N Hobolth

1.1k total citations
37 papers, 848 citations indexed

About

N Hobolth is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, N Hobolth has authored 37 papers receiving a total of 848 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in N Hobolth's work include Neonatal Health and Biochemistry (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Metabolism and Genetic Disorders (5 papers). N Hobolth is often cited by papers focused on Neonatal Health and Biochemistry (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Metabolism and Genetic Disorders (5 papers). N Hobolth collaborates with scholars based in Denmark, United States and Poland. N Hobolth's co-authors include Margareta Mikkelsen, N. Gregersen, Steen Kølvraa, Petrea Jacobsen, E. Christensen, J Philip, K. Henningsen, M. Hauge, Peter Karl Jacobsen and Flemming Pociot and has published in prestigious journals such as The Lancet, Diabetologia and The Journal of Pediatrics.

In The Last Decade

N Hobolth

35 papers receiving 792 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N Hobolth Denmark 14 369 308 212 154 127 37 848
E.I. Schwartz Russia 16 170 0.5× 164 0.5× 129 0.6× 150 1.0× 29 0.2× 40 665
Chris Carlson United States 12 271 0.7× 187 0.6× 152 0.7× 68 0.4× 55 0.4× 14 831
Akira Hirono Japan 18 212 0.6× 132 0.4× 94 0.4× 110 0.7× 634 5.0× 49 992
Libor Kozák Czechia 17 333 0.9× 150 0.5× 209 1.0× 96 0.6× 84 0.7× 37 769
Jean-Marie Saudubray France 14 383 1.0× 111 0.4× 397 1.9× 210 1.4× 115 0.9× 15 952
Maryellen C. Baluda United States 8 170 0.5× 67 0.2× 240 1.1× 42 0.3× 255 2.0× 11 670
S. Chalder United Kingdom 10 428 1.2× 179 0.6× 34 0.2× 66 0.4× 202 1.6× 14 963
Marcus G. Pezzolesi United States 23 590 1.6× 458 1.5× 59 0.3× 315 2.0× 52 0.4× 43 1.3k
Amin J. Barakat United States 15 362 1.0× 219 0.7× 14 0.1× 131 0.9× 185 1.5× 49 754
J. M. Saudubray France 18 717 1.9× 73 0.2× 615 2.9× 106 0.7× 100 0.8× 49 1.0k

Countries citing papers authored by N Hobolth

Since Specialization
Citations

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

Fields of papers citing papers by N Hobolth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N Hobolth

This figure shows the co-authorship network connecting the top 25 collaborators of N Hobolth. A scholar is included among the top collaborators of N Hobolth 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 N Hobolth. N Hobolth 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.
Pociot, Flemming, et al.. (1993). A nationwide population-based study of the familial aggregation of Type 1 (insulin-dependent) diabetes mellitus in Denmark. Diabetologia. 36(9). 870–875. 77 indexed citations
2.
Verder, Henrik, Lone Agertoft, Per Albertsen, et al.. (1992). [Surfactant treatment of newborn infants with respiratory distress syndrome primarily treated with nasal continuous positive air pressure. A pilot study].. PubMed. 154(31). 2136–9. 75 indexed citations
3.
Hobolth, N, et al.. (1988). Iatrogenic Intraspinal Epidermoid Tumour. Acta Paediatrica. 77(5). 759–759. 7 indexed citations
4.
Christiansen, Peter Munk, Ove Hansen, N Hobolth, et al.. (1988). Treatment of Cryptorchidism with Human Chorionic Gonadotropin or Gonadotropin Releasing Hormone. Hormone Research. 30(4-5). 187–192. 35 indexed citations
5.
Nielsen, Jytte Bieber, F. Güttler, N Hobolth, et al.. (1986). Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency. European Journal of Pediatrics. 145(6). 572–575. 2 indexed citations
6.
7.
Kølvraa, Steen, N. Gregersen, E. Christensen, & N Hobolth. (1982). In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase. Clinica Chimica Acta. 126(1). 53–67. 135 indexed citations
8.
Hobolth, N, et al.. (1980). Dysostosis Epiphysarea Peripherica. Scandinavian Journal of Rheumatology. 9(1). 269–276. 2 indexed citations
9.
Gregersen, Niels, et al.. (1980). Non-ketotic C6-C10-dicarboxylic aciduria: Biochemical investigations of two cases. Clinica Chimica Acta. 102(2-3). 179–189. 39 indexed citations
10.
Rasmussen, Jens, et al.. (1980). 4.2. Studies on the required analytical quality of TSH measurements in screening for congenital hypothyroidism. Scandinavian Journal of Clinical and Laboratory Investigation. 40(sup154). 85–93. 15 indexed citations
11.
Dulaney, John T., Aubrey Milunsky, James Sidbury, N Hobolth, & Hugo W. Moser. (1976). Diagnosis of lipogranulomatosis (Farber disease) by use of cultured fibroblasts. The Journal of Pediatrics. 89(1). 59–61. 31 indexed citations
12.
Mikkelsen, Margareta, et al.. (1975). Translocation (13q21q). Four generation family study with analysis of satellite associations, fluorescent markers, and prenatal diagnosis.. PubMed. 27(4). 303–7. 9 indexed citations
13.
Hobolth, N, Peter Karl Jacobsen, & Margareta Mikkelsen. (1974). Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother. Journal of Medical Genetics. 11(3). 299–303. 35 indexed citations
14.
Jacobsen, Petrea, M. Hauge, K. Henningsen, et al.. (1973). An (11;21) Translocation in Four Generations with Chromosome 11 Abnormalities in the Offspring. Human Heredity. 23(6). 568–585. 174 indexed citations
15.
Esmann, Viggo, et al.. (1969). Heredity of leukocyte phosphorylase andamylo-1,6-glucosidase deficiency. The Journal of Pediatrics. 74(1). 90–94. 7 indexed citations
16.
Hobolth, N. (1965). Haemoglobin Mårhus. Acta Paediatrica. 54(4). 363–368. 6 indexed citations
17.
Hobolth, N. (1965). 24. Treatment of the Respiratory Distress Syndrome in Prematures with Intravenous Infusion of Albumin. Acta Paediatrica. 54(S159). 60–62. 2 indexed citations
18.
Hobolth, N & Margareta Mikkelsen. (1965). “Maladie De Cri Du Chat”. Acta Obstetricia Et Gynecologica Scandinavica. 44(4). 572–578. 6 indexed citations
19.
Hobolth, N, et al.. (1964). ENZYME-STRIP ESTIMATION OF BLOOD-GLUCOSE. The Lancet. 284(7370). 1183–1183. 2 indexed citations
20.
Hobolth, N. (1963). DIABETES INSIPIDUS WITH MARKED MENTAL SYMPTOMS. Acta Psychiatrica Scandinavica. 39(4). 619–626. 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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