Michael Ludwig
Affiliations: | University of Chicago, Chicago, IL |
Area:
evolution of developmentGoogle:
"Michael Ludwig"Cross-listing: FlyTree
Collaborators
Sign in to add collaborator| Kevin P. White | collaborator | Chicago (FlyTree) | |
| Casey Bergman | collaborator | 1996-2001 | Chicago |
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Publications
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| Rieke JM, Zhang R, Braun D, et al. (2020) Is Involved in Urinary Tract and Urorectal Development. Frontiers in Cell and Developmental Biology. 8: 567 |
| Zhang R, Gehlen J, Kawalia A, et al. (2020) Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. Plos One. 15: e0234246 |
| Sharma A, Liu H, Tobar-Tosse F, et al. (2020) Ubiquitin Carboxyl-Terminal Hydrolases (UCHs): Potential Mediators for Cancer and Neurodegeneration. International Journal of Molecular Sciences. 21 |
| Güngör T, Eroğlu FK, Yazılıtaş F, et al. (2020) A case of Type 1 Dent disease presenting with isolated persistent proteinuria. Turk Pediatri Arsivi. 55: 72-75 |
| Sharma A, Biswas A, Liu H, et al. (2019) Mutational Landscape of the BAP1 Locus Reveals an Intrinsic Control to Regulate the miRNA Network and the Binding of Protein Complexes in Uveal Melanoma. Cancers. 11 |
| van de Putte R, Wijers CHW, Reutter H, et al. (2019) Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations. Plos One. 14: e0217477 |
| Kolvenbach CM, Dworschak GC, Frese S, et al. (2019) Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. American Journal of Human Genetics. 104: 994-1006 |
| Kause F, Zhang R, Ludwig M, et al. (2019) HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Research |
| Sharma A, Dakal TC, Ludwig M, et al. (2018) Towards a Central Role of in the Bladder Exstrophy⁻Epispadias Complex (BEEC): Computational Characterization of Genetic Variants and Structural Modelling. Genes. 9 |
| Weitensteiner V, Zhang R, Bungenberg J, et al. (2018) Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth Defects Research |