Michael Duyzend

2.2k total citations · 1 hit paper
16 papers, 673 citations indexed

About

Michael Duyzend is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Michael Duyzend has authored 16 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Michael Duyzend's work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Michael Duyzend is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Michael Duyzend collaborates with scholars based in United States, United Kingdom and Switzerland. Michael Duyzend's co-authors include Evan E. Eichler, Bradley P. Coe, Micha Hersch, Sven Bergmann, Niklas Krumm, J. Beckmann, Sébastien Jacquemont, Jill A. Rosenfeld, Martha L. Bulyk and Sidra Khan and has published in prestigious journals such as The American Journal of Human Genetics, Genome biology and Clinical Chemistry.

In The Last Decade

Michael Duyzend

14 papers receiving 662 citations

Hit Papers

A Higher Mutational Burden in Females Supports a “Female ... 2014 2026 2018 2022 2014 100 200 300
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.

  1. 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 →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael Duyzend United States 8 383 336 276 58 57 16 673
Daniel Moreno‐De‐Luca United States 9 413 1.1× 389 1.2× 179 0.6× 106 1.8× 22 0.4× 16 677
Regina Waltes Germany 13 345 0.9× 241 0.7× 481 1.7× 71 1.2× 36 0.6× 19 870
Karola Rehnström Finland 14 432 1.1× 256 0.8× 257 0.9× 62 1.1× 21 0.4× 21 760
Corneliu Bodea United States 4 514 1.3× 563 1.7× 284 1.0× 100 1.7× 50 0.9× 5 809
Dina Manaa United States 2 501 1.3× 563 1.7× 270 1.0× 100 1.7× 50 0.9× 2 793
Shannon Wake United Kingdom 13 569 1.5× 464 1.4× 310 1.1× 27 0.5× 25 0.4× 26 852
M. Pilar Trelles United States 9 237 0.6× 197 0.6× 221 0.8× 58 1.0× 26 0.5× 15 530
Katy Berg United Kingdom 10 432 1.1× 412 1.2× 205 0.7× 110 1.9× 30 0.5× 13 717
Ravinesh A. Kumar United States 10 508 1.3× 278 0.8× 364 1.3× 67 1.2× 20 0.4× 16 767
Catarina Correia Portugal 12 331 0.9× 352 1.0× 173 0.6× 116 2.0× 30 0.5× 18 639

Countries citing papers authored by Michael Duyzend

Since Specialization
Citations

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

Fields of papers citing papers by Michael Duyzend

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Duyzend

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

All Works

16 of 16 papers shown
1.
Cohen, Jennifer L., Michael Duyzend, Mark D. Fleming, et al.. (2025). Advancing precision care in pregnancy through a treatable fetal findings list. The American Journal of Human Genetics. 112(6). 1251–1269.
2.
Dobson, Lori, Sean A. Horan, Michael Duyzend, et al.. (2025). Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions. Clinical Chemistry. 71(1). 129–140. 3 indexed citations
3.
Duyzend, Michael, Pilar Cacheiro, Julius O.B. Jacobsen, et al.. (2024). Improving prenatal diagnosis through standards and aggregation. Prenatal Diagnosis. 44(4). 454–464. 3 indexed citations
4.
Duyzend, Michael, et al.. (2024). Going Back in Time: Prenatal Presentations of Postnatal Genetic Diagnoses Made in a Neonatal Intensive Care Unit. Prenatal Diagnosis. 45(10). 1292–1312.
5.
Cacheiro, Pilar, Ignatia B. Van den Veyver, Stephen A. Murray, et al.. (2024). Lethal phenotypes in Mendelian disorders. Genetics in Medicine. 26(7). 101141–101141. 1 indexed citations
6.
Duyzend, Michael. (2021). Genomic medicine in a community hospital setting. The Journal of Pediatrics. 239. 1–4. 1 indexed citations
7.
Hudac, Caitlin M., Michael Duyzend, Alastair J. Martin, et al.. (2020). Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers. Autism Research. 13(8). 1300–1310. 16 indexed citations
8.
Duyzend, Michael. (2020). Non-diagnostic results from rapid exome sequencing can change clinical management in the critical care setting. The Journal of Pediatrics. 226. 1–4. 1 indexed citations
9.
Guo, Hui, Michael Duyzend, Bradley P. Coe, et al.. (2018). Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes. Genetics in Medicine. 21(7). 1611–1620. 80 indexed citations
10.
Wallace, Arianne S., Caitlin M. Hudac, Kyle J. Steinman, et al.. (2017). Longitudinal report of child with de novo 16p11.2 triplication. Clinical Case Reports. 6(1). 147–154. 5 indexed citations
11.
Dougherty, Max L., Xander Nuttle, Osnat Penn, et al.. (2017). The birth of a human-specific neural gene by incomplete duplication and gene fusion. Genome biology. 18(1). 49–49. 29 indexed citations
12.
Duyzend, Michael, Xander Nuttle, Bradley P. Coe, et al.. (2015). Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV. The American Journal of Human Genetics. 98(1). 45–57. 44 indexed citations
13.
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 →
14.
Lozano, Reymundo, Randi J. Hagerman, Michael Duyzend, et al.. (2014). Genomic studies in fragile X premutation carriers. Journal of Neurodevelopmental Disorders. 6(1). 27–27. 21 indexed citations
15.
Duyzend, Michael, Aaron M. Leconte, Andrew W. Wills, et al.. (2011). Synthesis and evaluation of substrate analogue inhibitors of trypanothione reductase. Journal of Enzyme Inhibition and Medicinal Chemistry. 27(6). 784–794. 11 indexed citations
16.
Siggers, Trevor, Michael Duyzend, Jessica Reddy, Sidra Khan, & Martha L. Bulyk. (2011). Non‐DNA‐binding cofactors enhance DNA‐binding specificity of a transcriptional regulatory complex. Molecular Systems Biology. 7(1). 83 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Daniel Moreno‐De‐Luca Breakdown of academic impact, for papers by Regina Waltes Breakdown of academic impact, for papers by Karola Rehnström Breakdown of academic impact, for papers by Corneliu Bodea Breakdown of academic impact, for papers by Dina Manaa Breakdown of academic impact, for papers by Shannon Wake Breakdown of academic impact, for papers by M. Pilar Trelles Breakdown of academic impact, for papers by Katy Berg Breakdown of academic impact, for papers by Ravinesh A. Kumar Breakdown of academic impact, for papers by Catarina Correia
Rankless by CCL
2026