Anders Buchard

592 total citations
16 papers, 456 citations indexed

About

Anders Buchard is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anders Buchard has authored 16 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anders Buchard's work include Molecular Biology Techniques and Applications (5 papers), Forensic and Genetic Research (5 papers) and Glutathione Transferases and Polymorphisms (3 papers). Anders Buchard is often cited by papers focused on Molecular Biology Techniques and Applications (5 papers), Forensic and Genetic Research (5 papers) and Glutathione Transferases and Polymorphisms (3 papers). Anders Buchard collaborates with scholars based in Denmark, United Kingdom and Spain. Anders Buchard's co-authors include Niels Morling, Claus Børsting, Juan José Martínez Sánchez, Kim Dalhoff, Charlotte Hallenberg, Alexis Hernández, Marie‐Louise Kampmann, Helle Smidt Mogensen, Eszter Rockenbauer and Jill K. Olofsson and has published in prestigious journals such as Electrophoresis, BioTechniques and Forensic Science International.

In The Last Decade

Anders Buchard

16 papers receiving 444 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anders Buchard Denmark 12 301 262 69 33 27 16 456
Heinz‐Dieter Wehner Germany 10 92 0.3× 49 0.2× 4 0.1× 11 0.3× 28 1.0× 27 297
H. Thöle Germany 9 80 0.3× 166 0.6× 9 0.1× 44 1.3× 8 0.3× 28 393
Changmei Yang China 13 227 0.8× 26 0.1× 28 0.4× 24 0.7× 5 0.2× 21 436
Prashantha Hebbar Kuwait 14 164 0.5× 187 0.7× 6 0.1× 10 0.3× 1 0.0× 34 437
C. Eckhoff Germany 9 325 1.1× 125 0.5× 7 0.1× 36 1.1× 11 424
María Saiz Spain 10 119 0.4× 126 0.5× 25 0.4× 20 0.6× 30 262
Roberto Semeraro Italy 10 200 0.7× 59 0.2× 29 0.4× 7 0.2× 23 351
Sumi Elsa John Kuwait 14 141 0.5× 188 0.7× 6 0.1× 7 0.2× 30 409
Lina Cai China 11 104 0.3× 99 0.4× 16 0.2× 33 1.0× 1 0.0× 43 444
Zeynep Ocak Türkiye 11 117 0.4× 46 0.2× 3 0.0× 20 0.6× 15 0.6× 29 267

Countries citing papers authored by Anders Buchard

Since Specialization
Citations

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

Fields of papers citing papers by Anders Buchard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anders Buchard

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

All Works

16 of 16 papers shown
1.
Christiansen, Sofie Lindgren, Claus Børsting, Anders Buchard, et al.. (2019). Non-invasive prenatal paternity testing using a standard forensic genetic massively parallel sequencing assay for amplification of human identification SNPs. International Journal of Legal Medicine. 133(5). 1361–1368. 11 indexed citations
2.
Ullah, Inam, Jill K. Olofsson, Ashot Margaryan, et al.. (2017). High Y‐chromosomal Differentiation Among Ethnic Groups of Dir and Swat Districts, Pakistan. Annals of Human Genetics. 81(6). 234–248. 10 indexed citations
3.
Kampmann, Marie‐Louise, et al.. (2016). High-Throughput Sequencing of Forensic Genetic Samples Using Punches of FTA Cards with Buccal Swabs. BioTechniques. 61(3). 149–151. 19 indexed citations
4.
Schultz, André, Niels Høiby, Xiaohui Chen Nielsen, et al.. (2016). Individual pharmacokinetic variation leads to underdosing of ciprofloxacin in some cystic fibrosis patients. Pediatric Pulmonology. 52(3). 319–323. 10 indexed citations
5.
Buchard, Anders, et al.. (2016). ISO 17025 validation of a next‐generation sequencing assay for relationship testing. Electrophoresis. 37(21). 2822–2831. 52 indexed citations
6.
Olofsson, Jill K., Helle Smidt Mogensen, Anders Buchard, Claus Børsting, & Niels Morling. (2015). Forensic and population genetic analyses of Danes, Greenlanders and Somalis typed with the Yfiler® Plus PCR amplification kit. Forensic Science International Genetics. 16. 232–236. 39 indexed citations
7.
Buchard, Anders, et al.. (2015). Introduction of the Python script STRinNGS for analysis of STR regions in FASTQ or BAM files and expansion of the Danish STR sequence database to 11 STRs. Forensic Science International Genetics. 21. 68–75. 31 indexed citations
8.
Nielsen, Xiaohui Chen, Kim Dalhoff, Jan‐Willem C. Alffenaar, et al.. (2013). Pharmacokinetic variability of clarithromycin and differences in CYP3A4 activity in patients with cystic fibrosis. Journal of Cystic Fibrosis. 13(2). 179–185. 10 indexed citations
9.
Rockenbauer, Eszter, Anders Buchard, Helle Smidt Mogensen, et al.. (2013). Non-uniform phenotyping of D12S391 resolved by second generation sequencing. Forensic Science International Genetics. 8(1). 195–199. 29 indexed citations
10.
Buchard, Anders, Susanne Rosthøj, Peder Skov Wehner, et al.. (2012). Gene Dose Effects of GSTM1, GSTT1 and GSTP1 Polymorphisms on Outcome in Childhood Acute Lymphoblastic Leukemia. Journal of Pediatric Hematology/Oncology. 34(1). 38–42. 16 indexed citations
11.
Buchard, Anders, Martin Eefsen, Stig Ejdrup Andersen, et al.. (2011). The role of the glutathione S-transferase genes GSTT1, GSTM1, and GSTP1 in acetaminophen-poisoned patients. Clinical Toxicology. 50(1). 27–33. 11 indexed citations
12.
Buchard, Anders, et al.. (2011). Validation of the AmpFlSTR® Identifiler® Direct PCR Amplification kit in a laboratory accredited according to the ISO17025 standard. Forensic science international. Genetics supplement series. 3(1). e165–e166. 6 indexed citations
13.
Buchard, Anders, et al.. (2010). Postmortem Blood Concentrations of R‐ and S‐Enantiomers of Methadone and EDDP in Drug Users: Influence of Co‐Medication and P‐glycoprotein Genotype. Journal of Forensic Sciences. 55(2). 457–463. 23 indexed citations
14.
Línnet, Kristían, et al.. (2008). Dominance of pre-analytical over analytical variation for measurement of methadone and its main metabolite in postmortem femoral blood. Forensic Science International. 179(1). 78–82. 20 indexed citations
15.
Buchard, Anders, Juan José Martínez Sánchez, Kim Dalhoff, & Niels Morling. (2007). Multiplex PCR Detection of GSTM1, GSTT1, and GSTP1 Gene Variants. Journal of Molecular Diagnostics. 9(5). 612–617. 63 indexed citations
16.
Sánchez, Juan José Martínez, Claus Børsting, Charlotte Hallenberg, et al.. (2003). Multiplex PCR and minisequencing of SNPs—a model with 35 Y chromosome SNPs. Forensic Science International. 137(1). 74–84. 106 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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