Divergent connectivity of homologous command-like neurons mediates segment-specific touch responses in Drosophila S Takagi, BT Cocanougher, S Niki, D Miyamoto, H Kohsaka, H Kazama, ... Neuron 96 (6), 1373-1387. e6, 2017 | 75 | 2017 |
Circuits for integrating learned and innate valences in the insect brain C Eschbach, A Fushiki, M Winding, B Afonso, IV Andrade, ... Elife 10, e62567, 2021 | 50* | 2021 |
Facilitating Neuron-Specific Genetic Manipulations in Drosophila melanogaster Using a Split GAL4 Repressor MJ Dolan, H Luan, WC Shropshire, B Sutcliffe, B Cocanougher, RL Scott, ... Genetics 206 (2), 775-784, 2017 | 46 | 2017 |
Hidden concepts in the history and philosophy of origins-of-life studies: A workshop report C Mariscal, A Barahona, N Aubert-Kato, AU Aydinoglu, S Bartlett, ... Origins of Life and Evolution of Biospheres 49, 111-145, 2019 | 32 | 2019 |
A single-cell transcriptomic atlas of complete insect nervous systems across multiple life stages M Corrales, BT Cocanougher, AB Kohn, JD Wittenbach, XS Long, ... Neural Development 17 (1), 8, 2022 | 28 | 2022 |
Semiparametric spectral modeling of the Drosophila connectome CE Priebe, Y Park, M Tang, A Athreya, V Lyzinski, JT Vogelstein, Y Qin, ... arXiv preprint arXiv:1705.03297, 2017 | 28 | 2017 |
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 | 24 | 2023 |
Adult MTM1-related myopathy carriers: Classification based on deep phenotyping BT Cocanougher, L Flynn, P Yun, M Jain, M Waite, R Vasavada, ... Neurology 93 (16), e1535-e1542, 2019 | 22 | 2019 |
Increasing proportions of tyrosine hydroxylase-immunoreactive interneurons colocalize with choline acetyltransferase or vasoactive intestinal peptide in the developing rat … SE Asmus, BT Cocanougher, DL Allen, JB Boone, EA Brooks, ... Brain research 1383, 108-119, 2011 | 17 | 2011 |
Comparative single-cell transcriptomics of complete insect nervous systems BT Cocanougher, JD Wittenbach, XS Long, AB Kohn, TP Norekian, J Yan, ... BioRxiv, 785931, 2019 | 15 | 2019 |
Single cell RNA-seq analysis reveals temporally-regulated and quiescence-regulated gene expression in Drosophila larval neuroblasts N Dillon, B Cocanougher, C Sood, X Yuan, AB Kohn, LL Moroz, ... Neural Development 17 (1), 7, 2022 | 12 | 2022 |
MuscleViz: free open-source software for muscle weakness visualization JD Wittenbach, BT Cocanougher, P Yun, AR Foley, CG Bönnemann Journal of Neuromuscular Diseases 6 (2), 263-266, 2019 | 5 | 2019 |
Rapid whole genome sequencing in critically ill neonates enables precision medicine pipeline M Beaman, K Fisher, M McDonald, QKG Tan, D Jackson, ... Journal of Personalized Medicine 12 (11), 1924, 2022 | 4 | 2022 |
Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease B Cocanougher, U Aypar, A McDonald, L Hasadsri, MJ Bennett, ... Molecular Genetics and Metabolism Reports 2, 61-64, 2015 | 3 | 2015 |
Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemia B Cocanougher, U Aypar, A McDonald, L Hasadsri, MJ Bennett, ... Data in Brief 3, 34-39, 2015 | 2 | 2015 |
The severity of MUSK pathogenic variants is predicted by the protein domain they disrupt BT Cocanougher, SW Liu, L Francescatto, A Behura, M Anneling, ... Human Genetics and Genomics Advances 5 (3), 2024 | | 2024 |
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals DE Layo-Carris, EE Lubin, AK Sangree, KJ Clark, EL Durham, ... European Journal of Human Genetics, 1-10, 2024 | | 2024 |
Co-existing genetic disorders in Pompe disease: Exome analysis of a large Pompe disease cohort identifies disease-modifying cryptic dual diagnoses B Cocanougher, L Francescatto, E Huggins, SH Jung, PS Kishnani Molecular Genetics and Metabolism 141 (4), 108214, 2024 | | 2024 |
The recurrent deep intronic pseudoexon-inducing variant COL6A1 c. 930+ 189C> T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial … AR Foley, V Bolduc, F Guirguis, S Donkervoort, Y Hu, R Orbach, ... medRxiv, 2024 | | 2024 |
Statistical signature of subtle behavioural changes in large-scale behavioural assays A Blanc, F Laurent, A Barbier--Chebbah, BT Cocanougher, BMW Jones, ... bioRxiv, 2024.05. 03.591825, 2024 | | 2024 |