Hans C. Andersson

5.7k total citations · 1 hit paper
104 papers, 3.8k citations indexed

About

Hans C. Andersson is a scholar working on Molecular Biology, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hans C. Andersson has authored 104 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 19 papers in Plant Science and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hans C. Andersson's work include Metabolism and Genetic Disorders (16 papers), Carcinogens and Genotoxicity Assessment (15 papers) and DNA Repair Mechanisms (11 papers). Hans C. Andersson is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Carcinogens and Genotoxicity Assessment (15 papers) and DNA Repair Mechanisms (11 papers). Hans C. Andersson collaborates with scholars based in United States, Sweden and Cameroon. Hans C. Andersson's co-authors include Paige Kaplan, B.A. Kihlman, Joel Charrow, Neal J. Weinreb, Barry E. Rosenbloom, Pramod K. Mistry, Rebecca S. Wappner, Gregory M. Pastores, Edwin H. Kolodny and C. Ronald Scott and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Hans C. Andersson

99 papers receiving 3.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Phenylalanine hydroxylase deficiency: diagnosis and management guideline

2014 465 citations Hans C. Andersson et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hans C. Andersson United States	29	1.6k	1.5k	731	639	583	104	3.8k
Loranne Agius United Kingdom	42	1.3k 0.8×	2.9k 1.9×	513 0.7×	661 1.0×	380 0.7×	166	5.2k
Willy Stalmans Belgium	43	728 0.5×	3.7k 2.4×	1.1k 1.5×	313 0.5×	475 0.8×	123	6.1k
Efstathios S. Gonos Greece	42	1.5k 1.0×	3.2k 2.1×	841 1.2×	687 1.1×	213 0.4×	118	6.0k
Robert E. Pacifici United States	28	530 0.3×	2.4k 1.5×	491 0.7×	248 0.4×	220 0.4×	39	4.0k
Robert F. Newbold United Kingdom	36	827 0.5×	3.0k 2.0×	192 0.3×	230 0.4×	507 0.9×	84	4.5k
Philippa B. Mills United Kingdom	32	479 0.3×	1.9k 1.2×	337 0.5×	130 0.2×	1.1k 2.0×	71	3.7k
Hidetaka Morinaga Japan	28	1.2k 0.8×	2.5k 1.7×	256 0.4×	1.0k 1.6×	299 0.5×	46	5.4k
Jean Girard France	48	2.8k 1.8×	4.0k 2.6×	777 1.1×	2.6k 4.1×	619 1.1×	128	8.9k
Fumiki Katsuoka Japan	34	417 0.3×	3.8k 2.4×	343 0.5×	296 0.5×	112 0.2×	73	4.9k
Paolo Degan Italy	41	575 0.4×	4.1k 2.7×	205 0.3×	414 0.6×	200 0.3×	121	6.3k

Countries citing papers authored by Hans C. Andersson

Since Specialization

Citations

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

Fields of papers citing papers by Hans C. Andersson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans C. Andersson. 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 Hans C. Andersson. The network helps show where Hans C. Andersson may publish in the future.

Co-authorship network of co-authors of Hans C. Andersson

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

All Works

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20 of 20 papers shown

Cooney, Erin E., Laura Davis‐Keppen, Stephanie Sacharow, et al.. (2024). Lessons learned from 5 years of pegvaliase in US clinics: A case series. Molecular Genetics and Metabolism Reports. 42. 101181–101181.

Chang, Richard, Monica Boyer, Laura Davis‐Keppen, et al.. (2024). Outcomes in 14 live births resulting from Pegvaliase-treated pregnancies in PKU-affected females. Molecular Genetics and Metabolism. 141(3). 108152–108152. 7 indexed citations

Li, Yuwen, et al.. (2022). Genotype–phenotype correlation in IARS2‐related diseases: A case report and review of literature. SHILAP Revista de lepidopterología. 10(2). e05401–e05401. 7 indexed citations

Adams, Darius J., Hans C. Andersson, Kristin Lindstrom, et al.. (2021). Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics. Molecular Genetics and Metabolism Reports. 28. 100790–100790. 14 indexed citations

Jenkins, Brittany D., Catherine G. Fischer, Deborah Maiese, et al.. (2021). The 2019 US medical genetics workforce: a focus on clinical genetics. Genetics in Medicine. 23(8). 1458–1464. 96 indexed citations

Witters, Peter, K. Vande Kerckhove, Hans C. Andersson, et al.. (2016). Autism in patients with propionic acidemia. Molecular Genetics and Metabolism. 119(4). 317–321. 63 indexed citations

Andersson, Hans C., et al.. (2014). Multiple stressors threatening the future of the Baltic Sea–Kattegat marine ecosystem: Implications for policy and management actions. Marine Pollution Bulletin. 86(1-2). 468–480. 24 indexed citations

Andersson, Hans C., et al.. (2011). Emergency preparedness for genetics centers, laboratories, and patients: The Southeast Region Genetics Collaborative strategic plan. Genetics in Medicine. 13(10). 903–907. 1 indexed citations

Li, Marilyn M. & Hans C. Andersson. (2009). Clinical Application of Microarray-Based Molecular Cytogenetics: An Emerging New Era of Genomic Medicine. The Journal of Pediatrics. 155(3). 311–317. 23 indexed citations

10.

Andersson, Hans C.. (2009). Induction of sister chromatid exchanges by streptonigrin, an antibiotic and antineoplastic agent. Hereditas. 95(1). 141–148.

11.

Andersson, Hans C. & B.A. Kihlman. (2008). Localization of chemically induced chromosomal aberrations in three different karyotypes of Viciafaba. Hereditas. 107(1). 15–25. 3 indexed citations

12.

Andersson, Hans C.. (2008). G2 repair and the formation of chromosomal aberrations. Hereditas. 97(2). 193–209. 2 indexed citations

13.

Andersson, Hans C., Joel Charrow, Paige Kaplan, et al.. (2005). Individualization of long-term enzyme replacement therapy for Gaucher disease. Genetics in Medicine. 7(2). 105–110. 89 indexed citations

14.

Krousel‐Wood, Marie, et al.. (2003). Physicians’ perceived usefulness of and satisfaction with test reports for cystic fibrosis (ΔF508) and factor V Leiden. Genetics in Medicine. 5(3). 166–171. 13 indexed citations

15.

Andersson, Hans C., Marie Krousel‐Wood, Kelly E. Jackson, Janet C. Rice, & Ira M. Lubin. (2002). Medical genetic test reporting for cystic fibrosis (ΔF508) and factor V Leiden in North American laboratories. Genetics in Medicine. 4(5). 324–327. 13 indexed citations

16.

Andersson, Hans C., Rolf Lewensohn, & Eva Månsson‐Brahme. (1999). Chromosomal sensitivity to X-ray irradiation during the G2 phase in lymphocytes of patients with hereditary cutaneous malignant melanoma as compared to healthy controls. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 425(1). 9–20. 2 indexed citations

17.

Varela, Maria, et al.. (1997). Complex congenital heart malformations in mosaic tetrasomy 8p: Case report and review of the literature. American Journal of Medical Genetics. 73(3). 330–333. 10 indexed citations

18.

Kihlman, B.A. & Hans C. Andersson. (1992). Enhancement and reduction by methylated oxypurines of the frequencies of chromatid aberrations induced by camptothecin in root-tip cells of Vicia faba. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 269(2). 259–267. 2 indexed citations

19.

Kihlman, B.A. & Hans C. Andersson. (1985). Synergistic enhancement of the frequency of chromatid aberrations in cultured human lymphocytes by combinations of inhibitors of DNA repair. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 150(1-2). 313–325. 40 indexed citations

20.

Kihlman, B.A., A.T. Natarajan, & Hans C. Andersson. (1978). Use of the 5-bromodeoxyuridine-labelling technique for exploring mechanisms involved in the formation of chromosomal aberrations I. G2 experiments with root-tips of Vicia faba. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 52(2). 181–198. 41 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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