Random replication of the inactive X chromosome

Por Koren, Amnon, McCarroll, Steven A.
Publicado em 2014

Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for Neurobiology

Por McCarroll, Steven A., Hyman, Steven E.
Publicado em 2013

Complex and multi-allelic copy number variation in human disease

Por Usher, Christina L., McCarroll, Steven A.
Publicado no Brief Funct Genomics (2015)

Microtubules and Their Role in Cellular Stress in Cancer

Por Parker, Amelia L., Kavallaris, Maria, McCarroll, Joshua A.
Publicado em 2014

Movers and shakers: cell cytoskeleton in cancer metastasis

Por Fife, C M, McCarroll, J A, Kavallaris, M
Publicado no Br J Pharmacol (2014)

Genome-scale neurogenetics: methodology and meaning

Por McCarroll, Steven A, Feng, Guoping, Hyman, Steven E
Publicado no Nat Neurosci (2014)

On the level: IRGM gene function is all about expression

Por Huett, Alan, McCarroll, Steven A., Daly, Mark J., Xavier, Ramnik J.
Publicado em 2009

Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

Por Handsaker, Robert E., Korn, Joshua M., Nemesh, James, McCarroll, Steven A.
Publicado no Nat Genet (2011)

An Emerging Role for Tubulin Isotypes in Modulating Cancer Biology and Chemotherapy Resistance

Por Parker, Amelia L., Teo, Wee Siang, McCarroll, Joshua A., Kavallaris, Maria
Publicado no Int J Mol Sci (2017)

Structural haplotypes and recent evolution of the human 17q21.31 region

Por Boettger, Linda M., Handsaker, Robert E., Zody, Michael C., McCarroll, Steven A.
Publicado em 2012

Specific β-Tubulin Isotypes Can Functionally Enhance or Diminish Epothilone B Sensitivity in Non-Small Cell Lung Cancer Cells

Por Gan, Pei Pei, McCarroll, Joshua A., Byrne, Frances L., Garner, James, Kavallaris, Maria
Publicado em 2011

Mapping the Human Reference Genome’s Missing Sequence by Three-Way Admixture in Latino Genomes

Por Genovese, Giulio, Handsaker, Robert E., Li, Heng, Kenny, Eimear E., McCarroll, Steven A.
Publicado em 2013

Single-Tissue and Cross-Tissue Heritability of Gene Expression Via Identity-by-Descent in Related or Unrelated Individuals

Por Price, Alkes L., Helgason, Agnar, Thorleifsson, Gudmar, McCarroll, Steven A., Kong, Augustine, Stefansson, Kari
Publicado em 2011

Vitamin A inhibits pancreatic stellate cell activation: implications for treatment of pancreatic fibrosis

Por McCarroll, J A, Phillips, P A, Santucci, N, Pirola, R C, Wilson, J S, Apte, M V
Publicado em 2006

Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function

Por Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J.
Publicado em 2010

Differential Relationship of DNA Replication Timing to Different Forms of Human Mutation and Variation

Por Koren, Amnon, Polak, Paz, Nemesh, James, Michaelson, Jacob J., Sebat, Jonathan, Sunyaev, Shamil R., McCarroll, Steven A.
Publicado em 2012

Role of pancreatic stellate cells in chemoresistance in pancreatic cancer

Por McCarroll, Joshua A., Naim, Stephanie, Sharbeen, George, Russia, Nelson, Lee, Julia, Kavallaris, Maria, Goldstein, David, Phillips, Phoebe A.
Publicado em 2014

Genetic variation in human DNA replication timing

Por Koren, Amnon, Handsaker, Robert E., Kamitaki, Nolan, Karlić, Rosa, Ghosh, Sulagna, Polak, Paz, Eggan, Kevin, McCarroll, Steven A.
Publicado no Cell (2014)

Recurring exon deletions in the haptoglobin (HP) gene associate with lower blood cholesterol levels

Por Boettger, Linda M., Salem, Rany M., Handsaker, Robert E., Peloso, Gina, Kathiresan, Sekar, Hirschhorn, Joel, McCarroll, Steven A.
Publicado no Nat Genet (2016)

Rat pancreatic stellate cells secrete matrix metalloproteinases: implications for extracellular matrix turnover

Por Phillips, P A, McCarroll, J A, Park, S, Wu, M-J, Pirola, R, Korsten, M, Wilson, J S, Apte, M V
Publicado em 2003