ORCID as entered in ROS

Select Publications
2016, 'Cited2 regulates neocortical layer II/III generation and somatosensory callosal projection neuron development and connectivity', Journal of Neuroscience, 36, pp. 6403 - 6419, http://dx.doi.org/10.1523/JNEUROSCI.4067-15.2016
,2016, 'Notch1 endocytosis is induced by ligand and is required for signal transduction', Biochimica et Biophysica Acta - Molecular Cell Research, 1863, pp. 166 - 177, http://dx.doi.org/10.1016/j.bbamcr.2015.10.021
,2015, 'NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets', Elife, 4, pp. e06942, http://dx.doi.org/10.7554/eLife.06942
,2015, 'Mig-6 regulates endometrial genes involved in cell cycle and progesterone signaling', Biochemical and Biophysical Research Communications, 462, pp. 409 - 414, http://dx.doi.org/10.1016/j.bbrc.2015.04.146
,2015, 'Renal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signaling', Kidney International, 87, pp. 975 - 983, http://dx.doi.org/10.1038/ki.2014.394
,2015, 'TBX6 null variants and a common hypomorphic allele in congenital scoliosis', New England Journal of Medicine, 372, pp. 341 - 350, http://dx.doi.org/10.1056/NEJMoa1406829
,2015, 'Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects', Human Molecular Genetics, 24, pp. 1234 - 1242, http://dx.doi.org/10.1093/hmg/ddu534
,2014, 'Cited2 is required in trophoblasts for correct placental capillary patterning', Developmental Biology, 392, pp. 62 - 79, http://dx.doi.org/10.1016/j.ydbio.2014.04.023
,2014, 'Gene-environment interaction demonstrates the vulnerability of the embryonic heart', Developmental Biology, 391, pp. 99 - 110, http://dx.doi.org/10.1016/j.ydbio.2014.03.005
,2014, 'Cited2 is required for the maintenance of glycolytic metabolism in adult hematopoietic stem cells', Stem Cells and Development, 23, pp. 83 - 94, http://dx.doi.org/10.1089/scd.2013.0370
,2014, 'Cited2, a transcriptional modulator protein, regulates metabolism in murine embryonic stem cells', Journal of Biological Chemistry, 289, pp. 251 - 263, http://dx.doi.org/10.1074/jbc.M113.497594
,2014, 'Notch4 reveals a novel mechanism regulating Notch signal transduction', Biochimica Et Biophysica Acta Molecular Cell Research, 1843, pp. 1272 - 1284, http://dx.doi.org/10.1016/j.bbamcr.2014.03.015
,2014, 'Targeted Next-Generation Sequencing Identifies Pathogenic Variants in Familial Congenital Heart Disease', Journal of the American College of Cardiology, 64, pp. 2498 - 2506, http://dx.doi.org/10.1016/j.jacc.2014.09.048
,2013, 'Cited2 Is Required For The Maintenance Of Glycolytic Metabolism In Adult Hematopoietic Stem Cells', Blood, 122, pp. 794 - 794, http://dx.doi.org/10.1182/blood.v122.21.794.794
,2013, 'Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus', American Journal of Medical Genetics Part A, 161, pp. 2244 - 2249, http://dx.doi.org/10.1002/ajmg.a.36073
,2013, 'Cited1 Deficiency Suppresses Intestinal Tumorigenesis', Plos Genetics, 9, http://dx.doi.org/10.1371/journal.pgen.1003638
,2013, 'Ways, means and consequences of shaping morphogen gradients', Current Opinion in Genetics and Development, 23, pp. 361 - 362, http://dx.doi.org/10.1016/j.gde.2013.07.005
,2013, 'Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6', Human Molecular Genetics, 22, pp. 1625 - 1631, http://dx.doi.org/10.1093/hmg/ddt012
,2012, 'A mechanism for gene-environment interaction in the etiology of congenital scoliosis', Cell, 149, pp. 295 - 306, http://dx.doi.org/10.1016/j.cell.2012.02.054
,2012, 'Cited2 gene controls pluripotency and cardiomyocyte differentiation of murine embryonic stem cells through Oct4 gene', The Journal of Biological Chemistry, 287, pp. 29088 - 29100, http://dx.doi.org/10.1074/jbc.M112.378034
,2012, 'Deletion of HIF-1 alpha partially rescues the abnormal hyaloid vascular system in Cited2 conditional knockout mouse eyes', Molecular Vision, 18, pp. 1260 - 1270
,2012, 'HIF-1 deletion partially rescues defects of hematopoietic stem cell quiescence caused by Cited2 deficiency', Blood, 119, pp. 2789 - 2798, http://dx.doi.org/10.1182/blood-2011-10-387902
,2011, 'Cited2 Regulates Hematopoietic Stem Cell Quiescence Through HIF-1α Dependent and Independent Pathways', Blood, 118, pp. 912 - 912, http://dx.doi.org/10.1182/blood.v118.21.912.912
,2011, 'Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species', The Journal of Experimental Medicine, 208, pp. i20 - i20, http://dx.doi.org/10.1084/jem2087oia20
,2011, 'A cell autonomous role for the Notch ligand Delta-like 3 in alphabeta T-cell development', Immunology and Cell Biology, 89, pp. 696 - 705, http://dx.doi.org/10.1038/icb.2010.154
,2011, 'Complex SUMO-1 regulation of cardiac transcription factor Nkx2-5', PLoS ONE, 6, pp. e24812 - e24825, http://dx.doi.org/10.1371/journal.pone.0024812
,2011, 'Cooperation between somatic Ikaros and Notch1 mutations at the inception of T-ALL', Leukemia Research, 35, pp. 1512 - 1519, http://dx.doi.org/10.1016/j.leukres.2011.07.024
,2011, 'Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis', Human Molecular Genetics, 20, pp. 1097 - 1110, http://dx.doi.org/10.1093/hmg/ddq554
,2011, 'Notch inhibition by the ligand Delta-like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis', Human Molecular Genetics, 20, pp. 905 - 916, http://dx.doi.org/10.1093/hmg/ddq529
,2011, 'The mouse notches up another success: understanding the causes of human vertebral malformation', Mammalian Genome, 22, pp. 362 - 376, http://dx.doi.org/10.1007/s00335-011-9335-5
,2011, 'Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species', Journal of Cell Biology, 193, pp. 1181 - 1196, http://dx.doi.org/10.1083/jcb.201006114
,2010, 'Gonadal defects in Cited2-mutant mice indicate a role for SF1 in both testis and ovary differentiation', International Journal of Developmental Biology, 54, pp. 683 - 689, http://dx.doi.org/10.1387/ijdb.092920ac
,2009, 'Mutation of the fucose-specific beta 1,3 N-acetylglucosaminyltransferase UNG results in abnormal formation of the spine (Reprinted)', BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1792, pp. 862 - 873, http://dx.doi.org/10.1016/j.bbadis.2008.11.003
,2009, 'Conditional deletion of Cited2 results in defective corneal epithelial morphogenesis and maintenance', Developmental Biology, 334, pp. 243 - 252, http://dx.doi.org/10.1016/j.ydbio.2009.07.028
,2009, 'Cyclical expression of the Notch/Wnt regulator Nrarp requires modulation by Dll3 in somitogenesis', Developmental Biology, 329, pp. 400 - 409, http://dx.doi.org/10.1016/j.ydbio.2009.02.023
,2009, 'Mutation of the fucose-specific beta 1,3 N-acetylglucosaminyltransferase LFNG results in abnormal formation of the spine', Biochimica et Biophysica ACTA - Molecular Basis of Disease, 1792, pp. 100 - 111, http://dx.doi.org/10.1016/j.bbadis.2008.11.003
,2009, 'Placental insufficiency associated with loss of Cited1 causes renal medullary dysplasia', Journal of the American Society of Nephrology, 20, pp. 777 - 786, http://dx.doi.org/10.1681/ASN.2008050547
,2009, 'Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans', Annals of the New York Academy of Sciences, 1151, pp. 38 - 67, http://dx.doi.org/10.1111/j.1749-6632.2008.03452.x
,2009, 'The Role of Hypoxia in Development of the Mammalian Embryo', Developmental Cell, 17, pp. 755 - 773, http://dx.doi.org/10.1016/j.devcel.2009.11.008
,2009, 'The role of Notch in patterning the human vertebral column', Current Opinion in Genetics and Development, 19, pp. 329 - 337, http://dx.doi.org/10.1016/j.gde.2009.06.005
,2008, 'Molecular diagnosis of vertebral segmentation disorders in humans', Expert Opinion on Medical Diagnostics, 2, pp. 1107 - 1121, http://dx.doi.org/10.1517/17530059.2.10.1107
,2008, 'Dll3 and Notchl genetic interactions model axial segmental and craniofacial malformations of human birth defects (Developmental Dynamics 236, (2943-2951))', Developmental Dynamics, 237, pp. 1754, http://dx.doi.org/10.1002/dvdy.21580
,2008, 'BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4', Genes and Development, 22, pp. 3037 - 3049
,2008, 'Cited2 is required for fetal lung maturation', Developmental Biology, 317, pp. 95 - 105, http://dx.doi.org/10.1016/j.ydbio.2008.02.019
,2008, 'Cited2 is required for the proper formation of the hyaloid vasculature and for lens morphogenesis', Development (Cambridge), 135, pp. 2939 - 2948
,2008, 'Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis', Human Molecular Genetics, 17, pp. 3761 - 3766
,2008, 'SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation', Nature Genetics, 40, pp. 663 - 669, http://dx.doi.org/10.1038/ng.142
,2008, 'Spondylocostal dysostosis in a pregnancy complicated by confined placental mosaicism for tetrasomy 9p', American Journal of Medical Genetics Part A, 146A, pp. 1972 - 1976
,2007, 'Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo', The Journal of Experimental Medicine, 204, pp. i20 - i20, http://dx.doi.org/10.1084/jem2048oia20
,2007, 'Abnormal vertebral segmentation and the notch signaling pathway in man', Developmental Dynamics, 236, pp. 1456 - 1474
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