Publications | Lund University Publications

1 – 5 of 5

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+%22Rare+variants%22&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

2023
Mark Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Mueller, S.H. ; Augustinsson, A. ^LU ; Olsson, H. ^LU and Kuchenbaecker, Karoline B. (2023) In Genome Medicine 15(1).
- Contribution to journal › Article
2022
Mark A relatively common hypomorphic variant in WARS2 causes monogenic disease
Ilinca, Andreea ^LU ; Kafantari, Efthymia ^LU and Puschmann, Andreas ^LU (2022) In Parkinsonism and Related Disorders 94. p.129-131
- Contribution to journal › Debate/Note/Editorial
2017
Mark The functional effect of rare variants in complement genes on C3b degradation in patients with age-related macular degeneration
Geerlings, Maartje J. ; Kremlitzka, Mariann ^LU ; Bakker, Bjorn ; Nilsson, Sara C. ^LU ; Saksens, Nicole T. ; Lechanteur, Yara T E ; Pauper, Marc ; Corominas, Jordi ; Fauser, Sascha and Hoyng, Carel B. , et al. (2017) In JAMA Ophthalmology 135(1). p.39-46
- Contribution to journal › Article
Mark Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population
Henmyr, V. ^LU ; Carlberg, D ; Manderstedt, E. ^LU ; Lind-Halldén, C ; Säll, T. ^LU ; Cardell, L. O. ^LU and Halldén, C. ^LU (2017) In BMC Medical Genetics 18(1).
- Contribution to journal › Article
2011
Mark Heredity in Parkinson's disease. From rare mutations to common genetic risk factors.
Puschmann, Andreas ^LU (2011) In Lund University Faculty of Medicine Doctoral Dissertation Series 2011:95.
- Thesis › Doctoral thesis (compilation)

your query:: Remove keywords: Rare variants