J. M. Berg

1.9k total citations
57 papers, 1.4k citations indexed

About

J. M. Berg is a scholar working on Genetics, Physiology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, J. M. Berg has authored 57 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Physiology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in J. M. Berg's work include Genomic variations and chromosomal abnormalities (5 papers), Clinical Laboratory Practices and Quality Control (5 papers) and Family and Disability Support Research (5 papers). J. M. Berg is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Clinical Laboratory Practices and Quality Control (5 papers) and Family and Disability Support Research (5 papers). J. M. Berg collaborates with scholars based in United Kingdom, Canada and United States. J. M. Berg's co-authors include Loretta Ford, P. E. Polani, C. E. Ford, L. Crome, V. D. Marković, N. E. France, M. A. C. Ridler, R. G. Worton, Harry Karlinsky and B. H. Kirman and has published in prestigious journals such as Nature, The Lancet and Neurology.

In The Last Decade

J. M. Berg

54 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. M. Berg United Kingdom 20 383 310 239 237 195 57 1.4k
Alfred Tenore Italy 24 350 0.9× 317 1.0× 201 0.8× 383 1.6× 123 0.6× 73 1.8k
Pasquale De Franciscis Italy 30 276 0.7× 230 0.7× 467 2.0× 282 1.2× 104 0.5× 189 2.9k
Michele Reyes United States 22 245 0.6× 74 0.2× 142 0.6× 109 0.5× 73 0.4× 38 1.8k
Francesça Chiaffarino Italy 33 174 0.5× 211 0.7× 536 2.2× 401 1.7× 72 0.4× 108 3.1k
Kenneth Hughes Singapore 28 130 0.3× 279 0.9× 334 1.4× 93 0.4× 232 1.2× 70 2.3k
R. B. Ness United States 22 200 0.5× 182 0.6× 414 1.7× 424 1.8× 168 0.9× 39 2.0k
Patrice Lopès France 16 322 0.8× 274 0.9× 463 1.9× 184 0.8× 43 0.2× 78 1.7k
Marianne Hørby Jørgensen Denmark 23 182 0.5× 189 0.6× 225 0.9× 427 1.8× 187 1.0× 90 1.9k
Michel Druet‐Cabanac France 29 72 0.2× 146 0.5× 133 0.6× 843 3.6× 103 0.5× 73 2.4k
Carolina Medina‐Gómez Netherlands 19 240 0.6× 525 1.7× 147 0.6× 146 0.6× 315 1.6× 63 1.4k

Countries citing papers authored by J. M. Berg

Since Specialization
Citations

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

Fields of papers citing papers by J. M. Berg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. M. Berg

This figure shows the co-authorship network connecting the top 25 collaborators of J. M. Berg. A scholar is included among the top collaborators of J. M. 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 J. M. Berg. J. M. Berg 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.
Berg, J. M., John A. Duley, William E. Evans, et al.. (2013). Nomenclature for alleles of the thiopurine methyltransferase gene. Pharmacogenetics and Genomics. 23(4). 242–248. 97 indexed citations
2.
Berg, J. M.. (2001). Shakespeare as a geneticist1. Clinical Genetics. 59(3). 165–170.
3.
4.
Karlinsky, Harry, et al.. (1994). Molecular Genetic Predictive Testing for Alzheimerʼs Disease. Alzheimer Disease & Associated Disorders. 8(2). 126–126. 25 indexed citations
5.
Karlinsky, Harry, et al.. (1994). Issues in Molecular Genetic Testing of Individuals with Suspected Early-onset Familial Alzheimerʼs Disease. Alzheimer Disease & Associated Disorders. 8(2). 116–125. 14 indexed citations
6.
Karlinsky, Harry, J. M. Berg, Peter N. Ray, et al.. (1992). Monozygotic twins concordant for late‐onset probable alzheimer disease with suspected alzheimer disease in four sibs. American Journal of Medical Genetics. 44(5). 591–597. 9 indexed citations
7.
Berg, J. M. & Derek Armstrong. (1991). On the association of moyamoya disease with Down's syndrome. Journal of Intellectual Disability Research. 35(4). 398–403. 15 indexed citations
8.
Gama, Rousseau, Peter Nightingale, P M Broughton, et al.. (1991). Feedback of Laboratory Usage and Cost Data to Clinicians: Does it Alter Requesting Behaviour?. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 28(2). 143–149. 12 indexed citations
9.
Berg, J. M., et al.. (1988). The Genetics of mental retardation : biomedical, psychosocial and ethical issues. Kluwer Academic Publishers eBooks.
10.
Steketee, Richard W., Steven G.F. Wassilak, William N. Adkins, et al.. (1988). Evidence for a High Attack Rate and Efficacy of Erythromycin Prophylaxis in a Pertussis Outbreak in a Facility for the Developmentally Disabled. The Journal of Infectious Diseases. 157(3). 434–440. 81 indexed citations
11.
Berg, J. M., et al.. (1988). Twenty‐six years later: a woman with tetra‐X chromosomes. Journal of Intellectual Disability Research. 32(1). 67–74. 1 indexed citations
12.
Berg, J. M., et al.. (1986). Science and service in mental retardation : proceedings of the Seventh Congress of the International Association for the Scientific Study of Mental Deficiency (IASSMD). Methuen eBooks. 1 indexed citations
13.
Marković, V. D., R. G. Worton, & J. M. Berg. (1978). Evidence for the inheritance of silver-stained nucleolus organizer regions. Human Genetics. 41(2). 181–187. 71 indexed citations
14.
Berg, J. M., et al.. (1969). Mongolism and maternal menarche.. Journal of Medical Genetics. 6(2). 135–136. 2 indexed citations
15.
Berg, J. M.. (1968). OBSERVATIONS ON THENAR/FIRST INTERDIGITAL DERMATOGLYPHIC PATTERNS IN MONGOLISM. Journal of Intellectual Disability Research. 12(3-4). 307–311. 3 indexed citations
16.
Smith, George F., et al.. (1967). FAMILIAL TRANSMISSION OF AN ABERRANT SUBMETACENTRIC CHROMOSOME. Journal of Intellectual Disability Research. 11(1). 58–68. 1 indexed citations
17.
Berg, J. M. & B. H. Kirman. (1961). Risk of Dual Occurrence of Mongolism in Sibships. Archives of Disease in Childhood. 36(190). 645–648. 7 indexed citations
18.
Polani, P. E., et al.. (1960). A MONGOL GIRL WITH 46 CHROMOSOMES. The Lancet. 275(7127). 721–724. 229 indexed citations
19.
Berg, J. M. & B. H. Kirman. (1960). The Mentally Defective Twin. BMJ. 1(5190). 1911–1917. 8 indexed citations
20.
Berg, J. M., et al.. (1959). ATROPINE IN MONGOLISM. The Lancet. 274(7100). 441–442. 38 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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