Ryan Richholt

1.1k total citations
16 papers, 335 citations indexed

About

Ryan Richholt is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ryan Richholt has authored 16 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ryan Richholt's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Alzheimer's disease research and treatments (2 papers). Ryan Richholt is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Alzheimer's disease research and treatments (2 papers). Ryan Richholt collaborates with scholars based in United States, Belgium and Germany. Ryan Richholt's co-authors include Ashley L. Siniard, Matthew J. Huentelman, Chris Balak, Szabolcs Szelinger, Isabelle Schrauwen, Amanda Courtright, Elizabeth Hutchins, Elizabeth Carlson, Robert R. Kitchen and Rebecca Reiman and has published in prestigious journals such as Nature Communications, PLoS ONE and Scientific Reports.

In The Last Decade

Ryan Richholt

16 papers receiving 332 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ryan Richholt United States	11	218	108	54	44	43	16	335
Ken Matsuura Japan	8	257 1.2×	39 0.4×	45 0.8×	72 1.6×	16 0.4×	11	383
Michael J. Szego Canada	9	294 1.3×	64 0.6×	141 2.6×	42 1.0×	28 0.7×	16	454
Samantha Stora Lebanon	10	205 0.9×	19 0.2×	60 1.1×	92 2.1×	53 1.2×	16	326
Christy M. Hoffmann United States	4	306 1.4×	32 0.3×	25 0.5×	23 0.5×	44 1.0×	7	395
Christopher Stoddard United States	7	167 0.8×	33 0.3×	91 1.7×	41 0.9×	21 0.5×	11	258
Claire C. Homan Australia	11	271 1.2×	31 0.3×	185 3.4×	37 0.8×	19 0.4×	16	493
Monika L. Ignacak United States	8	322 1.5×	288 2.7×	86 1.6×	24 0.5×	51 1.2×	11	473
Lauryl M. J. Nutter Canada	11	249 1.1×	36 0.3×	90 1.7×	10 0.2×	14 0.3×	26	344
Kip D. Zimmerman United States	9	156 0.7×	33 0.3×	32 0.6×	9 0.2×	25 0.6×	25	309

Countries citing papers authored by Ryan Richholt

Since Specialization

Citations

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

Fields of papers citing papers by Ryan Richholt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryan Richholt

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

All Works

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16 of 16 papers shown

Hutchins, Elizabeth, Rebecca Reiman, Ryan Richholt, et al.. (2021). Extracellular circular RNA profiles in plasma and urine of healthy, male college athletes. Scientific Data. 8(1). 276–276. 11 indexed citations

Szelinger, Szabolcs, Janine LoBello, Jessica Aldrich, et al.. (2021). Analytic validation and clinical utilization of the comprehensive genomic profiling test, GEM ExTra®. Oncotarget. 12(8). 726–739. 16 indexed citations

Wie, Jinhong, Vinodh Narayanan, Keri Ramsey, et al.. (2020). Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex. Nature Communications. 11(1). 3351–3351. 19 indexed citations

Stonnington, Cynthia M., Yinghua Chen, Matt Huentelman, et al.. (2020). Interaction Between BDNF Val66Met and APOE4 on Biomarkers of Alzheimer’s Disease and Cognitive Decline. Journal of Alzheimer s Disease. 78(2). 721–734. 15 indexed citations

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

Huentelman, Matthew J., Ignazio S. Piras, Ashley L. Siniard, et al.. (2018). Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers. Frontiers in Aging Neuroscience. 10. 155–155. 22 indexed citations

Stickel, Ariana M., Katrin Walther, Elizabeth L. Glisky, et al.. (2018). Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults. Frontiers in Aging Neuroscience. 9. 431–431. 9 indexed citations

Wingo, Aliza P., Nikolaos P. Daskalakis, Isaac R. Galatzer‐Levy, et al.. (2018). 228. Transcriptome-Wide Analysis Identifies ICAM5 Differentially Expressed in Chronic PTSD Symptoms Versus Resiliency Post Trauma Exposure in a Longitudinal Study. Biological Psychiatry. 83(9). S91–S92. 3 indexed citations

Yeri, Ashish, Amanda Courtright, Rebecca Reiman, et al.. (2017). Total Extracellular Small RNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects. Scientific Reports. 7(1). 44061–44061. 123 indexed citations

10.

Ramsey, Keri, Newell Belnap, Szabolcs Szelinger, et al.. (2017). Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results. Seminars in Pediatric Neurology. 26. 28–32. 9 indexed citations

11.

Huentelman, Matthew J., Ignazio S. Piras, Ashley L. Siniard, et al.. (2017). [P4–081]: ASSOCIATION OF MAP2K3 GENE VARIATION AND THE SUPERAGING PHENOTYPE DETECTED BY WHOLE EXOME SEQUENCING. Alzheimer s & Dementia. 13(7S_Part_27). 1 indexed citations

12.

You, Jing, Nara Sobreira, Dustin L. Gable, et al.. (2016). A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2 , a Gene Encoding a Component of the TTT Complex. The American Journal of Human Genetics. 98(5). 909–918. 26 indexed citations

13.

Belnap, Newell, Ashley L. Siniard, Szabolcs Szelinger, et al.. (2016). A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia. Molecular Case Studies. 2(5). a000851–a000851. 15 indexed citations

14.

Schrauwen, Isabelle, Szabolcs Szelinger, Ashley L. Siniard, et al.. (2015). A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome. PLoS ONE. 10(7). e0131797–e0131797. 35 indexed citations

15.

Kalani, M. Yashar S., Ashley L. Siniard, Jason J. Corneveaux, et al.. (2015). Rare Variants in Cardiomyopathy Genes Associated With Stress-Induced Cardiomyopathy. Neurosurgery. 78(6). 835–843. 5 indexed citations

16.

Schrauwen, Isabelle, Szabolcs Szelinger, Ashley L. Siniard, et al.. (2015). A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome. Investigative Ophthalmology & Visual Science. 56(6). 3896–3896. 14 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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