The evidential statistical paradigm in genetics

por Strug, Lisa J.
Publicado 2018

Reply to: Is a microRNA‐328 binding site in PAX6 associated with Rolandic epilepsy?

por Strug, Lisa J., Pal, Deb K.
Publicado 2017

Testing Calibration of Cox Survival Models at Extremes of Event Risk

por Soave, David M., Strug, Lisa J.
Publicado 2018

The X factor: A robust and powerful approach to X‐chromosome‐inclusive whole‐genome association studies

por Chen, Bo, Craiu, Radu V., Strug, Lisa J., Sun, Lei
Publicado 2021

A flexible summary statistics-based colocalization method with application to the mucin cystic fibrosis lung disease modifier locus

por Wang, Fan, Panjwani, Naim, Wang, Cheng, Sun, Lei, Strug, Lisa J.
Publicado 2022

SLC26A9 Gene Is Associated With Lung Function Response to Ivacaftor in Patients With Cystic Fibrosis

por Corvol, Harriet, Mésinèle, Julie, Douksieh, Isman-Hassan, Strug, Lisa J., Boëlle, Pierre-Yves, Guillot, Loïc
Publicado 2018

VikNGS: a C++ variant integration kit for next generation sequencing association analysis

por Baskurt, Zeynep, Mastromatteo, Scott, Gong, Jiafen, Wintle, Richard F, Scherer, Stephen W, Strug, Lisa J
Publicado 2020

Construction of the model for the Genetic Analysis Workshop 14 simulated data: genotype-phenotype relationships, gene interaction, linkage, association, disequilibrium, and ascerta...

por Greenberg, David A, Zhang, Junying, Shmulewitz, Dvora, Strug, Lisa J, Zimmerman, Regina, Singh, Veena, Marathe, Sudhir
Publicado 2005

Immunomodulatory function of the cystic fibrosis modifier gene BPIFA1

por Saferali, Aabida, Tang, Anthony C., Strug, Lisa J., Quon, Bradley S., Zlosnik, James, Sandford, Andrew J., Turvey, Stuart E.
Publicado 2020

Collaborative Cross Mice Yield Genetic Modifiers for Pseudomonas aeruginosa Infection in Human Lung Disease

por Lorè, Nicola Ivan, Sipione, Barbara, He, Gengming, Strug, Lisa J., Atamni, Hanifa J., Dorman, Alexandra, Mott, Richard, Iraqi, Fuad A., Bragonzi, Alessandra
Publicado 2020

LocusFocus: Web-based colocalization for the annotation and functional follow-up of GWAS

por Panjwani, Naim, Wang, Fan, Mastromatteo, Scott, Bao, Allen, Wang, Cheng, He, Gengming, Gong, Jiafen, Rommens, Johanna M., Sun, Lei, Strug, Lisa J.
Publicado 2020

A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways

por Soave, David, Corvol, Harriet, Panjwani, Naim, Gong, Jiafen, Li, Weili, Boëlle, Pierre-Yves, Durie, Peter R., Paterson, Andrew D., Rommens, Johanna M., Strug, Lisa J., Sun, Lei
Publicado 2015

Statistical power in COVID-19 case-control host genomic study design

por Lin, Yu-Chung, Brooks, Jennifer D., Bull, Shelley B., Gagnon, France, Greenwood, Celia M. T., Hung, Rayjean J., Lawless, Jerald, Paterson, Andrew D., Sun, Lei, Strug, Lisa J.
Publicado 2020

Evidence for a Causal Relationship Between Early Exocrine Pancreatic Disease and Cystic Fibrosis–Related Diabetes: A Mendelian Randomization Study

por Soave, David, Miller, Melissa R., Keenan, Katherine, Li, Weili, Gong, Jiafen, Ip, Wan, Accurso, Frank, Sun, Lei, Rommens, Johanna M., Sontag, Marci, Durie, Peter R., Strug, Lisa J.
Publicado 2014

Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputation

por Dang, Hong, Polineni, Deepika, Pace, Rhonda G., Stonebraker, Jaclyn R., Corvol, Harriet, Cutting, Garry R., Drumm, Mitchell L., Strug, Lisa J., O’Neal, Wanda K., Knowles, Michael R.
Publicado 2020

The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

por Strug, Lisa J., Addis, Laura, Chiang, Theodore, Baskurt, Zeynep, Li, Weili, Clarke, Tara, Hardison, Huntley, Kugler, Steven L., Mandelbaum, David E., Novotny, Edward J., Wolf, Steven M., Pal, Deb K.
Publicado 2012

Identification of brain cell types underlying genetic association with word reading and correlated traits

por Price, Kaitlyn M., Wigg, Karen G., Nigam, Anukrati, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N., Guger, Sharon L., Lovett, Maureen W., Strug, Lisa J., Tripathy, Shreejoy J., Barr, Cathy L.
Publicado 2023

Novel variation at chr11p13 associated with cystic fibrosis lung disease severity

por Dang, Hong, Gallins, Paul J, Pace, Rhonda G, Guo, Xue-liang, Stonebraker, Jaclyn R, Corvol, Harriet, Cutting, Garry R, Drumm, Mitchell L, Strug, Lisa J, Knowles, Michael R, O’Neal, Wanda K
Publicado 2016

Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severity

por Dang, Hong, Gallins, Paul J, Pace, Rhonda G, Guo, Xue-liang, Stonebraker, Jaclyn R, Corvol, Harriet, Cutting, Garry R, Drumm, Mitchell L, Strug, Lisa J, Knowles, Michael R, O’Neal, Wanda K
Publicado 2017

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

por Price, Kaitlyn M., Wigg, Karen G., Eising, Else, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N., Guger, Sharon L., Fisher, Simon E., Lovett, Maureen W., Strug, Lisa J., Barr, Cathy L.
Publicado 2022