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 | 1698 | 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 | 674 | 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 | 426 | 2013 |
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 | 272 | 2011 |
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis H Corvol, SM Blackman, PY Boëlle, PJ Gallins, RG Pace, JR Stonebraker, ... Nature communications 6 (1), 8382, 2015 | 271 | 2015 |
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 | 238 | 2009 |
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 | 233 | 2013 |
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 | 221 | 2012 |
Genetic modifiers of cystic fibrosis–related diabetes SM Blackman, CW Commander, C Watson, KM Arcara, LJ Strug, ... Diabetes 62 (10), 3627-3635, 2013 | 178 | 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 | 169 | 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 | 135 | 2007 |
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 | 125 | 2014 |
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 | 125 | 2005 |
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 | 116 | 2010 |
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 | 108 | 2005 |
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 | 105 | 2005 |
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 | 101 | 2007 |
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 | 97 | 2016 |
Possible Interaction Between HLA-DRβ1 and Thyroglobulin Variants in Graves' Disease SE Hodge, Y Ban, LJ Strug, DA Greenberg, TF Davies, ES Concepcion, ... Thyroid 16 (4), 351-355, 2006 | 92 | 2006 |
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 | 90 | 2016 |