| 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 |
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| 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 |
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| 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 |
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| 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 |
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