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2013
Mark Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
Meyer, Kerstin B. ; O'Reilly, Martin ; Michailidou, Kyriaki ; Carlebur, Saskia ; Edwards, Stacey L. ; French, Juliet D. ; Prathalingham, Radhika ; Dennis, Joe ; Bolla, Manjeet K. and Wang, Qin , et al. (2013) In American Journal of Human Genetics 93(6). p.1046-1060
- Contribution to journal › Article
2012
Mark SHANK1 Deletions in Males with Autism Spectrum Disorder
Sato, Daisuke ; Lionel, Anath C. ; Leblond, Claire S. ; Prasad, Aparna ; Pinto, Dalila ; Walker, Susan ; O'Connor, Irene ; Russell, Carolyn ; Drmic, Irene E. and Hamdan, Fadi F. , et al. (2012) In American Journal of Human Genetics 90(5). p.879-887
- Contribution to journal › Article
Mark Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci
Asselbergs, Folkert W. ; Guo, Yiran ; van Iperen, Erik P. A. ; Sivapalaratnam, Suthesh ; Tragante, Vinicius ; Lanktree, Matthew B. ; Lange, Leslie A. ; Almoguera, Berta ; Appelman, Yolande E. and Barnard, John , et al. (2012) In American Journal of Human Genetics 91(5). p.823-838
- Contribution to journal › Article
Mark Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci
Saxena, Richa ; Elbers, Clara C. ; Guo, Yiran ; Peter, Inga ; Gaunt, Tom R. ; Mega, Jessica L. ; Lanktree, Matthew B. ; Tare, Archana ; Almoguera Castillo, Berta and Li, Yun R. , et al. (2012) In American Journal of Human Genetics 90(3). p.410-425
- Contribution to journal › Article
Mark Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death
Nyegaard, Mette ; Overgaard, Michael T. ; Sendergaard, Mads T. ; Vranas, Marta ; Behr, Elijah R. ; Hildebrandt, Lasse L. ; Lund, Jacob ; Hedley, Paula L. ; Camm, A. John and Wettrell, Göran GWE ^LU , et al. (2012) In American Journal of Human Genetics 91(4). p.703-712
- Contribution to journal › Article
2011
Mark Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height
Lanktree, Matthew B. ; Guo, Yiran ; Murtaza, Muhammed ; Glessner, Joseph T. ; Bailey, Swneke D. ; Onland-Moret, N. Charlotte ; Lettre, Guillaume ; Ongen, Halit ; Rajagopalan, Ramakrishnan and Johnson, Toby , et al. (2011) In American Journal of Human Genetics 88(1). p.41443-41443
- Contribution to journal › Article
Mark VPS35 Mutations in Parkinson Disease
Vilarino-Gueell, Carles ; Wider, Christian ; Ross, Owen A. ; Dachsel, Justus C. ; Kachergus, Jennifer M. ; Lincoln, Sarah J. ; Soto-Ortolaza, Alexandra I. ; Cobb, Stephanie A. ; Wilhoite, Greggory J. and Bacon, Justin A. , et al. (2011) In American Journal of Human Genetics 89(1). p.162-167
- Contribution to journal › Article
Mark Blood Pressure Loci Identified with a Gene-Centric Array
Johnson, Toby ; Gaunt, Tom R. ; Newhouse, Stephen J. ; Padmanabhan, Sandosh ; Tomaszewski, Maciej ; Kumari, Meena ; Morris, Richard W. ; Tzoulaki, Ioanna ; O'Brien, Eoin T. and Poulter, Neil R. , et al. (2011) In American Journal of Human Genetics 89(6). p.688-700
- Contribution to journal › Article
2010
Mark A Missense Mutation in the Aggrecan C-type Lectin Domain Disrupts Extracellular Matrix Interactions and Causes Dominant Familial Osteochondritis Dissecans
Stattin, Eva-Lena ; Wiklund, Fredrik ; Lindblom, Karin ^LU ; Önnerfjord, Patrik ^LU ; Jonsson, Bjorn-Anders ; Tegner, Yelverton ; Sasaki, Takako ; Struglics, André ^LU ; Lohmander, Stefan ^LU and Dahl, Niklas , et al. (2010) In American Journal of Human Genetics 86(2). p.126-137
- Contribution to journal › Article
2009
Mark Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
Friedman, James S. ; Ray, Joseph W. ; Waseem, Naushin ; Johnson, Kory ; Brooks, Matthew J. ; Hugosson, Therése ^LU ; Breuer, Debra ; Branham, Kari E. ; Krauth, Daniel S. and Bowne, Sara J. , et al. (2009) In American Journal of Human Genetics 84(6). p.792-800
- Contribution to journal › Article

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