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Lisa J. Strug, Ph.D. - Publications

Affiliations: 
2003 University of Toronto, Toronto, ON, Canada 
Area:
Biostatistics Biology
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Year Citation  Score
2022 Price KM, Wigg KG, Eising E, Feng Y, Blokland K, Wilkinson M, Kerr EN, Guger SL, Fisher SE, Lovett MW, Strug LJ, Barr CL. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Translational Psychiatry. 12: 495. PMID 36446759 DOI: 10.1038/s41398-022-02250-z  0.308
2022 Sun Q, Liu W, Rosen JD, Huang L, Pace RG, Dang H, Gallins PJ, Blue EE, Ling H, Corvol H, Strug LJ, Bamshad MJ, Gibson RL, Pugh EW, Blackman SM, et al. Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients. Hgg Advances. 3: 100090. PMID 35128485 DOI: 10.1016/j.xhgg.2022.100090  0.316
2022 Wang F, Panjwani N, Wang C, Sun L, Strug LJ. A flexible summary statistics-based colocalization method with application to the mucin cystic fibrosis lung disease modifier locus. American Journal of Human Genetics. PMID 35065708 DOI: 10.1016/j.ajhg.2021.12.012  0.306
2021 Burton CL, Lemire M, Xiao B, Corfield EC, Erdman L, Bralten J, Poelmans G, Yu D, Shaheen SM, Goodale T, Sinopoli VM, Soreni N, Hanna GL, Fitzgerald KD, ... ... Strug LJ, et al. Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder. Translational Psychiatry. 11: 91. PMID 33531474 DOI: 10.1038/s41398-020-01121-9  0.303
2020 Laselva O, Moraes TJ, He G, Bartlett C, Szàrics I, Ouyang H, Gunawardena TNA, Strug L, Bear CE, Gonska T. The CFTR Mutation c.3453G > C (D1152H) Confers an Anion Selectivity Defect in Primary Airway Tissue that Can Be Rescued by Ivacaftor. Journal of Personalized Medicine. 10. PMID 32414100 DOI: 10.3390/Jpm10020040  0.343
2020 Lorè NI, Sipione B, He G, Strug LJ, Atamni HJ, Dorman A, Mott R, Iraqi FA, Bragonzi A. Collaborative Cross Mice Yield Genetic Modifiers for Pseudomonas aeruginosa Infection in Human Lung Disease. Mbio. 11. PMID 32127447 DOI: 10.1128/Mbio.00097-20  0.387
2020 Price KM, Wigg KG, Feng Y, Blokland K, Wilkinson M, He G, Kerr EN, Carter TC, Guger SL, Lovett MW, Strug LJ, Barr CL. Genome-Wide Association Study of Word Reading: Overlap with Risk Genes for Neurodevelopmental Disorders. Genes, Brain, and Behavior. e12648. PMID 32108986 DOI: 10.1111/Gbb.12648  0.381
2020 Saferali A, Tang AC, Strug LJ, Quon BS, Zlosnik J, Sandford AJ, Turvey SE. Immunomodulatory function of the cystic fibrosis modifier gene BPIFA1. Plos One. 15: e0227067. PMID 31931521 DOI: 10.1371/Journal.Pone.0227067  0.339
2019 Baskurt Z, Mastromatteo S, Gong J, Wintle RF, Scherer SW, Strug LJ. VikNGS: A C ++ Variant Integration Kit for Next Generation Sequencing Association Analysis. Bioinformatics (Oxford, England). PMID 31580400 DOI: 10.1093/Bioinformatics/Btz716  0.732
2019 Trost B, Walker S, Haider SA, Sung WWL, Pereira S, Phillips CL, Higginbotham EJ, Strug LJ, Nguyen C, Raajkumar A, Szego MJ, Marshall CR, Scherer SW. Impact of DNA source on genetic variant detection from human whole-genome sequencing data. Journal of Medical Genetics. PMID 31515274 DOI: 10.1136/Jmedgenet-2019-106281  0.306
2019 Gong J, Wang F, Xiao B, Panjwani N, Lin F, Keenan K, Avolio J, Esmaeili M, Zhang L, He G, Soave D, Mastromatteo S, Baskurt Z, Kim S, O'Neal WK, ... ... Strug LJ, et al. Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci. Plos Genetics. 15: e1008007. PMID 30807572 DOI: 10.1371/Journal.Pgen.1008007  0.741
2019 Corfield E, Burton C, Strug L, Xiao B, Arnold P, Crosbie J, Schachar R. SU4CHARACTERIZING THE GENETICS OF ADHD TRAITS WITH COGNITIVE DEFICITS USING A MULTIVARIATE APPROACH European Neuropsychopharmacology. 29: S1270. DOI: 10.1016/J.Euroneuro.2018.08.368  0.301
2019 Barr C, Price K, Wigg K, Feng Y, Blokland K, Wilkinson M, He G, Kerr E, Guger S, Lovett M, Strug L. SA101GENOME-WIDE ASSOCIATION OF WORD READING: OVERLAP WITH RISK GENES FOR NEURODEVELOPMENTAL DISORDERS European Neuropsychopharmacology. 29: S1243-S1244. DOI: 10.1016/J.Euroneuro.2018.08.323  0.306
2019 Burton C, Zarrei M, Enghuan W, Merico D, MacDonald J, Xiao B, Paterson A, Strug L, Marshall C, Crosbie J, Arnold P, Schachar R, Scherer S. Copy Number Variants In Brain-Related Genes Are Associated With Neuropsychiatric Traits In Childhood European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.078  0.393
2018 Baskurt Z, Strug LJ. Genetic association analysis with pedigrees: Direct inference using the composite likelihood ratio. Genetic Epidemiology. PMID 30221395 DOI: 10.1002/Gepi.22153  0.744
2018 Corvol H, Mésinèle J, Douksieh IH, Strug LJ, Boëlle PY, Guillot L. Gene Is Associated With Lung Function Response to Ivacaftor in Patients With Cystic Fibrosis. Frontiers in Pharmacology. 9: 828. PMID 30140228 DOI: 10.3389/Fphar.2018.00828  0.337
2018 Strug LJ. The evidential statistical paradigm in genetics. Genetic Epidemiology. PMID 30120797 DOI: 10.1002/gepi.22151  0.307
2018 Strug LJ, Stephenson AL, Panjwani N, Harris A. Recent advances in developing therapeutics for cystic fibrosis. Human Molecular Genetics. 27: R173-R186. PMID 30060192 DOI: 10.1093/Hmg/Ddy188  0.362
2018 Darrah RJ, Jacono FJ, Joshi N, Mitchell AL, Sattar A, Campanaro CK, Litman P, Frey J, Nethery DE, Barbato ES, Hodges CA, Corvol H, Cutting GR, Knowles MR, Strug LJ, et al. AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29937318 DOI: 10.1016/J.Jcf.2018.05.013  0.35
2018 Eckford PDW, McCormack J, Munsie L, He G, Stanojevic S, Pereira SL, Ho K, Avolio J, Bartlett C, Yang JY, Wong AP, Wellhauser L, Huan LJ, Jiang JX, Ouyang H, ... ... Strug LJ, et al. The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29685812 DOI: 10.1016/J.Jcf.2018.03.013  0.302
2018 Panjwani N, Xiao B, Xu L, Gong J, Keenan K, Lin F, He G, Baskurt Z, Kim S, Zhang L, Esmaeili M, Blackman S, Scherer SW, Corvol H, Drumm M, ... ... Strug LJ, et al. Improving imputation in disease-relevant regions: lessons from cystic fibrosis. Npj Genomic Medicine. 3: 8. PMID 29581887 DOI: 10.1038/S41525-018-0047-6  0.75
2017 Hagemeijer MC, Siegwart DJ, Strug LJ, Cebotaru L, Torres MJ, Sofoluwe A, Beekman JM. Translational research to enable personalized treatment of cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29275953 DOI: 10.1016/J.Jcf.2017.10.017  0.31
2017 Polineni D, Dang H, Gallins PJ, Jones LC, Pace RG, Stonebraker JR, Commander LA, Krenicky JE, Zhou YH, Corvol H, Cutting GR, Drumm ML, Strug LJ, Boyle MP, Durie PR, et al. Airway Mucosal Host Defense is Key to Genomic Regulation of Cystic Fibrosis Lung Disease Severity. American Journal of Respiratory and Critical Care Medicine. PMID 28853905 DOI: 10.1164/Rccm.201701-0134Oc  0.372
2017 Dang H, Gallins PJ, Pace RG, Guo XL, Stonebraker JR, Corvol H, Cutting GR, Drumm ML, Strug LJ, Knowles MR, O'Neal WK. Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severity. Human Genome Variation. 4: 17016. PMID 28674633 DOI: 10.1038/Hgv.2017.16  0.333
2017 Dennis J, Medina-Rivera A, Truong V, Antounians L, Zwingerman N, Carrasco G, Strug L, Wells P, Trégouët DA, Morange PE, Wilson MD, Gagnon F. Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels. Genetic Epidemiology. PMID 28421636 DOI: 10.1002/Gepi.22049  0.347
2017 C Yuen RK, Merico D, Bookman M, L Howe J, Thiruvahindrapuram B, Patel RV, Whitney J, Deflaux N, Bingham J, Wang Z, Pellecchia G, Buchanan JA, Walker S, Marshall CR, Uddin M, ... ... Strug LJ, et al. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nature Neuroscience. PMID 28263302 DOI: 10.1038/Nn.4524  0.403
2017 Schachar R, Burton C, Zarrei M, MacDonald J, Merico D, Paterson A, Strug L, Marshall C, Crosbie J, Arnold P, Scherer S. Copy Number Variant Analysis Of Psychiatric Traits In A Community-Based Pediatric Sample European Neuropsychopharmacology. 27: S491-S492. DOI: 10.1016/J.Euroneuro.2016.09.585  0.391
2016 Strug LJ, Gonska T, He G, Keenan K, Ip W, Boëlle PY, Lin F, Panjwani N, Gong J, Li W, Soave D, Xiao B, Tullis E, Rabin H, Parkins MD, et al. Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics. Human Molecular Genetics. 25: 4590-4600. PMID 28171547 DOI: 10.1093/Hmg/Ddw290  0.35
2016 Pal DK, Ferrie C, Addis L, Akiyama T, Capovilla G, Caraballo R, de Saint-Martin A, Fejerman N, Guerrini R, Hamandi K, Helbig I, Ioannides AA, Kobayashi K, Lal D, Lesca G, ... ... Strug LJ, et al. Idiopathic focal epilepsies: the "lost tribe". Epileptic Disorders : International Epilepsy Journal With Videotape. PMID 27435520 DOI: 10.1684/Epd.2016.0839  0.355
2016 Dang H, Gallins PJ, Pace RG, Guo XL, Stonebraker JR, Corvol H, Cutting GR, Drumm ML, Strug LJ, Knowles MR, O'Neal WK. Novel variation at chr11p13 associated with cystic fibrosis lung disease severity. Human Genome Variation. 3: 16020. PMID 27408752 DOI: 10.1038/Hgv.2016.20  0.412
2016 Panjwani N, Wilson MD, Addis L, Crosbie J, Wirrell E, Auvin S, Caraballo RH, Kinali M, McCormick D, Oren C, Taylor J, Trounce J, Clarke T, Akman CI, Kugler SL, ... ... Strug LJ, et al. A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy. Annals of Clinical and Translational Neurology. 3: 512-522. PMID 27386500 DOI: 10.1002/Acn3.320  0.364
2016 Collaco JM, Blackman SM, Raraigh KS, Corvol H, Rommens JM, Pace RG, Boelle PY, McGready J, Sosnay PR, Strug LJ, Knowles MR, Cutting GR. Sources of Variation in Sweat Chloride Measurements in Cystic Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 27258095 DOI: 10.1164/Rccm.201603-0459Oc  0.307
2016 Borges K, Vasilevska-Ristovska J, Hussain-Shamsy N, Patel V, Banh T, Hebert D, Pearl RJ, Radhakrishnan S, Piscione TD, Licht CP, Langlois V, Levin L, Strug L, Parekh RS. Parental attitudes to genetic testing differ by ethnicity and immigration in childhood nephrotic syndrome: a cross-sectional study. Canadian Journal of Kidney Health and Disease. 3: 16. PMID 26998310 DOI: 10.1186/S40697-016-0104-Y  0.325
2015 Vega YH, Smith A, Cockerill H, Tang S, Agirre-Arrizubieta Z, Goyal S, Pina M, Akman CI, Jolleff N, McGinnity C, Gomez K, Gupta R, Hughes E, Jackman J, McCormick D, ... ... Strug LJ, et al. Risk factors for reading disability in families with rolandic epilepsy. Epilepsy & Behavior : E&B. 53: 174-179. PMID 26580214 DOI: 10.1016/J.Yebeh.2015.10.016  0.317
2015 Corvol H, Blackman SM, Boëlle PY, Gallins PJ, Pace RG, Stonebraker JR, Accurso FJ, Clement A, Collaco JM, Dang H, Dang AT, Franca A, Gong J, Guillot L, Keenan K, ... ... Strug LJ, et al. Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis. Nature Communications. 6: 8382. PMID 26417704 DOI: 10.1038/Ncomms9382  0.403
2015 Soave D, Corvol H, Panjwani N, Gong J, Li W, Boëlle PY, Durie PR, Paterson AD, Rommens JM, Strug LJ, Sun L. A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways. American Journal of Human Genetics. 97: 125-38. PMID 26140448 DOI: 10.1016/J.Ajhg.2015.05.015  0.41
2015 Dupuis A, Keenan K, Ooi CY, Dorfman R, Sontag MK, Naehrlich L, Castellani C, Strug LJ, Rommens JM, Gonska T. Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26087176 DOI: 10.1038/Gim.2015.79  0.321
2015 Addis L, Ahn JW, Dobson R, Dixit A, Ogilvie CM, Pinto D, Vaags AK, Coon H, Chaste P, Wilson S, Parr JR, Andrieux J, Lenne B, Tumer Z, Leuzzi V, ... ... Strug LJ, et al. Microdeletions of ELP4 are Associated with Language Impairment, Autism Spectrum Disorder and Mental Retardation. Human Mutation. PMID 26010655 DOI: 10.1002/Humu.22816  0.353
2015 Dávila-Román VG, Sung YJ, Basson J, Cheng N, Nguyen KH, Nandakumar P, Hunt SC, Arnett DK, Rao DC, Chakravarti A, Badii R, Alkowari MK, Girotto G, Gasparini P, Mezzavilla M, ... ... Strug LJ, et al. 43rd European Mathematical Genetics Meeting (EMGM) 2015. April 16-17, 2015, Brest, France: Abstracts Human Heredity. 79: 28-52. PMID 25791167 DOI: 10.1159/000381109  0.32
2015 Miller MR, Soave D, Li W, Gong J, Pace RG, Boëlle PY, Cutting GR, Drumm ML, Knowles MR, Sun L, Rommens JM, Accurso F, Durie PR, Corvol H, Levy H, ... ... Strug LJ, et al. Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis. The Journal of Pediatrics. 166: 1152-1157.e6. PMID 25771386 DOI: 10.1016/J.Jpeds.2015.01.044  0.314
2015 Li W, Dobbins S, Tomlinson I, Houlston R, Pal DK, Strug LJ. Prioritizing rare variants with conditional likelihood ratios. Human Heredity. 79: 5-13. PMID 25659987 DOI: 10.1159/000371579  0.378
2015 O'Neal WK, Gallins P, Pace RG, Dang H, Wolf WE, Jones LC, Guo X, Zhou YH, Madar V, Huang J, Liang L, Moffatt MF, Cutting GR, Drumm ML, Rommens JM, ... Strug LJ, et al. Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypes. American Journal of Human Genetics. 96: 318-28. PMID 25640674 DOI: 10.1016/J.Ajhg.2014.12.022  0.396
2014 Pal DK, Strug LJ. The genetics of common epilepsies: common or distinct? The Lancet. Neurology. 13: 859-60. PMID 25087077 DOI: 10.1016/S1474-4422(14)70124-3  0.369
2014 Soave D, Miller MR, Keenan K, Li W, Gong J, Ip W, Accurso F, Sun L, Rommens JM, Sontag M, Durie PR, Strug LJ. Evidence for a causal relationship between early exocrine pancreatic disease and cystic fibrosis-related diabetes: a Mendelian randomization study. Diabetes. 63: 2114-9. PMID 24550193 DOI: 10.2337/Db13-1464  0.358
2014 Addis L, Chiang T, Clarke T, Hardison H, Kugler S, Mandelbaum DE, Novotny E, Wolf S, Strug LJ, Pal DK. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci. Genes, Brain, and Behavior. 13: 333-40. PMID 24286483 DOI: 10.1111/Gbb.12110  0.429
2014 Li W, Soave D, Miller MR, Keenan K, Lin F, Gong J, Chiang T, Stephenson AL, Durie P, Rommens J, Sun L, Strug LJ. Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities. Human Genetics. 133: 151-61. PMID 24057835 DOI: 10.1007/S00439-013-1363-7  0.41
2013 Lesca G, Rudolf G, Bruneau N, Lozovaya N, Labalme A, Boutry-Kryza N, Salmi M, Tsintsadze T, Addis L, Motte J, Wright S, Tsintsadze V, Michel A, Doummar D, Lascelles K, ... Strug L, et al. GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nature Genetics. 45: 1061-6. PMID 23933820 DOI: 10.1038/Ng.2726  0.325
2013 Blackman SM, Commander CW, Watson C, Arcara KM, Strug LJ, Stonebraker JR, Wright FA, Rommens JM, Sun L, Pace RG, Norris SA, Durie PR, Drumm ML, Knowles MR, Cutting GR. Genetic modifiers of cystic fibrosis-related diabetes. Diabetes. 62: 3627-35. PMID 23670970 DOI: 10.2337/Db13-0510  0.368
2013 Crosbie J, Arnold P, Paterson A, Swanson J, Dupuis A, Li X, Shan J, Goodale T, Tam C, Strug LJ, Schachar RJ. Response inhibition and ADHD traits: correlates and heritability in a community sample. Journal of Abnormal Child Psychology. 41: 497-507. PMID 23315233 DOI: 10.1007/S10802-012-9693-9  0.315
2012 Strug LJ, Addis L, Chiang T, Baskurt Z, Li W, Clarke T, Hardison H, Kugler SL, Mandelbaum DE, Novotny EJ, Wolf SM, Pal DK. The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy. Plos One. 7: e40696. PMID 22815793 DOI: 10.1371/Journal.Pone.0040696  0.733
2012 Sun L, Rommens JM, Corvol H, Li W, Li X, Chiang TA, Lin F, Dorfman R, Busson PF, Parekh RV, Zelenika D, Blackman SM, Corey M, Doshi VK, Henderson L, ... ... Strug LJ, et al. Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis. Nature Genetics. 44: 562-9. PMID 22466613 DOI: 10.1038/Ng.2221  0.38
2011 Hodge SE, Baskurt Z, Strug LJ. Using parametric multipoint lods and mods for linkage analysis requires a shift in statistical thinking. Human Heredity. 72: 264-75. PMID 22189469 DOI: 10.1159/000331463  0.741
2011 Wright FA, Strug LJ, Doshi VK, Commander CW, Blackman SM, Sun L, Berthiaume Y, Cutler D, Cojocaru A, Collaco JM, Corey M, Dorfman R, Goddard K, Green D, Kent JW, et al. Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Nature Genetics. 43: 539-46. PMID 21602797 DOI: 10.1038/Ng.838  0.416
2011 Taylor C, Commander CW, Collaco JM, Strug LJ, Li W, Wright FA, Webel AD, Pace RG, Stonebraker JR, Naughton K, Dorfman R, Sandford A, Blackman SM, Berthiaume Y, Paré P, et al. A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studies. Pediatric Pulmonology. 46: 857-69. PMID 21462361 DOI: 10.1002/Ppul.21456  0.418
2011 Li W, Sun L, Corey M, Zou F, Lee S, Cojocaru AL, Taylor C, Blackman SM, Stephenson A, Sandford AJ, Dorfman R, Drumm ML, Cutting GR, Knowles MR, Durie P, ... ... Strug LJ, et al. Understanding the population structure of North American patients with cystic fibrosis. Clinical Genetics. 79: 136-46. PMID 20681990 DOI: 10.1111/J.1399-0004.2010.01502.X  0.335
2011 Hodge SE, Baskurt Z, Strug LJ, Greenberg DA, Vieland VJ, Huang Y, Seok S, Burian J, Catalyurek U, O’Connell J, Segre A, Valentine-Cooper W, Bailey-Wilson JE, Wilson AF, Devoto M, et al. Contents Vol. 72, 2011 Human Heredity. 72. DOI: 10.1159/000334420  0.682
2010 Pal DK, Li W, Clarke T, Lieberman P, Strug LJ. Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves. Genes, Brain, and Behavior. 9: 1004-12. PMID 20825490 DOI: 10.1111/J.1601-183X.2010.00648.X  0.38
2010 Strug LJ, Hodge SE, Chiang T, Pal DK, Corey PN, Rohde C. A pure likelihood approach to the analysis of genetic association data: an alternative to Bayesian and frequentist analysis. European Journal of Human Genetics : Ejhg. 18: 933-41. PMID 20424645 DOI: 10.1038/Ejhg.2010.47  0.617
2010 Strug LJ, Suresh R, Fyer AJ, Talati A, Adams PB, Li W, Hodge SE, Gilliam TC, Weissman MM. Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR). Molecular Psychiatry. 15: 166-76. PMID 18663369 DOI: 10.1038/Mp.2008.79  0.315
2010 Pal DK, Strug LJ, Veliskova J, Chachua T, Velisek L, Greenberg DA. ELP4 in rolandic epilepsy and BRD2 in juvenile myoclonic epilepsy Epilepsia. 51: 73-73. DOI: 10.1111/J.1528-1167.2010.02859.X  0.349
2009 Clarke T, Baskurt Z, Strug LJ, Pal DK. Evidence of shared genetic risk factors for migraine and rolandic epilepsy. Epilepsia. 50: 2428-33. PMID 19674062 DOI: 10.1111/J.1528-1167.2009.02240.X  0.729
2009 Dorfman R, Li W, Sun L, Lin F, Wang Y, Sandford A, Paré PD, McKay K, Kayserova H, Piskackova T, Macek M, Czerska K, Sands D, Tiddens H, Margarit S, ... ... Strug LJ, et al. Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results. Human Genetics. 126: 763-78. PMID 19662435 DOI: 10.1007/S00439-009-0724-8  0.424
2009 Strug LJ, Clarke T, Chiang T, Chien M, Baskurt Z, Li W, Dorfman R, Bali B, Wirrell E, Kugler SL, Mandelbaum DE, Wolf SM, McGoldrick P, Hardison H, Novotny EJ, et al. Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4). European Journal of Human Genetics : Ejhg. 17: 1171-81. PMID 19172991 DOI: 10.1038/Ejhg.2008.267  0.738
2008 Hodge SE, Rodriguez-Murillo L, Strug LJ, Greenberg DA. Multipoint lods provide reliable linkage evidence despite unknown limiting distribution: type I error probabilities decrease with sample size for multipoint lods and mods. Genetic Epidemiology. 32: 800-15. PMID 18613118 DOI: 10.1002/Gepi.20350  0.338
2008 Kugler SL, Bali B, Lieberman P, Strug L, Gagnon B, Murphy PL, Clarke T, Greenberg DA, Pal DK. An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder. Epilepsia. 49: 1086-90. PMID 18248446 DOI: 10.1111/J.1528-1167.2007.01517.X  0.398
2008 Pal DK, Strug LJ, Greenberg DA. Evaluating candidate genes in common epilepsies and the nature of evidence. Epilepsia. 49: 386-92. PMID 18028406 DOI: 10.1111/J.1528-1167.2007.01416.X  0.401
2007 Clarke T, Strug LJ, Murphy PL, Bali B, Carvalho J, Foster S, Tremont G, Gagnon BR, Dorta N, Pal DK. High risk of reading disability and speech sound disorder in rolandic epilepsy families: case-control study. Epilepsia. 48: 2258-65. PMID 17850323 DOI: 10.1111/J.1528-1167.2007.01276.X  0.361
2007 Bali B, Kull LL, Strug LJ, Clarke T, Murphy PL, Akman CI, Greenberg DA, Pal DK. Autosomal dominant inheritance of centrotemporal sharp waves in rolandic epilepsy families. Epilepsia. 48: 2266-72. PMID 17662063 DOI: 10.1111/J.1528-1167.2007.01221.X  0.319
2006 Strug LJ, Hodge SE. An alternative foundation for the planning and evaluation of linkage analysis. II. Implications for multiple test adjustments. Human Heredity. 61: 200-9. PMID 16877867 DOI: 10.1159/000094775  0.342
2006 Strug LJ, Hodge SE. An alternative foundation for the planning and evaluation of linkage analysis. I. Decoupling "error probabilities" from "measures of evidence". Human Heredity. 61: 166-88. PMID 16865000 DOI: 10.1159/000094709  0.402
2006 Hodge SE, Ban Y, Strug LJ, Greenberg DA, Davies TF, Concepcion ES, Villanueva R, Tomer Y. Possible interaction between HLA-DRbeta1 and thyroglobulin variants in Graves' disease. Thyroid : Official Journal of the American Thyroid Association. 16: 351-5. PMID 16646680 DOI: 10.1089/Thy.2006.16.351  0.341
2005 Greenberg DA, Zhang J, Shmulewitz D, Strug LJ, Zimmerman R, Singh V, Marathe S. Construction of the model for the Genetic Analysis Workshop 14 simulated data: genotype-phenotype relationships, gene interaction, linkage, association, disequilibrium, and ascertainment effects for a complex phenotype. Bmc Genetics. 6: S3. PMID 16451639 DOI: 10.1186/1471-2156-6-S1-S3  0.413
2005 Greenberg DA, Cayanis E, Strug L, Marathe S, Durner M, Pal DK, Alvin GB, Klotz I, Dicker E, Shinnar S, Bromfield EB, Resor S, Cohen J, Moshe SL, Harden C, et al. Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy. American Journal of Human Genetics. 76: 139-46. PMID 15532013 DOI: 10.1086/426735  0.4
Low-probability matches (unlikely to be authored by this person)
2018 Kim SO, Corey M, Stephenson AL, Strug LJ. Reference percentiles of FEV1 for the Canadian cystic fibrosis population: comparisons across time and countries. Thorax. PMID 29434047 DOI: 10.1136/Thoraxjnl-2017-210899  0.3
2022 Mastromatteo S, Chen A, Gong J, Lin F, Thiruvahindrapuram B, Sung WWL, Whitney J, Wang Z, Patel RV, Keenan K, Halevy A, Panjwani N, Avolio J, Wang C, Côté-Maurais G, ... ... Strug LJ, et al. High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification. Hgg Advances. 4: 100156. PMID 36386424 DOI: 10.1016/j.xhgg.2022.100156  0.296
2004 Katz SL, Strug LJ, Coates AL, Corey M. Disease severity in siblings with cystic fibrosis. Pediatric Pulmonology. 37: 407-12. PMID 15095323 DOI: 10.1002/Ppul.20007  0.296
2003 Strug L, Sun L, Corey M. The genetics of cross-sectional and longitudinal body mass index. Bmc Genetics. 4: S14. PMID 14975082 DOI: 10.1186/1471-2156-4-S1-S14  0.296
2019 Aksit MA, Pace RG, Vecchio-Pagan B, Ling H, Rommens JM, Boelle PY, Guillot L, Raraigh KS, Pugh E, Zhang P, Strug LJ, Drumm ML, Knowles MR, Cutting GR, Corvol H, et al. Genetic modifiers of cystic fibrosis-related diabetes have extensive overlap with type 2 diabetes and related traits. The Journal of Clinical Endocrinology and Metabolism. PMID 31697830 DOI: 10.1210/Clinem/Dgz102  0.293
2016 Tang AC, Saferali A, He G, Sandford AJ, Strug LJ, Turvey SE. Endoplasmic reticulum stress regulates chemokine production in cystic fibrosis airway cells through STAT3 modulation. The Journal of Infectious Diseases. PMID 27799352 DOI: 10.1093/Infdis/Jiw516  0.291
2020 Dang H, Polineni D, Pace RG, Stonebraker JR, Corvol H, Cutting GR, Drumm ML, Strug LJ, O'Neal WK, Knowles MR. Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputation. Plos One. 15: e0239189. PMID 33253230 DOI: 10.1371/journal.pone.0239189  0.289
2023 Tadros R, Zheng SL, Grace C, Jordà P, Francis C, Jurgens SJ, Thomson KL, Harper AR, Ormondroyd E, West DM, Xu X, Theotokis PI, Buchan RJ, McGurk KA, Mazzarotto F, ... ... Strug LJ, et al. Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy. Medrxiv : the Preprint Server For Health Sciences. PMID 36778260 DOI: 10.1101/2023.01.28.23285147  0.289
2018 Soave DM, Strug LJ. Testing Calibration of Cox Survival Models at Extremes of Event Risk. Frontiers in Genetics. 9: 177. PMID 29872446 DOI: 10.3389/Fgene.2018.00177  0.285
2006 Bali B, Kull L, Strug L, Clarke T, Greenberg D, Pal D. AUTOSOMAL DOMINANT TRANSMISSION OF CENTROTEMPORAL SPIKES IN ROLANDIC EPILEPSY FAMILIES Neuropediatrics. 37. DOI: 10.1055/S-2006-945563  0.283
2008 Talati A, Ponniah K, Strug LJ, Hodge SE, Fyer AJ, Weissman MM. Panic disorder, social anxiety disorder, and a possible medical syndrome previously linked to chromosome 13. Biological Psychiatry. 63: 594-601. PMID 17920564 DOI: 10.1016/J.Biopsych.2007.07.021  0.283
2007 Strug LJ, Rohde CA, Corey PN. An Introduction to Evidential Sample Size Calculations The American Statistician. 61: 207-212. DOI: 10.1198/000313007X222488  0.28
2005 Clark LN, Nicolai A, Afridi S, Harris J, Mejia-Santana H, Strug L, Cote LJ, Louis ED, Andrews H, Waters C, Ford B, Frucht S, Fahn S, Mayeux R, Ottman R, et al. Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 100-3. PMID 15517591 DOI: 10.1002/Mds.20320  0.278
2018 Reuter MS, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, Yuen RKC, Trost B, Paton TA, Pereira SL, Herbrick JA, Wintle RF, Merico D, Howe J, MacDonald JR, ... ... Strug LJ, et al. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 190: E126-E136. PMID 29431110 DOI: 10.1503/Cmaj.171151  0.277
2020 Panjwani N, Wang F, Mastromatteo S, Bao A, Wang C, He G, Gong J, Rommens JM, Sun L, Strug LJ. LocusFocus: Web-based colocalization for the annotation and functional follow-up of GWAS. Plos Computational Biology. 16: e1008336. PMID 33090994 DOI: 10.1371/journal.pcbi.1008336  0.277
2022 Casalino S, Frangione E, Chung M, MacDonald G, Chowdhary S, Mighton C, Faghfoury H, Bombard Y, Strug L, Pugh TJ, Simpson J, Arnoldo S, Aujla N, Bearss E, Binnie A, et al. Genome screening, reporting, and genetic counseling for healthy populations. Human Genetics. PMID 36331656 DOI: 10.1007/s00439-022-02480-7  0.275
2022 Trost B, Thiruvahindrapuram B, Chan AJS, Engchuan W, Higginbotham EJ, Howe JL, Loureiro LO, Reuter MS, Roshandel D, Whitney J, Zarrei M, Bookman M, Somerville C, Shaath R, Abdi M, ... ... Strug LJ, et al. Genomic architecture of autism from comprehensive whole-genome sequence annotation. Cell. 185: 4409-4427.e18. PMID 36368308 DOI: 10.1016/j.cell.2022.10.009  0.272
2008 Kavros PM, Clarke T, Strug LJ, Halperin JM, Dorta NJ, Pal DK. Attention impairment in rolandic epilepsy: systematic review. Epilepsia. 49: 1570-80. PMID 18410358 DOI: 10.1111/J.1528-1167.2008.01610.X  0.271
2005 Schneiderman-Walker J, Wilkes DL, Strug L, Lands LC, Pollock SL, Selvadurai HC, Hay J, Coates AL, Corey M. Sex differences in habitual physical activity and lung function decline in children with cystic fibrosis. The Journal of Pediatrics. 147: 321-6. PMID 16182669 DOI: 10.1016/J.Jpeds.2005.03.043  0.266
2022 Frangione E, Chung M, Casalino S, MacDonald G, Chowdhary S, Mighton C, Faghfoury H, Bombard Y, Strug L, Pugh T, Simpson J, Hao L, Lebo M, Lane WJ, Taher J, et al. Genome Reporting for Healthy Populations-Pipeline for Genomic Screening from the GENCOV COVID-19 Study. Current Protocols. 2: e534. PMID 36205462 DOI: 10.1002/cpz1.534  0.263
2006 Clarke T, Bali B, Carvalho J, Foster S, Tremont G, Hawash K, Strug L, Murphy P, Dorta N, Pal D. SPEECH AND LANGUAGE DISORDERS AGGREGATE IN ROLANDIC EPILEPSY FAMILIES Neuropediatrics. 37. DOI: 10.1055/S-2006-945564  0.261
2023 Roshandel D, Sanders EJ, Shakeshaft A, Panjwani N, Lin F, Collingwood A, Hall A, Keenan K, Deneubourg C, Mirabella F, Topp S, Zarubova J, Thomas RH, Talvik I, Syvertsen M, ... ... Strug LJ, et al. SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy. Npj Genomic Medicine. 8: 28. PMID 37770509 DOI: 10.1038/s41525-023-00370-z  0.26
2022 Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, ... ... Strug LJ, et al. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America. 119: e2202764119. PMID 35998220 DOI: 10.1073/pnas.2202764119  0.256
2011 Gonska T, Keenan K, Dorfman R, Taylor C, Sun L, Ooi C, Ooi C, Zielenski J, Corey M, Rommens J, Strug L, Durie P. 12* The relation between meconium ileus prevalence score and functional severity of CFTR mutations Journal of Cystic Fibrosis. 10: S3. DOI: 10.1016/S1569-1993(11)60034-9  0.252
2023 Zhou YH, Gallins PJ, Pace RG, Dang H, Aksit MA, Blue EE, Buckingham KJ, Collaco JM, Faino AV, Gordon WW, Hetrick KN, Ling H, Liu W, Onchiri FM, Pagel K, ... ... Strug LJ, et al. Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole Genome Analysis of 7,840 Patients. American Journal of Respiratory and Critical Care Medicine. PMID 36921087 DOI: 10.1164/rccm.202209-1653OC  0.251
2018 Syme C, Pelletier S, Shin J, Abrahamowicz M, Leonard G, Perron M, Richer L, Veillette S, Gaudet D, Pike B, Strug LJ, Wang Y, Xu H, Taylor G, Bennett S, et al. Visceral fat-related systemic inflammation and the adolescent brain: a mediating role of circulating glycerophosphocholines. International Journal of Obesity (2005). PMID 30206338 DOI: 10.1038/S41366-018-0202-2  0.247
2022 Gong J, He G, Wang C, Bartlett C, Panjwani N, Mastromatteo S, Lin F, Keenan K, Avolio J, Halevy A, Shaw M, Esmaeili M, Côté-Maurais G, Adam D, Bégin S, ... ... Strug LJ, et al. Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease. Npj Genomic Medicine. 7: 28. PMID 35396391 DOI: 10.1038/s41525-022-00299-9  0.247
2017 Chin M, Strug L, Stephenson AL. Editorial to Don't judge a book by its cover: the emerging challenge of diagnosing CF in non-Caucasians. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 28599956 DOI: 10.1016/J.Jcf.2017.05.007  0.244
2015 Saferali A, Obeidat M, Bérubé JC, Lamontagne M, Bossé Y, Laviolette M, Hao K, Nickle DC, Timens W, Sin DD, Postma DS, Strug LJ, Gallins PJ, Paré PD, Bingle CD, et al. Polymorphisms associated with expression of BPIFA1/BPIFB1 and lung disease severity in cystic fibrosis. American Journal of Respiratory Cell and Molecular Biology. 53: 607-14. PMID 25574903 DOI: 10.1165/rcmb.2014-0182OC  0.243
2017 Strug LJ, Pal DK. Reply to: Is a microRNA-328 binding site in PAX6 associated with Rolandic epilepsy? Annals of Clinical and Translational Neurology. 4: 278-280. PMID 28382310 DOI: 10.1002/Acn3.403  0.242
2020 Lin YC, Brooks JD, Bull SB, Gagnon F, Greenwood CMT, Hung RJ, Lawless J, Paterson AD, Sun L, Strug LJ. Statistical power in COVID-19 case-control host genomic study design. Genome Medicine. 12: 115. PMID 33371892 DOI: 10.1186/s13073-020-00818-2  0.24
2006 Huang Q, Ng MYM, Cheung C, Chan V, Sham P, Chung R, Hauser ER, Martin ER, Njajou OT, Alizadeh BZ, Aulchenko Y, Zillikens MC, Strug LJ, Hodge SE, Guedj M, et al. Contents Vol. 61, 2006 Human Heredity. 61: 247-248. DOI: 10.1159/000095745  0.238
2016 Syme C, Czajkowski S, Shin J, Abrahamowicz M, Leonard G, Perron M, Richer L, Veillette S, Gaudet D, Strug L, Wang Y, Xu H, Taylor G, Paus T, Bennett S, et al. Glycerophosphocholine Metabolites and Cardiovascular Disease Risk Factors in Adolescents: A Cohort Study. Circulation. PMID 27756781 DOI: 10.1161/Circulationaha.116.022993  0.237
2021 Chen B, Craiu RV, Strug LJ, Sun L. The X factor: A robust and powerful approach to X-chromosome-inclusive whole-genome association studies. Genetic Epidemiology. PMID 34224641 DOI: 10.1002/gepi.22422  0.231
2016 Strug LJ, Gonska T, He G, Keenan K, Ip W, Boelle PY, Lin F, Panjwani N, Gong J, Li W, Soave D, Xiao B, Tullis E, Rabin H, Parkins MD, et al. Cystic Fibrosis Gene Modifier SLC26A9 Modulates Airway Response to CFTR-directed Therapeutics. Human Molecular Genetics. PMID 27571897 DOI: 10.1093/hmg/ddw290  0.225
2020 Shakeshaft A, Panjwani N, McDowall R, Crudgington H, Peña Ceballos J, Andrade DM, Beier CP, Fong CY, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Orsini A, Rees MI, ... ... Strug LJ, et al. Trait impulsivity in Juvenile Myoclonic Epilepsy. Annals of Clinical and Translational Neurology. PMID 33264519 DOI: 10.1002/acn3.51255  0.224
2002 Curriero FC, Heiner KS, Samet JM, Zeger SL, Strug L, Patz JA. Temperature and mortality in 11 cities of the eastern United States. American Journal of Epidemiology. 155: 80-7. PMID 11772788 DOI: 10.1093/Aje/155.1.80  0.215
2023 Zhong L, Strug LJ. RoPE: A robust profile likelihood method for differential gene expression analysis. Genetic Epidemiology. PMID 37042632 DOI: 10.1002/gepi.22526  0.212
2021 Povysil G, Butler-Laporte G, Shang N, Wang C, Khan A, Alaamery M, Nakanishi T, Zhou S, Forgetta V, Eveleigh RJM, Bourgey M, Aziz N, Jones SJ, Knoppers B, Scherer SW, ... Strug LJ, et al. Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19. The Journal of Clinical Investigation. PMID 34043590 DOI: 10.1172/JCI147834  0.208
2020 Povysil G, Butler-Laporte G, Shang N, Weng C, Khan A, Alaamery M, Nakanishi T, Zhou S, Forgetta V, Eveleigh R, Bourgey M, Aziz N, Jones S, Knoppers B, Scherer S, ... Strug L, et al. Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19. Medrxiv : the Preprint Server For Health Sciences. PMID 33398295 DOI: 10.1101/2020.12.18.20248226  0.207
2014 Derkach A, Chiang T, Gong J, Addis L, Dobbins S, Tomlinson I, Houlston R, Pal DK, Strug LJ. Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic. Bioinformatics (Oxford, England). 30: 2179-88. PMID 24733292 DOI: 10.1093/bioinformatics/btu196  0.204
2006 Huang Q, Ng MYM, Cheung C, Chan V, Sham P, Chung R, Hauser ER, Martin ER, Njajou OT, Alizadeh BZ, Aulchenko Y, Zillikens MC, Strug LJ, Hodge SE, Guedj M, et al. Subject Index Vol. 61, 2006 Human Heredity. 61: 245-246. DOI: 10.1159/000095744  0.193
2023 Zarrei M, Burton CL, Engchuan W, Higginbotham EJ, Wei J, Shaikh S, Roslin NM, MacDonald JR, Pellecchia G, Nalpathamkalam T, Lamoureux S, Manshaei R, Howe J, Trost B, Thiruvahindrapuram B, ... ... Strug LJ, et al. Gene copy number variation and pediatric mental health/neurodevelopment in a general population. Human Molecular Genetics. PMID 37154571 DOI: 10.1093/hmg/ddad074  0.188
2021 Rauscher R, Bampi GB, Guevara-Ferrer M, Santos LA, Joshi D, Mark D, Strug LJ, Rommens JM, Ballmann M, Sorscher EJ, Oliver KE, Ignatova Z. Positive epistasis between disease-causing missense mutations and silent polymorphism with effect on mRNA translation velocity. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33468668 DOI: 10.1073/pnas.2010612118  0.182
2022 He G, Panjwani N, Avolio J, Ouyang H, Keshavjee S, Rommens JM, Gonska T, Moraes TJ, Strug LJ. Expression of cystic fibrosis lung disease modifier genes in human airway models. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 35190293 DOI: 10.1016/j.jcf.2022.02.007  0.181
2023 Rubboli G, Beier CP, Selmer KK, Syvertsen M, Shakeshaft A, Collingwood A, Hall A, Andrade DM, Fong CY, Gesche J, Greenberg DA, Hamandi K, Lim KS, Ng CC, Orsini A, ... ... Strug LJ, et al. Variation in prognosis and treatment outcome in juvenile myoclonic epilepsy: a Biology of Juvenile Myoclonic Epilepsy Consortium proposal for a practical definition and stratified medicine classifications. Brain Communications. 5: fcad182. PMID 37361715 DOI: 10.1093/braincomms/fcad182  0.174
2021 Lin YC, Keenan K, Gong J, Panjwani N, Avolio J, Lin F, Adam D, Barrett P, Bégin S, Berthiaume Y, Bilodeau L, Bjornson C, Brusky J, Burgess C, Chilvers M, ... ... Strug LJ, et al. Cystic fibrosis-related diabetes onset can be predicted using biomarkers measured at birth. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33500570 DOI: 10.1038/s41436-020-01073-x  0.174
2023 Price KM, Wigg KG, Nigam A, Feng Y, Blokland K, Wilkinson M, Kerr EN, Guger SL, Lovett MW, Strug LJ, Tripathy SJ, Barr CL. Identification of brain cell types underlying genetic association with word reading and correlated traits. Molecular Psychiatry. PMID 36750735 DOI: 10.1038/s41380-023-01970-y  0.174
2023 Sahakyan Y, Abrahamyan L, Ratjen F, Bear C, Strug L, Eckford PDW, Peel JK, Krahn M, Sander B. Cost-effectiveness analysis of genetic tools to predict treatment response in patients with cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 37100704 DOI: 10.1016/j.jcf.2023.04.013  0.172
2020 Corbett RD, Eveleigh R, Whitney J, Barai N, Bourgey M, Chuah E, Johnson J, Moore RA, Moradin N, Mungall KL, Pereira S, Reuter MS, Thiruvahindrapuram B, Wintle RF, Ragoussis J, ... Strug LJ, et al. A Distributed Whole Genome Sequencing Benchmark Study. Frontiers in Genetics. 11: 612515. PMID 33335541 DOI: 10.3389/fgene.2020.612515  0.17
2022 Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, ... ... Strug LJ, et al. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Scientific Reports. 12: 2785. PMID 35190554 DOI: 10.1038/s41598-022-06324-2  0.148
2023 Birimberg-Schwartz L, Ip W, Bartlett C, Avolio J, Vonk AM, Gunawardena T, Du K, Esmaeili M, Beekman JM, Rommens J, Strug L, Bear CE, Moraes TJ, Gonska T. Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis. Life Science Alliance. 6. PMID 37024122 DOI: 10.26508/lsa.202201857  0.145
2023 Abbondanza F, Dale PS, Wang CA, Hayiou-Thomas ME, Toseeb U, Koomar TS, Wigg KG, Feng Y, Price KM, Kerr EN, Guger SL, Lovett MW, Strug LJ, van Bergen E, Dolan CV, et al. Language and reading impairments are associated with increased prevalence of non-right-handedness. Child Development. PMID 36780127 DOI: 10.1111/cdev.13914  0.131
2023 Morgan G, Casalino S, Chowdhary S, Frangione E, Fung CYJ, Haller S, Lapadula E, Scott M, Wolday D, Young J, Arnoldo S, Aujla N, Bearss E, Binnie A, Bombard Y, ... ... Strug L, et al. Characterizing Risk Factors for Hospitalization and Clinical Characteristics in a Cohort of COVID-19 Patients Enrolled in the GENCOV Study. Viruses. 15. PMID 37632107 DOI: 10.3390/v15081764  0.119
2021 Taher J, Mighton C, Chowdhary S, Casalino S, Frangione E, Arnoldo S, Bearss E, Binnie A, Bombard Y, Borgundvaag B, Chertkow H, Clausen M, Devine L, Faghfoury H, Friedman SM, ... ... Strug L, et al. Implementation of serological and molecular tools to inform COVID-19 patient management: protocol for the GENCOV prospective cohort study. Bmj Open. 11: e052842. PMID 34593505 DOI: 10.1136/bmjopen-2021-052842  0.104
2021 Lin YC, Keenan K, Gong J, Panjwani N, Avolio J, Lin F, Adam D, Barrett P, Bégin S, Berthiaume Y, Bilodeau L, Bjornson C, Brusky J, Burgess C, Chilvers M, ... ... Strug LJ, et al. Correction to: Cystic fibrosis-related diabetes onset can be predicted using biomarkers measured at birth. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 34389817 DOI: 10.1038/s41436-021-01281-z  0.097
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