Dr Peter Kullar Dr Ian Wilson Professor Johannes Attems Dr Christopher Morris
| Frequency and signature of somatic variants in 1461 human brain exomes | 2019 |
|
Dr Peter Kullar Emerita Professor Janet Wilson Professor Patrick Chinnery
| Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family | 2018 |
|
Dr Peter Kullar Emerita Professor Janet Wilson Professor Rita Horvath Dr Patrick Yu Wai Man Professor Patrick Chinnery et al. | Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction | 2016 |
|
Dr Peter Kullar Professor Robert Taylor Dr Charlotte Alston Dr Emma Watson Professor Patrick Chinnery et al. | The frequency of the m.1555A > G (MTRNR1) variant in UK patients with suspected mitochondrial deafness | 2016 |
|
Dr Peter Kullar Philip Yates
| Actinomycosis of the middle ear | 2013 |
|