Haghighi, A., Tiwari, A., Piri, N., Nürnberg, G., Saleh-Gohari, N., Haghighi, A., . . . Berger, W. (2014). Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome. PLoS One.

Haghighi, Alireza, Amit Tiwari, Niloofar Piri, Gudrun Nürnberg, Nasrollah Saleh-Gohari, Amirreza Haghighi, John Neidhardt, Peter Nürnberg, e Wolfgang Berger. "Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome." PLoS One 2014.

Haghighi, Alireza, et al. "Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome." PLoS One 2014.