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2014
Mark IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes
Boggio, E. ; Clemente, N. ; Mondino, A. ; Cappellano, G. ; Orilieri, E. ; Gigliotti, C.L. ; Toth, E. ^LU ; Ramenghi, Ugo ; Dianzani, U. and Chiocchetti, Andreas (2014) In Blood 123(8). p.1178-1186
- Contribution to journal › Article
Mark Hereditary myopathy with early respiratory failure: occurrence in various populations
Palmio, Johanna ; Evila, Anni ; Chapon, Francoise ; Tasca, Giorgio ; Xiang, Fengqing ; Brådvik, Björn ^LU ; Eymard, Bruno ; Echaniz-Laguna, Andoni ; Laporte, Jocelyn and Karppa, Mikko , et al. (2014) In Journal of Neurology, Neurosurgery and Psychiatry 85(3). p.345-353
- Contribution to journal › Article
2013
Mark High Familial Risk of Atrial Fibrillation/Atrial Flutter in Multiplex Families: A Nationwide Family Study in Sweden
Zöller, Bengt ^LU ; Ohlsson, Henrik ^LU ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2013) In Journal of the American Heart Association 2(1). p.003384-003384
- Contribution to journal › Article
Mark Heritability Estimates Identify a Substantial Genetic Contribution to Risk and Outcome of Intracerebral Hemorrhage
Devan, William J. ; Falcone, Guido J. ; Anderson, Christopher D. ; Jagiella, Jeremiasz M. ; Schmidt, Helena ; Hansen, Björn ^LU ; Jimenez-Conde, Jordi ; Giralt-Steinhauer, Eva ; Cuadrado-Godia, Elisa and Soriano, Carolina , et al. (2013) In Stroke: a journal of cerebral circulation 44(6). p.1578-1583
- Contribution to journal › Article
Mark Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women
Koller, Daniel L. ; Zheng, Hou-Feng ; Karasik, David ; Yerges-Armstrong, Laura ; Liu, Ching-Ti ; McGuigan, Fiona ^LU ; Kemp, John P. ; Giroux, Sylvie ; Lai, Dongbing and Edenberg, Howard J. , et al. (2013) In Journal of Bone and Mineral Research 28(3). p.547-558
- Contribution to journal › Article
Mark Role of Gα(olf) in Familial and Sporadic Adult-Onset Primary Dystonia.
Vemula, Satya R ; Puschmann, Andreas ^LU ; Xiao, Jianfeng ; Rudzinska, Monika ; Frei, Karen P ; Truong, Daniel D ; Wszolek, Zbigniew K and LeDoux, Mark S (2013) In Human Molecular Genetics 22(12). p.2510-2519
- Contribution to journal › Article
Mark Familial Risk of Small Intestinal Carcinoid and Adenocarcinoma
Kharazmi, Elham ; Pukkala, Eero ; Sundquist, Kristina ^LU and Hemminki, Kari ^LU (2013) In Clinical Gastroenterology and Hepatology 11(8). p.944-949
- Contribution to journal › Article
Mark Population-specific Frequencies for LRRK2 Susceptibility Variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium
Heckman, Michael G. ; Soto-Ortolaza, Alexandra I. ; Aasly, Jan O. ; Abahuni, Nadine ; Annesi, Grazia ; Bacon, Justin A. ; Bardien, Soraya ; Bozi, Maria ; Brice, Alexis and Brighina, Laura , et al. (2013) In Movement Disorders 28(12). p.1740-1744
- Contribution to journal › Article
Mark Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
Albrechtsen, A. ; Grarup, N. ; Li, Y. ; Sparso, T. ; Tian, G. ; Cao, H. ; Jiang, T. ; Kim, S. Y. ; Korneliussen, T. and Li, Q. , et al. (2013) In Diabetologia 56(2). p.298-310
- Contribution to journal › Article
Mark Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease
Lindquist, SG ; Duno, M ; Batbayli, M ; Puschmann, Andreas ^LU ; Braendgaard, H ; Mardosiene, S ; Svenstrup, K ; Pinborg, LH ; Vestergaard, K and Hjermind, LE , et al. (2013) In Clinical Genetics 83(3). p.279-283
- Contribution to journal › Article

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