Medical College of Wisconsin
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Danielle Sidjanin Maier PhD

APP Inpatient 2

Institution: Medical College of Wisconsin
Department: Medicine
Division: General Internal Medicine
Program: Hospitalist

Member of the Neuroscience Research Center

Publications (32)

  • TBC1D20 mediates autophagy as a key regulator of autophagosome maturation. (Sidjanin DJ, Park AK, Ronchetti A, Martins J, Jackson WT) Autophagy 2016 Oct 02;12(10):1759-1775 PMID: 27487390 PMCID: PMC5079675 SCOPUS ID: 2-s2.0-84980378961 08/04/2016       66 Citations
  • A Disintegrin and Metalloproteinase10 (ADAM10) Regulates NOTCH Signaling during Early Retinal Development. (Toonen JA, Ronchetti A, Sidjanin DJ) PLoS One 2016;11(5):e0156184 PMID: 27224017 PMCID: PMC4880208 SCOPUS ID: 2-s2.0-84971422194 05/26/2016       17 Citations
  • Type I Interferon Counteracts Antiviral Effects of Statins in the Context of Gammaherpesvirus Infection. (Lange PT, Darrah EJ, Vonderhaar EP, Mboko WP, Rekow MM, Patel SB, Sidjanin DJ, Tarakanova VL) J Virol 2016 Jan 06;90(7):3342-54 PMID: 26739055 PMCID: PMC4794672 SCOPUS ID: 2-s2.0-84960977475 01/08/2016       14 Citations
  • Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation. (Handley MT, Carpanini SM, Mali GR, Sidjanin DJ, Aligianis IA, Jackson IJ, FitzPatrick DR) Open Biol 2015 Jun;5(6):150047 PMID: 26063829 PMCID: PMC4632505 SCOPUS ID: 2-s2.0-84934923305 06/13/2015       45 Citations
  • Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice. (Park AK, Liegel RP, Ronchetti A, Ebert AD, Geurts A, Sidjanin DJ) BMC Genet 2014 Dec 05;15:135 PMID: 25476608 PMCID: PMC4266191 SCOPUS ID: 2-s2.0-84964313193 12/06/2014       19 Citations
  • Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome. (Liegel RP, Ronchetti A, Sidjanin DJ) Mol Genet Metab Rep 2014;1:299-311 PMID: 25197626 PMCID: PMC4151185 SCOPUS ID: 2-s2.0-84905675045 09/10/2014       25 Citations
  • Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans. (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, Accorsi P, Giordano L, Pinelli L, Hartmann B, Ebert AD, Barr FA, Aligianis IA, Sidjanin DJ) Am J Hum Genet 2013 Dec 05;93(6):1001-14 PMID: 24239381 PMCID: PMC3852926 SCOPUS ID: 2-s2.0-84890310034 11/19/2013       112 Citations
  • Functional analysis of HSF4 mutations found in patients with autosomal recessive congenital cataracts. (Merath K, Ronchetti A, Sidjanin DJ) Invest Ophthalmol Vis Sci 2013 Oct 11;54(10):6646-54 PMID: 24045990 PMCID: PMC3796937 SCOPUS ID: 2-s2.0-84885441288 09/21/2013       14 Citations
  • ADAM17 transactivates EGFR signaling during embryonic eyelid closure. (Hassemer EL, Endres B, Toonen JA, Ronchetti A, Dubielzig R, Sidjanin DJ) Invest Ophthalmol Vis Sci 2013 Jan 07;54(1):132-40 PMID: 23211830 PMCID: PMC3544417 SCOPUS ID: 2-s2.0-84874531665 12/06/2012       15 Citations
  • Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene. (Toonen J, Liang L, Sidjanin DJ) BMC Genet 2012 Aug 28;13:76 PMID: 22928477 PMCID: PMC3469352 SCOPUS ID: 2-s2.0-84865337053 08/30/2012       19 Citations
  • Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice. (Liang L, Liegel R, Endres B, Ronchetti A, Chang B, Sidjanin DJ) Mol Vis 2011;17:3062-71 PMID: 22162625 PMCID: PMC3233385 SCOPUS ID: 2-s2.0-83055198499 12/14/2011       6 Citations
  • A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse. (Merath KM, Chang B, Dubielzig R, Jeannotte R, Sidjanin DJ) Mamm Genome 2011 Dec;22(11-12):661-73 PMID: 21858719 PMCID: PMC3251904 SCOPUS ID: 2-s2.0-84655163481 08/23/2011       11 Citations
  • Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice. (Liegel R, Chang B, Dubielzig R, Sidjanin DJ) Mol Genet Metab 2011 May;103(1):51-9 PMID: 21353609 PMCID: PMC3081956 SCOPUS ID: 2-s2.0-79955164331 03/01/2011       38 Citations
  • The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17. (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) Genetics 2010 May;185(1):245-55 PMID: 20194968 PMCID: PMC2870960 SCOPUS ID: 2-s2.0-77956635945 03/03/2010       40 Citations
  • Genetic and clinical evaluation of juvenile retinoschisis. (Kim JE, Ruttum MS, Koeberl MJ, Hassemer EL, Sidjanin DJ) J AAPOS 2009 Apr;13(2):215-7 PMID: 19393523 PMCID: PMC3926297 SCOPUS ID: 2-s2.0-64749084909 04/28/2009       5 Citations
  • Pharmacogenetics of ophthalmic topical beta-blockers. (Sidjanin DJ, McCarty CA, Patchett R, Smith E, Wilke RA) Per Med 2008;5(4):377-385 PMID: 19266054 PMCID: PMC2650848 SCOPUS ID: 2-s2.0-50549086113 01/01/2008       15 Citations
  • Identification of two novel mutations in families with X-linked ocular albinism. (Iannaccone A, Gallaher KT, Buchholz J, Jennings BJ, Neitz M, Sidjanin DJ) Mol Vis 2007 Oct 02;13:1856-61 PMID: 17960122 SCOPUS ID: 2-s2.0-34948893453 10/26/2007       4 Citations
  • Cloning and characterization of canine PAX6 and evaluation as a candidate gene in a canine model of aniridia. (Hunter LS, Sidjanin DJ, Hijar MV, Johnson JL, Kirkness E, Acland GM, Aguirre GD) Mol Vis 2007 Mar 26;13:431-42 PMID: 17417604 PMCID: PMC2647561 SCOPUS ID: 2-s2.0-33947582652 04/10/2007       3 Citations
  • Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod-cone degeneration interval and identifies ancestral disease-transmitting chromosome. (Goldstein O, Zangerl B, Pearce-Kelling S, Sidjanin DJ, Kijas JW, Felix J, Acland GM, Aguirre GD) Genomics 2006 Nov;88(5):541-50 PMID: 16859891 PMCID: PMC4006154 SCOPUS ID: 2-s2.0-33749430640 07/25/2006       63 Citations
  • Radiation hybrid mapping of cataract genes in the dog. (Hunter LS, Sidjanin DJ, Johnson JL, Zangerl B, Galibert F, Andre C, Kirkness E, Talamas E, Acland GM, Aguirre GD) Mol Vis 2006 May 24;12:588-96 PMID: 16760895 PMCID: PMC1509099 SCOPUS ID: 2-s2.0-33646870097 06/09/2006       9 Citations
  • Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice. (Talamas E, Jackson L, Koeberl M, Jackson T, McElwee JL, Hawes NL, Chang B, Jablonski MM, Sidjanin DJ) Genomics 2006 Jul;88(1):44-51 PMID: 16595169 PMCID: PMC1509100 SCOPUS ID: 2-s2.0-33744911966 04/06/2006       21 Citations
  • Cloning of canine galactokinase (GALK1) and evaluation as a candidate gene for hereditary cataracts in Labrador retrievers. (Sidjanin DJ, McElwee J, Miller B, Aguirre GD) Anim Genet 2005 Jun;36(3):265-6 PMID: 15932415 PMCID: PMC1509098 SCOPUS ID: 2-s2.0-20444371986 06/04/2005       5 Citations
  • Radiation hybrid map, physical map, and low-pass genomic sequence of the canine prcd region on CFA9 and comparative mapping with the syntenic region on human chromosome 17. (Sidjanin DJ, Miller B, Kijas J, McElwee J, Pillardy J, Malek J, Pai G, Feldblyum T, Fraser C, Acland G, Aguirre G) Genomics 2003 Feb;81(2):138-48 PMID: 12620391 SCOPUS ID: 2-s2.0-0037294866 03/07/2003       15 Citations
  • Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3. (Sidjanin DJ, Lowe JK, McElwee JL, Milne BS, Phippen TM, Sargan DR, Aguirre GD, Acland GM, Ostrander EA) Hum Mol Genet 2002 Aug 01;11(16):1823-33 PMID: 12140185 SCOPUS ID: 2-s2.0-0036667730 07/26/2002       173 Citations
  • Cloning of the canine delta tubulin cDNA (TUBD) and mapping to CFA9. (Sidjanin DJ, Zangerl B, Johnson JL, Xue F, Mellersh C, Ostrander EA, Acland G, Aguirre GD) Anim Genet 2002 Apr;33(2):161-2 PMID: 12047234 SCOPUS ID: 2-s2.0-0036010113 06/06/2002       3 Citations
  • Cloning of canine gamma-tubulin (TUBG1) cDNA and mapping to CFA9. (Sidjanin DJ, Xue F, McElwee J, Johnson JL, Holmgren C, Mellersh C, Ostrander E, Acland G, Aguirre GD) Anim Genet 2001 Oct;32(5):328-9 PMID: 11683730 SCOPUS ID: 2-s2.0-0034772176 10/31/2001       2 Citations
  • A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice. (Sidjanin DJ, Parker-Wilson DM, Neuhäuser-Klaus A, Pretsch W, Favor J, Deen PM, Ohtaka-Maruyama C, Lu Y, Bragin A, Skach WR, Chepelinsky AB, Grimes PA, Stambolian DE) Genomics 2001 Jun 15;74(3):313-9 PMID: 11414759 SCOPUS ID: 2-s2.0-0035874985 06/21/2001       40 Citations
  • Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16. (Sidjanin DJ, Grimes PA, Pretsch W, Neuhäuser-Klaus A, Favor J, Stambolian DE) Invest Ophthalmol Vis Sci 1997 Nov;38(12):2502-7 PMID: 9375568 SCOPUS ID: 2-s2.0-0030731478 12/31/1997       14 Citations
  • Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4. (Zhou E, Grimes P, Favor J, Koeberlein B, Pretsch W, Neuhauser-Klaus A, Sidjanin D, Stambolian D) Mamm Genome 1997 Mar;8(3):178-81 PMID: 9069117 SCOPUS ID: 2-s2.0-0031089330 03/01/1997       19 Citations
  • UV-induced changes in cell cycle and gene expression within rabbit lens epithelial cells. (Sidjanin D, Grdina D, Woloschak GE) Photochem Photobiol 1996 Jan;63(1):79-85 PMID: 8577869 SCOPUS ID: 2-s2.0-0030041844 01/01/1996       10 Citations
  • Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts. (Stambolian D, Ai Y, Sidjanin D, Nesburn K, Sathe G, Rosenberg M, Bergsma DJ) Nat Genet 1995 Jul;10(3):307-12 PMID: 7670469 SCOPUS ID: 2-s2.0-0029011131 07/01/1995       93 Citations
  • DNA damage and repair in rabbit lens epithelial cells following UVA radiation. (Sidjanin D, Zigman S, Reddan J) Curr Eye Res 1993 Sep;12(9):773-81 PMID: 8261789 SCOPUS ID: 2-s2.0-0027492965 09/01/1993       40 Citations
    • Last update: 05/04/2025