Licensed Certified Genetic Counselor (LCGC)
BS in Cell Biology, Molecular Biology, and Genetics - Boston University, Boston, MA
MS in Genetic Counseling - Arcadia University, Glenside, PA
Licensed Genetic Counselor II
Six New Cases of CRB2-Related Syndrome and a Review of Clinical Findings in 28 Reported Patients. Adutwum, A, Seifert, M, Mirzaa, G, Kushner, JD, Rogers, C, Schnur, R, Khalek, N, Cristancho, AG, Burrill, N, Slavotinek, A. Clinical Genetics. Clin Genet. 2022 Sep 7. doi: 10.1111/cge.14222. Epub ahead of print. PMID: 36071576.
Mitochondrial disease patient motivations and barriers to participate in clinical trials. Zolkipli-Cunningham, Z, Xiao, R, Stoddart, A, McCormick, EM, Holberts, AR, Burrill, N, McCormack, S, Williams, L, Wang, X, Thompson, JLP, Falk, MJ. May 5, 2018.
Beslow LA, Pukenas BA, Borst AB, Britt A, Vossough A, Teefey CP, Agarwal S, Burrill N, Goldmuntz B, Fuller S, Lang SS (August 2023). Brain arteriovenous fistula presenting as ventriculomegaly and cystic encephalomalacia in a fetus with HHT. Oral presentation at HHT International Expert Case Conference: Brain: An Advanced Management Forum for HHT Clinical Cases. August 15, 2023.
Presented important cases seen at the CFDT to the Genetics community and sub-specialties at CHOP, providing education on genetic conditions seen at the center in addition to genetic testing options in pregnancy. CHOP Genetics Grand Rounds, Philadelphia, PA, 2018 – Present.
Burrill, N. What’s New in Fetal Therapy. Presented at the Human Genetics Association of New Jersey Annual Conference, held virtually. May 2, 2023.
Burrill, N. Fetal Interventions and the Role of Genetic Counselors at Fetal Centers. Presented virtually at Kean University Genetic Counseling Graduate Program Presentation, March 2021-April 2023.
Burrill, N. Fetal Limb Anomalies. Presented for University of Pennsylvania Graduate Genetic Counseling Program, Philadelphia, PA, April 2021-2023.
Dicicco, R, Burrill, N, Crane, H, Khalek, N, Gebb, J, Agarwal, S, Whitehead, M, Zarnow, D, Oliver, ER, Bach, A, Moldenhauer, J. Two Cases of Prenatally Diagnosed Cri-du-Chat Syndrome and Associated MRI Findings. Poster at American College of Medical Genetics Annual Conference, Salt Lake City, UT, March 14-18, 2023.
Burrill, N, Khalek, N, Oliver, E, Dicicco, R, Moldenhauer, J. Prenatal Presentation of Baraitser-Winter Syndrome: A New Lymphatic Multiple Congenital Anomaly Syndrome. Poster at American College of Medical Genetics Annual Conference, Salt Lake City, UT, March 14-18, 2023.
Burrill, N, Schindewolf, E, Pilchman, L, Dicicco, R, Khalek, N, Gebb, J, Paidas C, Soni, S, Oliver E, Linn, R, Moldenhauer, J. Whole Exome Sequencing in an Enriched Population of Fetuses with Structural Anomalies. Poster at Society of Maternal Fetal Medicine Conference, San Francisco, CA; February 6-11, 2023
Burrill, N. Information about Abortion. Presented for University of Pennsylvania Genetic Counseling Program, Philadelphia, PA; Nov 2, 2022.
Burrill, N, Khalek, N, Cristancho, A, Coleman, B, Moldenhauer, J. Novel Biallelic CRB2 Variants Identified in a Fetus With Severe Fetal Ventriculomegaly and Markedly Elevated AF-AFP. Virtual poster at National Society of Genetic Counseling Conference, Nashville, TN; November 16-20, 2022.
Burrill, N, Khalek, N, Cristancho, A, Coleman, B, Moldenhauer, J. Fetus with a Multiple Congenital Anomaly Syndrome Caused by Novel Variants in ATP1A2. Virtual poster at National Society of Genetic Counseling Conference, Nashville, TN; November 16-20, 2022.
Burrill, N, Schindewolf, E, Pilchman, L, Khalek, N, Gebb, J, Paidas, C, Coleman, B, Oliver, ER, Horii, S, Strong, A, Medne, L, Bedoukian, E, Rintoul, N, Maschhoff, K, Moldenhauer, J. Expansion of the Prenatal Phenotype of PIEZO1 mutations. Poster at American College of Medical Genetics Annual Conference, Nashville, TN; March 22-26, 2022.
Burrill, N, Gebb J, Oliver, E, Moldenhauer, J. Multiple Pregnancies with Fetal Akinesia Deformation Sequence Caused by Mutations in MUSK. Poster at American College of Medical Genetics Annual Conference, Nashville, TN; March 22-26, 2022.
Burrill, N, Khalek, N, Oliver, E, Linn, R, Victoria, T, Moldenhauer, J. Family History Helps Solve the Case: Prenatal Case Report of Lowe Syndrome. Poster at American College of Medical Genetics Annual Conference, Nashville, TN; March 22-26, 2022.
Schindewolf, E, Burrill, N, Krahling, S, Pilchman, L, Linn, R, Khalek N, Gebb, J, Paidas Teefey, C, Soni, S, Moldenhauer, J. Clinical utility of postmortem whole exome sequencing in fetal cases of multiple congenital anomalies. Poster at International Society of Prenatal Diagnosis, held virtually; June 6-9 2021.
Burrill, N. Genetic Counselor Role in Postmortem Evaluation of Fetal Anomaly. Presented at the Psychosocial Mental Health and Early Childhood Psychological Conference, held virtually; May 4, 2021.
Burrill, N. Use of Whole Exome Sequencing in NICU/Prenatal Setting – The Clinic Perspective. Presented virtually at the Pennsylvania Genetic Counseling Conference; April 22, 2021.
Burrill, N, Kasperski, S, Savla, JJ, Didier, R, Oliver, ER, Santani, A, Gebb, J, Hartung, E, Christ, L, Soni, S, Moldenhauer, J. Recurrent Affected Pregnancies Ultimately Leads to Genetic Diagnosis: A Case Report Involving Candidate Gene CYS1. Virtual poster presentation at American College of Medical Genetics Annual Conference, Los Angeles, CA; April 13-16 2021.
Burrill, N, Coleman, B, Agarwal, S, Moldenhauer, J, Khalek, N. Prenatal Diagnosis of Two Co-Occurring Genetic Conditions: FOGX1 Contiguous Deletion and Becker Muscular Dystrophy. Virtual poster presentation at American College of Medical Genetics Annual Conference, Los Angeles, CA; April 13-16 2021.
Burrill, N, DeBari, S, Coleman, B, Zarnow, D, Warner, A, Moldenhauer, J, Paidas Teefey, C. Whole Exome Sequencing Identifies Numerous Variants in a Deceased Fetus with Multiple Congenital Anomalies: Which One(s) is Our Likely Answer? Virtual poster presentation at American College of Medical Genetics Annual Conference, Los Angeles, CA; April 13-16 2021.
Burrill, N, Coleman, B, Moldenhauer, J, Khalek, N. Case Report of Severe Prenatal Presentation of Osteogenesis Imperfecta Caused by Uncommon IFITM5 mutation. Virtual poster presentation at American College of Medical Genetics Annual Conference, Los Angeles, CA; April 13-16 2021.
Burrill, N, Carreon, KC, Oliver, ER, Looney, D, Hoffman, JA, Kasperski, S, Wang, Q, Moldenhauer, J, Johnson, MP. Prenatal Diagnosis of Harlequin Ichthyosis Resulting in Third Trimester Termination. Virtual poster presentation at American College of Medical Genetics Annual Conference, San Antonio, TX; March 17-20 2020.
Burrill, N, Johnson, MP, Soni, S, Gebb, J, Khalek, N, Paidas Teefey, C, Schindewolf, E, Moldenhauer, E. Challenges in Prenatal Counseling of Congenital Adrenal Hyperplasia. Virtual poster presentation at American College of Medical Genetics Annual Conference, San Antonio, TX; March 17-20 2020.
Graduate Dean’s Distinguished Honors list, Arcadia University
Dean’s Scholarship, Boston University
Dean’s List, Boston University