Garvan-Weizmann Centre for Cellular Genomics (GWCCG) – Research

Selected Publications

  1. Freidman C, Nguyen Q, Lukowski S, Helfer A, Chiu H, Voges H, Suo S, Han J, Osteil P, Peng G, Jing N, Murry C, Wong E, Ding J, Bar-Joseph Z, Wang Y, Hudson J, Tam P, Powell J*, Palpant N*. *Joint senior. Cardiac-directed differential using small molecule Wnt modulation at single cell resolution. Cell Stem Cell, Accepted.
  2. Nguyen Q, Lukowski S, Chiu H, Senabouth A, Bruxner T, Christ A, Palpant N, Powell J. Single-cell transcriptome sequencing of 18,787 human induced pluripotent stem cells identifies differentially primed subpopulations. Genome Research, (2018)
  3. Lukowski S, Tuong K, Noske K, Senabouth A, Nguyen Q, Soyer P, Frazer I, Powell J. Detection of HPV E7 transcription at single cell resolution in epidermis. Journal of Investigative Dermatology, (2018)
  4. Yap C, Lloyd-Jones L, Holloway A, Smartt P, Wray N, Gratten J, Powell J. Independent trans-eQTL identified in whole blood have limited influence on complex disease biology. European Journal of Human Genetics, (2018)
  5. Lukowski S, [16], Powell J. Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood. Nature Communications, 8, 483-492 (2017).
  6. Lloyd-Jones L, [14], Powell J. The genetic architecture of gene expression in peripheral blood. American Journal of Human Genetics, 100, 228-237 (2017)
  7. Powell J, [17], Montgomery. Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. Human Molecular Genomics, 25, 5054-5058 (2016)
  8. Hemani G, Shakhbazov K, Westra H, Esko, T, Henders A, McRae A, Yang J, Gibson G, Martin N, Metspalu A, Franke L, Montgomery G, Visscher P, Powell J. Detection and replication of epistasis influencing transcription in humans. Nature, 508, 249-253 (2014)
  9. Powell J, Henders A, McRae A, Kim J, Hemani G, Martin N, Dermitzakis M, Gibson G, Montgomery G, Visscher P. Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics, 9, e1003502
(2013)
  10. Westra H, [6], Powell J, [46], Franke L. Systematic identification of trans eQTLs as putative drivers of known disease associations Nature Genetics, 45, 1238-43 (2013)
  11. Powell J, Henders A, McRae A, Wright M, Martin N, Dermitzakis E, Montgomery G, Visscher P. Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22, 456-66
(2012)
  12. Powell J, Henders, McRae, Caracella A, Smith S, Wright M, Whitfield J, Martin N, Dermitzakis E, Visscher P, Montgomery G. The Brisbane Systems Genetics Study: Genetical genomics meets complex trait genetics PLoS One, 7, e35430
(2012)
  13. Yang J, Loos R, Powell J, [122], Visscher P. FTO genotype is associated with phenotypic variability of body mass index. Nature, 490, 267-72 (2012)
  14. Powell J*, McEvoy B*, Goddard M, Visscher P. *Joint first. Human population dispersal “out of Africa” estimated from linkage disequilibrium and allele frequencies of SNPs. Genome Research, 21, 821-829 (2011)
  15. Powell J, Visscher P, Goddard M. Reconciling the analysis of IBD and IBS in complex trait studies. Nature Reviews Genetics, 11, 800-805 (2010)

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Garvan-Weizmann Centre for Cellular Genomics (GWCCG) – Research News