IW
Ian Welsh
Jackson Laboratory, Cornell University
Research areas: Social Sciences · Sociology and Political Science · Anarchism and Radical Politics · Developmental Biology and Gene Regulation · Communism, Protests, Social Movements
0000-0002-5685-3235
Employment
Education
- 2008 - 2015
Projects & Funding
-
Genomic regulation of midfacial outgrowth variation in evolution and pathology National Institute of Dental and Craniofacial Research2017 - 2020
Publications (19)
- Evolutionary transfer learning enables organism-wide inference of mammalian enhancer landscapes Save
- Palatal segment contributions to midfacial anterior-posterior growth Save
- A single-cell transcriptional timelapse of mouse embryonic development, from gastrula to pup Save
- Mendelian gene identification through mouse embryo viability screening. Save
- Systematic reconstruction of cellular trajectories across mouse embryogenesis. Save
- Loss of Extreme Long-Range Enhancers in Human Neural Crest Drives a Craniofacial Disorder. Save
- Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface. Save
- Chromatin Architecture of the Pitx2 Locus Requires CTCF- and Pitx2-Dependent Asymmetry that Mirrors Embryonic Gut Laterality. Save
- The left-right Pitx2 pathway drives organ-specific arterial and lymphatic development in the intestine. Save
- Integration of left-right Pitx2 transcription and Wnt signaling drives asymmetric gut morphogenesis via Daam2. Save
- Reproductive and developmental genomics retreat at Cornell University, 2012. Save
- Signaling integration in the rugae growth zone directs sequential SHH signaling center formation during the rostral outgrowth of the palate. Save
- Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. Save
- A dosage-dependent role for Spry2 in growth and patterning during palate development. Save
- Analysis of the gene regulatory program induced by the homeobox transcription factor distal-less 3 in mouse placenta. Save
- Evidence for a conserved function in synapse formation reveals Phr1 as a candidate gene for respiratory failure in newborn mice. Save
- Development of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in mice. Save
- Notch signaling regulates left-right asymmetry determination by inducing Nodal expression. Save
- Loss of late primitive streak mesoderm and interruption of left-right morphogenesis in the Ednrb(s-1Acrg) mutant mouse. Save