| Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice EA Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, ... Nature 410 (6824), 97-101, 2001 | 1113 | 2001 |
| Timing of surgery following SARS‐CoV‐2 infection: an international prospective cohort study H Gacaferi, GS Collaborative, COVIDSurg Collaborative Anaesthesia 76 (6), 2021 | 534* | 2021 |
| Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus PJ Scambler, D Kelly, E Lindsay, R Williamson, R Goldberg, R Shprintzen, ... The Lancet 339 (8802), 1138-1139, 1992 | 506 | 1992 |
| Congenital heart disease in mice deficient for the DiGeorge syndrome region EA Lindsay, A Botta, V Jurecic, S Carattini-Rivera, YC Cheah, ... Nature 401 (6751), 379-383, 1999 | 472 | 1999 |
| Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract H Xu, M Morishima, JN Wylie, RJ Schwartz, BG Bruneau, EA Lindsay, ... Oxford University Press for The Company of Biologists Limited 131 (13), 3217 …, 2004 | 428 | 2004 |
| Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways F Vitelli, M Morishima, I Taddei, EA Lindsay, A Baldini Human molecular genetics 11 (8), 915-922, 2002 | 381 | 2002 |
| Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome R Paylor, B Glaser, A Mupo, P Ataliotis, C Spencer, A Sobotka, C Sparks, ... Proceedings of the National Academy of Sciences 103 (20), 7729-7734, 2006 | 342 | 2006 |
| Chromosomal microdeletions: dissecting del22q11 syndrome EA Lindsay Nature Reviews Genetics 2 (11), 858-868, 2001 | 322 | 2001 |
| A genetic link between Tbx1 and fibroblast growth factor signaling F Vitelli, I Taddei, M Morishima, EN Meyers, EA Lindsay, A Baldini Oxford University Press for The Company of Biologists Limited 129 (19), 4605 …, 2002 | 321 | 2002 |
| Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11 D Kelly, R Goldberg, D Wilson, E Lindsay, A Carey, J Goodship, J Burn, ... American journal of medical genetics 45 (3), 308-312, 1993 | 195 | 1993 |
| Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments R Paylor, KL McIlwain, R McAninch, A Nellis, LA Yuva-Paylor, A Baldini, ... Human molecular genetics 10 (23), 2645-2650, 2001 | 166 | 2001 |
| Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease S Halford, R Wadey, C Roberts, SCM Daw, JA Whiting, H O'Donnell, ... Human molecular genetics 2 (12), 2099-2107, 1993 | 166 | 1993 |
| Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice V Randall, K McCue, C Roberts, V Kyriakopoulou, S Beddow, AN Barrett, ... The Journal of clinical investigation 119 (11), 3301-3310, 2009 | 162 | 2009 |
| Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions EA Lindsay, R Goldberg, V Jurecic, B Morrow, C Carlson, ... American journal of medical genetics 57 (3), 514-522, 1995 | 158 | 1995 |
| TBX1 is required for inner ear morphogenesis F Vitelli, A Viola, M Morishima, T Pramparo, A Baldini, E Lindsay Human molecular genetics 12 (16), 2041-2048, 2003 | 148 | 2003 |
| Submicroscopic deletions at 22q11. 2: variability of the clinical picture and delineation of a commonly deleted region EA Lindsay, F Greenberg, LG Shaffer, SK Shapira, PJ Scambler, A Baldini American journal of medical genetics 56 (2), 191-197, 1995 | 146 | 1995 |
| Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm A Calmont, S Ivins, KL Van Bueren, I Papangeli, V Kyriakopoulou, ... Development 136 (18), 3173-3183, 2009 | 145 | 2009 |
| Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development Z Zhang, F Cerrato, H Xu, F Vitelli, M Morishima, J Vincentz, Y Furuta, ... Oxford University Press for The Company of Biologists Limited 132 (23), 5307 …, 2005 | 143 | 2005 |
| Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes I Taddei, M Morishima, T Huynh, EA Lindsay Proceedings of the National Academy of Sciences 98 (20), 11428-11431, 2001 | 127 | 2001 |
| A genetic etiology for interruption of the aortic arch type B MB Lewin, EA Lindsay, V Jurecic, V Goytia, JA Towbin, A Baldini The American journal of cardiology 80 (4), 493-497, 1997 | 127 | 1997 |
