Daniel Kelberman

3.5k total citations
43 papers, 2.2k citations indexed

About

Daniel Kelberman is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Daniel Kelberman has authored 43 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 24 papers in Molecular Biology and 13 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Daniel Kelberman's work include Growth Hormone and Insulin-like Growth Factors (11 papers), Ocular Disorders and Treatments (9 papers) and Hedgehog Signaling Pathway Studies (8 papers). Daniel Kelberman is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (11 papers), Ocular Disorders and Treatments (9 papers) and Hedgehog Signaling Pathway Studies (8 papers). Daniel Kelberman collaborates with scholars based in United Kingdom, United States and France. Daniel Kelberman's co-authors include Mehul Dattani, Iain C. A. F. Robinson, Robin Lovell‐Badge, Karine Rizzoti, Juan Pedro Martı́nez-Barberá, Steve E. Humphries, Jane C. Sowden, Kyriaki S. Alatzoglou, John C. Achermann and Patricia Woo and has published in prestigious journals such as Journal of Clinical Investigation, Development and Endocrine Reviews.

In The Last Decade

Daniel Kelberman

42 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Kelberman United Kingdom 28 1.1k 967 717 269 219 43 2.2k
Bruno Leheup France 29 1.1k 1.0× 758 0.8× 234 0.3× 239 0.9× 215 1.0× 97 2.2k
Koji Muroya Japan 28 1.9k 1.7× 1.9k 1.9× 719 1.0× 377 1.4× 158 0.7× 119 3.1k
Yoshio Makita Japan 24 916 0.8× 797 0.8× 185 0.3× 213 0.8× 131 0.6× 77 1.8k
Alexander A.L. Jorge Brazil 36 2.0k 1.8× 1.7k 1.7× 1.5k 2.1× 467 1.7× 154 0.7× 185 3.8k
Peter Wieacker Germany 35 2.4k 2.2× 1.6k 1.7× 255 0.4× 191 0.7× 119 0.5× 141 3.8k
Guillermo Antiñolo Spain 30 2.0k 1.8× 792 0.8× 244 0.3× 913 3.4× 193 0.9× 179 3.3k
Henning B. Boldt Denmark 23 833 0.8× 231 0.2× 744 1.0× 145 0.5× 275 1.3× 44 2.2k
Dvorah Abeliovich Israel 31 1.5k 1.3× 1.4k 1.4× 148 0.2× 340 1.3× 158 0.7× 98 3.0k
Anne Camus France 20 1.6k 1.4× 387 0.4× 259 0.4× 260 1.0× 57 0.3× 32 2.4k
Sarina G. Kant Netherlands 26 1.4k 1.3× 1.3k 1.3× 451 0.6× 193 0.7× 70 0.3× 70 2.7k

Countries citing papers authored by Daniel Kelberman

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Daniel Kelberman

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Kelberman. A scholar is included among the top collaborators of Daniel Kelberman 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 Daniel Kelberman. Daniel Kelberman 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.
Wilkinson, Meredyth, Dale Moulding, Thomas McDonnell, et al.. (2022). Role of CD14+ monocyte-derived oxidised mitochondrial DNA in the inflammatory interferon type 1 signature in juvenile dermatomyositis. Annals of the Rheumatic Diseases. 82(5). 658–669. 26 indexed citations
2.
Gagunashvili, Andrey, Louise Ocaka, Daniel Kelberman, et al.. (2019). Novel missense variants in the RNF213 gene from a European family with Moyamoya disease. Human Genome Variation. 6(1). 35–35. 10 indexed citations
3.
Kelberman, Daniel, Lily Islam, Jörn Lakowski, et al.. (2014). Mutation of SALL2 causes recessive ocular coloboma in humans and mice. Human Molecular Genetics. 23(10). 2511–2526. 37 indexed citations
4.
Prasov, Lev, Tehmina Masud, Shagufta Khaliq, et al.. (2012). ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Human Molecular Genetics. 21(16). 3681–3694. 51 indexed citations
5.
Alatzoglou, Kyriaki S., Cynthia L. Andoniadou, Daniel Kelberman, et al.. (2011). SOX2 haploinsufficiency is associated with slow progressing hypothalamo‐pituitary tumours. Human Mutation. 32(12). 1376–1380. 33 indexed citations
6.
Gaston‐Massuet, Carles, Daniel Kelberman, Mehul Dattani, & Juan Pedro Martı́nez-Barberá. (2009). Absence of SIX3 mutations in patients with congenital hypopituitarism. American Journal of Medical Genetics Part A. 149A(12). 2874–2876. 5 indexed citations
7.
Kelberman, Daniel & Mehul Dattani. (2009). Role of Transcription Factors in Midline Central Nervous System and Pituitary Defects. Endocrine development. 14. 67–82. 21 indexed citations
8.
Kelberman, Daniel & Mehul Dattani. (2008). Septo-Optic Dysplasia – Novel Insights into the Aetiology. Hormone Research in Paediatrics. 69(5). 257–265. 58 indexed citations
9.
Samuel, Jane, Daniel Kelberman, Andrew J. Smith, Steve E. Humphries, & Patricia Woo. (2008). Identification of a novel regulatory region in the interleukin-6 gene promoter. Cytokine. 42(2). 256–264. 31 indexed citations
10.
Kelberman, Daniel, Sandra C. de Castro, Heike Biebermann, et al.. (2008). Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss. Human Molecular Genetics. 17(14). 2150–2159. 65 indexed citations
11.
Kelberman, Daniel, James Turton, Mona Alkhawari, et al.. (2008). Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD). Clinical Endocrinology. 70(1). 96–103. 34 indexed citations
12.
Lin, Lin, Pascal Philibert, Bruno Ferraz‐de‐Souza, et al.. (2007). Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function. The Journal of Clinical Endocrinology & Metabolism. 92(3). 991–999. 150 indexed citations
13.
Kelberman, Daniel & Mehul Dattani. (2007). Hypopituitarism Oddities: Congenital Causes. Hormone Research in Paediatrics. 68(Suppl. 5). 138–144. 46 indexed citations
14.
Kelberman, Daniel & Mehul Dattani. (2007). Genetics of septo-optic dysplasia. Pituitary. 10(4). 393–407. 58 indexed citations
15.
Fife, M, Emma Ogilvie, Daniel Kelberman, et al.. (2005). Novel IL-6 haplotypes and disease association. Genes and Immunity. 6(4). 367–370. 47 indexed citations
16.
Kelberman, Daniel, M Fife, Matthew V. Rockman, et al.. (2004). Analysis of common IL-6 promoter SNP variants and the AnTn tract in humans and primates and effects on plasma IL-6 levels following coronary artery bypass graft surgery. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1688(2). 160–167. 29 indexed citations
17.
18.
Kelberman, Daniel, Jess Tyson, David Chandler, et al.. (2001). Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome. Human Genetics. 109(6). 638–645. 92 indexed citations
19.
Kelberman, Daniel, et al.. (2000). Mapping of a locus for autosomal dominant Hemifacial Microsomia. UCL Discovery (University College London). 1 indexed citations
20.
Prescott, Natalie J., et al.. (1999). Candidate gene analysis of TGFA, EDN-1, and MTHFR, and the influence of maternal smoking in nonsyndromic cleft lip and palate. UCL Discovery (University College London). 1 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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