DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 LA Jerome, VE Papaioannou Nature genetics 27 (3), 286-291, 2001 | 1250 | 2001 |
Mammary gland, limb and yolk sac defects in mice lacking Tbx3,the gene mutated in human ulnar mammary syndrome TG Davenport, LA Jerome-Majewska, VE Papaioannou Oxford University Press for The Company of Biologists Limited 130 (10), 2263 …, 2003 | 370 | 2003 |
The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis RG Kelly, LA Jerome-Majewska, VE Papaioannou Human molecular genetics 13 (22), 2829-2840, 2004 | 270 | 2004 |
High intake of folic acid disrupts embryonic development in mice L Pickell, K Brown, D Li, XL Wang, L Deng, Q Wu, J Selhub, L Luo, ... Birth Defects Research Part A: Clinical and Molecular Teratology 91 (1), 8-19, 2011 | 140 | 2011 |
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11. 2DS DM McDonald-McGinn, S Fahiminiya, T Revil, BA Nowakowska, J Suhl, ... Journal of medical genetics 50 (2), 80-90, 2013 | 127 | 2013 |
Tbx3, the ulnar‐mammary syndrome gene, and Tbx2 interact in mammary gland development through a p19Arf/p53‐independent pathway LA Jerome‐Majewska, GP Jenkins, E Ernstoff, F Zindy, CJ Sherr, ... Developmental dynamics: an official publication of the American Association …, 2005 | 114 | 2005 |
Alternative splicing is frequent during early embryonic development in mouse T Revil, D Gaffney, C Dias, J Majewski, LA Jerome-Majewska BMC genomics 11, 1-17, 2010 | 103 | 2010 |
Barriers to horizontal cell transformation by extracellular vesicles containing oncogenic H-ras TH Lee, S Chennakrishnaiah, B Meehan, L Montermini, D Garnier, ... Oncotarget 7 (32), 51991, 2016 | 102 | 2016 |
Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation CB Gurumurthy, AR O’brien, RM Quadros, J Adams, P Alcaide, S Ayabe, ... Genome biology 20 (1), 1-14, 2019 | 88 | 2019 |
The trafficking protein Tmed2/p24β1 is required for morphogenesis of the mouse embryo and placenta LA Jerome-Majewska, T Achkar, L Luo, F Lupu, E Lacy Developmental biology 341 (1), 154-166, 2010 | 82 | 2010 |
Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development F Moraes, A Nóvoa, LA Jerome-Majewska, VE Papaioannou, M Mallo Mechanisms of development 122 (2), 199-212, 2005 | 80 | 2005 |
Methylenetetrahydrofolate reductase deficiency and low dietary folate increase embryonic delay and placental abnormalities in mice L Pickell, D Li, K Brown, LG Mikael, XL Wang, Q Wu, L Luo, ... Birth Defects Research Part A: Clinical and Molecular Teratology 85 (6), 531-541, 2009 | 79 | 2009 |
Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome N Anastasio, T Ben-Omran, A Teebi, KCH Ha, E Lalonde, R Ali, ... The American Journal of Human Genetics 87 (4), 553-559, 2010 | 74 | 2010 |
Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro–costo–mandibular syndrome DC Lynch, T Revil, J Schwartzentruber, EJ Bhoj, AM Innes, RE Lamont, ... Nature communications 5 (1), 4483, 2014 | 73 | 2014 |
Control of anterior GR adient 2 (AGR 2) dimerization links endoplasmic reticulum proteostasis to inflammation M Maurel, J Obacz, T Avril, YP Ding, O Papadodima, X Treton, F Daniel, ... EMBO molecular medicine 11 (6), e10120, 2019 | 65 | 2019 |
Transmembrane emp24 domain proteins in development and disease. R Aber, W Chan, S Mugisha, LA Jerome-Majewska Genetics Research 101, e14, 2019 | 58 | 2019 |
Aortic arch and pharyngeal phenotype in the absence of BMP-dependent neural crest in the mouse S Ohnemus, B Kanzler, LA Jerome-Majewska, VE Papaioannou, ... Mechanisms of development 119 (2), 127-135, 2002 | 57 | 2002 |
A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development KE Christensen, L Deng, KY Leung, E Arning, T Bottiglieri, OV Malysheva, ... Human molecular genetics 22 (18), 3705-3719, 2013 | 51 | 2013 |
Spliceosomopathies and neurocristopathies: Two sides of the same coin? MC Beauchamp, SS Alam, S Kumar, LA Jerome‐Majewska Developmental Dynamics 249 (8), 924-945, 2020 | 49 | 2020 |
Single substitution in H3. 3G34 alters DNMT3A recruitment to cause progressive neurodegeneration S Khazaei, CCL Chen, AF Andrade, N Kabir, P Azarafshar, SM Morcos, ... Cell 186 (6), 1162-1178. e20, 2023 | 38 | 2023 |