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Ryan P. Liegel, Ph.D. - Publications

Affiliations: 
2013 Cell Biology, Neurobiology, and Anatomy Medical College of Wisconsin, Milwaukee, WI, United States 
Area:
Genetics, Cell Biology, Molecular Biology
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9 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
2023 Liegel RP, Michalski MN, Vaidya S, Bittermann E, Finnerty E, Menke CA, Diegel CR, Zhong ZA, Williams BO, Stottmann RW. Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformations. Development (Cambridge, England). 150. PMID 36789910 DOI: 10.1242/dev.201038  0.684
2019 Bittermann E, Abdelhamed Z, Liegel RP, Menke C, Timms A, Beier DR, Stottmann RW. Differential requirements of tubulin genes in mammalian forebrain development. Plos Genetics. 15: e1008243. PMID 31386652 DOI: 10.1371/Journal.Pgen.1008243  0.653
2018 Liegel RP, Finnerty E, Ward L, DiStasio A, Hufnagel RB, Saal HM, Sund KL, Prows CA, Stottmann R. Using human sequencing to guide craniofacial research. Genesis (New York, N.Y. : 2000). PMID 30375152 DOI: 10.1002/Dvg.23259  0.742
2014 Park AK, Liegel RP, Ronchetti A, Ebert AD, Geurts A, Sidjanin DJ. Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice. Bmc Genetics. 15: 135. PMID 25476608 DOI: 10.1186/S12863-014-0135-2  0.805
2014 Liegel RP, Ronchetti A, Sidjanin DJ. Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome. Molecular Genetics and Metabolism Reports. 1: 299-311. PMID 25197626 DOI: 10.1016/J.Ymgmr.2014.06.003  0.771
2013 Liegel RP, Handley MT, Ronchetti A, Brown S, Langemeyer L, Linford A, Chang B, Morris-Rosendahl DJ, Carpanini S, Posmyk R, Harthill V, Sheridan E, Abdel-Salam GM, Terhal PA, Faravelli F, et al. Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans. American Journal of Human Genetics. 93: 1001-14. PMID 24239381 DOI: 10.1016/J.Ajhg.2013.10.011  0.793
2011 Liang L, Liegel R, Endres B, Ronchetti A, Chang B, Sidjanin DJ. Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice. Molecular Vision. 17: 3062-71. PMID 22162625  0.727
2011 Liegel R, Chang B, Dubielzig R, Sidjanin DJ. Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice. Molecular Genetics and Metabolism. 103: 51-9. PMID 21353609 DOI: 10.1016/J.Ymgme.2011.02.002  0.791
2010 Hassemer EL, Le Gall SM, Liegel R, McNally M, Chang B, Zeiss CJ, Dubielzig RD, Horiuchi K, Kimura T, Okada Y, Blobel CP, Sidjanin DJ. The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17. Genetics. 185: 245-55. PMID 20194968 DOI: 10.1534/Genetics.109.113167  0.711
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