Recent publications

  1. Oliver KL, Franceschetti S, Milligan CJ, Muona M, Mandelstam SA, Canafoglia L, Boguszewska-Chachulska AM, Korczyn AD, Bisulli F, Di Bonaventura C, Ragona F, Michelucci R, Ben-Zeev B, Straussberg R, Panzica F, Massano J, Friedman D, Crespel A, Engelsen BA, Andermann F, Andermann E, Spodar K, Lasek-Bal A, Riguzzi P, Pasini E, Tinuper P, Licchetta L, Gardella E, Lindenau M, Wulf A, Moller RS, Benninger F, Afawi Z, Rubboli G, Reid CA, Maljevic S, Lerche H, Lehesjoki A-E, Petrou S, Berkovic S. Myoclonus Epilepsy and Ataxia due to KCNC1 Mutation: Analysis of 20 Cases and K plus Channel Properties. ANNALS OF NEUROLOGY. Wiley-Liss. 2017, Vol. 81, Issue 5.
  2. Stamp L, Gwynne RM, Foong JPP, Lomax AE, Hao M, Kaplan DI, Reid CA, Petrou S, Allen AM, Bornstein JC, Young H. Optogenetic Demonstration of Functional Innervation of Mouse Colon by Neurons Derived From Transplanted Neural Cells. GASTROENTEROLOGY. WB Saunders Co. 2017, Vol. 152, Issue 6.
  3. Sadovnick AD, Gu B, Traboulsee AL, Bernales CQ, Encarnacion M, Yee IM, Criscuoli MG, Huang X, Ou A, Milligan CJ, Petrou S, Wiley JS, Vilarino-Guell C. Purinergic receptors P2RX4 and P2RX7 in familial multiple sclerosis. HUMAN MUTATION. Wiley-Liss. 2017, Vol. 38, Issue 6.
  4. Reid C, Hildebrand MS, Mullen SA, Hildebrand JM, Berkovic S, Petrou S. Synaptic Zn2+ and febrile seizure susceptibility. BRITISH JOURNAL OF PHARMACOLOGY. Nature Publishing Group. 2017, Vol. 174, Issue 2.
  5. Allen AS, Bellows ST, Berkovic S, Bridgers J, Burgess R, Cavalleri G, Chung SK, Cossette P, Delanty N, Dlugos D, Epstein MP, Freyer C, Goldstein DB, Heinzen EL, Hildebrand MS, Johnson MR, Kuzniecky R, Lowenstein DH, Marson AG, Mayeux R, Mebane C, Mefford HC, O'Brien T, Ottman R, Petrou S, Petrovski S, Pickrell WO, Radtke RA, Rees MI, Regan BM, Ren Z, Scheffer I, Sills GJ, Thomas RH, Wang Q, Abou-Khalil B, Alldredge BK, Amrom D, Andermann E, Andermann F, Bautista JF, Bluvstein J, Boro A, Cascino GD, Consalvo D, Crumrine P, Devinsky O, Fiol M, Fountain NB, French J, Friedman D, Geller EB, Glauser T, Glynn S, Haas K, Haut SR, Hayward J, Helmers SL, Joshi S, Kanner A, Kirsch HE, Knowlton RC, Kossoff EH, Kuperman R, Motika PV, Novotny EJ, Paolicchi JM, Parent JM, Park K, Poduri A, Sadleir LG, Shellhaas RA, Sherr EH, Shih JJ, Shinnar S, Singh RK, Sirven J, Smith MC, Sullivan J, Thio LL, Venkat A, Vining EPG, Von Allmen GK, Weisenberg JL, Widdess-Walsh P, Winawer MR. Ultra-rare genetic variation in common epilepsies: a case-control sequencing study. The Lancet Neurology. The Lancet Publishing Group. 2017, Vol. 16, Issue 2.
  6. Howden S, McColl B, Glaser A, Vadolas J, Petrou S, Little M, Elefanty A, Stanley E. A Cas9 Variant for Efficient Generation of Indel-Free Knockin or Gene-Corrected Human Pluripotent Stem Cells. STEM CELL REPORTS. Cell Press. 2016, Vol. 7, Issue 3.
  7. Hildebrand M, Myers CT, Carvill GL, Regan B, Damiano J, Mullen S, Newton M, Nair U, Gazina E, Milligan C, Reid C, Petrou S, Scheffer I, Berkovic S, Mefford HC. A targeted resequencing gene panel for focal epilepsy. NEUROLOGY. Lippincott Williams & Wilkins. 2016, Vol. 86, Issue 17.
  8. Phelan D, Anderson DJ, Howden S, Wong R, Hickey PF, Pope K, Wilson G, Pebay A, Davis A, Petrou S, Elefanty A, Stanley E, James P, MacCiocca I, Bahlo M, Cheung M, Amor D, Elliott D, Lockhart P. ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy(aEuro). EUROPEAN HEART JOURNAL. WB Saunders Co. 2016, Vol. 37, Issue 33.
  9. Myers CT, McMahon JM, Schneider AL, Petrovski S, Allen AS, Carvill GL, Zemel M, Saykally JE, Lacroix AJ, Heinzen EL, Hollingsworth G, Nikanorova M, Corbett M, Gecz J, Coman D, Freeman J, Calvert S, Gill D, Carney P, Lerman-Sagie T, Sampaio H, Cossette P, Delanty N, Dlugos D, Eichler EE, Epstein MP, Glauser T, Johnson MR, Kuzniecky R, Marson AG, O'Brien T, Ottman R, Petrou S, Poduri A, Pickrell WO, Chung SK, Rees MI, Sherr E, Sadleir LG, Goldstein DB, Lowenstein DH, M├śller RS, Berkovic S, Scheffer I, Mefford HC. De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. American Journal of Human Genetics. University of Chicago Press. 2016, Vol. 99, Issue 2.
  10. Corbett MA, Bellows S, Li M, Carroll R, Micallef S, Carvill GL, Myers CT, Howell K, Maljevic S, Lerche H, Gazina E, Mefford HC, Bahlo M, Berkovic S, Petrou S, Scheffer I, Gecz J. Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy. NEUROLOGY. Lippincott Williams & Wilkins. 2016, Vol. 87, Issue 19.
  11. Simpson D, Tetienne J, McCoey J, Ganesan K, Hall L, Petrou S, Scholten R, Hollenberg L. Magneto-optical imaging of thin magnetic films using spins in diamond. SCIENTIFIC REPORTS. Nature Publishing Group. 2016, Vol. 6.
  12. Helbig I, Heinzen EL, Mefford HC, Berkovic S, Lowenstein DH, Kato M, Helen Cross J, Satishchandra P, De Jonghe P, Jiang Y, Goldman A, Petrou S, Tan N. Primer Part 1 - The building blocks of epilepsy genetics. Epilepsia. Blackwell Science. 2016, Vol. 57, Issue 6.
  13. Delahaye-Duriez A, Srivastava P, Shkura K, Langley SR, Laaniste L, Moreno-Moral A, Danis B, Mazzuferi M, Foerch P, Gazina E, Richards K, Petrou S, Kaminski RM, Petretto E, Johnson MR. Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery. GENOME BIOLOGY. Biomed Central. 2016, Vol. 17, Issue 1.
  14. Kaplan DI, Isom LL, Petrou S. Role of Sodium Channels in Epilepsy. COLD SPRING HARBOR PERSPECTIVES IN MEDICINE. Cold Spring Harbor Laboratory Press, Publications Department. 2016, Vol. 6, Issue 6.
  15. Petty S, Milligan CJ, Todaro M, Richards KL, Kularathna PK, Pagel C, French C, Hill E, O'Brien T, Wark J, MacKie E, Petrou S. The antiepileptic medications carbamazepine and phenytoin inhibit native sodium currents in murine osteoblasts. EPILEPSIA. Blackwell Science. 2016, Vol. 57, Issue 9.

View a full list of publications on the University of Melbourne’s ‘Find An Expert’ profile