Niklas Krumm

11.1k total citations · 2 hit papers
23 papers, 2.0k citations indexed

About

Niklas Krumm is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Niklas Krumm has authored 23 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Niklas Krumm's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Cancer Genomics and Diagnostics (5 papers). Niklas Krumm is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Cancer Genomics and Diagnostics (5 papers). Niklas Krumm collaborates with scholars based in United States, Switzerland and Slovakia. Niklas Krumm's co-authors include Evan E. Eichler, Brian J. O’Roak, Bradley P. Coe, Jay Shendure, Deborah A. Nickerson, Sébastien Jacquemont, Tychele N. Turner, Micha Hersch, J. Beckmann and Jill A. Rosenfeld and has published in prestigious journals such as New England Journal of Medicine, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Niklas Krumm

22 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders

2014 375 citations Sébastien Jacquemont, Bradley P. Coe et al. The American Journal of Human Genetics profile →
Excess of rare, inherited truncating mutations in autism

2015 345 citations Niklas Krumm, Tychele N. Turner et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Niklas Krumm United States	12	1.3k	871	705	193	152	23	2.0k
Zohreh Talebizadeh United States	17	1.0k 0.8×	973 1.1×	422 0.6×	157 0.8×	134 0.9×	31	1.7k
Tiziano Pramparo United States	27	1.2k 0.9×	1.7k 1.9×	503 0.7×	136 0.7×	112 0.7×	50	2.7k
Francesca Ariani Italy	29	1.6k 1.2×	1.3k 1.5×	581 0.8×	127 0.7×	60 0.4×	70	2.4k
Tychele N. Turner United States	20	1.1k 0.8×	915 1.1×	530 0.8×	125 0.6×	136 0.9×	47	1.7k
Ilaria Meloni Italy	29	1.7k 1.3×	1.3k 1.5×	759 1.1×	110 0.6×	70 0.5×	60	2.4k
Kaitlin E. Samocha United States	17	1.3k 1.0×	917 1.1×	178 0.3×	210 1.1×	94 0.6×	23	1.9k
Martine Raynaud France	25	2.1k 1.6×	1.9k 2.2×	757 1.1×	80 0.4×	101 0.7×	57	3.0k
Vinodh Narayanan United States	25	749 0.6×	1.2k 1.3×	398 0.6×	89 0.5×	117 0.8×	67	2.3k
Siddharth Srivastava United States	21	1000 0.8×	700 0.8×	392 0.6×	53 0.3×	177 1.2×	80	1.7k
Jinong Feng United States	27	725 0.6×	1.3k 1.4×	411 0.6×	428 2.2×	82 0.5×	44	2.1k

Countries citing papers authored by Niklas Krumm

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Niklas Krumm

This figure shows the co-authorship network connecting the top 25 collaborators of Niklas Krumm. A scholar is included among the top collaborators of Niklas Krumm 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 Niklas Krumm. Niklas Krumm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Kadri, Sabah, Kelly E. Craven, Elaine P.S. Gee, et al.. (2025). Clinical Bioinformatician Body of Knowledge—Bioinformatics and Software Core. Journal of Molecular Diagnostics. 27(7). 566–582. 2 indexed citations

Krumm, Niklas, Marc R. Radke, Kalyan Banda, et al.. (2023). Diagnosis of Ovarian Carcinoma Homologous Recombination DNA Repair Deficiency From Targeted Gene Capture Oncology Assays. JCO Precision Oncology. 7(7). e2200720–e2200720. 3 indexed citations

Krumm, Niklas, Lindsay Bazydlo, Dustin R. Bunch, Shannon Haymond, & Daniel T. Holmes. (2023). Diving into Data Science: A Clinical Laboratory Update. The Journal of Applied Laboratory Medicine. 8(1). 1–2.

Krumm, Niklas. (2022). Organizational and Technical Security Considerations for Laboratory Cloud Computing. The Journal of Applied Laboratory Medicine. 8(1). 180–193. 1 indexed citations

Bosch, Dustin E., Patrick C. Mathias, Niklas Krumm, et al.. (2021). Elevated White Blood Cell Count Does Not Predict Clostridium difficile Nucleic Acid Testing Results. Clinical Infectious Diseases. 73(4). 699–705. 3 indexed citations

Krumm, Niklas & Noah G. Hoffman. (2020). Practical estimation of cloud storage costs for clinical genomic data. Practical Laboratory Medicine. 21. e00168–e00168. 29 indexed citations

Krumm, Niklas & Brian H. Shirts. (2019). Technical, Biological, and Systems Barriers for Molecular Clinical Decision Support. Clinics in Laboratory Medicine. 39(2). 281–294. 3 indexed citations

Steineck, Angela, Niklas Krumm, Jay F. Sarthy, et al.. (2019). Response to Pembrolizumab in a Patient With Xeroderma Pigmentosum and Advanced Squamous Cell Carcinoma. JCO Precision Oncology. 3(3). 1–6. 9 indexed citations

Krumm, Niklas & Noah G. Hoffman. (2019). Practical Cost Analysis of Genomic Data in the Cloud. American Journal of Clinical Pathology. 152(Supplement_1). S2–S3. 2 indexed citations

10.

Ling, Albee Y., Tychele N. Turner, Maria X. Sosa, et al.. (2019). Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease. New England Journal of Medicine. 380(15). 1421–1432. 113 indexed citations

11.

Turner, Tychele N., Yi Qian, Niklas Krumm, et al.. (2016). denovo-db: a compendium of humande novovariants. Nucleic Acids Research. 45(D1). D804–D811. 120 indexed citations

12.

Krumm, Niklas, Tychele N. Turner, Carl Baker, et al.. (2015). Excess of rare, inherited truncating mutations in autism. Nature Genetics. 47(6). 582–588. 345 indexed citations breakdown →

13.

Minot, Samuel S., et al.. (2015). One Codex: A Sensitive and Accurate Data Platform for. 1 indexed citations

14.

Jacquemont, Sébastien, Bradley P. Coe, Micha Hersch, et al.. (2014). A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders. The American Journal of Human Genetics. 94(3). 415–425. 375 indexed citations breakdown →

15.

Krumm, Niklas, Brian J. O’Roak, Jay Shendure, & Evan E. Eichler. (2014). A de novo convergence of autism genetics and molecular neuroscience. Trends in Neurosciences. 37(2). 95–105. 317 indexed citations

16.

Hoischen, Alexander, Niklas Krumm, & Evan E. Eichler. (2014). Prioritization of neurodevelopmental disease genes by discovery of new mutations. Nature Neuroscience. 17(6). 764–772. 107 indexed citations

17.

Walsh, Tom, Süleyman Gülsüner, Alex S. Nord, et al.. (2013). Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia. The American Journal of Human Genetics. 93(4). 697–710. 28 indexed citations

18.

Krumm, Niklas, Brian J. O’Roak, Emre Karakoç, et al.. (2013). Transmission Disequilibrium of Small CNVs in Simplex Autism. The American Journal of Human Genetics. 93(4). 595–606. 65 indexed citations

19.

Krumm, Niklas, Peter H. Sudmant, Arthur Ko, et al.. (2012). Copy number variation detection and genotyping from exome sequence data. Genome Research. 22(8). 1525–1532. 411 indexed citations

20.

Thomas, Brandon J., Eric D. Rubio, Niklas Krumm, et al.. (2011). Allele-specific transcriptional elongation regulates monoallelic expression of the IGF2BP1 gene. Epigenetics & Chromatin. 4(1). 14–14. 8 indexed citations

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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