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Myers, Candace T, McMahon, Jacinta M, Schneider, Amy L, Petrovski, Slave, Allen, Andrew S, Carvill, Gemma L, Zemel, Matthew, Say-Kally, Julia E, LaCroix, Amy J, Heinzen, Erin L
et al (show 34 more authors) (2016) De Novo Mutations in <i>SLC1A2</i> and <i>CACNA1A</i> Are Important Causes of Epileptic Encephalopathies. AMERICAN JOURNAL OF HUMAN GENETICS, 99 (2). pp. 287-298.


Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L, Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Bruenger, Tobias, Thomas, Rhys H
et al (show 313 more authors) (2023) Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals. NATURE COMMUNICATIONS, 14 (1). 4392-.


Abou-Khalil, Bassel, Afawi, Zaid, Allen, Andrew S, Bautista, Jocelyn F, Bellows, Susannah T, Berkovic, Samuel F, Bluvstein, Judith, Burgess, Rosemary, Cascino, Gregory, Cops, Elisa J
et al (show 58 more authors) (2017) Phenotypic analysis of 303 multiplex families with common epilepsies. BRAIN, 140 (8). pp. 2144-2156.

This list was generated on Tue Apr 16 07:52:27 2024 BST.