Detection of cis-acting regulatory SNPs using allelic expression data

av Xiao, Rui, Scott, Laura J.
I publikationen Genet Epidemiol (2011)

What Will Diabetes Genomes Tell Us?

av Mohlke, Karen L., Scott, Laura J.
Publicerad 2012

Assessing Whether an Allele Can Account in Part for a Linkage Signal: The Genotype-IBD Sharing Test (GIST)

av Li, Chun, Scott, Laura J., Boehnke, Michael
Publicerad 2004

Recommended joint and meta-analysis strategies for case-control association testing of single low-count variants

av Ma, Clement, Blackwell, Tom, Boehnke, Michael, Scott, Laura J.
Publicerad 2013

Identifying Plausible Genetic Models Based on Association and Linkage Results: Application to Type 2 Diabetes

av Guan, Weihua, Boehnke, Michael, Pluzhnikov, Anna, Cox, Nancy J., Scott, Laura J.
Publicerad 2012

Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK

av Fogarty, Marie P., Xiao, Rui, Prokunina-Olsson, Ludmila, Scott, Laura J., Mohlke, Karen L.
Publicerad 2010

A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank

av Dutta, Diptavo, VandeHaar, Peter, Fritsche, Lars G., Zöllner, Sebastian, Boehnke, Michael, Scott, Laura J., Lee, Seunggeun
I publikationen Am J Hum Genet (2021)

Broad-Enrich: functional interpretation of large sets of broad genomic regions

av Cavalcante, Raymond G., Lee, Chee, Welch, Ryan P., Patil, Snehal, Weymouth, Terry, Scott, Laura J., Sartor, Maureen A.
Publicerad 2014

CIP2A- and SETBP1-mediated PP2A inhibition reveals AKT S473 phosphorylation to be a new biomarker in AML

av Lucas, Claire M., Scott, Laura J., Carmell, Natasha, Holcroft, Alison K., Hills, Robert K., Burnett, Alan K., Clark, Richard E.
I publikationen Blood Adv (2018)

ChIP-Enrich: gene set enrichment testing for ChIP-seq data

av Welch, Ryan P., Lee, Chee, Imbriano, Paul M., Patil, Snehal, Weymouth, Terry E., Smith, R. Alex, Scott, Laura J., Sartor, Maureen A.
Publicerad 2014

High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools

av Mohlke, Karen L., Erdos, Michael R., Scott, Laura J., Fingerlin, Tasha E., Jackson, Anne U., Silander, Kaisa, Hollstein, Pablo, Boehnke, Michael, Collins, Francis S.
Publicerad 2002

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

av Zhang, Fan, Flickinger, Matthew, Taliun, Sarah A. Gagliano, Abecasis, Gonçalo R., Scott, Laura J., McCaroll, Steven A., Pato, Carlos N., Boehnke, Michael, Kang, Hyun Min
I publikationen Genome Res (2020)

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

av Carlson, Jedidiah, Locke, Adam E., Flickinger, Matthew, Zawistowski, Matthew, Levy, Shawn, Myers, Richard M., Boehnke, Michael, Kang, Hyun Min, Scott, Laura J., Li, Jun Z., Zöllner, Sebastian
I publikationen Nat Commun (2018)

Subsets of Finns with High HDL to Total Cholesterol Ratio Show Evidence for Linkage to Type 2 Diabetes on Chromosome 6q

av Shtir, Corina, Nagakawa, I. Sharon, Duren, William L., Conneely, Karen N., Scott, Laura J., Silander, Kaisa, Valle, Timo T., Tuomilehto, Jaakko, Buchanan, Thomas A., Bergman, Richard N., Collins, Francis S., Boehnke, Michael, Watanabe, Richard M.
Publicerad 2006

Circulating β-carotene levels and Type 2 diabetes: Cause or effect?

av Perry, John R.B., Ferrucci, Luigi, Bandinelli, Stefania, Guralnik, Jack, Semba, Richard D., Rice, Neil, Melzer, David, Saxena, Richa, Scott, Laura J, McCarthy, Mark I, Hattersley, Andrew T, Zeggini, Ele, Weedon, Michael N, Frayling, Timothy M
Publicerad 2009

Global epigenomic analysis of primary human pancreatic islets provides insights into type 2 diabetes susceptibility loci

av Stitzel, Michael L., Sethupathy, Praveen, Pearson, Daniel S., Chines, Peter S., Song, Lingyun, Erdos, Michael R., Welch, Ryan, Parker, Stephen C. J., Boyle, Alan P., Scott, Laura J., Margulies, Elliott H., Boehnke, Michael, Furey, Terrence S., Crawford, Gregory E., Collins, Francis S.
Publicerad 2010

A Partial Loss-of-Function Variant in AKT2 Is Associated With Reduced Insulin-Mediated Glucose Uptake in Multiple Insulin-Sensitive Tissues: A Genotype-Based Callback Positron Emis...

av Latva-Rasku, Aino, Honka, Miikka-Juhani, Stančáková, Alena, Koistinen, Heikki A., Kuusisto, Johanna, Guan, Li, Manning, Alisa K., Stringham, Heather, Gloyn, Anna L., Lindgren, Cecilia M., Collins, Francis S., Mohlke, Karen L., Scott, Laura J., Karjalainen, Tomi, Nummenmaa, Lauri, Boehnke, Michael, Nuutila, Pirjo, Laakso, Markku
I publikationen Diabetes (2018)

Heritable Individual-Specific and Allele-Specific Chromatin Signatures in Humans

av McDaniell, Ryan, Lee, Bum-Kyu, Song, Lingyun, Liu, Zheng, Boyle, Alan P., Erdos, Michael R., Scott, Laura J., Morken, Mario A., Kucera, Katerina S., Battenhouse, Anna, Keefe, Damian, Collins, Francis S., Willard, Huntington F., Lieb, Jason D., Furey, Terrence S., Crawford, Gregory E., Iyer, Vishwanath R., Birney, Ewan
Publicerad 2010

Tissue-specific alternative splicing of TCF7L2

av Prokunina-Olsson, Ludmila, Welch, Cullan, Hansson, Ola, Adhikari, Neeta, Scott, Laura J., Usher, Nicolle, Tong, Maurine, Sprau, Andrew, Swift, Amy, Bonnycastle, Lori L., Erdos, Michael R., He, Zhi, Saxena, Richa, Harmon, Brennan, Kotova, Olga, Hoffman, Eric P., Altshuler, David, Groop, Leif, Boehnke, Michael, Collins, Francis S., Hall, Jennifer L.
Publicerad 2009

Next-generation genotype imputation service and methods

av Das, Sayantan, Forer, Lukas, Schönherr, Sebastian, Sidore, Carlo, Locke, Adam E, Kwong, Alan, Vrieze, Scott I, Chew, Emily Y, Levy, Shawn, McGue, Matt, Schlessinger, David, Stambolian, Dwight, Loh, Po-Ru, Iacono, William G, Swaroop, Anand, Scott, Laura J, Cucca, Francesco, Kronenberg, Florian, Boehnke, Michael, Abecasis, Gonçalo R, Fuchsberger, Christian
I publikationen Nat Genet (2016)