Erwin Pauws
Impact in
- Genetics top 5%
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Congenital Ear and Nasal Anomalies
-
- Thyroid Disorders and Treatments
- Thyroid Cancer Diagnosis and Treatment
Papers in
-
- dental development and anomalies 9
- RNA modifications and cancer 6
- Congenital heart defects research 4
- RNA and protein synthesis mechanisms 4
- Genetics 29
- Cleft Lip and Palate Research 23
- Craniofacial Disorders and Treatments 19
- Congenital Ear and Nasal Anomalies 8
- Co-authors
- Philip Stanier (18 shared papers)Carrie Ris‐Stalpers (7 shared papers)Gudrun E. Moore (7 shared papers)Jan J. M. de Vijlder (5 shared papers)Héctor M. Targovnik (1 shared paper)Fernando Mendive (1 shared paper)Frank Baas (3 shared papers)Peter Hammond (2 shared papers)
- Journals
- Human Molecular Genetics (4 papers)Journal of Anatomy (4 papers)Disease Models & Mechanisms (3 papers)International Journal of Oral and Maxillofacial Surgery (2 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)
- Partner nations
- United KingdomNetherlandsUnited States
In The Last Decade
Erwin Pauws
45 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 88
- Genetics 647
- Genetics 136
- Endocrinology, Diabetes and Metabolism 190
- Molecular Biology 753
- Speech and Hearing 28
Countries citing papers authored by Erwin Pauws
This map shows the geographic impact of Erwin Pauws'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 Erwin Pauws with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erwin Pauws more than expected).
Fields of papers citing papers by Erwin Pauws
This network shows the impact of papers produced by Erwin Pauws. 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 Erwin Pauws. The network helps show where Erwin Pauws may publish in the future.
Co-authors
The 25 scholars most cited alongside Erwin Pauws, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 124 | |
| 2 | 2001 | 93 | |
| 3 | 2009 | 75 | |
| 4 | 1999 | 73 | |
| 5 | 2007 | 72 | |
| 6 | 2007 | 70 | |
| 7 | 2010 | 60 | |
| 8 | 2007 | 59 | |
| 9 | 2013 | 54 | |
| 10 | 2008 | 53 | |
| 11 | Tbx22 null マウスは,口蓋骨形成の低下により粘膜下口蓋裂を有し,そしてまた舌小帯短縮症および後鼻孔閉鎖表現型を示す | 2009 | 49 |
| 12 | 2015 | 49 | |
| 13 | 2012 | 48 | |
| 14 | 2001 | 46 | |
| 15 | 2000 | 39 | |
| 16 | 2011 | 38 | |
| 17 | 2019 | 31 | |
| 18 | 1997 | 30 | |
| 19 | 2000 | 28 | |
| 20 | 2015 | 26 |
About Erwin Pauws
Erwin Pauws is a scholar working on Molecular Biology, Genetics, Genetics, Pulmonary and Respiratory Medicine and Endocrinology, Diabetes and Metabolism, having authored 46 papers that have together received 1.3k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (23 papers), Craniofacial Disorders and Treatments (19 papers), dental development and anomalies (9 papers), Congenital Ear and Nasal Anomalies (8 papers), RNA modifications and cancer (6 papers), Congenital heart defects research (4 papers), RNA and protein synthesis mechanisms (4 papers) and Tracheal and airway disorders (4 papers). The work is most often cited by research in Genetics (647 citations), Genetics (136 citations), Endocrinology, Diabetes and Metabolism (190 citations), Molecular Biology (753 citations) and Speech and Hearing (28 citations). Erwin Pauws has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Philip Stanier, Carrie Ris‐Stalpers, Gudrun E. Moore, Jan J. M. de Vijlder, Héctor M. Targovnik, Fernando Mendive, Frank Baas, Peter Hammond, Juan Pedro Martı́nez-Barberá and Nicholas D. E. Greene. Their work appears in journals such as Human Molecular Genetics, Journal of Anatomy, Disease Models & Mechanisms, International Journal of Oral and Maxillofacial Surgery and The Journal of Clinical Endocrinology & Metabolism.
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.