| HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle MA Deardorff, M Bando, R Nakato, E Watrin, T Itoh, M Minamino, K Saitoh, ... Nature 489 (7415), 313-317, 2012 | 641 | 2012 |
| RAD21 mutations cause a human cohesinopathy MA Deardorff, JJ Wilde, M Albrecht, E Dickinson, S Tennstedt, ... The American Journal of Human Genetics 90 (6), 1014-1027, 2012 | 320 | 2012 |
| Genetic, epigenetic, and environmental contributions to neural tube closure JJ Wilde, JR Petersen, L Niswander Annual review of genetics 48, 583-611, 2014 | 239 | 2014 |
| Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked … FJ Kaiser, M Ansari, D Braunholz, M Concepción Gil-Rodríguez, ... Human molecular genetics 23 (11), 2888-2900, 2014 | 177 | 2014 |
| Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size JF Chen, Y Zhang, J Wilde, KC Hansen, F Lai, L Niswander Nature communications 5 (1), 3885, 2014 | 165 | 2014 |
| Scribble is required for normal epithelial cell–cell contacts and lumen morphogenesis in the mammalian lung LL Yates, C Schnatwinkel, L Hazelwood, L Chessum, A Paudyal, H Hilton, ... Developmental biology 373 (2), 267-280, 2013 | 95 | 2013 |
| Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repair JJ Wilde, T Aida, RCH Del Rosario, T Kaiser, P Qi, M Wienisch, Q Zhang, ... Cell 184 (12), 3267-3280. e18, 2021 | 47 | 2021 |
| X-linked bulbo-spinal neuronopathy: a family study of three patients. J Wilde, T Moss, D Thrush Journal of Neurology, Neurosurgery & Psychiatry 50 (3), 279-284, 1987 | 47 | 1987 |
| Prime editing primarily induces undesired outcomes in mice T Aida, JJ Wilde, L Yang, Y Hou, M Li, D Xu, J Lin, P Qi, Z Lu, G Feng BioRxiv, 2020.08. 06.239723, 2020 | 36 | 2020 |
| Diencephalic size is restricted by a novel interplay between GCN5 acetyltransferase activity and retinoic acid signaling JJ Wilde, JA Siegenthaler, SYR Dent, LA Niswander Journal of Neuroscience 37 (10), 2565-2579, 2017 | 21 | 2017 |
| Efficient zygotic genome editing via RAD51-enhanced interhomolog repair JJ Wilde, T Aida, M Wienisch, Q Zhang, P Qi, G Feng BioRxiv, 263699, 2018 | 14 | 2018 |
| Potassium dependent rescue of a myopathy with core-like structures in mouse MG Hanson, JJ Wilde, RL Moreno, AD Minic, L Niswander Elife 4, e02923, 2015 | 9 | 2015 |
| Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms M Kaur, J Blair, B Devkota, S Fortunato, D Clark, A Lawrence, J Kim, W Do, ... American Journal of Medical Genetics Part A 191 (8), 2113-2131, 2023 | 8 | 2023 |
| Circuit-specific gene therapy reverses core symptoms in a primate Parkinson’s disease model Y Chen, Z Hong, J Wang, K Liu, J Liu, J Lin, S Feng, T Zhang, L Shan, ... Cell 186 (24), 5394-5410. e18, 2023 | 7 | 2023 |
| Mixed Phenotype of Langer–Giedion's and Cornelia de Lange's Syndromes in an 8q23. 3-q24. 1 Microdeletion without TRPS1 Deletion A Herrero-García, P Marín-Reina, G Cabezuelo-Huerta, ... Journal of Pediatric Genetics 9 (01), 053-057, 2020 | 3 | 2020 |
| Enhancement of mediodorsal thalamus rescues aberrant belief dynamics in a mouse model with schizophrenia-associated mutation T Zhou, YY Ho, RX Lee, AB Fath, K He, J Scott, N Bajwa, ND Hartley, ... bioRxiv, 2024 | 1 | 2024 |
| Methods of enhancing chromosomal homologous recombination G Feng, J Wilde, A Tomomi, M Wienisch, Q Zhang US Patent 11,643,670, 2023 | 1 | 2023 |
| Enhancement of mediodorsal thalamus rescues aberrant belief dynamics in a mouse model with schizophrenia-associated mutation T Zhou, YY Ho, RX Lee, AB Fath, K He, J Scott, N Bajwa, ND Hartley, ... bioRxiv: the preprint server for biology, 2024 | | 2024 |
| STAG2 MUTATIONS CAUSE A VARIABLE SYNDROMIC X-LINKED INTELLECTUAL DISABILITY MA Deardorff, AN Redding, J Bradley, ID Krantz, JJ Wilde AMERICAN JOURNAL OF MEDICAL GENETICS PART A 182 (4), 900-900, 2020 | | 2020 |
| Identification of Novel Roles of the Acetyltransferase GCN5 in Forebrain Development and Function JJ Wilde University of Colorado, 2016 | | 2016 |
