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Last Name


TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Obstetrics & Gynecology
DivisionObstetrics and Gynecology
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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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    1. 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.
      View in: PubMed
    2. 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.
      View in: PubMed
    3. 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.
      View in: PubMed
    4. 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.
      View in: PubMed
    5. 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.
      View in: PubMed
    6. 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.
      View in: PubMed
    7. Knutzen D. Genetic counseling through hope. J Genet Couns. 2012 Apr; 21(2):205-6. PMID: 22160403.
      View in: PubMed
    8. 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.
      View in: PubMed
    9. 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, Top├žu 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.
      View in: PubMed
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