Jonathan Berg

784 total citations
7 papers, 160 citations indexed

About

Jonathan Berg is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Genetics. According to data from OpenAlex, Jonathan Berg has authored 7 papers receiving a total of 160 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Pulmonary and Respiratory Medicine, 2 papers in Genetics and 2 papers in Genetics. Recurrent topics in Jonathan Berg's work include Vascular Anomalies and Treatments (2 papers), Tracheal and airway disorders (2 papers) and Genetic Syndromes and Imprinting (1 paper). Jonathan Berg is often cited by papers focused on Vascular Anomalies and Treatments (2 papers), Tracheal and airway disorders (2 papers) and Genetic Syndromes and Imprinting (1 paper). Jonathan Berg collaborates with scholars based in United Kingdom, France and Denmark. Jonathan Berg's co-authors include Gail Kirby, Louise Tee, Fiona MacDonald, Renuka Dias, Peter Nightingale, Eamonn R. Maher, Abdulla Ibrahim, Carol Hardy, Derek Lim and John Foerster and has published in prestigious journals such as Breast Cancer Research, European Journal of Human Genetics and Frontiers in Genetics.

In The Last Decade

Jonathan Berg

5 papers receiving 138 citations

Peers

Jonathan Berg

MB

GENET

PPCH

IMMUN

DERMA

Marta Guindo-Martínez Spain

M. Tuchman United States

Jingning Zhang United States

Michelle McBean Australia

Sophie R. Wang United States

José Ricardo Magliocco Ceroni Brazil

Katayoon Shirneshan Germany

Lara Al-Olabi United Kingdom

David Baudry France

Marta Guindo-Martínez Spain

Jonathan Berg

125 ×1.6

MB

42 ×0.6

GENET

63 ×1.2

PPCH

20 ×0.6

IMMUN

5 ×0.3

DERMA

Citations per year, relative to Jonathan Berg Jonathan Berg (= 1×) peers Marta Guindo-Martínez

Countries citing papers authored by Jonathan Berg

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan Berg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Berg

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan Berg. A scholar is included among the top collaborators of Jonathan Berg 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 Jonathan Berg. Jonathan Berg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Turnpenny, Peter D., Ute Moog, Edward S. Tobias, et al.. (2025). The European Certificate in Medical Genetics and Genomics (ECMGG). European Journal of Human Genetics. 33(9). 1113–1120.

2.

McGowan, Ruth, et al.. (2024). Outcomes of patients with Juvenile Polyposis-Hereditary Haemorrhagic Telangiectasia caused by pathogenic SMAD4 variants in a pan-Scotland cohort. European Journal of Human Genetics. 32(6). 731–735.

3.

Ogston, S., et al.. (2017). HLA-Cw6-positive patients with psoriasis show improved response to methotrexate treatment. Clinical and Experimental Dermatology. 42(6). 651–655. 37 indexed citations

4.

Letteboer, Tom G.W., Michael Benzinou, David A. Quigley, et al.. (2015). Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14. Frontiers in Genetics. 6. 67–67. 16 indexed citations

5.

Ibrahim, Abdulla, Gail Kirby, Carol Hardy, et al.. (2014). Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects. Clinical Epigenetics. 6(1). 11–11. 87 indexed citations

6.

Whelehan, Patricia, et al.. (2011). Improving the validity of breast density assessment. Breast Cancer Research. 13(S1). 1 indexed citations

7.

Berg, Jonathan, et al.. (1990). Geochemistry of the Mamainse Point volcanics, Ontario, and implications for the Keweenawan paleomagnetic record. Canadian Journal of Earth Sciences. 27(9). 1194–1199. 19 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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