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2019
Mark The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism : Association study and meta-analysis
Grünblatt, Edna ; Nemoda, Zsofia ; Werling, Anna Maria ; Roth, Alexander ; Angyal, Nora ; Tarnok, Zsanett ; Thomsen, Hauke ^LU ; Peters, Triinu ; Hinney, Anke and Hebebrand, Johannes , et al. (2019) In American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 80(6).
- Contribution to journal › Article
Mark Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke
Pfeiffer, Dorothea ; Chen, Bowang ^LU ; Schlicht, Kristina ; Ginsbach, Philip ; Abboud, Sherine ; Bersano, Anna ; Bevan, Steve ; Brandt, Tobias ; Caso, Valeria and Debette, Stéphanie , et al. (2019) In Stroke 50(2). p.298-304
- Contribution to journal › Article
Mark Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
Sabater-Lleal, Maria ; Lindgren, Arne ^LU and Smith, Nicholas L (2019) In Circulation 139(5). p.620-635
- Contribution to journal › Article
Mark Nature vs nurture in knee osteoarthritis – the importance of age, sex and body mass index
Magnusson, K. ^LU ; Turkiewicz, A. ^LU and Englund, M. ^LU (2019) In Osteoarthritis and Cartilage 27(4). p.586-592
- Contribution to journal › Article
Mark International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology : Report of the Dubai, Copenhagen and Toronto meetings
Storry, Jill R. ^LU ; Clausen, Frederik Banch ; Castilho, Lilian ; Chen, Qing ; Daniels, Geoff ; Denomme, Greg ; Flegel, Willy A. ; Gassner, Christoph ; de Haas, Masja and Hyland, Catherine , et al. (2019) In Vox Sanguinis 114(1). p.95-102
- Contribution to journal › Article
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 A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
Ahluwalia, Tarunveer S. ; Schulz, Christina Alexandra ^LU ; Waage, Johannes ; Skaaby, Tea ; Sandholm, Niina ; van Zuydam, Natalie ; Charmet, Romain ; Bork-Jensen, Jette ; Almgren, Peter ^LU and Thuesen, Betina H. , et al. (2019) In Diabetologia 62(2). p.292-305
- Contribution to journal › Article
Mark Advancing research toward faster diagnosis, better treatment, and end of stigma in epilepsy
Pitkänen, Asla ; Henshall, David C. ; Cross, J. Helen ; Guerrini, Renzo ; Jozwiak, Sergiusz ; Kokaia, Merab ^LU ; Simonato, Michele ; Sisodiya, Sanjay and Mifsud, Janet (2019) In Epilepsia
- Contribution to journal › Article
Mark Models and Nomenclature for Cytoplasmic Incompatibility : Caution over Premature Conclusions – A Response to Beckmann et al.
Shropshire, J. Dylan ; Leigh, Brittany ; Bordenstein, Sarah R. ; Duplouy, Anne ^LU ; Riegler, Markus ; Brownlie, Jeremy C. and Bordenstein, Seth R. (2019) In Trends in Genetics 35(6). p.397-399
- Contribution to journal › Letter
Mark Heritability of glomerulonephritis : A Swedish adoption study
Akrawi, Delshad Saleh ^LU ; Zöller, Bengt ^LU ; Fjellstedt, Erik ^LU ; Sundquist, Jan ^LU ; Sundquist, Kristina ^LU and PirouziFard, Mir Nabi ^LU (2019) In European Journal of Clinical Investigation 49(8).
- Contribution to journal › Article

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