Nadia Carstens

8PUBLICATIONS
25CO-AUTHORS
Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Forensic epidemiologyMedical biotechnology diagnostics (incl. biosensors)Medical biotechnology not elsewhere classified
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Publications (8)

|Sep 08, 2026
Molecular Characterisation of Treacher Collins Syndrome in a South African Cohort: Novel Disease-Causing Variants in TCOF1 and POLR1D.

|Jul 09, 2026
Copy number variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders-the DDD-Africa study.

|Jun 26, 2026
The expected utility and psychological impacts of exome sequencing results in the DDD-Africa study.

|Apr 27, 2026
Confirmation of Exome Sequencing Results Using Sanger Sequencing-Considerations in a Low-Resource Setting.

|Apr 09, 2026
Implementation of an Inherited Diseases Gene Panel to Accelerate Precision Medicine in the South African Public Healthcare System.

Nadia Carstens, Maria Mudau, Fahmida Essop

|Feb 12, 2026
Copy Number Variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders - the DDD-Africa study.

Nadja Louw, Prince Makay, Phelelani T Mpangase

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Frequent Collaborators

7 joint publications

Amanda Krause

5 joint publications

Zané Lombard

2 joint publications

Nadja Louw

2 joint publications

Prince Makay