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

Andrew Dauber
Comparison fields: 5 of 115
  • Genetics 1.3k
  • Molecular Biology 1.3k
  • Endocrinology, Diabetes and Metabolism 962
  • Pediatrics, Perinatology and Child Health 354
  • Pathology and Forensic Medicine 241
Alicia Belgorosky Argentina
Emanuele Ferrante Italy
Horacio M. Domené Argentina
M. Jansen Netherlands
Alessandra Vottero Italy
Graziella Pinto France
Jan Lebl Czechia
Tülay Güran Türkiye
U. Heinrich Germany
Sharron Gargosky United States
Alicia Belgorosky Argentina View profile →
Citations per field, relative to Andrew Dauber
Andrew Dauber · 1×
Citations per year, relative to Andrew Dauber
Andrew Dauber · 1×

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
# Title Journal Authors Indexed citations
1 Vosoritide treatment for children with hypochondroplasia: a phase 2 trial EClinicalMedicine Andrew Dauber, Roopa Kanakatti Shankar et al. 4
2 Clinical Predictors of Good/Poor Response to Growth Hormone Treatment in Children with Idiopathic Short Stature Hormone Research in Paediatrics Andrew Dauber, Moshe Phillip et al. 4
3 Phase 2 Trial of Vosoritide Use in Patients with Hypochondroplasia: A Pharmacokinetic/Pharmacodynamic Analysis Hormone Research in Paediatrics Roopa Kanakatti Shankar, Niti Dham et al. 1
4 Recombinant Human Insulin-Like Growth Factor-1 Treatment of Severe Growth Failure in Three Siblings with STAT5B Deficiency Hormone Research in Paediatrics Andrew Dauber, Vivian Hwa et al. 0
5 Shedding New Light Pediatric Clinics of North America Andrew Dauber et al. 2
6 Longitudinal Associations between Low Serum Bicarbonate and Linear Growth in Children with CKD Kidney360 Megan K. Carroll, Derek K. Ng et al. 7
7 Using Human Induced Pluripotent Stem Cell–Derived Organoids to Identify New Pathologies in Patients With PDX1 Mutations Gastroenterology Mansa Krishnamurthy, Daniel O. Kechele et al. 14
8 Protein QTL analysis of IGF-I and its binding proteins provides insights into growth biology Human Molecular Genetics Eric Bartell, Masanobu Fujimoto et al. 1
9 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 Timothy P. Foster, Daniel J. Perry et al. 4
10 Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation Endocrinology Masanobu Fujimoto, Melissa Andrew et al. 14
11 A Novel Homozygous Mutation of the Acid-Labile Subunit <i>(IGFALS)</i> Gene in a Male Adolescent Journal of Clinical Research in Pediatric Endocrinology Şükran Poyrazoğlu, Vivian Hwa et al. 9
12 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 Colin P. Hawkes, Melissa Andrew et al. 5
13 DLK1 Is a Novel Link Between Reproduction and Metabolism The Journal of Clinical Endocrinology & Metabolism Larissa Garcia Gomes, Marina Cunha-Silva et al. 91
14 Mosaic variegated aneuploidy syndrome caused by a CEP57 mutation diagnosed by whole exome sequencing Clinical Case Reports Andrew Dauber et al. 13
15 Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study Cellular Physiology and Biochemistry Zhuo Huang, Yu Sun et al. 28
16 Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation Nature Communications Jürgen Klammt, David Neumann et al. 79
17 High Frequency of <b><i>MKRN3</i></b> Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic Neuroendocrinology Danielle S. Bessa, Delanie B. Macedo et al. 56
18 Whole Exome Sequencing to Identify Genetic Causes of Short Stature Hormone Research in Paediatrics Michael H. Guo, Yiping Shen et al. 58
19 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 Andrew Dauber, Yongguo Yu et al. 56
20 [The incidence of postoperative pain on general surgical wards. Results of different evaluation procedures]. PubMed Andrew Dauber, Benno Ure et al. 8

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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