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Marshall Lukacs - Publications

Affiliations: 
Cincinnati Children's Hospital Medical Center, University of Cincinnati 
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Abdelhamed Z, Lukacs M, Cindric S, Ali S, Omran H, Stottmann RW. Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice. Disease Models & Mechanisms. 14. PMID 34115122 DOI: 10.1242/dmm.048645  0.642
2021 Abdelhamed Z, Lukacs M, Cindric S, Ali S, Omran H, Stottmann RW. Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice Disease Models & Mechanisms. 14: dmm048645. DOI: 10.1242/dmm.048645  0.682
2020 Abdelhamed Z, Lukacs M, Cindric S, Omran H, Stottmann RW. A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice. Disease Models & Mechanisms. PMID 34005086 DOI: 10.1242/dmm.045344  0.546
2020 Abdelhamed Z, Lukacs M, Cindric S, Omran H, Stottmann RW. A novel hypomorphic allele of causes primary ciliary dyskinesia phenotypes in mice. Disease Models & Mechanisms. PMID 32988999 DOI: 10.1242/Dmm.045344  0.675
2020 Lukacs M, Blizzard LE, Stottmann RW. CNS Glycosylphosphatidylinositol Deficiency Results in Delayed White Matter Development, Ataxia, and Premature Death in a Novel Mouse Model. Human Molecular Genetics. PMID 32179897 DOI: 10.1093/Hmg/Ddaa046  0.649
2019 Lukacs M, Roberts T, Chatuverdi P, Stottmann RW. Glycosylphosphatidylinositol biosynthesis and remodeling are required for neural tube closure, heart development, and cranial neural crest cell survival. Elife. 8. PMID 31232685 DOI: 10.7554/Elife.45248  0.641
2019 Lukacs M, Gilley J, Zhu Y, Orsomando G, Angeletti C, Liu J, Yang X, Park J, Hopkin RJ, Coleman MP, Zhai RG, Stottmann RW. Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence. Experimental Neurology. 112961. PMID 31136762 DOI: 10.1016/J.Expneurol.2019.112961  0.617
2016 Gelineau-Morel R, Lukacs M, Weaver KN, Hufnagel RB, Gilbert DL, Stottmann RW. Congenital Cataracts and Gut Dysmotility in a DYNC1H1 Dyneinopathy Patient. Genes. 7. PMID 27754416 DOI: 10.3390/Genes7100085  0.612
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