| WNT5A mutations in patients with autosomal dominant Robinow syndrome AD Person, S Beiraghi, CM Sieben, S Hermanson, AN Neumann, ... Developmental Dynamics 239 (1), 327-337, 2009 | 278 | 2009 |
| Bone morphogenic protein 2 directly enhances differentiation of murine osteoclast precursors ED Jensen, L Pham, CJ Billington Jr, K Espe, AE Carlson, JJ Westendorf, ... Journal of cellular biochemistry 109 (4), 672-682, 2010 | 161 | 2010 |
| Drosophila target of rapamycin kinase functions as a multimer Y Zhang, CJ Billington Jr, D Pan, TP Neufeld Genetics 172 (1), 355-362, 2006 | 101 | 2006 |
| Twisted gastrulation limits apoptosis in the distal region of the mandibular arch in mice BA MacKenzie, R Wolff, N Lowe, CJ Billington Jr, A Peterson, B Schmidt, ... Developmental biology 328 (1), 13-23, 2009 | 41 | 2009 |
| Hypoxia induces cardiac malformations via A1 adenosine receptor activation in chicken embryos SK Ghatpande, CJ Billington Jr, SA Rivkees, CC Wendler Birth Defects Research Part A: Clinical and Molecular Teratology 82 (3), 121-130, 2008 | 26 | 2008 |
| A case of VEXAS syndrome associated with EBV-associated hemophagocytic lymphohistiocytosis RL Kao, AA Jacobsen, CJ Billington Jr, SL Yohe, AK Beckman, ... Blood Cells, Molecules, and Diseases 93, 102636, 2022 | 20 | 2022 |
| Impact of retinoic acid exposure on midfacial shape variation and manifestation of holoprosencephaly in Twsg1 mutant mice CJ Billington Jr, B Schmidt, RS Marcucio, B Hallgrimsson, ... Disease models & mechanisms 8 (2), 139-146, 2015 | 20 | 2015 |
| Whole exome sequencing in patients with Williams–Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk PCR Parrish, D Liu, RH Knutsen, CJ Billington Jr, RP Mecham, YP Fu, ... Human molecular genetics 29 (12), 2035-2050, 2020 | 19 | 2020 |
| Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams–Beuren syndrome M Lugo, ZC Wong, CJ Billington Jr, PCR Parrish, G Muldoon, D Liu, ... American journal of medical genetics Part A 182 (5), 1008-1020, 2020 | 19 | 2020 |
| Glycosylation of twisted gastrulation is required for BMP binding and activity during craniofacial development CJ Billington Jr, JE Fiebig, CL Forsman, L Pham, N Burbach, M Sun, ... Frontiers in Physiology 2, 59, 2011 | 19 | 2011 |
| The molecular and cellular basis of variable craniofacial phenotypes and their genetic rescue in< i> Twisted gastrulation</i> mutant mice CJ Billington, B Ng, C Forsman, B Schmidt, A Bagchi, DE Symer, ... Developmental biology 355 (1), 21-31, 2011 | 16 | 2011 |
| Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency M Davids, M Menezes, Y Guo, SD McLean, H Hakonarson, F Collins, ... Molecular genetics and metabolism 130 (1), 49-57, 2020 | 15 | 2020 |
| The function of twisted gastrulation in regulating osteoclast differentiation is dependent on BMP binding R Huntley, J Davydova, A Petryk, CJ Billington Jr, ED Jensen, KC Mansky, ... Journal of cellular biochemistry 116 (10), 2239-2246, 2015 | 15 | 2015 |
| Maternal diet supplementation with methyl donors and increased parity affect the incidence of craniofacial defects in the offspring of twisted gastrulation mutant mice CJ Billington Jr, B Schmidt, L Zhang, JS Hodges, MK Georgieff, G Schotta, ... The Journal of nutrition 143 (3), 332-339, 2013 | 14 | 2013 |
| Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders N Di Donato, R Guerrini, CJ Billington Jr, AJ Barkovich, P Dinkel, E Freri, ... Brain 145 (9), 3274-3287, 2022 | 13 | 2022 |
| Use of dexamethasone in idiopathic, acute pediatric rhabdomyolysis ML Summerlin, DS Regier, JL Fraser, KA Chapman, D Kafashzadeh, ... American Journal of Medical Genetics Part A 185 (2), 500-507, 2021 | 6 | 2021 |
| Frequency of QTc interval prolongation in children and adults with Williams syndrome BD Brink, R Feinn, BA Kozel, CJ Billington Jr, D Liu, E Yu, S Sindhar, J He, ... Pediatric Cardiology 43 (7), 1559-1567, 2022 | 5 | 2022 |
| Copper-binding domain variation in a novel murine lysyl oxidase model produces structurally inferior aortic elastic fibers whose failure is modified by age, sex, and blood pressure KM Tsang, RH Knutsen, CJ Billington Jr, E Lindberg, H Steenbock, YP Fu, ... International journal of molecular sciences 23 (12), 6749, 2022 | 4 | 2022 |
| Rare presentation of FDX2‐related disorder and untargeted global metabolomics findings A Aggarwal, NR Pillai, CJ Billington Jr, L Schema, SA Berry American Journal of Medical Genetics Part A 188 (4), 1239-1244, 2022 | 4 | 2022 |
| Genomic and biochemical analysis of repeatedly observed variants in DBT in individuals with maple syrup urine disease of Central American ancestry CJ Billington Jr, KA Chapman, E Leon, BW Meltzer, SI Berger, M Olson, ... American Journal of Medical Genetics Part A 188 (9), 2738-2749, 2022 | 3 | 2022 |
