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2014
Mark Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland
Wang, Sophie R ; Agarwala, Vineeta ; Flannick, Jason ; Chiang, Charleston W K ; Altshuler, David and Hirschhorn, Joel N (2014) In American Journal of Human Genetics 94(5). p.20-710
- Contribution to journal › Article
2013
Mark Origin of Swedish hemophilia B mutations
Hallden, C. ; Mårtensson, Annika ^LU ; Nilsson, D. ; Säll, Torbjörn ^LU ; Lind-Hallden, C. ; Liden, A. C. and Ljung, Rolf ^LU (2013) In Journal of Thrombosis and Haemostasis 11(11). p.2001-2008
- Contribution to journal › Article
2011
Mark Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
Im, Kate M ; Kirchhoff, Tomas ; Wang, Xianshu ; Green, Todd ; Chow, Clement Y ; Vijai, Joseph ; Korn, Joshua ; Gaudet, Mia M ; Fredericksen, Zachary and Shane Pankratz, V , et al. (2011) In Human Genetics 130(5). p.99-685
- Contribution to journal › Article
2010
Mark Caloplaca phlogina, a lichen with two facies; an example of infraspecific variability resulting in the description of a redundant species
Vondrak, Jan ; Soun, Jaroslav ; Sogaard, Majbrit Zeuthen ; Sochting, Ulrik and Arup, Ulf ^LU (2010) In Lichenologist 42(6). p.685-692
- Contribution to journal › Article
1997
Mark Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
Hakansson, Sara ; Johannsson, O ^LU ; Johansson, Ulla ^LU ; Sellberg, G ^LU ; Loman, N ^LU ; Gerdes, A M ; Holmberg, E ; Dahl, N ; Pandis, N and Kristoffersson, U ^LU , et al. (1997) In American Journal of Human Genetics 60(5). p.1068-1078
- Contribution to journal › Article

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