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2019
Mark The Applicability of Mouse Models to the Study of Human Disease
Rydell-Törmänen, Kristina ^LU and Johnson, Jill R. (2019) In Methods in molecular biology (Clifton, N.J.) 1940. p.3-22
- Contribution to journal › Article
Mark Nomenclature of Genetically Determined Myoclonus Syndromes : Recommendations of the International Parkinson and Movement Disorder Society Task Force
van der Veen, Sterre ; Zutt, Rodi ; Klein, Christine ; Marras, Connie ; Berkovic, Samuel F. ; Caviness, John N. ; Shibasaki, Hiroshi ; de Koning, Tom J. ^LU and Tijssen, Marina A.J. (2019) In Movement Disorders 34(11). p.1602-1613
- Contribution to journal › Scientific review
2018
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 Examining the Association Between Autistic Traits and Atypical Sensory Reactivity : A Twin Study
Taylor, Mark J. ; Gustafsson, Peik ^LU ; Larsson, Henrik ; Gillberg, Christopher ; Lundström, Sebastian ^LU and Lichstenstein, Paul (2018) In Journal of the American Academy of Child and Adolescent Psychiatry 57(2). p.96-102
- Contribution to journal › Article
Mark Heritability of End-Stage Renal Disease : A Swedish Adoption Study
Akrawi, Delshad Saleh ^LU ; PirouziFard, Mir Nabi ^LU ; Fjellstedt, Erik ; Sundquist, Jan ^LU ; Sundquist, Kristina ^LU and Zöller, Bengt ^LU (2018) In Nephron 138(2). p.157-165
- Contribution to journal › Article
Mark Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway : a meta-analysis
McKeown, Nicola M. ; Dashti, Hassan S. ; Ma, Jiantao ; Haslam, Danielle E. ; Kiefte-de Jong, Jessica C. ; Smith, Caren E. ; Tanaka, Toshiko ; Graff, Mariaelisa ; Lemaitre, Rozenn N. and Rybin, Denis , et al. (2018) In Diabetologia 61(2). p.317-330
- 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 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 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 Sources of Parent-Child Transmission of Drug Abuse : Path Analyses of Not-Lived-With Parental, Stepparental, Triparental, and Adoptive Families
Kendler, Kenneth S. ^LU ; Ohlsson, Henrik ^LU ; Sundquist, Kristina ^LU and Sundquist, Jan ^LU (2018) In Journal of Nervous and Mental Disease 206(4). p.239-244
- Contribution to journal › Article

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