Marcus Naymik

1.6k total citations
23 papers, 378 citations indexed

About

Marcus Naymik is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Marcus Naymik has authored 23 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Surgery. Recurrent topics in Marcus Naymik's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), RNA regulation and disease (3 papers) and Head and Neck Anomalies (3 papers). Marcus Naymik is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), RNA regulation and disease (3 papers) and Head and Neck Anomalies (3 papers). Marcus Naymik collaborates with scholars based in United States, Norway and Australia. Marcus Naymik's co-authors include Matthew J. Huentelman, Ashley L. Siniard, Isabelle Schrauwen, Matthew De Both, Ignazio S. Piras, Candace R. Lewis, Jared M. Dickinson, Andrew C. D’Lugos, Chad C. Carroll and Wendy Winslow and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Applied Physiology.

In The Last Decade

Marcus Naymik

21 papers receiving 373 citations

Peers

Marcus Naymik
Matt Huentelman United States
Marika Bianchi Italy
Zhaozeng Lu China
Kelli L. Vaughan United States
Andy Brooks United States
Veronika Borbélyová Slovakia
Daniela Rodrígues-Amorím Spain
Nasrin Azad United States
R. Franceschini Italy
Seetharamaiah Chittiprol India
Matt Huentelman United States
Marcus Naymik
Citations per year, relative to Marcus Naymik Marcus Naymik (= 1×) peers Matt Huentelman

Countries citing papers authored by Marcus Naymik

Since Specialization
Citations

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

Fields of papers citing papers by Marcus Naymik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcus Naymik

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

All Works

20 of 20 papers shown
1.
Ghisays, Valentina, Ignazio S. Piras, Marcus Naymik, et al.. (2025). Phenome-wide association of APOE alleles in the All of Us Research Program. EBioMedicine. 117. 105768–105768. 1 indexed citations
2.
Belnap, Newell, Keri Ramsey, Alon Abraham, et al.. (2024). Expanded carrier screening for inherited genetic disease using exome and genome sequencing. Journal of Genetic Counseling. 34(2). e1964–e1964.
3.
Ramsey, Keri, Marcus Naymik, Jennifer L. Sloan, et al.. (2024). Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD Gene. International Journal of Molecular Sciences. 25(22). 11922–11922.
4.
Thapaliya, Gita, Elena Jansen, Marcus Naymik, et al.. (2023). FTO variation and early frontostriatal brain development in children. Obesity. 32(1). 156–165. 1 indexed citations
5.
Jansen, Elena, Marcus Naymik, Gita Thapaliya, et al.. (2023). Parent-reported child appetite moderates relationships between child genetic obesity risk and parental feeding practices. Frontiers in Nutrition. 10. 1174441–1174441. 5 indexed citations
6.
Belnap, Newell, Marcus Naymik, Jennifer L. Sloan, et al.. (2023). Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: A novel SMS gene variant. SHILAP Revista de lepidopterología. 2. 100017–100017. 2 indexed citations
7.
Windsor, Rebecca, Joshua S. Talboom, Candace R. Lewis, et al.. (2021). Leukocyte and cytokine variables in asymptomatic Pugs at genetic risk of necrotizing meningoencephalitis. Journal of Veterinary Internal Medicine. 35(6). 2846–2852. 8 indexed citations
8.
Lewis, Candace R., Joshua S. Talboom, Matt De Both, et al.. (2021). Smoking is associated with impaired verbal learning and memory performance in women more than men. Scientific Reports. 11(1). 10248–10248. 19 indexed citations
9.
Talboom, Joshua S., Matt De Both, Marcus Naymik, et al.. (2021). Two separate, large cohorts reveal potential modifiers of age-associated variation in visual reaction time performance. SHILAP Revista de lepidopterología. 7(1). 14–14. 16 indexed citations
10.
Wang, Qi, Bessie Meechoovet, Ashley L. Siniard, et al.. (2021). DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s Disease. Frontiers in Genetics. 12. 640266–640266. 53 indexed citations
11.
12.
Piras, Ignazio S., Isabelle Schrauwen, Joshua S. Talboom, et al.. (2020). Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the disease. Acta Neuropathologica Communications. 8(1). 76–76. 20 indexed citations
13.
Velázquez, Ramón, Eric Ferreira, Wendy Winslow, et al.. (2019). Maternal choline supplementation ameliorates Alzheimer’s disease pathology by reducing brain homocysteine levels across multiple generations. Molecular Psychiatry. 25(10). 2620–2629. 61 indexed citations
14.
Llaci, Lorida, Keri Ramsey, Newell Belnap, et al.. (2019). Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD). Human Genetics. 138(11-12). 1409–1417. 12 indexed citations
15.
Peter, Beate, Valentin Dinu, Li Liu, et al.. (2019). Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects. Behavior Genetics. 49(4). 399–414. 16 indexed citations
16.
Kari, Elina, Lorida Llaci, John L. Go, et al.. (2019). A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing loss. Molecular Genetics & Genomic Medicine. 7(12). e995–e995. 3 indexed citations
17.
Talboom, Joshua S., Asta K. Håberg, Matthew De Both, et al.. (2019). Family history of Alzheimer’s disease alters cognition and is modified by medical and genetic factors. eLife. 8. 30 indexed citations
18.
Schrauwen, Isabelle, Elina Kari, Lorida Llaci, et al.. (2018). De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness. Human Genetics. 137(6-7). 459–470. 28 indexed citations
19.
Das, Arup, Sampathkumar Rangasamy, Marcus Naymik, et al.. (2018). Novel Genetic Variants in Extreme Phenotypes of Diabetic Retinopathy: DRGen Study. Investigative Ophthalmology & Visual Science. 59(9). 1911–1911. 4 indexed citations
20.
Dickinson, Jared M., Andrew C. D’Lugos, Marcus Naymik, et al.. (2018). Transcriptome response of human skeletal muscle to divergent exercise stimuli. Journal of Applied Physiology. 124(6). 1529–1540. 57 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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