Anders O.H. Nygren

4.8k total citations · 2 hit papers
38 papers, 3.2k citations indexed

About

Anders O.H. Nygren is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Anders O.H. Nygren has authored 38 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 16 papers in Genetics and 7 papers in Oncology. Recurrent topics in Anders O.H. Nygren's work include Epigenetics and DNA Methylation (10 papers), DNA Repair Mechanisms (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Anders O.H. Nygren is often cited by papers focused on Epigenetics and DNA Methylation (10 papers), DNA Repair Mechanisms (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Anders O.H. Nygren collaborates with scholars based in Netherlands, United States and Germany. Anders O.H. Nygren's co-authors include Jos Jonkers, Piet Borst, Sven Rottenberg, Ariena Kersbergen, Eline van der Burg, Aaron Cranston, Mark J. O’Connor, Niall M.B. Martin, Alan Lau and Jan P. Schouten and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and The Journal of Experimental Medicine.

In The Last Decade

Anders O.H. Nygren

38 papers receiving 3.2k 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.

High sensitivity of BRCA1-deficient mammary tumors to the PARP inhibitor AZD2281 alone and in combination with platinum drugs

2008 762 citations Sven Rottenberg, Janneke E. Jaspers et al. profile →
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

2011 371 citations Mathias Ehrich, Anders O.H. Nygren et al. profile →

Peers

Anders O.H. Nygren

ONCOL

GENET

PPCH

Hans Herweijer United States

Andrew Wilber United States

Christian Hagemeier Germany

Eric Wang United States

Robert Lucito United States

Frank O. Fackelmayer Germany

Anne Dubart‐Kupperschmitt France

K. D. Zang Germany

Sandra Offner Switzerland

Chad May United States

Hans Herweijer United States

Anders O.H. Nygren

1.9k ×1.0

760 ×0.7

ONCOL

823 ×1.1

GENET

159 ×0.3

PPCH

191 ×0.4

Citations per year, relative to Anders O.H. Nygren Anders O.H. Nygren (= 1×) peers Hans Herweijer

Countries citing papers authored by Anders O.H. Nygren

Since Specialization

Citations

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

Fields of papers citing papers by Anders O.H. Nygren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anders O.H. Nygren

This figure shows the co-authorship network connecting the top 25 collaborators of Anders O.H. Nygren. A scholar is included among the top collaborators of Anders O.H. Nygren 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 O.H. Nygren. Anders O.H. Nygren 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

Nakorchevsky, Aleksey, et al.. (2015). Ultrasensitive Detection of Multiplexed Somatic Mutations Using MALDI-TOF Mass Spectrometry. Journal of Molecular Diagnostics. 18(1). 23–31. 68 indexed citations

Shapiro, Adam J., Karen E. Weck, Margaret Rosenfeld, et al.. (2014). Cri du Chat Syndrome and Primary Ciliary Dyskinesia: A Common Genetic Cause on Chromosome 5p. The Journal of Pediatrics. 165(4). 858–861. 7 indexed citations

Zander, Serge A.L., Ariena Kersbergen, Eline van der Burg, et al.. (2010). Sensitivity and Acquired Resistance of BRCA1;p53-Deficient Mouse Mammary Tumors to the Topoisomerase I Inhibitor Topotecan. Cancer Research. 70(4). 1700–1710. 66 indexed citations

Meienberg, Janine, Marianne Rohrbach, Stefan Neuenschwander, et al.. (2010). Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency. European Journal of Human Genetics. 18(12). 1315–1321. 28 indexed citations

Hay, Trevor, James R. Matthews, Alan Lau, et al.. (2009). Poly(ADP-Ribose) Polymerase-1 Inhibitor Treatment Regresses Autochthonous Brca2/p53 -Mutant Mammary Tumors In vivo and Delays Tumor Relapse in Combination with Carboplatin. Cancer Research. 69(9). 3850–3855. 94 indexed citations

Pajic, Marina, Jayasree K. Iyer, Ariena Kersbergen, et al.. (2009). Moderate Increase in Mdr1a/1b Expression Causes In vivo Resistance to Doxorubicin in a Mouse Model for Hereditary Breast Cancer. Cancer Research. 69(16). 6396–6404. 77 indexed citations

Alsum, Zobaida, Leen Abu Safieh, Anders O.H. Nygren, Mohamed H. Al‐Hamed, & Fowzan S. Alkuraya. (2009). Methylation-Specific Multiplex-Ligation-Dependent Probe Amplification as a Rapid Molecular Diagnostic Tool for Pseudohypoparathyroidism Type 1b. Genetic Testing and Molecular Biomarkers. 14(1). 135–139. 7 indexed citations

Тодоров, Т., et al.. (2009). Fragile X mosaic male full mutation/normal allele detected by PCR/MS-MLPA. BMJ Case Reports. 2009. bcr0620080139–bcr0620080139. 12 indexed citations

Özalp, Veli Cengiz, Anders O.H. Nygren, & Ciara K. O’Sullivan. (2008). Fluorescent resonance energy transfer (FRET) based detection of a multiplex ligation-dependent probe amplification assay (MLPA) product. Molecular BioSystems. 4(9). 950–954. 3 indexed citations

10.

Groth, Marco, Karol Szafranski, Stefan Taudien, et al.. (2008). High-resolution mapping of the 8p23.1 beta-defensin cluster reveals strictly concordant copy number variation of all genes. Human Mutation. 29(10). 1247–1254. 50 indexed citations

11.

Nygren, Anders O.H., et al.. (2008). Methylation-Specific Multiplex Ligation-Dependent Probe Amplification Enables a Rapid and Reliable Distinction between Male FMR1 Premutation and Full-Mutation Alleles. Journal of Molecular Diagnostics. 10(6). 496–501. 23 indexed citations

12.

Murthy, Sabita K., et al.. (2007). Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment. Cytogenetic and Genome Research. 116(1-2). 135–140. 55 indexed citations

13.

Møller, Lisbeth Birk, Anders O.H. Nygren, Patrick Scott, et al.. (2007). Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany. Human Mutation. 28(2). 207–207. 23 indexed citations

14.

Dikow, Nicola, et al.. (2007). Quantification of the methylation status of the PWS/AS imprinted region: Comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA. Molecular and Cellular Probes. 21(3). 208–215. 46 indexed citations

15.

Djarmati, Ana, Miodrag Gužvić, Anne Grünewald, et al.. (2007). Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation‐dependent probe amplification. Movement Disorders. 22(12). 1708–1714. 9 indexed citations

16.

Worsham, Maria J., Kang Mei Chen, Anders O.H. Nygren, et al.. (2006). Epigenetic Events of Disease Progression in Head and Neck Squamous Cell Carcinoma. Archives of Otolaryngology - Head and Neck Surgery. 132(6). 668–668. 74 indexed citations

17.

Kluwe, Lan, Anders O.H. Nygren, Abdellatif Errami, et al.. (2005). Screening for large mutations of the NF2 gene. Genes Chromosomes and Cancer. 42(4). 384–391. 36 indexed citations

18.

Nygren, Anders O.H.. (2005). Methylation-Specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences. Nucleic Acids Research. 33(14). e128–e128. 302 indexed citations

19.

Meuller, Johan, Gunilla Kanter-Smoler, Anders O.H. Nygren, et al.. (2004). Identification of Genomic Deletions of the APC Gene in Familial Adenomatous Polyposis by Two Independent Quantitative Techniques. Genetic Testing. 8(3). 248–256. 20 indexed citations

20.

Beysen, Diane, Jean‐Pierre Fryns, Miranda Splitt, et al.. (2004). Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis. European Journal of Human Genetics. 12. 248–248. 2 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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