Rolf W. Stottmann, Ph.D.

Affiliations: 
1998-2004 Cell Biology Duke Medical School, Durham, NC, United States 
 2004-2001 Pediatrics Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States 
 2011- Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States 
Area:
cortical and craniofacial development, genetics
Website:
http://www.cincinnatichildrens.org/research/divisions/h/genetics/labs/stottmann/default/
Google:
"Rolf Stottmann"
Mean distance: 18.54 (cluster 32)
 
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Publications

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Abdelhamed Z, Lukacs M, Cindric S, et al. (2021) Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice. Disease Models & Mechanisms. 14
Abdelhamed Z, Lukacs M, Cindric S, et al. (2020) A novel hypomorphic allele of causes primary ciliary dyskinesia phenotypes in mice. Disease Models & Mechanisms
Lukacs M, Blizzard LE, Stottmann RW. (2020) CNS Glycosylphosphatidylinositol Deficiency Results in Delayed White Matter Development, Ataxia, and Premature Death in a Novel Mouse Model. Human Molecular Genetics
DiStasio A, Paulding D, Chaturvedi P, et al. (2019) Nubp2 is required for cranial neural crest survival in the mouse. Developmental Biology
Snedeker J, Gibbons WJ, Paulding DF, et al. (2019) Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants. Plos Genetics. 15: e1008467
Bittermann E, Abdelhamed Z, Liegel RP, et al. (2019) Differential requirements of tubulin genes in mammalian forebrain development. Plos Genetics. 15: e1008243
Lukacs M, Roberts T, Chatuverdi P, et al. (2019) Glycosylphosphatidylinositol biosynthesis and remodeling are required for neural tube closure, heart development, and cranial neural crest cell survival. Elife. 8
Lukacs M, Gilley J, Zhu Y, et al. (2019) Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence. Experimental Neurology. 112961
Liegel RP, Finnerty E, Ward L, et al. (2018) Using human sequencing to guide craniofacial research. Genesis (New York, N.Y. : 2000)
Abdelhamed Z, Vuong SM, Hill L, et al. (2018) A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development (Cambridge, England). 145
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