Garrett Allington

774 total citations
13 papers, 195 citations indexed

About

Garrett Allington is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Garrett Allington has authored 13 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Garrett Allington's work include Fetal and Pediatric Neurological Disorders (5 papers), Cerebrospinal fluid and hydrocephalus (5 papers) and Craniofacial Disorders and Treatments (3 papers). Garrett Allington is often cited by papers focused on Fetal and Pediatric Neurological Disorders (5 papers), Cerebrospinal fluid and hydrocephalus (5 papers) and Craniofacial Disorders and Treatments (3 papers). Garrett Allington collaborates with scholars based in United States, Canada and United Kingdom. Garrett Allington's co-authors include Kristopher T. Kahle, Sheng Chih Jin, Nicholas S. Diab, Shujuan Zhao, Weilai Dong, Martina Brueckner, Adam J. Kundishora, Phan Q. Duy, Philip B. Verghese and Pankaj Mehta and has published in prestigious journals such as Brain, Hepatology and Scientific Reports.

In The Last Decade

Garrett Allington

12 papers receiving 194 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Garrett Allington United States 8 83 52 50 48 45 13 195
Mauricio De Castro United States 9 51 0.6× 78 1.5× 32 0.6× 35 0.7× 15 0.3× 20 230
Elena Gianetti Italy 12 98 1.2× 53 1.0× 34 0.7× 19 0.4× 13 0.3× 13 309
Brian J. Shayota United States 10 127 1.5× 68 1.3× 29 0.6× 11 0.2× 31 0.7× 23 321
Jose C. Florez United States 6 40 0.5× 30 0.6× 13 0.3× 187 3.9× 44 1.0× 10 295
Ana Carolina Proença da Fonseca Brazil 11 83 1.0× 109 2.1× 16 0.3× 38 0.8× 15 0.3× 31 292
Teresia Wangensteen Norway 10 97 1.2× 120 2.3× 24 0.5× 59 1.2× 9 0.2× 16 295
Bregje Jaeger Netherlands 9 80 1.0× 16 0.3× 26 0.5× 19 0.4× 19 0.4× 22 216
Hiroyasu Iwasa Japan 8 149 1.8× 48 0.9× 49 1.0× 5 0.1× 40 0.9× 9 272
María Obón Spain 5 58 0.7× 49 0.9× 52 1.0× 34 0.7× 9 0.2× 11 132
Miroslav Kapuscinski Australia 6 48 0.6× 36 0.7× 18 0.4× 10 0.2× 40 0.9× 11 167

Countries citing papers authored by Garrett Allington

Since Specialization
Citations

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

Fields of papers citing papers by Garrett Allington

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Garrett Allington

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

All Works

13 of 13 papers shown
1.
Allington, Garrett, Neel H. Mehta, Evan Dennis, et al.. (2024). De novo variants disrupt an LDB1 -regulated transcriptional network in congenital ventriculomegaly. Brain. 148(5). 1817–1828.
2.
Mehta, Neel H., et al.. (2023). Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus. JAMA Network Open. 6(11). e2343384–e2343384. 7 indexed citations
3.
Timberlake, Andrew T., Garrett Allington, Emre Kiziltug, et al.. (2023). De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis. The American Journal of Human Genetics. 110(5). 846–862. 11 indexed citations
4.
Kiziltug, Emre, Phan Q. Duy, Garrett Allington, et al.. (2023). Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis. Journal of Neurosurgery Pediatrics. 33(1). 59–72. 5 indexed citations
5.
Allington, Garrett, et al.. (2022). Genomic medicine for liver disease. Hepatology. 76(3). 860–868. 12 indexed citations
6.
Allington, Garrett, Aladine A. Elsamadicy, Phan Q. Duy, et al.. (2022). Familial and syndromic forms of arachnoid cyst implicate genetic factors in disease pathogenesis. Cerebral Cortex. 33(6). 3012–3025. 7 indexed citations
7.
Wu, Yuchang, Julie Choi, Garrett Allington, et al.. (2022). Computational Genomics in the Era of Precision Medicine: Applications to Variant Analysis and Gene Therapy. Journal of Personalized Medicine. 12(2). 175–175. 8 indexed citations
8.
Allington, Garrett, Phan Q. Duy, Amrita Singh, et al.. (2022). Genomic approaches to improve the clinical diagnosis and management of patients with congenital hydrocephalus. Journal of Neurosurgery Pediatrics. 29(2). 168–177. 9 indexed citations
9.
Robert, Stephanie M., Benjamin C. Reeves, Arnaud Marlier, et al.. (2021). Inflammatory hydrocephalus. Child s Nervous System. 37(11). 3341–3353. 9 indexed citations
10.
Diab, Nicholas S., Weilai Dong, Garrett Allington, et al.. (2021). Analysis workflow to assess de novo genetic variants from human whole-exome sequencing. STAR Protocols. 2(1). 100383–100383. 4 indexed citations
11.
Kundishora, Adam J., Amrita Singh, Garrett Allington, et al.. (2021). Genomics of human congenital hydrocephalus. Child s Nervous System. 37(11). 3325–3340. 18 indexed citations
12.
Diab, Nicholas S., Weilai Dong, Shujuan Zhao, et al.. (2021). Molecular Genetics and Complex Inheritance of Congenital Heart Disease. Genes. 12(7). 1020–1020. 58 indexed citations
13.
Liu, Shan, Garrett Allington, Frances Prelli, et al.. (2017). Targeting Apolipoprotein E/Amyloid β Binding by Peptoid CPO_Aβ17-21 P Ameliorates Alzheimer’s Disease Related Pathology and Cognitive Decline. Scientific Reports. 7(1). 8009–8009. 47 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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