Andrew Dauber

6.4k total citations
109 papers, 2.8k citations indexed

About

Andrew Dauber is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Andrew Dauber has authored 109 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Genetics, 51 papers in Molecular Biology and 44 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Andrew Dauber's work include Growth Hormone and Insulin-like Growth Factors (33 papers), Genetic Syndromes and Imprinting (17 papers) and Connective tissue disorders research (13 papers). Andrew Dauber is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (33 papers), Genetic Syndromes and Imprinting (17 papers) and Connective tissue disorders research (13 papers). Andrew Dauber collaborates with scholars based in United States, United Kingdom and Brazil. Andrew Dauber's co-authors include Joel N. Hirschhorn, Ron G. Rosenfeld, Vivian Hwa, Ola Nilsson, Michael H. Guo, Jeffrey Baron, Jan M. Wit, Jennifer Moon, Moshe Phillip and Lars Sävendahl and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Gastroenterology.

In The Last Decade

Andrew Dauber

105 papers receiving 2.7k 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 Dauber United States 31 1.3k 1.3k 962 354 241 109 2.8k
Alicia Belgorosky Argentina 30 917 0.7× 1.1k 0.8× 1.2k 1.2× 322 0.9× 74 0.3× 127 2.5k
Emanuele Ferrante Italy 26 1.2k 0.9× 1.1k 0.9× 1.6k 1.7× 137 0.4× 128 0.5× 132 3.4k
Horacio M. Domené Argentina 28 665 0.5× 655 0.5× 1.4k 1.5× 318 0.9× 82 0.3× 77 2.0k
M. Jansen Netherlands 29 1.1k 0.8× 1.6k 1.2× 1.7k 1.7× 749 2.1× 63 0.3× 55 3.3k
Alessandra Vottero Italy 27 787 0.6× 811 0.6× 895 0.9× 143 0.4× 58 0.2× 49 2.5k
Graziella Pinto France 26 717 0.5× 1.0k 0.8× 873 0.9× 238 0.7× 59 0.2× 65 2.1k
Jan Lebl Czechia 35 1.8k 1.3× 1.5k 1.2× 1.4k 1.5× 278 0.8× 85 0.4× 178 3.5k
Tülay Güran Türkiye 25 452 0.3× 833 0.6× 667 0.7× 222 0.6× 414 1.7× 131 2.3k
U. Heinrich Germany 26 1.2k 0.9× 1.2k 1.0× 1.3k 1.3× 461 1.3× 51 0.2× 70 2.8k
Sharron Gargosky United States 30 534 0.4× 917 0.7× 1.8k 1.9× 629 1.8× 68 0.3× 67 2.9k

Countries citing papers authored by Andrew Dauber

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Dauber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Dauber

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Dauber. A scholar is included among the top collaborators of Andrew Dauber 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 Dauber. Andrew Dauber 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.
Dauber, Andrew, et al.. (2024). Vosoritide treatment for children with hypochondroplasia: a phase 2 trial. EClinicalMedicine. 71. 102591–102591. 4 indexed citations
2.
Dauber, Andrew, et al.. (2024). Clinical Predictors of Good/Poor Response to Growth Hormone Treatment in Children with Idiopathic Short Stature. Hormone Research in Paediatrics. 1–20. 4 indexed citations
3.
Shankar, Roopa Kanakatti, et al.. (2024). Phase 2 Trial of Vosoritide Use in Patients with Hypochondroplasia: A Pharmacokinetic/Pharmacodynamic Analysis. Hormone Research in Paediatrics. 99(1). 131–137. 1 indexed citations
4.
Dauber, Andrew, et al.. (2023). Recombinant Human Insulin-Like Growth Factor-1 Treatment of Severe Growth Failure in Three Siblings with STAT5B Deficiency. Hormone Research in Paediatrics. 97(2). 195–202.
5.
Dauber, Andrew, et al.. (2023). Shedding New Light. Pediatric Clinics of North America. 70(5). 951–961. 2 indexed citations
6.
Carroll, Megan K., Derek K. Ng, Rebecca V. Levy, et al.. (2022). Longitudinal Associations between Low Serum Bicarbonate and Linear Growth in Children with CKD. Kidney360. 3(4). 666–676. 7 indexed citations
7.
Krishnamurthy, Mansa, Daniel O. Kechele, Taylor Broda, et al.. (2022). Using Human Induced Pluripotent Stem Cell–Derived Organoids to Identify New Pathologies in Patients With PDX1 Mutations. Gastroenterology. 163(4). 1053–1063.e7. 14 indexed citations
8.
Bartell, Eric, Masanobu Fujimoto, Jane Khoury, et al.. (2020). Protein QTL analysis of IGF-I and its binding proteins provides insights into growth biology. Human Molecular Genetics. 29(15). 2625–2636. 1 indexed citations
9.
Foster, Timothy P., Daniel J. Perry, Ron G. Rosenfeld, et al.. (2020). A Novel Mutation in Insulin-Like Growth Factor 1 Receptor (c.641-2A>G) Is Associated with Impaired Growth, Hypoglycemia, and Modified Immune Phenotypes. Hormone Research in Paediatrics. 93(5). 322–334. 4 indexed citations
10.
Fujimoto, Masanobu, Melissa Andrew, Dongsheng Zhang, et al.. (2019). Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation. Endocrinology. 160(6). 1363–1376. 14 indexed citations
11.
Poyrazoğlu, Şükran, Vivian Hwa, Firdevs Baş, et al.. (2019). A Novel Homozygous Mutation of the Acid-Labile Subunit <i>(IGFALS)</i> Gene in a Male Adolescent. Journal of Clinical Research in Pediatric Endocrinology. 11(4). 432–438. 9 indexed citations
12.
Hawkes, Colin P., Melissa Andrew, Diego Campos, et al.. (2019). Targeted Searches of the Electronic Health Record and Genomics Identify an Etiology in Three Patients with Short Stature and High IGF-I Levels. Hormone Research in Paediatrics. 92(3). 186–195. 5 indexed citations
13.
Gomes, Larissa Garcia, Marina Cunha-Silva, Carolina Ramos, et al.. (2018). DLK1 Is a Novel Link Between Reproduction and Metabolism. The Journal of Clinical Endocrinology & Metabolism. 104(6). 2112–2120. 91 indexed citations
14.
Dauber, Andrew, et al.. (2018). Mosaic variegated aneuploidy syndrome caused by a CEP57 mutation diagnosed by whole exome sequencing. Clinical Case Reports. 6(8). 1531–1534. 13 indexed citations
15.
Huang, Zhuo, Yu Sun, Yanjie Fan, et al.. (2018). Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study. Cellular Physiology and Biochemistry. 49(1). 295–305. 28 indexed citations
16.
Klammt, Jürgen, David Neumann, Evelien Gevers, et al.. (2018). Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation. Nature Communications. 9(1). 2105–2105. 79 indexed citations
17.
Bessa, Danielle S., Delanie B. Macedo, Vinícius Nahime Brito, et al.. (2016). High Frequency of <b><i>MKRN3</i></b> Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic. Neuroendocrinology. 105(1). 17–25. 56 indexed citations
18.
Guo, Michael H., Yiping Shen, Emily C. Walvoord, et al.. (2014). Whole Exome Sequencing to Identify Genetic Causes of Short Stature. Hormone Research in Paediatrics. 82(1). 44–52. 58 indexed citations
19.
Dauber, Andrew, Yongguo Yu, Michael C. Turchin, et al.. (2011). Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions. The American Journal of Human Genetics. 89(6). 751–759. 56 indexed citations
20.
Dauber, Andrew, et al.. (1993). [The incidence of postoperative pain on general surgical wards. Results of different evaluation procedures].. PubMed. 42(7). 448–54. 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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