Søren Besenbacher

发表

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

Paolo Vineis, Abbas Ghaderi, Simonetta Guarrera, 2011, Human molecular genetics.

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

William Wheeler, Tony Fletcher, Paolo Vineis, 2010, Nature Genetics.

Proteomic profiling identifies outcome-predictive markers in patients with peripheral T-cell lymphoma, not otherwise specified.

Søren Besenbacher, Knud Bendix, S. Besenbacher, 2018, Blood advances.

RBT - a tool for building refined Buneman trees

Thomas Mailund, Christian N. S. Pedersen, Søren Besenbacher, 2005, Bioinform..

Rate of de novo mutations and the importance of father’s age to disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

Large-scale whole-genome sequencing of the Icelandic population

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2015, Nature Genetics.

Rate of de novo mutations, father’s age, and disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

Expression patterns and prognostic potential of circular RNAs in mantle cell lymphoma: a study of younger patients from the MCL2 and MCL3 clinical trials

J. Kjems, S. Besenbacher, L. Kristensen, 2021, Leukemia.

Mutations in BRIP1 confer high risk of ovarian cancer

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2011, Nature Genetics.

Identification of low-frequency variants associated with gout and serum uric acid levels

H. Stefánsson, A. Gylfason, D. Gudbjartsson, 2011, Nature Genetics.

Common variants at 19p13 are associated with susceptibility to ovarian cancer

A. Whittemore, D. Hernandez, L. Kiemeney, 2010, Nature Genetics.

Pathway Analysis of Skin from Psoriasis Patients after Adalimumab Treatment Reveals New Early Events in the Anti-Inflammatory Mechanism of Anti-TNF-α

P. Sætrom, S. Besenbacher, F. Drabløs, 2016, PloS one.

Multi-nucleotide de novo Mutations in Humans

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2016, PLoS genetics.

Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus

Clement Adebamowo, Olufunmilayo I. Olopade, Robert Johansson, 2010, PLoS genetics.

Whole genome association mapping by incompatibilities and local perfect phylogenies

Thomas Mailund, Søren Besenbacher, Mikkel H. Schierup, 2006, BMC Bioinformatics.

Sequencing and de novo assembly of 150 genomes from Denmark as a population reference

Anders E. Halager, P. Sullivan, A. Krogh, 2017, Nature.

The Mutationathon highlights the importance of reaching standardization in estimates of pedigree-based germline mutation rates

P. Moorjani, S. Besenbacher, M. Schierup, 2022, eLife.

Mutationathon: towards standardization in estimates of pedigree-based germline mutation rates

P. Moorjani, S. Besenbacher, M. Schierup, 2021, bioRxiv.

The germline mutational process in rhesus macaque and its implications for phylogenetic dating

S. Besenbacher, M. Schierup, M. Gilbert, 2020, bioRxiv.

Direct estimation of mutations in great apes reconciles phylogenetic dating

T. Mailund, M. Schierup, C. Hvilsom, 2019, Nature Ecology & Evolution.

Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios

Anders E. Halager, P. Sullivan, A. Krogh, 2018, BMC Bioinformatics.

Direct estimation of mutations in great apes reveals significant recent human slowdown in the yearly mutation rate

T. Marquès-Bonet, S. Besenbacher, T. Mailund, 2018, bioRxiv.

The mutationathon highlights the importance of reaching standardization 1 in estimates of pedigree-based germline mutation rates 2

Matthew W. Hahn, M. Schierup, A. Yoder, 2022 .

Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population

Lars Bolund, Anders Albrechtsen, Jun Wang, 2014, European Journal of Human Genetics.

Parental origin of sequence variants associated with complex diseases

Daniel F. Gudbjartsson, Michael L. Frigge, Kari Stefansson, 2009, Nature.

Whole genome characterization of sequence diversity of 15,220 Icelanders

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2017, Scientific Data.

The Proteome of Seed Development in the Model Legume Lotus japonicus1[C][W]

J. Enghild, S. Besenbacher, S. Tabata, 2009, Plant Physiology.

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2010, Nature Genetics.

Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2010, Science Translational Medicine.

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.

D. Gudbjartsson, T. Thorgeirsson, L. Kiemeney, 2011, Cancer research.

A novel combined miRNA and methylation marker panel (miMe) for prediction of prostate cancer outcome after radical prostatectomy

K. D. Sørensen, Peter Mouritzen, Michael Borre, 2019, International journal of cancer.

Prognostic miRNA classifier in early-stage mycosis fungoides: development and validation in a Danish nationwide study.

T. Litman, S. Besenbacher, A. H. Rittig, 2018, Blood.

Identifying disease associated genes by network propagation

Yu Qian, Thomas Mailund, Søren Besenbacher, 2014, BMC Systems Biology.

Association mapping and disease: evolutionary perspectives.

S. Besenbacher, T. Mailund, M. Schierup, 2012, Methods in molecular biology.

Association Mapping and Disease: Evolutionary Perspectives.

S. Besenbacher, T. Mailund, M. Schierup, 2019, Methods in molecular biology.