Publications | Lund University Publications

161 – 170 of 417

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
…
42
next »

2018
Mark Genetic variation of acquired structural chromosomal aberrations
Vodicka, Pavel ; Musak, Ludovit ; Vodickova, Ludmila ; Vodenkova, Sona ; Catalano, Calogerina ; Kroupa, Michal ; Naccarati, Alessio ; Polivkova, Zdena ; Vymetalkova, Veronika and Försti, Asta ^LU , et al. (2018) In Mutation Research - Genetic Toxicology and Environmental Mutagenesis 836. p.13-21
- Contribution to journal › Article
Mark Fifth Åland Island conference on von Willebrand disease
Berntorp, E. ^LU ; Ågren, A. ; Aledort, L. ; Blombäck, M. ; Cnossen, M. H. ; Croteau, S. E. ; von Depka, M. ; Federici, A. B. ; Goodeve, A. and Goudemand, J. , et al. (2018) In Haemophilia 24. p.5-19
- Contribution to journal › Article
Mark 17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage
Marini, Sandro ; Devan, William J. ; Radmanesh, Farid ; Miyares, Laura ; Poterba, Timothy ; Hansen, Björn M. ^LU ; Norrving, Bo ^LU ; Jimenez-Conde, Jordi ; Giralt-Steinhauer, Eva and Elosua, Roberto , et al. (2018) In Stroke 49(7). p.1618-1625
- Contribution to journal › Article
Mark Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome
Bonfiglio, Ferdinando ; Zheng, Tenghao ; Garcia-Etxebarria, Koldo ; Hadizadeh, Fatemeh ; Bujanda, Luis ; Bresso, Francesca ; Agreus, Lars ; Andreasson, Anna ; Dlugosz, Aldona and Lindberg, Greger , et al. (2018) In Gastroenterology 155(1). p.168-179
- Contribution to journal › Article
Mark The lived experience of Huntington’s disease : A phenomenological perspective on genes, the body and the lived experience of a genetic disease
Hagen, Niclas ^LU (2018) In Health 22(1). p.72-86
- Contribution to journal › Article
Mark Gestational diabetes and maternal obesity are associated with epigenome-wide methylation changes in children
Hjort, Line ^LU ; Martino, David ; Grunnet, Louise Groth ; Naeem, Haroon ; Maksimovic, Jovana ; Olsson, Anders Henrik ^LU ; Zhang, Cuilin ; Ling, Charlotte ^LU ; Olsen, Sjurdur Frodi and Saffery, Richard , et al. (2018) In JCI Insight 3(17).
- Contribution to journal › Article
Mark Immunogenetics of Parkinson's disease
Swanberg, Maria ^LU and Jimenez-Ferrer, Itzia ^LU (2018) p.27-44
- Chapter in Book/Report/Conference proceeding › Book chapter
Mark Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
Duffy, David L. and Martin, Nicholas G (2018) In Nature Communications 9(1). p.1-10
- Contribution to journal › Article
2017
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
Mark Naumovozyma castellii: an alternative model for budding yeast molecular biology
Karademir Andersson, Ahu ^LU and Cohn, Marita ^LU (2017) In Yeast 34(3). p.95-109
- Contribution to journal › Article

« previous
1
…
16
17
18
19
…
42
next »

your query:: Remove keywords: Genetics