DANA KNUTZEN

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Obstetrics & Gynecology
Address333 NORTH SANTA ROSA ST.
San Antonio, TX 78207
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Shields AD, Wagner RK, Knutzen D, Deering S, Nielsen PE. Maintaining access to maternal fetal medicine care by telemedicine during a global pandemic. J Telemed Telecare. 2020 Sep 26; 1357633X20957468. PMID: 32985379.
      Citations: 4     Fields:    
    2. Bachmann-Gagescu R, Dempsey JC, Bulgheroni S, Chen ML, D'Arrigo S, Glass IA, Heller T, Héon E, Hildebrandt F, Joshi N, Knutzen D, Kroes HY, Mack SH, Nuovo S, Parisi MA, Snow J, Summers AC, Symons JM, Zein WM, Boltshauser E, Sayer JA, Gunay-Aygun M, Valente EM, Doherty D. Healthcare recommendations for Joubert syndrome. Am J Med Genet A. 2020 01; 182(1):229-249. PMID: 31710777.
      Citations: 9     Fields:    Translation:Humans
    3. Knutzen D, Stoll K. Beyond the Brochure: Innovations in Clinical Counseling Practices for Prenatal Genetic Testing Options. J Perinat Neonatal Nurs. 2019 Jan/Mar; 33(1):12-25. PMID: 30676459.
      Citations: 1     Fields:    Translation:Humans
    4. Zelig CM, Knutzen DM, Ennen CS, Dolinsky BM, Napolitano PG. Chorionic Villus Sampling, Early Amniocentesis, and Termination of Pregnancy Without Diagnostic Testing: Comparison of Fetal Risk Following Positive Non-invasive Prenatal Testing. J Obstet Gynaecol Can. 2016 05; 38(5):441-445.e2. PMID: 27261219.
      Citations: 1     Fields:    Translation:Humans
    5. Slaats GG, Isabella CR, Kroes HY, Dempsey JC, Gremmels H, Monroe GR, Phelps IG, Duran KJ, Adkins J, Kumar SA, Knutzen DM, Knoers NV, Mendelsohn NJ, Neubauer D, Mastroyianni SD, Vogt J, Worgan L, Karp N, Bowdin S, Glass IA, Parisi MA, Otto EA, Johnson CA, Hildebrandt F, van Haaften G, Giles RH, Doherty D. MKS1 regulates ciliary INPP5E levels in Joubert syndrome. J Med Genet. 2016 Jan; 53(1):62-72. PMID: 26490104.
      Citations: 22     Fields:    Translation:HumansAnimalsCells
    6. Bachmann-Gagescu R, Dempsey JC, Phelps IG, O'Roak BJ, Knutzen DM, Rue TC, Ishak GE, Isabella CR, Gorden N, Adkins J, Boyle EA, de Lacy N, O'Day D, Alswaid A, Ramadevi A R, Lingappa L, Lourenço C, Martorell L, Garcia-Cazorla À, Ozyürek H, Haliloglu G, Tuysuz B, Topçu M, Chance P, Parisi MA, Glass IA, Shendure J, Doherty D. Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity. J Med Genet. 2015 Aug; 52(8):514-22. PMID: 26092869.
      Citations: 73     Fields:    Translation:Humans
    7. Lutgendorf MA, Stoll KA, Knutzen DM, Foglia LM. Noninvasive prenatal testing: limitations and unanswered questions. Genet Med. 2014 Apr; 16(4):281-5. PMID: 24009001.
      Citations: 14     Fields:    Translation:Humans
    8. Stoll K, Lutgendorf M, Knutzen D, Nielsen PE. Questioning the costs and benefits of non-invasive prenatal testing. J Matern Fetal Neonatal Med. 2014 Apr; 27(6):633-4. PMID: 23808328.
      Citations:    Fields:    Translation:Humans
    9. Knutzen DM, Stoll KA, McClellan MW, Deering SH, Foglia LM. Improving knowledge about prenatal screening options: can group education make a difference? J Matern Fetal Neonatal Med. 2013 Dec; 26(18):1799-803. PMID: 23662746.
      Citations: 5     Fields:    Translation:Humans
    10. Knutzen D. Genetic counseling through hope. J Genet Couns. 2012 Apr; 21(2):205-6. PMID: 22160403.
      Citations:    Fields:    Translation:Humans
    11. Collie AM, Landsverk ML, Ruzzo E, Mefford HC, Buysse K, Adkins JR, Knutzen DM, Barnett K, Brown RH, Parry GJ, Yum SW, Simpson DA, Olney RK, Chinnery PF, Eichler EE, Chance PF, Hannibal MC. Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy. J Med Genet. 2010 Sep; 47(9):601-7. PMID: 19939853.
      Citations: 8     Fields:    Translation:HumansCells
    12. Doherty D, Parisi MA, Finn LS, Gunay-Aygun M, Al-Mateen M, Bates D, Clericuzio C, Demir H, Dorschner M, van Essen AJ, Gahl WA, Gentile M, Gorden NT, Hikida A, Knutzen D, Ozyurek H, Phelps I, Rosenthal P, Verloes A, Weigand H, Chance PF, Dobyns WB, Glass IA. Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis). J Med Genet. 2010 Jan; 47(1):8-21. PMID: 19574260.
      Citations: 56     Fields:    Translation:Humans
    13. Hannibal MC, Ruzzo EK, Miller LR, Betz B, Buchan JG, Knutzen DM, Barnett K, Landsverk ML, Brice A, LeGuern E, Bedford HM, Worrall BB, Lovitt S, Appel SH, Andermann E, Bird TD, Chance PF. SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy. Neurology. 2009 May 19; 72(20):1755-9. PMID: 19451530.
      Citations: 11     Fields:    Translation:HumansCells
    14. Landsverk ML, Ruzzo EK, Mefford HC, Buysse K, Buchan JG, Eichler EE, Petty EM, Peterson EA, Knutzen DM, Barnett K, Farlow MR, Caress J, Parry GJ, Quan D, Gardner KL, Hong M, Simmons Z, Bird TD, Chance PF, Hannibal MC. Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Hum Mol Genet. 2009 Apr 01; 18(7):1200-8. PMID: 19139049.
      Citations: 9     Fields:    Translation:HumansCells
    15. Gorden NT, Arts HH, Parisi MA, Coene KL, Letteboer SJ, van Beersum SE, Mans DA, Hikida A, Eckert M, Knutzen D, Alswaid AF, Ozyurek H, Dibooglu S, Otto EA, Liu Y, Davis EE, Hutter CM, Bammler TK, Farin FM, Dorschner M, Topçu M, Zackai EH, Rosenthal P, Owens KN, Katsanis N, Vincent JB, Hildebrandt F, Rubel EW, Raible DW, Knoers NV, Chance PF, Roepman R, Moens CB, Glass IA, Doherty D. CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290. Am J Hum Genet. 2008 Nov; 83(5):559-71. PMID: 18950740.
      Citations: 110     Fields:    Translation:HumansCells
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