Andrew T. Timberlake

1.7k total citations
35 papers, 492 citations indexed

About

Andrew T. Timberlake is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Andrew T. Timberlake has authored 35 papers receiving a total of 492 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Andrew T. Timberlake's work include Craniofacial Disorders and Treatments (15 papers), Cleft Lip and Palate Research (10 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Andrew T. Timberlake is often cited by papers focused on Craniofacial Disorders and Treatments (15 papers), Cleft Lip and Palate Research (10 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Andrew T. Timberlake collaborates with scholars based in United States, Austria and France. Andrew T. Timberlake's co-authors include John A. Persing, James R. Monaghan, Craig M. Crews, Robin T. Wu, Irvin M. Modlin, Richard P. Lifton, Roswitha Pfragner, Mark Kidd, Kristopher T. Kahle and Kyle S. Gabrick and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gastroenterology and Development.

In The Last Decade

Andrew T. Timberlake

30 papers receiving 485 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew T. Timberlake United States 12 235 183 95 41 35 35 492
Gaëtan Riou France 11 86 0.4× 192 1.0× 18 0.2× 19 0.5× 22 0.6× 20 472
Matthew Pollard United States 11 115 0.5× 76 0.4× 38 0.4× 35 0.9× 16 0.5× 16 590
Silvia Marino Italy 11 114 0.5× 86 0.5× 37 0.4× 35 0.9× 105 3.0× 51 417
Katherine Rose United States 10 73 0.3× 180 1.0× 64 0.7× 20 0.5× 19 0.5× 22 427
C Conti Italy 12 53 0.2× 75 0.4× 67 0.7× 43 1.0× 10 0.3× 31 394
Chaowei Tian China 7 161 0.7× 136 0.7× 37 0.4× 11 0.3× 13 0.4× 12 415
F. T. A. Fitzpatrick France 10 153 0.7× 65 0.4× 49 0.5× 21 0.5× 20 0.6× 10 698
S.A. Guttormsen United States 12 182 0.8× 125 0.7× 59 0.6× 20 0.5× 17 0.5× 25 436
Sawa Yasumoto Japan 17 345 1.5× 344 1.9× 31 0.3× 253 6.2× 190 5.4× 44 947

Countries citing papers authored by Andrew T. Timberlake

Since Specialization
Citations

This map shows the geographic impact of Andrew T. Timberlake'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 Andrew T. Timberlake with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew T. Timberlake more than expected).

Fields of papers citing papers by Andrew T. Timberlake

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew T. Timberlake. 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 Andrew T. Timberlake. The network helps show where Andrew T. Timberlake may publish in the future.

Co-authorship network of co-authors of Andrew T. Timberlake

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew T. Timberlake. A scholar is included among the top collaborators of Andrew T. Timberlake 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 Andrew T. Timberlake. Andrew T. Timberlake 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.
2.
Timberlake, Andrew T., Kshipra Hemal, Le Hao, et al.. (2024). AXIN1 mutations in nonsyndromic craniosynostosis. Journal of Neurosurgery Pediatrics. 34(3). 246–251.
3.
Yang, Jenny F., et al.. (2024). The role of genetics on behavioral outcomes in nonsyndromic sagittal synostosis. Journal of Neurosurgery Pediatrics. 34(3). 234–245.
4.
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
5.
Timberlake, Andrew T., et al.. (2023). Quantifying the Impact of Genetics on Neurocognition in Nonsyndromic Sagittal Craniosynostosis. Plastic & Reconstructive Surgery. 152(2). 300e–306e. 3 indexed citations
6.
Timberlake, Andrew T., Daniel Quiat, Michael L. Cunningham, et al.. (2023). 1. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia. Plastic & Reconstructive Surgery Global Open. 11(5S). 1–1. 1 indexed citations
7.
Duy, Phan Q., Andrew T. Timberlake, Richard P. Lifton, & Kristopher T. Kahle. (2022). Molecular genetics of human developmental neurocranial anomalies: towards “precision surgery”. Cerebral Cortex. 33(6). 2912–2918. 4 indexed citations
8.
Kerner, Gaspard, Matthieu Bouaziz, Aurélie Cobat, et al.. (2020). A genome-wide case-only test for the detection of digenic inheritance in human exomes. Proceedings of the National Academy of Sciences. 117(32). 19367–19375. 17 indexed citations
9.
Gabrick, Kyle S., et al.. (2019). The Effect of Autologous Fat Grafting on Edema and Ecchymoses in Primary Open Rhinoplasty. Aesthetic Surgery Journal. 40(4). 359–366. 10 indexed citations
10.
Sawh‐Martinez, Rajendra, Alex M. Lin, Andrew T. Timberlake, et al.. (2019). Immediate plastic surgery closure at index spinal surgery minimizes complications compared to delayed reconstruction: A retrospective cohort review. Journal of Plastic Reconstructive & Aesthetic Surgery. 73(8). 1499–1505. 5 indexed citations
11.
Furey, Charuta G., Xue Zeng, Weilai Dong, et al.. (2018). Human Genetics and Molecular Mechanisms of Congenital Hydrocephalus. World Neurosurgery. 119. 441–443. 9 indexed citations
12.
Chesler, David A., et al.. (2018). Non-syndromic single-suture craniosynostosis in triplets. Child s Nervous System. 34(6). 1241–1245. 3 indexed citations
13.
Persing, Sarah, et al.. (2018). Three-Dimensional Imaging in Rhinoplasty: A Comparison of the Simulated versus Actual Result. Aesthetic Plastic Surgery. 42(5). 1331–1335. 24 indexed citations
14.
Timberlake, Andrew T., Robin T. Wu, Carol Nelson‐Williams, et al.. (2018). Co-occurrence of frameshift mutations in SMAD6 and TCF12 in a child with complex craniosynostosis. Human Genome Variation. 5(1). 14–14. 14 indexed citations
15.
Furey, Charuta G., Prince Antwi, Daniel Durán, et al.. (2018). 9p24 triplication in syndromic hydrocephalus with diffuse villous hyperplasia of the choroid plexus. Molecular Case Studies. 4(5). a003145–a003145. 6 indexed citations
16.
Timberlake, Andrew T. & John A. Persing. (2018). Genetics of Nonsyndromic Craniosynostosis. Plastic & Reconstructive Surgery. 141(6). 1508–1516. 43 indexed citations
17.
Timberlake, Andrew T., Charuta G. Furey, Jungmin Choi, et al.. (2017). De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis. Proceedings of the National Academy of Sciences. 114(35). E7341–E7347. 61 indexed citations
18.
Champaneria, Manish C., Roswitha Pfragner, Irvin M. Modlin, et al.. (2015). reference genes for real-time PCR GeneChip, geNorm, and gastrointestinal tumors: novel.
19.
Timberlake, Andrew T., et al.. (2014). Highly efficient targeted mutagenesis in axolotl using Cas9 RNA-guided nuclease. Development. 141(10). 2165–2171. 80 indexed citations
20.

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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