| Loss of δ-catenin function in severe autism TN Turner, K Sharma, EC Oh, YP Liu, RL Collins, MX Sosa, DR Auer, ... Nature 520 (7545), 51-56, 2015 | 166 | 2015 |
| Enhancer variants synergistically drive dysfunction of a gene regulatory network in Hirschsprung disease S Chatterjee, A Kapoor, JA Akiyama, DR Auer, D Lee, S Gabriel, ... Cell 167 (2), 355-368. e10, 2016 | 116 | 2016 |
| Gene-and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease S Chatterjee, P Nandakumar, DR Auer, SB Gabriel, A Chakravarti Proceedings of the National Academy of Sciences 116 (52), 26697-26708, 2019 | 18 | 2019 |
| State MW, Talkowski ME, Cook E., Huganir R., Katsanis N., Chakravarti A. Loss of δ-catenin function in severe autism TN Turner, K Sharma, EC Oh, YP Liu, RL Collins, MX Sosa, DR Auer, ... Nature 520 (7545), 51-56, 2015 | 18 | 2015 |
| Human genome meeting 2016: houston, TX, USA. 28 February-2 March 2016 AK Srivastava, Y Wang, R Huang, C Skinner, T Thompson, L Pollard, ... Human genomics 10, 1-40, 2016 | 17 | 2016 |
| Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system development A Kapoor, DR Auer, D Lee, S Chatterjee, A Chakravarti Human molecular genetics 26 (10), 1811-1820, 2017 | 6 | 2017 |
| Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects A Kapoor, P Nandakumar, DR Auer, MX Sosa, H Ross, J Bollinger, J Yan, ... Journal of pediatric surgery 56 (12), 2286-2294, 2021 | 5 | 2021 |
| Generation of a cre recombinase-conditional Nos1ap over-expression transgenic mouse DR Auer, P Sysa-Shah, D Bedja, JL Simmers, E Pak, A Dutra, R Cohn, ... Biotechnology letters 36, 1179-1185, 2014 | 4 | 2014 |
| Ret deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development E Vincent, S Chatterjee, GH Cannon, D Auer, H Ross, A Chakravarti, ... Proceedings of the National Academy of Sciences 120 (34), e2211986120, 2023 | 3 | 2023 |
| Ret loss-of-function decreases neural crest progenitor proliferation and restricts developmental fate potential during enteric nervous system development E Vincent, S Chatterjee, GH Cannon, D Auer, H Ross, A Chakravarti, ... bioRxiv, 2021.12. 28.474390, 2021 | 1 | 2021 |
| Multiple, independent, common variants overlapping known and putative gut enhancers at RET, SEMA3 and NRG1 underlie Hirschsprung disease risk in … A Kapoor, P Nandakumar, DR Auer, MX Sosa, H Ross, J Bollinger, J Yan, ... bioRxiv, 2020.06. 07.138719, 2020 | 1 | 2020 |
| Cardiac muscle–restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features A Smith, D Auer, M Johnson, E Sanchez, H Ross, C Ward, A Chakravarti, ... G3: Genes, Genomes, Genetics 13 (11), jkad208, 2023 | | 2023 |
| Cardiac muscle-restricted partial loss of Nos1ap expression has limited impact on electro- and echo-cardiographic features A Smith, D Auer, M Johnson, E Sanchez, H Ross, C Ward, A Chakravarti, ... bioRxiv, 2022.09. 27.509782, 2022 | | 2022 |
| The gastrointestinal development ‘parts list’: transcript profiling of embryonic gut development in wildtype and Ret-deficient mice S Chatterjee, P Nandakumar, DR Auer, SB Gabriel, A Chakravarti bioRxiv, 730010, 2019 | | 2019 |
| Multiple enhancer variants disrupt gene regulatory network in Hirschsprung disease S Chatterjee, A Kapoor, J Akiyama, D Auer, C Berrios, L Pennacchio, ... HUMAN GENOMICS 10, 2016 | | 2016 |
| Loss of δ-catenin function in severe autism S Sanders, TN Turner, K Sharma, EC Oh, YP Liu, RL Collins, MX Sosa, ... | | 2015 |
