Terry Bertin

5.0k total citations
55 papers, 3.5k citations indexed

About

Terry Bertin is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Terry Bertin has authored 55 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 29 papers in Molecular Biology and 13 papers in Rheumatology. Recurrent topics in Terry Bertin's work include Connective tissue disorders research (12 papers), Virus-based gene therapy research (7 papers) and Bone and Dental Protein Studies (7 papers). Terry Bertin is often cited by papers focused on Connective tissue disorders research (12 papers), Virus-based gene therapy research (7 papers) and Bone and Dental Protein Studies (7 papers). Terry Bertin collaborates with scholars based in United States, Canada and Germany. Terry Bertin's co-authors include Brendan Lee, Tao Yang, Elda Munivez, Brian Dawson, Yuqing Chen, William J. Schull, Craig L. Hanis, Brendan Lee, Jianning Tao and Roy Morello and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Terry Bertin

55 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Terry Bertin United States 31 1.8k 1.5k 818 675 529 55 3.5k
Paula S. Henthorn United States 35 2.2k 1.2× 1.1k 0.8× 920 1.1× 176 0.3× 423 0.8× 105 5.0k
Laurence Legeai‐Mallet France 36 2.7k 1.5× 2.5k 1.7× 760 0.9× 291 0.4× 467 0.9× 87 4.7k
Efthimia K. Basdra Greece 32 1.6k 0.9× 552 0.4× 333 0.4× 375 0.6× 343 0.6× 89 3.1k
Jürgen W. Spranger Germany 44 2.4k 1.4× 2.7k 1.8× 1.1k 1.3× 312 0.5× 674 1.3× 171 5.8k
Pierre Moffatt Canada 31 1.3k 0.7× 1000 0.7× 1.2k 1.4× 209 0.3× 331 0.6× 76 2.7k
Sherrill Adams United States 35 1.7k 0.9× 578 0.4× 1.1k 1.3× 283 0.4× 269 0.5× 56 3.2k
Takako Hattori Japan 31 1.8k 1.0× 434 0.3× 691 0.8× 393 0.6× 222 0.4× 103 2.7k
Leonard Rifas United States 27 1.7k 0.9× 480 0.3× 630 0.8× 341 0.5× 941 1.8× 49 3.5k
Donna D. Strong United States 35 1.8k 1.0× 595 0.4× 259 0.3× 453 0.7× 422 0.8× 78 3.5k
Wei Hsu United States 37 3.3k 1.8× 1.1k 0.7× 214 0.3× 314 0.5× 552 1.0× 66 4.3k

Countries citing papers authored by Terry Bertin

Since Specialization
Citations

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

Fields of papers citing papers by Terry Bertin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Terry Bertin

This figure shows the co-authorship network connecting the top 25 collaborators of Terry Bertin. A scholar is included among the top collaborators of Terry Bertin 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 Terry Bertin. Terry Bertin 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.
Jin, Zixue, Lindsay C. Burrage, Ming‐Ming Jiang, et al.. (2018). Whole‐Exome Sequencing Identifies an Intronic Cryptic Splice Site in SERPINF1 Causing Osteogenesis Imperfecta Type VI. JBMR Plus. 2(4). 235–239. 3 indexed citations
2.
Bae, Yangjin, Brian C. Dawson, Yuqing Chen, et al.. (2017). MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-β signalling in osteoblasts. Nature Communications. 8(1). 15000–15000. 82 indexed citations
3.
Rajagopal, Abbhirami, Erica P. Homan, Kyu Sang Joeng, et al.. (2015). Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice. Molecular Genetics and Metabolism. 117(3). 378–382. 11 indexed citations
4.
Lietman, Caressa, Abbhirami Rajagopal, Erica P. Homan, et al.. (2014). Connective tissue alterations in Fkbp10−/− mice. Human Molecular Genetics. 23(18). 4822–4831. 48 indexed citations
5.
Ruan, Merry Z. C., Ayelet Erez, Kilian Guse, et al.. (2013). Proteoglycan 4 expression protects against the development of osteoarthritis. Osteoarthritis and Cartilage. 21. S18–S18. 25 indexed citations
6.
Guse, Kilian, Masataka Suzuki, Gautam Sule, et al.. (2012). Capsid-Modified Adenoviral Vectors for Improved Muscle-Directed Gene Therapy. Human Gene Therapy. 23(10). 1065–1070. 21 indexed citations
7.
Bae, Yangjin, Tao Yang, Philippe M. Campeau, et al.. (2012). miRNA-34c regulates Notch signaling during bone development. Human Molecular Genetics. 21(13). 2991–3000. 200 indexed citations
8.
Homan, Erica P., Frank Rauch, Ingo Grafe, et al.. (2011). Mutations in SERPINF1 cause osteogenesis imperfecta type VI. Journal of Bone and Mineral Research. 26(12). 2798–2803. 135 indexed citations
9.
Keller, Bettina G., Tao Yang, Yuqing Chen, et al.. (2011). Interaction of TGFβ and BMP Signaling Pathways during Chondrogenesis. PLoS ONE. 6(1). e16421–e16421. 119 indexed citations
10.
Yang, Tao, Roberto Mendoza‐Londono, Jianning Tao, et al.. (2010). E-selectin ligand–1 regulates growth plate homeostasis in mice by inhibiting the intracellular processing and secretion of mature TGF-β. Journal of Clinical Investigation. 120(7). 2474–2485. 25 indexed citations
11.
Vetrini, Francesco, Nicola Brunetti‐Pierri, Donna Palmer, et al.. (2010). Vasoactive Intestinal Peptide Increases Hepatic Transduction and Reduces Innate Immune Response Following Administration of Helper-dependent Ad. Molecular Therapy. 18(7). 1339–1345. 7 indexed citations
12.
Morello, Roy, Terry Bertin, Silke Schlaubitz, et al.. (2008). Brachy–syndactyly caused by loss of Sfrp2 function. Journal of Cellular Physiology. 217(1). 127–137. 56 indexed citations
13.
Cerullo, Vincenzo, Michael P. Seiler, Viraj Mane, et al.. (2007). Toll-like Receptor 9 Triggers an Innate Immune Response to Helper-dependent Adenoviral Vectors. Molecular Therapy. 15(2). 378–385. 116 indexed citations
14.
McCormack, William M., Terry Bertin, Donna Palmer, et al.. (2006). Helper‐dependent adenoviral gene therapy mediates long‐term correction of the clotting defect in the canine hemophilia A model. Journal of Thrombosis and Haemostasis. 4(6). 1218–1225. 49 indexed citations
15.
Morello, Roy, Terry Bertin, Yuqing Chen, et al.. (2006). CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis Imperfecta. Cell. 127(2). 291–304. 366 indexed citations
16.
Hermanns, Pia, Alison A. Bertuch, Terry Bertin, et al.. (2005). Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia. Human Molecular Genetics. 14(23). 3723–3740. 86 indexed citations
17.
Blanton, Susan H., et al.. (2003). Nonsyndromic cleft lip and palate: Four chromosomal regions of interest. American Journal of Medical Genetics Part A. 125A(1). 28–37. 22 indexed citations
18.
Sutton, V. Reid, William H. McAlister, Terry Bertin, et al.. (2003). Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12). Human Genetics. 113(5). 447–451. 38 indexed citations
19.
Hanis, Craig L. & Terry Bertin. (1992). Juxtaposed short sequence repeat types and haplotypes near exon 3 of the insulin receptor locus among Mexican Americans. Genomics. 12(4). 842–845. 11 indexed citations
20.
Bertin, Terry, Jennifer Harris, R E Ferrell, & William J. Schull. (1978). The Nubians of Kom Ombo: Serum and Red Cell Protein Types. Human Heredity. 28(1). 66–71. 8 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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