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Number of items: 9.


Allen, Andrew S, Berkovic, Samuel F, Bridgers, Joshua, Cossette, Patrick, Dlugos, Dennis, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Heinzen, Erin L, Jiang, Yu
et al (show 104 more authors) (2017) Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (7). pp. 894-899.


Koko, Mahmoud ORCID: 0000-0001-9512-0184, Motelow, Joshua E ORCID: 0000-0002-4367-4182, Stanley, Kate E ORCID: 0000-0002-2861-9660, Bobbili, Dheeraj R ORCID: 0000-0002-1368-9623, Dhindsa, Ryan S ORCID: 0000-0002-8965-0813, May, Patrick ORCID: 0000-0001-8698-3770, Canadian Epilepsy Network, , Epi4K Consortium, , Epilepsy Phenome/Genome Project, , EpiPGX Consortium,
et al (show 1 more authors) (2022) Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia, 63 (3). pp. 723-735.


Koko, Mahmoud ORCID: 0000-0001-9512-0184, Krause, Roland ORCID: 0000-0001-9938-7126, Sander, Thomas, Bobbili, Dheeraj Reddy ORCID: 0000-0002-1368-9623, Nothnagel, Michael, May, Patrick ORCID: 0000-0001-8698-3770, Lerche, Holger and Epi25 Collaborative,
(2021) Distinct gene-set burden patterns underlie common generalized and focal epilepsies. EBioMedicine, 72. 103588-.


Grover, Sandeep, Kumar Sreelatha, Ashwin Ashok, Pihlstrom, Lasse, Domenighetti, Cloe, Schulte, Claudia, Sugier, Pierre-Emmanuel, Radivojkov-Blagojevic, Milena, Lichtner, Peter, Mohamed, Oceane, Portugal, Berta
et al (show 73 more authors) (2022) Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium. NEUROLOGY, 99 (7). E698-E710.


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-.


Domenighetti, Cloe, Douillard, Venceslas, Sugier, Pierre-Emmanuel, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep, May, Patrick, Bobbili, Dheeraj R, Radivojkov-Blagojevic, Milena, Lichtner, Peter
et al (show 70 more authors) (2022) The Interaction between <i>HLA-DRB1</i> and Smoking in Parkinson's Disease Revisited. MOVEMENT DISORDERS, 37 (9). pp. 1929-1937.


Sugier, Pierre-Emmanuel, Lucotte, Elise H, Domenighetti, Cloe M, Law, Matthew, Iles, Mark, Brown, Kevin D, Amos, Christopher J, McKay, James, Hung, Rayjean, Karimi, Mojgan
et al (show 84 more authors) (2023) Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. MOVEMENT DISORDERS, 38 (4). pp. 604-615.


Blauwendraat, Cornelis, Faghri, Faraz, Pihlstrom, Lasse, Geiger, Joshua T, Elbaz, Alexis, Lesage, Suzanne, Corvol, Jean-Christophe, May, Patrick, Nicolas, Aude, Abramzon, Yevgeniya
et al (show 31 more authors) (2017) NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases. Neurobiology of Aging, 57. 247.e9-247.e13.


May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline
et al (show 88 more authors) (2018) Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study. LANCET NEUROLOGY, 17 (8). pp. 699-708.

This list was generated on Sat Dec 23 12:42:52 2023 GMT.