Helge Boman

3.2k total citations
73 papers, 2.1k citations indexed

About

Helge Boman is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Helge Boman has authored 73 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 19 papers in Genetics and 11 papers in Clinical Biochemistry. Recurrent topics in Helge Boman's work include Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (5 papers) and Peroxisome Proliferator-Activated Receptors (5 papers). Helge Boman is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (5 papers) and Peroxisome Proliferator-Activated Receptors (5 papers). Helge Boman collaborates with scholars based in Norway, United States and Canada. Helge Boman's co-authors include Per M. Knappskog, Cecilie Bredrup, Eyvind Rødahl, Stefan Johansson, Hans Geir Eiken, Arno G. Motulsky, Bjørn Ivar Haukanes, Jacek Majewski, Laurence A. Bindoff and Jaran Apold and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Helge Boman

70 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Helge Boman Norway 26 1.1k 488 241 231 214 73 2.1k
Patrick G. Quinn United States 24 831 0.8× 305 0.6× 267 1.1× 92 0.4× 152 0.7× 38 2.0k
Sarah K. Bronson United States 26 1.8k 1.8× 370 0.8× 509 2.1× 243 1.1× 428 2.0× 44 3.2k
Yang Hu China 27 1.0k 1.0× 443 0.9× 316 1.3× 130 0.6× 317 1.5× 80 2.3k
M Toga France 29 691 0.7× 531 1.1× 177 0.7× 60 0.3× 163 0.8× 124 2.7k
Dennis L. Guberski United States 26 579 0.6× 762 1.6× 142 0.6× 191 0.8× 355 1.7× 39 2.1k
Huseyin Mehmet United Kingdom 25 1.2k 1.1× 106 0.2× 122 0.5× 111 0.5× 143 0.7× 52 2.6k
Alex Agrotis Australia 35 1.2k 1.1× 167 0.3× 182 0.8× 325 1.4× 311 1.5× 62 3.3k
M. Aguennouz Italy 27 1.4k 1.3× 115 0.2× 95 0.4× 147 0.6× 364 1.7× 85 2.2k
Diane Gesty‐Palmer United States 22 1.8k 1.7× 189 0.4× 128 0.5× 108 0.5× 129 0.6× 34 2.6k
Nazar Mashtalir United States 26 1.9k 1.8× 378 0.8× 70 0.3× 94 0.4× 653 3.1× 33 3.0k

Countries citing papers authored by Helge Boman

Since Specialization
Citations

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

Fields of papers citing papers by Helge Boman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helge Boman

This figure shows the co-authorship network connecting the top 25 collaborators of Helge Boman. A scholar is included among the top collaborators of Helge Boman 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 Helge Boman. Helge Boman 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.
Haugarvoll, Kristoffer, Stefan Johansson, Carlos E. Rodríguez, et al.. (2017). GBA2 Mutations Cause a Marinesco-Sjögren-Like Syndrome: Genetic and Biochemical Studies. PLoS ONE. 12(1). e0169309–e0169309. 13 indexed citations
2.
Bredrup, Cecilie, Stefan Johansson, Laurence A. Bindoff, et al.. (2015). High Myopia–Excavated Optic Disc Anomaly Associated With a Frameshift Mutation in the MYC-Binding Protein 2 Gene (MYCBP2). American Journal of Ophthalmology. 159(5). 973–979.e2. 9 indexed citations
3.
Rødahl, Eyvind, Per M. Knappskog, Jacek Majewski, et al.. (2013). Variants of Anterior Segment Dysgenesis and Cerebral Involvement in a Large Family With a Novel COL4A1 Mutation. American Journal of Ophthalmology. 155(5). 946–953.e2. 23 indexed citations
4.
Tzoulis, Charalampos, Stefan Johansson, Bjørn Ivar Haukanes, et al.. (2013). Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. PLoS ONE. 8(6). e66145–e66145. 18 indexed citations
5.
Rødahl, Eyvind, Per M. Knappskog, Jacek Majewski, et al.. (2011). Variants Of Anterior Segment Dysgenesis In A Large Family With A Novel COL4A1 Mutation. Investigative Ophthalmology & Visual Science. 52(14). 68–68. 1 indexed citations
6.
Christensen, Anne Estmann, Per M. Knappskog, Marit Midtbø, et al.. (2010). Brittle Cornea Syndrome Associated with a Missense Mutation in the Zinc-Finger 469 Gene. Investigative Ophthalmology & Visual Science. 51(1). 47–47. 42 indexed citations
7.
Yamazaki, Masanori, Tomoki Kosho, Shigeo Kawachi, et al.. (2010). Cold‐induced sweating syndrome with neonatal features of Crisponi syndrome: Longitudinal observation of a patient homozygous for a CRLF1 mutation. American Journal of Medical Genetics Part A. 152A(3). 764–769. 12 indexed citations
8.
Sövik, Oddmund & Helge Boman. (2008). Co‐occurrence of vitamin D‐dependent rickets type 1 and phenylketonuria. Acta Paediatrica. 97(5). 665–667. 2 indexed citations
9.
Løvås, Kristian, et al.. (2004). Retarded bone growth in thyroid hormone resistance. A clinical study of a large family with a novel thyroid hormone receptor mutation. European Journal of Endocrinology. 150(4). 425–430. 13 indexed citations
10.
Paulsen, Aksel, et al.. (2002). Parathyroid Adenoma in a Subject with Familial Hypocalciuric Hypercalcemia: Coincidence or Causality?. The Journal of Clinical Endocrinology & Metabolism. 87(3). 1015–1016. 45 indexed citations
11.
Korvatska, Elena, Francis L. Munier, Béatrice E. Frueh, et al.. (1998). Mutation Hot Spots in 5q31-Linked Corneal Dystrophies. The American Journal of Human Genetics. 62(2). 320–324. 107 indexed citations
12.
Løvlie, Roger, et al.. (1996). The Ca 2+ -sensing receptor gene (PCAR1) mutation T151M in isolated autosomal dominant hypoparathyroidism. Human Genetics. 98(2). 129–133. 41 indexed citations
13.
14.
Kate, Leo P. ten, Helge Boman, Stephen P. Daiger, & Arno G. Motulsky. (1982). Familial aggregation of coronary heart disease and its relation to known genetic risk factors. The American Journal of Cardiology. 50(5). 945–953. 111 indexed citations
15.
16.
Boman, Helge, et al.. (1976). Hereditary retinoschisis linkage studies in a family and considerations in genetic counselling.. PubMed. 11(1). 11–6. 4 indexed citations
17.
Hoehn, Holger, Eileen Bryant, Kit Sing Au, et al.. (1975). Variegated translocation mosaicism in human skin fibroblast cultures. Cytogenetic and Genome Research. 15(5). 282–298. 124 indexed citations
18.
Torsvik, Harald, A L Børresen, K. Berg, & Helge Boman. (1972). Preliminary assignment of the inherited Hl 1 antigen to the apoA‐I polypeptide of rabbit high density lipoprotein. FEBS Letters. 28(2). 153–155. 6 indexed citations
19.
Boman, Helge. (1971). Studies on Inherited Antigenic Variation of Human Serum <i>β</i>-Lipoprotein by Passive Hemagglutination. Human Heredity. 21(6). 614–623. 1 indexed citations
20.
Torsvik, Harald & Helge Boman. (1971). Amino acid composition of serum high density lipoprotein in patients with familial lecithin:cholesterol acyltransferase deficiency. Clinical Genetics. 2(2). 91–94. 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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