Publications | Lund University Publications

161 – 170 of 403

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/publication?embed=1&q=keywords+exact+%22Genetics%22&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
…
16
17
18
19
…
41
next »

2017
Mark Family history of venous thromboembolism and mortality after venous thromboembolism : a Swedish population-based cohort study
Zöller, Bengt ^LU ; Pirouzifard, Mirnabi ^LU ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2017) In Journal of Thrombosis and Thrombolysis 43(4). p.469-475
- Contribution to journal › Article
Mark Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
Wheeler, Eleanor ; Leong, Aaron ; Liu, Ching-Ti ; Hivert, Marie-France ; Strawbridge, Rona J. ; Podmore, Clara ; Ladenvall, Claes ^LU ; Lyssenko, Valeriya ^LU ; Groop, Leif ^LU and Meigs, James B (2017) In PLoS Medicine 14(9).
- Contribution to journal › Article
Mark DNA methylation links genetics, fetal environment, and an unhealthy lifestyle to the development of type 2 diabetes
Nilsson, Emma ^LU and Ling, Charlotte ^LU (2017) In Clinical Epigenetics 9(1).
- Contribution to journal › Scientific review
Mark Molecular Epidemiology of Heart Failure : Translational Challenges and Opportunities
Smith, J. Gustav ^LU (2017) In JACC: Basic to Translational Science 2(6). p.757-769
- Contribution to journal › Scientific review
Mark Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction
Jabbari, Reza ; Jabbari, Javad ; Glinge, Charlotte ; Risgaard, Bjarke ; Sattler, Stefan ; Winkel, Bo Gregers ; Terkelsen, Christian Juhl ; Tilsted, Hans Henrik ; Jensen, Lisette Okkels and Hougaard, Mikkel , et al. (2017) In BMC Medical Genetics 18(1).
- Contribution to journal › Article
Mark Allelic difference in Mhc2ta confers altered microglial activation and susceptibility to α-synuclein-induced dopaminergic neurodegeneration
Jimenez, Itzia ^LU ; Jewett, Michael ^LU ; Tontanahal, Ashmita ^LU ; Romero-Ramos, Marina ^LU and Swanberg, Maria ^LU (2017) In Neurobiology of Disease 106. p.279-290
- Contribution to journal › Article
Mark Cerebellar mutism syndrome in children with brain tumours of the posterior fossa
Wibroe, Morten ; Cappelen, Johan ; Castor, Charlotte ^LU ; Clausen, Niels ; Grillner, Pernilla ; Gudrunardottir, Thora ; Gupta, Ramneek ; Gustavsson, Bengt ; Heyman, Mats and Holm, Stefan , et al. (2017) In BMC Cancer 17(1).
- Contribution to journal › Article
Mark An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott, Robert A. ; Scott, Laura J ; Mägi, Reedik ; Marullo, Letizia ; Gaulton, Kyle J ; Kaakinen, Marika ; Almgren, Peter ^LU ; Lyssenko, Valeriya ^LU ; Groop, Leif ^LU and Franks, Paul ^LU (2017) In Diabetes 66(11). p.2888-2902
- Contribution to journal › Article
Mark Genetics of complex disease
Henmyr, Viktor ^LU (2017)
- Thesis › Doctoral thesis (compilation)
Mark Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Webb, Thomas R. ; Erdmann, Jeanette ; Stirrups, Kathleen E. ; Stitziel, Nathan O. ; Masca, Nicholas G D ; Jansen, Henning ; Kanoni, Stavroula ; Nelson, Christopher P ; Ferrario, Paola G. and König, Inke R. , et al. (2017) In Journal of the American College of Cardiology 69(7). p.823-836
- Contribution to journal › Article

« previous
1
…
16
17
18
19
…
41
next »

your query:: Remove keywords: Genetics