Author

Anders O.H. Nygren

Observed names: A Nygren, A O H Nygren, A O Nygren, A. Nygren, A. O. H. Nygren, A. O. Nygren, A.O.H. Nygren, Anders Nygren, Anders O H Nygren, Anders O. H. Nygren, Anders OH Nygren, Nygren, Anders O. H.

Observed institutions: University College Dublin, Statens Serum Institut, Uppsala University, University of Copenhagen, Université Libre de Bruxelles, Radboud University Nijmegen, University of Antwerp, Duke University, Rigshospitalet, The Netherlands Cancer Institute, Maastricht University, MRC Holland (Netherlands), Jena University Hospital, Hertie Institute for Clinical Brain Research, Sequenom (United States), Génome Québec, University of Tübingen

OpenAlex ID: A5066160219

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

2008 · Sven Rottenberg, Janneke E. Jaspers, et al. · Proceedings of the National Academy of Sciences · 975

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

2011 · Mathias Ehrich, Cosmin Deciu, et al. · American Journal of Obstetrics and Gynecology · 470

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Methylation-Specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences

2005 · A. O. H. Nygren · Nucleic Acids Research · 404

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In situ genotyping individual DNA molecules by target-primed rolling-circle amplification of padlock probes

2004 · Chatarina Larsson, Jørn Koch, et al. · Nature Methods · 330

Quantitative comparison of DNA methylation assays for biomarker development and clinical applications

2016 · Christoph Bock, Florian Halbritter, et al. · Nature Biotechnology · 327

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Selective induction of chemotherapy resistance of mammary tumors in a conditional mouse model for hereditary breast cancer

2007 · Sven Rottenberg, Anders O. H. Nygren, et al. · Proceedings of the National Academy of Sciences · 306

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

2008 · Christian Beetz, Rebecca Schüle, et al. · Brain · 185

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A/T mutagenesis in hypermutated immunoglobulin genes strongly depends on PCNAK164 modification

2007 · Petra Langerak, Anders O.H. Nygren, et al. · The Journal of Experimental Medicine · 166

Quantification of Fetal DNA by Use of Methylation-Based DNA Discrimination

2010 · Anders OH Nygren, Jarrod Dean, et al. · Clinical Chemistry · 142

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

2006 · C. Beetz, A.O.H. Nygren, et al. · Neurology · 142

Sequential gene promoter methylation during HPV-induced cervical carcinogenesis

2007 · F E Henken, S M Wilting, et al. · British Journal of Cancer · 127

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Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation

2007 · R H Scott, J Douglas, et al. · Journal of Medical Genetics · 127

Poly(ADP-Ribose) Polymerase-1 Inhibitor Treatment Regresses Autochthonous Brca2/p53 -Mutant Mammary Tumors In vivo and Delays Tumor Relapse in Combination with Carboplatin

2009 · Trevor Hay, James R. Matthews, et al. · Cancer Research · 114

Moderate Increase in Mdr1a/1b Expression Causes In vivo Resistance to Doxorubicin in a Mouse Model for Hereditary Breast Cancer

2009 · Marina Pajic, Jayasree K. Iyer, et al. · Cancer Research · 93

Epigenetic Events of Disease Progression in Head and Neck Squamous Cell Carcinoma

2006 · Maria J. Worsham, Kang Mei Chen, et al. · Archives of Otolaryngology - Head and Neck Surgery · 85

Sensitivity and Acquired Resistance of BRCA1;p53-Deficient Mouse Mammary Tumors to the Topoisomerase I Inhibitor Topotecan

2010 · Serge A.L. Zander, Ariena Kersbergen, et al. · Cancer Research · 84

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

2007 · S.K. Murthy, A.O.H. Nygren, et al. · Cytogenetic and Genome Research · 83

Ultrasensitive Detection of Multiplexed Somatic Mutations Using MALDI-TOF Mass Spectrometry

2015 · Michael J. Mosko, Aleksey A. Nakorchevsky, et al. · Journal of Molecular Diagnostics · 81

Screening for large mutations of the NF2 gene

2005 · Lan Kluwe, Anders O.H. Nygren, et al. · Genes Chromosomes and Cancer · 62

High-resolution mapping of the 8p23.1 beta-defensin cluster reveals strictly concordant copy number variation of all genes

2008 · Marco Groth, Karol Szafranski, et al. · Human Mutation · 60

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Quantification of the methylation status of the PWS/AS imprinted region: Comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA

2007 · Nicola Dikow, Anders OH Nygren, et al. · Molecular and Cellular Probes · 58

Concurrent methylation of promoters from tumor associated genes predicts outcome in acute myeloid leukemia

2008 · Corine J. Hess, Abdellatif Errami, et al. · Leukemia & lymphoma/Leukemia and lymphoma · 45

Multiplex Ligation-Dependent Probe Amplification Technique for Copy Number Analysis on Small Amounts of DNA Material

2008 · Karina Meden Sørensen, Paal Skytt Andersen, et al. · Analytical Chemistry · 42

Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency

2010 · Janine Meienberg, Marianne Rohrbach, et al. · European Journal of Human Genetics · 38

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Strategies for Validation and Testing of DNA Methylation Biomarkers

2014 · Christa Noehammer, Walter Pulverer, et al. · Epigenomics · 34

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Works count: 80

Citation count: 4,884

H-index: 28

I10-index: 38