Molecular Biology, Cancer Research, Cognitive Neuroscience and Surgery, having authored 23 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (5 papers), Autism Spectrum Disorder Research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Prenatal Screening and Diagnostics (2 papers), Scientific Computing and Data Management (2 papers) and Helicobacter pylori-related gastroenterology studies (2 papers). The work is most often cited by research in Genetics (1.3k citations), Cognitive Neuroscience (705 citations), Cancer Research (193 citations), Molecular Biology (871 citations) and Developmental Neuroscience (35 citations). Niklas Krumm has collaborated with scholars based in United States, Switzerland and Slovakia. Frequent co-authors include Evan E. Eichler, Brian J. O’Roak, Bradley P. Coe, Jay Shendure, Deborah A. Nickerson, Sébastien Jacquemont, Tychele N. Turner, Sven Bergmann, Jill A. Rosenfeld and J. Beckmann. Their work appears in journals such as The American Journal of Human Genetics, JCO Precision Oncology, American Journal of Clinical Pathology, Clinical Infectious Diseases and Nature 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.