Robert Haws

1.7k total citations
33 papers, 785 citations indexed

About

Robert Haws is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Robert Haws has authored 33 papers receiving a total of 785 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 19 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Robert Haws's work include Genetic Syndromes and Imprinting (18 papers), Genetic and Kidney Cyst Diseases (18 papers) and Hedgehog Signaling Pathway Studies (13 papers). Robert Haws is often cited by papers focused on Genetic Syndromes and Imprinting (18 papers), Genetic and Kidney Cyst Diseases (18 papers) and Hedgehog Signaling Pathway Studies (13 papers). Robert Haws collaborates with scholars based in United States, Canada and Spain. Robert Haws's co-authors include Michel Baum, Guojun Yuan, Jack A. Yanovski, Andrea M. Haqq, Anthony D. Krentz, Gregory Gordon, Murray Stewart, John C. Morrison, Michael Grimley and Jeremy Pomeroy and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Radiology.

In The Last Decade

Robert Haws

31 papers receiving 770 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert Haws United States 15 331 266 136 116 114 33 785
Liliya M. Yamaleyeva United States 18 155 0.5× 121 0.5× 247 1.8× 139 1.2× 139 1.2× 38 833
Fabian Hammer Germany 15 285 0.9× 147 0.6× 396 2.9× 138 1.2× 35 0.3× 28 840
L. Zazzeron United States 14 402 1.2× 69 0.3× 41 0.3× 90 0.8× 39 0.3× 27 780
F.C. Logue United Kingdom 17 198 0.6× 76 0.3× 111 0.8× 62 0.5× 51 0.4× 37 748
Glenn Matfin United States 13 188 0.6× 139 0.5× 350 2.6× 121 1.0× 32 0.3× 40 692
Gökhan Üçkaya Türkiye 17 134 0.4× 78 0.3× 228 1.7× 164 1.4× 28 0.2× 38 694
Fang Luo China 16 223 0.7× 116 0.4× 76 0.6× 196 1.7× 36 0.3× 63 875
Valerio Podio Italy 17 307 0.9× 27 0.1× 111 0.8× 153 1.3× 56 0.5× 30 923
Sébastien Thalmann Switzerland 11 141 0.4× 110 0.4× 59 0.4× 92 0.8× 195 1.7× 17 761
Kyung Hoon Paik South Korea 12 97 0.3× 101 0.4× 33 0.2× 88 0.8× 45 0.4× 26 546

Countries citing papers authored by Robert Haws

Since Specialization
Citations

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

Fields of papers citing papers by Robert Haws

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Haws

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Haws. A scholar is included among the top collaborators of Robert Haws 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 Robert Haws. Robert Haws 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.
Mallya, Usha G., Sheri Fehnel, Robert S. Mittleman, et al.. (2023). Interview-Based Patient- and Caregiver-Reported Experiences of Hunger and Improved Quality of Life with Setmelanotide Treatment in Bardet-Biedl Syndrome. Advances in Therapy. 40(5). 2394–2411. 14 indexed citations
2.
Haws, Robert, et al.. (2023). Early development and adaptive functioning in children with Bardet‐Biedl syndrome. American Journal of Medical Genetics Part A. 194(1). 31–38. 4 indexed citations
3.
Forsythe, Elizabeth, Robert Haws, Jesús Argente, et al.. (2023). Quality of life improvements following one year of setmelanotide in children and adult patients with Bardet–Biedl syndrome: phase 3 trial results. Orphanet Journal of Rare Diseases. 18(1). 12–12. 27 indexed citations
4.
Krentz, Anthony D., et al.. (2022). Kidney failure in Bardet – Biedl syndrome. Clinical Genetics. 101(4). 429–441. 22 indexed citations
5.
6.
Pomeroy, Jeremy, et al.. (2021). Sleep and physical activity patterns in adults and children with Bardet–Biedl syndrome. Orphanet Journal of Rare Diseases. 16(1). 276–276. 6 indexed citations
7.
Haws, Robert, Gregory Gordon, Joan C. Han, et al.. (2021). The efficacy and safety of setmelanotide in individuals with Bardet-Biedl syndrome or Alström syndrome: Phase 3 trial design. Contemporary Clinical Trials Communications. 22. 100780–100780. 31 indexed citations
8.
Haws, Robert, et al.. (2019). Cutaneous findings in Bardet‐Biedl syndrome. International Journal of Dermatology. 58(10). 1160–1164. 7 indexed citations
9.
Olson, Andrew, et al.. (2018). Thoraco-Abdominal Abnormalities in Bardet-Biedl Syndrome: Situs Inversus and Heterotaxy. The Journal of Pediatrics. 204. 31–37. 25 indexed citations
10.
Haws, Robert, et al.. (2016). Renal transplantation in Bardet–Biedl Syndrome. Pediatric Nephrology. 31(11). 2153–2161. 11 indexed citations
11.
Schrodi, Steven J., Andrea E. DeBarber, Max M. He, et al.. (2015). Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data. Human Genetics. 134(6). 659–669. 24 indexed citations
12.
Resnick, Jeffrey M., et al.. (2013). Diarrhea in a post-renal transplant child: Questions. Pediatric Nephrology. 30(4). 589–590.
13.
Bleyer, Anthony J., Martina Živná, Helena Hůlková, et al.. (2010). Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone. Clinical Nephrology. 74(12). 411–422. 30 indexed citations
14.
Haws, Robert, Mark Joseph, & Raymond D. Adelman. (2007). Two cases of pheochromocytoma presenting with ADHD (attention deficit hyperactivity disorder)-like symptoms. Pediatric Nephrology. 23(3). 473–475. 8 indexed citations
15.
Geller, David S., Junhui Zhang, Maria‐Christina Zennaro, et al.. (2006). Autosomal Dominant Pseudohypoaldosteronism Type 1. Journal of the American Society of Nephrology. 17(5). 1429–1436. 83 indexed citations
16.
Pennington, Daniel J., et al.. (1998). Childhood pyelonephritis: comparison of gadolinium-enhanced MR imaging and renal cortical scintigraphy for diagnosis.. Radiology. 207(2). 377–384. 63 indexed citations
17.
Haws, Robert, et al.. (1997). RAPIDLY PROGRESSIVE T CELL LYMPHOMA PRESENTING AS ACUTE RENAL FAILURE: Case Report and Review of the Literature. Fetal and Pediatric Pathology. 17(3). 449–460. 1 indexed citations
18.
Neuhauser, Thomas S., et al.. (1997). RAPIDLY PROGRESSIVE T CELL LYMPHOMA PRESENTING AS ACUTE RENAL FAILURE: Case Report and Review of the Literature. Pediatric Pathology & Laboratory Medicine. 17(3). 449–460. 7 indexed citations
19.
Haws, Robert, Philip W. Shaul, Billy S. Arant, Bassam Atiyeh, & Mouin G. Seikaly. (1994). Glomerular Losartan (DuP 753)-Sensitive Angiotensin II Receptor Density Is Increased in Young Spontaneously Hypertensive Rats. Pediatric Research. 35(6). 671–676. 13 indexed citations
20.
Haws, Robert, Arthur G. Weinberg, & Michel Baum. (1992). Spontaneous remission of congenital nephrotic syndrome: a case report and review of the literature. Pediatric Nephrology. 6(1). 82–84. 9 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Liliya M. Yamaleyeva Breakdown of academic impact, for papers by Fabian Hammer Breakdown of academic impact, for papers by L. Zazzeron Breakdown of academic impact, for papers by F.C. Logue Breakdown of academic impact, for papers by Glenn Matfin Breakdown of academic impact, for papers by Gökhan Üçkaya Breakdown of academic impact, for papers by Fang Luo Breakdown of academic impact, for papers by Valerio Podio Breakdown of academic impact, for papers by Sébastien Thalmann Breakdown of academic impact, for papers by Kyung Hoon Paik
Rankless by CCL
2026