lisa strug
lisa strug
Professor, University of Toronto and Senior Scientist, SickKids Research Institute
Verified email at - Homepage
Cited by
Cited by
Temperature and mortality in 11 cities of the eastern United States
FC Curriero, KS Heiner, JM Samet, SL Zeger, L Strug, JA Patz
American journal of epidemiology 155 (1), 80-87, 2002
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RK C Yuen, D Merico, M Bookman, J L Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
G Lesca, G Rudolf, N Bruneau, N Lozovaya, A Labalme, N Boutry-Kryza, ...
Nature genetics 45 (9), 1061-1066, 2013
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis
H Corvol, SM Blackman, PY BoŽlle, PJ Gallins, RG Pace, JR Stonebraker, ...
Nature communications 6 (1), 8382, 2015
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13. 2
FA Wright, LJ Strug, VK Doshi, CW Commander, SM Blackman, L Sun, ...
Nature genetics 43 (6), 539-546, 2011
Response inhibition and ADHD traits: correlates and heritability in a community sample
J Crosbie, P Arnold, A Paterson, J Swanson, A Dupuis, X Li, J Shan, ...
Journal of abnormal child psychology 41, 497-507, 2013
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)
LJ Strug, T Clarke, T Chiang, M Chien, Z Baskurt, W Li, R Dorfman, B Bali, ...
European Journal of Human Genetics 17 (9), 1171-1181, 2009
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis
L Sun, JM Rommens, H Corvol, W Li, X Li, TA Chiang, F Lin, R Dorfman, ...
Nature genetics 44 (5), 562-569, 2012
Genetic modifiers of cystic fibrosis–related diabetes
SM Blackman, CW Commander, C Watson, KM Arcara, LJ Strug, ...
Diabetes 62 (10), 3627-3635, 2013
Attention impairment in rolandic epilepsy: systematic review
PM Kavros, T Clarke, LJ Strug, JM Halperin, NJ Dorta, DK Pal
Epilepsia 49 (9), 1570-1580, 2008
High risk of reading disability and speech sound disorder in rolandic epilepsy families: case–control study
T Clarke, LJ Strug, PL Murphy, B Bali, J Carvalho, S Foster, G Tremont, ...
Epilepsia 48 (12), 2258-2265, 2007
Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy
DA Greenberg, E Cayanis, L Strug, S Marathe, M Durner, DK Pal, ...
The American Journal of Human Genetics 76 (1), 139-146, 2005
Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities
W Li, D Soave, MR Miller, K Keenan, F Lin, J Gong, T Chiang, ...
Human genetics 133, 151-161, 2014
Sex differences in habitual physical activity and lung function decline in children with cystic fibrosis
J Schneiderman-Walker, DL Wilkes, L Strug, LC Lands, SL Pollock, ...
The Journal of pediatrics 147 (3), 321-326, 2005
Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics
LJ Strug, T Gonska, G He, K Keenan, W Ip, PY Boelle, F Lin, N Panjwani, ...
Human molecular genetics 25 (20), 4590-4600, 2016
Autosomal dominant inheritance of centrotemporal sharp waves in rolandic epilepsy families
B Bali, LL Kull, LJ Strug, T Clarke, PL Murphy, CI Akman, DA Greenberg, ...
Epilepsia 48 (12), 2266-2272, 2007
Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR)
LJ Strug, R Suresh, AJ Fyer, A Talati, PB Adams, W Li, SE Hodge, ...
Molecular psychiatry 15 (2), 166-176, 2010
Pilot association study of the β‐glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity
LN Clark, A Nicolai, S Afridi, J Harris, H Mejia‐Santana, L Strug, LJ Cote, ...
Movement disorders: official journal of the Movement Disorder Society 20 (1†…, 2005
Idiopathic focal epilepsies: the “lost tribe”
DK Pal, C Ferrie, L Addis, T Akiyama, G Capovilla, R Caraballo, ...
Epileptic Disorders 18 (3), 252-288, 2016
Genomic architecture of autism from comprehensive whole-genome sequence annotation
B Trost, B Thiruvahindrapuram, AJS Chan, W Engchuan, ...
Cell 185 (23), 4409-4427. e18, 2022
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