Nerine Gregersen

Articles:

1. Gregersen NE, Ballot DE, Guidozzi F, Cooper PA. Birth asphyxia: presenting the case for “a stitch in time…” S Afr Med J 1999; 89: 326-332.
2. Gregersen NE, Van Nierop WH, Von Gottberg A, Duse A, Davies VA, Cooper PA. Klebsiella pneumoniae with extended spectrum beta-lactamase activity associated with a necrotizing enterocolitis outbreak. Pediatr Infect Dis J 1999; 18: 963-967.
3. Gregersen N, Viljoen D. Costello syndrome with growth hormone deficiency and hypoglycemia: a new report and review of the endocrine associations. Am J Med Genet 2004; 129 A: 171-175.
4. Gregersen NE, Krause A. An approach to the genetic causes of the hypotonic infant. Paediatric Review 2005; 2: 6-17.
5. Gregersen, N. Facial asymmetry with colon atresia. Clin Dysmorphol 2006; 15: 45-46.
6. Mitchell C, Gregersen N, Krause A. Novel CYP2C9 and VKORC1 gene variants associated with warfarin dosage variability in the South African black population. Pharmacogenomics 2011;12(7): 953-63
7. Macaulay S, Gregersen N, Krause A. Uptake of genetic counselling services by patients with cystic fibrosis and their families. S Afr Fam Pract 2012; 54 (3): 250-255
8. Gregersen NE, Isaacson Z, Roose S. Diamonds in the defects: logotherapy in medical genetics. Int Forum Logotherapy 2012; 35: 29-32
9. Gregersen N, Lampret J, Lane A, Christianson A. The Greater Sekhukhune-CAPABILITY Outreach Project. J Community Genet 2013 Jul; 4 (3): 335-41
10. Sheath KL, Mazzaschi RL, Aftimos S, Gregersen NE, George AM, Love DR. Clinical outcomes and counselling issues regarding partial trisomy of terminal Xp in a child with developmental delay. Sultan Qaboos University Med J 2013; 13 (2): 311-317. Epub. 9th May 13
11. Doherty E, O’Connor R, Zhang A, Lim C, Love JM, Aston F, Claxton K, Gregersen N, George AM, Love DR. Developmental delay referrals and the roles of Fragile X testing and molecular karyotyping: A New Zealand perspective. Mol Med Report 2013; 7: 1710-1714
12. Mc Cormack A, Taylor J, Gregersen N, George AM, Love DR. Delineation of 2q32q35 Deletion Phenotypes: Two Apparent ‘‘Proximal’’ and ‘‘Distal’’ Syndromes. Case Rep Genet 2013, Article ID 823451
13. Moosa S, Segal D, Christianson AL, Gregersen NE. Thyroid dysfunction in a cohort of South African children with Down syndrome. SAMJ 2013; 103 (12 Suppl 1): 966-70
14. Mc Cormack A, Sharpe C, Gregersen N, Smith W, Hayes I, George AM and Love DR. 12q14 microdeletions: additional case series with confirmation of a macrocephaly region. Case Rep Genet 2015; Volume 2015, Article ID 192071
15. Eric Lee, TrangLe, Ying Zhu, […], Nerine Gregersen, et al. A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations. Genetics in Medicine 2018; 20: 1061–1068
16. Ngoc Minh Phuong Nguyen, Yassemine Khawajkie, Nawel Mechtouf, […], Nerine Gregersen et al. The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients. Modern Pathology 2018; 31: 1116-1130
17. Futoshi Sekiguchi, Yoshinori Tsurusaki, Nobuhiko Okamoto, […] Nerine Gregersen, et al. Genetic abnormalities in a large cohort of Coffin–Siris syndrome patients. J Hum Genet 2019; 64: 1173-1186
18. Maria Ercu, Lajos Markó, Carolin Schächterle, Dmitry Tsvetkov, Yingqiu Cui, Sara Maghsodi, Theda U.P. Bartolomaeus, Philipp G. Maass, Kerstin Zühlke, Nerine Gregersen, et al. Phosphodiesterase 3A and Arterial Hypertension. Circulation 2020

Book chapters:

1. Gregersen NE, Krause A. Molecular basis for phenotypic variation. In: Molecular Medicine for Clinicians. Mendelow B, Ramsay M, Chetty N, Stevens W (eds). Johannesburg, Wits University Press 2009: 187-193.
2. Gregersen NE, Krause A. Medical Genetics. In: Molecular Medicine for Clinicians. Mendelow B, Ramsay M, Chetty N, Stevens W (eds). Johannesburg, Wits University Press 2009: 194-202.
3. Walters S, Gregersen NE. Chromosome disorders. In: Molecular Medicine for Clinicians. Mendelow B, Ramsay M, Chetty N, Stevens W (eds). Johannesburg, Wits University Press 2009: 133-142.
4. Gregersen, NE and Christianson, AL. Medical genetics and birth defects. In: Coovadia’s Paediatrics and Child Health. Wittenberg DF (ed.). Cape Town, Oxford University Press. 6th edition 2009: 39 – 59; 7th edition 2014: 34-51

Qualifications

• 2019 Certified Dare to Lead™ Facilitator, Brené Brown Education and Research Group, USA
• 2018 Advanced Leadership Program, Women and Leadership Australia
• 2017 Diplomate in Logotherapy, Viktor Frankl Institute of Logotherapy, USA. Title of research report: “Gratitude: A Pathway to Meaning-Discovery”
• 2013 Supervision Skills for Health Care Professionals, Unitec (University of Technology), New Zealand
• 2013–2014 Yoga Teacher training level 1 and 2 (RYT200), Ashram Yoga, New Zealand
• 2012 Yoga Nidra (deep relaxation) training level 1 and 2, Ashram Yoga, New Zealand
• 2009 Associate Clinician in Logotherapy, University of South Africa (UNISA) under auspices of Viktor Frankl Institute of Logotherapy, USA
• 2009 Clinical Training in Mind/Body Medicine, Harvard Medical School Benson-Henry Institute for Mind Body Medicine, USA
• 2005 Master of Science in Medicine (Genetic Counselling), with distinction. University of the Witwatersrand, South Africa. Title of research report: “The implications to women of childbearing age taking warfarin anticoagulation”
• 2003 Certificate in Medical Genetics, with distinction. Colleges of Medicine of South Africa (CMSA), South Africa
• 1997 Fellow of the College of Paediatricians, Colleges of Medicine of South Africa (CMSA), South Africa
• 1991 Bachelor of Medicine and Surgery (MBBCH), University of the Witwatersrand, South Africa