Genetic studies of Crohn's disease: Past, present and future

Por Liu, Jimmy Z., Anderson, Carl A.
Publicado em 2014

Determination of figures of merit for near-infrared and raman spectrometry by net analyte signal analysis for a 4-component solid dosage system

Por Short, Steven M., Cogdill, Robert P., Anderson, Carl A.
Publicado em 2007

Process analytical technology case study, part III: Calibration monitoring and transfer

Por Cogdill, Robert P., Anderson, Carl A., Drennen, James K.
Publicado em 2005

A Simple Linear Regression Method for Quantitative Trait Loci Linkage Analysis With Censored Observations

Por Anderson, Carl A., McRae, Allan F., Visscher, Peter M.
Publicado em 2006

Synthetic Associations Are Unlikely to Account for Many Common Disease Genome-Wide Association Signals

Por Anderson, Carl A., Soranzo, Nicole, Zeggini, Eleftheria, Barrett, Jeffrey C.
Publicado em 2011

Generation of primary human intestinal T cell transcriptomes reveals differential expression at genetic risk loci for immune-mediated disease

Por Raine, Tim, Liu, Jimmy Z, Anderson, Carl A, Parkes, Miles, Kaser, Arthur
Publicado no Gut (2015)

Data quality control in genetic case-control association studies

Por Anderson, Carl A., Pettersson, Fredrik H, Clarke, Geraldine M, Cardon, Lon R, Morris, Andrew P., Zondervan, Krina T.
Publicado em 2010

Marker selection for genetic case-control association studies

Por Pettersson, Fredrik H, Anderson, Carl A, Clarke, Geraldine M, Cardon, Lon R, Morris, Andrew P, Zondervan, Krina T
Publicado em 2009

Basic statistical analysis in genetic case-control studies

Por Clarke, Geraldine M, Anderson, Carl A, Pettersson, Fredrik H, Cardon, Lon R, Morris, Andrew P, Zondervan, Krina T
Publicado em 2011

Host Genetic Variants and Gene Expression Patterns Associated with Epstein-Barr Virus Copy Number in Lymphoblastoid Cell Lines

Por Houldcroft, Charlotte J., Petrova, Velislava, Liu, Jimmy Z., Frampton, Dan, Anderson, Carl A., Gall, Astrid, Kellam, Paul
Publicado em 2014

Evaluating the Effects of Imputation on the Power, Coverage, and Cost Efficiency of Genome-wide SNP Platforms

Por Anderson, Carl A., Pettersson, Fredrik H., Barrett, Jeffrey C., Zhuang, Joanna J., Ragoussis, Jiannis, Cardon, Lon R., Morris, Andrew P.
Publicado em 2008

Process analytical technology case study: Part II. Development and validation of quantitative near-infrared calibrations in support of a process analytical technology application f...

Por Cogdill, Robert P., Anderson, Carl A., Delgado, Miriam, Chisholm, Robert, Bolton, Raymond, Herkert, Thorsten, Afnan, Ali M., Drennen, James K.
Publicado em 2005

Process analytical technology case study part I: Feasibility studies for quantitative near-infrared method development

Por Cogdill, Robert P., Anderson, Carl A., Delgado-Lopez, Miriam, Molseed, David, Chisholm, Robert, Bolton, Raymond, Herkert, Thorsten, Afnán, Ali M., Drennen, James K.
Publicado em 2005

Development of a Neuroscience-oriented “Methods” Course for Graduate Students of Pharmacology and Toxicology

Por Surratt, Christopher K., Witt-Enderby, Paula A., Johnson, David A., Anderson, Carl A., Bricker, J. Douglas, Davis, Vicki L., Firestine, Steven M., Meng, Wilson S.
Publicado em 2006

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

Por Saadati, Hamid Reza, Wittig, Michael, Helbig, Ingo, Häsler, Robert, Anderson, Carl A., Mathew, Christopher G., Kupcinskas, Limas, Parkes, Miles, Karlsen, Tom Hemming, Rosenstiel, Philip, Schreiber, Stefan, Franke, Andre
Publicado no BMC Med Genet (2016)

A Genome-Wide Linkage Scan for Age at Menarche in Three Populations of European Descent

Por Anderson, Carl A., Zhu, Gu, Falchi, Mario, van den Berg, Stéphanie M., Treloar, Susan A., Spector, Timothy D., Martin, Nicholas G., Boomsma, Dorret I., Visscher, Peter M., Montgomery, Grant W.
Publicado em 2008

Combined Influence of B-Cell Receptor Rearrangement and Somatic Hypermutation on B-Cell Class-Switch Fate in Health and in Chronic Lymphocytic Leukemia

Por Petrova, Velislava N., Muir, Luke, McKay, Paul F., Vassiliou, George S., Smith, Kenneth G. C., Lyons, Paul A., Russell, Colin A., Anderson, Carl A., Kellam, Paul, Bashford-Rogers, Rachael J. M.
Publicado no Front Immunol (2018)

Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis

Por Darlay, Rebecca, Ayers, Kristin L., Mells, George F., Hall, Lynsey S., Liu, Jimmy Z., Almarri, Mohamed A., Alexander, Graeme J., Jones, David E., Sandford, Richard N., Anderson, Carl A., Cordell, Heather J.
Publicado no PLoS Genet (2018)

Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease

Por Lee, James C., Biasci, Daniele, Roberts, Rebecca, Gearry, Richard B., Mansfield, John C., Ahmad, Tariq, Prescott, Natalie J., Satsangi, Jack, Wilson, David C., Jostins, Luke, Anderson, Carl A., Traherne, James A., Lyons, Paul A., Parkes, Miles, Smith, Kenneth G.C.
Publicado no Nat Genet (2017)

Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects

Por Williamson, Kathleen A., Rainger, Joe, Floyd, James A.B., Ansari, Morad, Meynert, Alison, Aldridge, Kishan V., Rainger, Jacqueline K., Anderson, Carl A., Moore, Anthony T., Hurles, Matthew E., Clarke, Angus, van Heyningen, Veronica, Verloes, Alain, Taylor, Martin S., Wilkie, Andrew O.M., FitzPatrick, David R.
Publicado em 2014