Daniel Kelberman
Impact in
-
- Growth Hormone and Insulin-like Growth Factors
- Pituitary Gland Disorders and Treatments
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Ocular Disorders and Treatments
- Genetic Syndromes and Imprinting
- Congenital Ear and Nasal Anomalies
Papers in
- Genetics 20
- Ocular Disorders and Treatments 9
- Congenital Ear and Nasal Anomalies 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Craniofacial Disorders and Treatments 3
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- Hedgehog Signaling Pathway Studies 6
- Congenital heart defects research 3
- Co-authors
- Mehul Dattani (24 shared papers)Iain C. A. F. Robinson (2 shared papers)Robin Lovell‐Badge (2 shared papers)Karine Rizzoti (2 shared papers)Juan Pedro Martı́nez-Barberá (6 shared papers)Jane C. Sowden (7 shared papers)Kyriaki S. Alatzoglou (3 shared papers)John C. Achermann (3 shared papers)
- Journals
- The Journal of Clinical Endocrinology & Metabolism (6 papers)Human Molecular Genetics (3 papers)Human Mutation (3 papers)Hormone Research in Paediatrics (2 papers)Clinical Endocrinology (2 papers)
- Partner nations
- United KingdomUnited StatesGreece
In The Last Decade
Daniel Kelberman
42 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 96
- Endocrinology, Diabetes and Metabolism 889
- Genetics 913
- Reproductive Medicine 162
- Genetics 175
- Molecular Biology 1.0k
Countries citing papers authored by Daniel Kelberman
This map shows the geographic impact of Daniel Kelberman'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 Daniel Kelberman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Kelberman more than expected).
Fields of papers citing papers by Daniel Kelberman
This network shows the impact of papers produced by Daniel Kelberman. 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 Daniel Kelberman. The network helps show where Daniel Kelberman may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel Kelberman, 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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 360 | |
| 2 | 2006 | 280 | |
| 3 | 2007 | 174 | |
| 4 | 2008 | 134 | |
| 5 | 2006 | 132 | |
| 6 | 2001 | 97 | |
| 7 | 2008 | 83 | |
| 8 | 2007 | 77 | |
| 9 | 2018 | 75 | |
| 10 | 2007 | 73 | |
| 11 | 2007 | 72 | |
| 12 | 2008 | 71 | |
| 13 | 2007 | 58 | |
| 14 | 2012 | 56 | |
| 15 | 2005 | 51 | |
| 16 | 2006 | 49 | |
| 17 | 2011 | 42 | |
| 18 | 2008 | 41 | |
| 19 | 2004 | 40 | |
| 20 | 2008 | 40 |
About Daniel Kelberman
Daniel Kelberman is a scholar working on Genetics, Molecular Biology, Endocrinology, Diabetes and Metabolism, Genetics and Surgery, having authored 43 papers that have together received 2.5k indexed citations. Recurring topics across this work include Growth Hormone and Insulin-like Growth Factors (10 papers), Ocular Disorders and Treatments (9 papers), Hedgehog Signaling Pathway Studies (6 papers), Congenital Ear and Nasal Anomalies (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Congenital heart defects research (3 papers), Craniofacial Disorders and Treatments (3 papers) and Pituitary Gland Disorders and Treatments (3 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (889 citations), Genetics (913 citations), Reproductive Medicine (162 citations), Genetics (175 citations) and Molecular Biology (1.0k citations). Daniel Kelberman has collaborated with scholars based in United Kingdom, United States and Greece. Frequent co-authors include Mehul Dattani, Iain C. A. F. Robinson, Robin Lovell‐Badge, Karine Rizzoti, Juan Pedro Martı́nez-Barberá, Jane C. Sowden, Kyriaki S. Alatzoglou, John C. Achermann, Steve E. Humphries and Sandra C. de Castro. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Human Molecular Genetics, Human Mutation, Hormone Research in Paediatrics and Clinical Endocrinology.
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.