Publications | Lund University Publications

11 – 17 of 17

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=issn+exact+%221018-4813%22&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
2
next »

2019
Mark A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
Farias, Fabiana H.G. ; Dahlqvist, Johanna ; Kozyrev, Sergey V. ; Leonard, Dag ; Wilbe, Maria ; Abramov, Sergei N. ; Alexsson, Andrei ; Pielberg, Gerli R. ; Hansson-Hamlin, Helene and Andersson, Göran , et al. (2019) In European Journal of Human Genetics 27(3). p.432-441
- Contribution to journal › Article
Mark A stroke gene panel for whole-exome sequencing
Ilinca, Andreea ^LU ; Samuelsson, Sofie ^LU ; Piccinelli, Paul ^LU ; Soller, Maria ^LU ; Kristoffersson, Ulf ^LU and Lindgren, Arne G. ^LU (2019) In European Journal of Human Genetics 27(2). p.317-324
- Contribution to journal › Article
Mark Motivations for data sharing—views of research participants from four European countries : A DIRECT study
Shah, Nisha ; Coathup, Victoria ; Teare, Harriet ; Forgie, Ian ; Giordano, Giuseppe Nicola ^LU ; Hansen, Tue Haldor ; Groeneveld, Lenka ; Hudson, Michelle ; Pearson, Ewan and Ruetten, Hartmut , et al. (2019) In European Journal of Human Genetics
- Contribution to journal › Article
2018
Mark Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
Vears, Danya F. ; Niemiec, Emilia ^LU ; Howard, Heidi Carmen ^LU and Borry, Pascal (2018) In European Journal of Human Genetics 26(12). p.1743-1751
- Contribution to journal › Article
2017
Mark From Mendel to Medical Genetics
Kristoffersson, Ulf ^LU and Macek, Milan (2017) In European Journal of Human Genetics 25(s2). p.53-59
- Contribution to journal › Scientific review
2016
Mark Rare novel variants in the ZIC3 gene cause X-linked heterotaxy
Paulussen, Aimee D C ; Steyls, Anja ; Vanoevelen, Jo ; Van Tienen, Florence H J ; Krapels, Ingrid P C ; Claes, Godelieve R F ; Chocron, Sonja ; Velter, Crool ; Tan-Sindhunata, Gita M. and Lundin, Catarina ^LU , et al. (2016) In European Journal of Human Genetics 24(12). p.1783-1791
- Contribution to journal › Article
2003
Mark Finnish and Swedish genotypes and risk of cancer in Sweden
Hemminki, Kari ^LU and Li, Xinjun ^LU (2003) In European Journal of Human Genetics 11(3). p.207-209
- Contribution to journal › Letter

« previous
1
2
next »

your query:: Remove issn: 1018-4813