Hauke Thomsen

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2020
Mark Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis
Blunk, Inga ^LU ; Thomsen, Hauke ^LU ; Reinsch, Norbert ; Mayer, Manfred ; Försti, Asta ^LU ; Sundquist, Jan ^LU ; Sundquist, Kristina ^LU and Hemminki, Kari ^LU (2020) In Scientific Reports 10(1).
- Contribution to journal › Article
Mark Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden
Thomsen, Hauke ^LU ; Li, Xinjun ^LU ; Sundquist, Kristina ^LU ; Sundquist, Jan ^LU ; Försti, Asta ^LU and Hemminki, Kari ^LU (2020) In Journal of Translational Autoimmunity 3.
- Contribution to journal › Article
Mark Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1
Thomsen, Hauke ^LU ; Chattopadhyay, Subhayan ^LU ; Hoffman, Per ; Nöthen, Markus M ; Kalirai, Helen ; Coupland, Sarah E. ; Jonas, Jost B. ; Hemminki, Kari ^LU and Försti, Asta ^LU (2020) In Melanoma Research 30(2). p.166-172
- Contribution to journal › Article
Mark Performance of individual and joint risk stratification by an environmental risk score and a genetic risk score in a colorectal cancer screening setting
Balavarca, Yesilda ; Weigl, Korbinian ; Thomsen, Hauke ^LU and Brenner, Hermann (2020) In International Journal of Cancer 146(3). p.627-634
- Contribution to journal › Article
2019
Mark Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
Chattopadhyay, Subhayan ^LU ; Thomsen, Hauke ^LU ; Weinhold, Niels ; Meziane, Iman ^LU ; Huhn, Stefanie ; da Silva Filho, Miguel Inacio ^LU ; Vodicka, Pavel ; Vodickova, Ludmila ; Hoffmann, Per and Nöthen, Markus M , et al. (2019) In Leukemia p.1-5
- Contribution to journal › Letter
Mark Quantification and detection of genetic risk factors in the familial aggregation of cancer : Habilitation thesis
Thomsen, Hauke ^LU (2019)
- Thesis › Doctoral thesis (compilation)
Mark Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer, Alexander ; Li, Yong ; Ghasemi, Sahar ; Prins, Bram P. ; Wuttke, Matthias ; Hermle, Tobias ; Giri, Ayush ; Sieber, Karsten B. ; Qiu, Chengxiang and Kirsten, Holger , et al. (2019) In Nature Communications 10(1).
- Contribution to journal › Article
Mark Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population
Niazi, Yasmeen ; Thomsen, Hauke ^LU ; Smolkova, Bozena ; Vodickova, Ludmila ; Vodenkova, Soňa ; Kroupa, Michal ; Vymetalkova, Veronika ; Kazimirova, Alena ; Barancokova, Magdalena and Volkovova, Katarina , et al. (2019) In Mutagenesis 34(4). p.323-330
- Contribution to journal › Article
Mark Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes
Went, Molly ; Kinnersley, Ben ; Sud, Amit ; Johnson, David C ; Weinhold, Niels ; Försti, Asta ^LU ; van Duin, Mark ; Orlando, Giulia ; Mitchell, Jonathan S and Kuiper, Rowan , et al. (2019) In Human Genomics 13(1).
- Contribution to journal › Article
Mark Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk
Sud, Amit ^LU ; Chattopadhyay, Subhayan ^LU ; Thomsen, Hauke ^LU ; Sundquist, Kristina ^LU ; Sundquist, Jan ^LU ; Houlston, Richard and Hemminki, Kari ^LU (2019) In Blood 134(12). p.960-969
- Contribution to journal › Article

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