Cathy Barr, PhD - Publications

Affiliations: 
SickKids Hospital 

121 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.4
2019 Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, ... ... Barr CL, et al. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. The American Journal of Psychiatry. 176: 217-227. PMID 30818990 DOI: 10.1176/appi.ajp.2018.18070857  0.32
2018 Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Barr CL, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/science.aap8757  0.44
2017 Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/j.neuron.2017.06.010  0.32
2015 Barr CL, Misener VL. Decoding the Non-Coding Genome: Elucidating Genetic Risk Outside the Coding Genome. Genes, Brain, and Behavior. PMID 26515765 DOI: 10.1111/gbb.12269  0.52
2015 Rimay T, Benak I, Kiss E, Baji I, Feher A, Juhasz A, Strauss J, Kennedy J, Barr C, Kovacs M, Vetro A, Kapornai K. BDNF Val66Met polymorphism and stressful life events in melancholic childhood-onset depression. Psychiatric Genetics. 25: 249-55. PMID 26462036 DOI: 10.1097/YPG.0000000000000107  0.52
2015 Liu F, Hon GC, Villa GR, Turner KM, Ikegami S, Yang H, Ye Z, Li B, Kuan S, Lee AY, Zanca C, Wei B, Lucey G, Jenkins D, Zhang W, ... Barr CL, et al. EGFR Mutation Promotes Glioblastoma through Epigenome and Transcription Factor Network Remodeling. Molecular Cell. PMID 26455392 DOI: 10.1016/j.molcel.2015.09.002  0.52
2015 Hirschtritt ME, Lee PC, Pauls DL, Dion Y, Grados MA, Illmann C, King RA, Sandor P, McMahon WM, Lyon GJ, Cath DC, Kurlan R, Robertson MM, Osiecki L, Scharf JM, et al. Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome. Jama Psychiatry. 72: 325-33. PMID 25671412 DOI: 10.1001/jamapsychiatry.2014.2650  0.52
2015 Zhang K, Feng Y, Wigg KG, Sandor P, Barr CL. Association study of the SLITRK5 gene and Tourette syndrome. Psychiatric Genetics. 25: 31-4. PMID 25426764 DOI: 10.1097/YPG.0000000000000067  0.52
2015 Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Barr CL, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/appi.ajp.2014.13101306  0.52
2014 McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, ... ... Barr CL, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/j.jaac.2014.04.022  0.52
2014 Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, ... ... Barr C, et al. Genetic association signal near NTN4 in Tourette syndrome. Annals of Neurology. 76: 310-5. PMID 25042818 DOI: 10.1002/ana.24215  0.52
2014 Gomez L, Wigg K, Zhang K, Lopez L, Sandor P, Malone M, Barr CL. Association of the KCNJ5 gene with Tourette Syndrome and Attention-Deficit/Hyperactivity Disorder. Genes, Brain, and Behavior. 13: 535-42. PMID 24840790 DOI: 10.1111/gbb.12141  0.52
2014 Tran C, Wigg KG, Zhang K, Cate-Carter TD, Kerr E, Field LL, Kaplan BJ, Lovett MW, Barr CL. Association of the ROBO1 gene with reading disabilities in a family-based analysis. Genes, Brain, and Behavior. 13: 430-8. PMID 24612512 DOI: 10.1111/gbb.12126  0.52
2014 Bisceglia R, Jenkins J, Barr CL, Wigg KG, Schmidt LA. Arginine Vasopressin Gene Variation and Behavioural Inhibition in Children: An Exploratory Study Infant and Child Development. 23: 249-258. DOI: 10.1002/icd.1866  0.52
2013 Spencer BW, Prainsack B, Rujescu D, Giegling I, Collier DA, Gaughran F, MacCabe JH, Barr CL, Sigurdsson E, Stovring H, Malhotra AK, Curran SR. Opening Pandora's box in the UK: a hypothetical pharmacogenetic test for clozapine. Pharmacogenomics. 14: 1907-14. PMID 24236489 DOI: 10.2217/pgs.13.182  0.52
2013 Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/journal.pgen.1003864  0.52
2013 Karagiannidis I, Dehning S, Sandor P, Tarnok Z, Rizzo R, Wolanczyk T, Madruga-Garrido M, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Szymanska U, Anastasiou Z, Stathias V, ... ... Barr C, et al. Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families. Journal of Medical Genetics. 50: 760-4. PMID 23825391 DOI: 10.1136/jmedgenet-2013-101637  0.52
2013 Tran C, Gagnon F, Wigg KG, Feng Y, Gomez L, Cate-Carter TD, Kerr EN, Field LL, Kaplan BJ, Lovett MW, Barr CL. A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 146-56. PMID 23341075 DOI: 10.1002/ajmg.b.32123  0.52
2013 Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Barr CL, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/mp.2012.69  0.52
2012 Xie W, Barr CL, Kim A, Yue F, Lee AY, Eubanks J, Dempster EL, Ren B. Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome. Cell. 148: 816-31. PMID 22341451 DOI: 10.1016/j.cell.2011.12.035  0.52
2012 Bisceglia R, Jenkins JM, Wigg KG, O'Connor TG, Moran G, Barr CL. Arginine vasopressin 1a receptor gene and maternal behavior: evidence of association and moderation. Genes, Brain, and Behavior. 11: 262-8. PMID 22288734 DOI: 10.1111/j.1601-183X.2012.00769.x  0.52
2012 Karagiannidis I, Rizzo R, Tarnok Z, Wolanczyk T, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Barta C, Szymanska U, Panteloglou G, Miranda DM, Feng Y, Sandor P, ... Barr C, et al. Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families. Molecular Psychiatry. 17: 665-8. PMID 22083730 DOI: 10.1038/mp.2011.151  0.52
2011 Tobe SW, Baker B, Hunter K, Kiss A, Perkins N, Gomez L, Feng Y, Wigg K, Barr CL. The impact of endothelin-1 genetic analysis and job strain on ambulatory blood pressure. Journal of Psychosomatic Research. 71: 97-101. PMID 21767690 DOI: 10.1016/j.jpsychores.2011.01.003  0.52
2011 Elbert A, Lovett MW, Cate-Carter T, Pitch A, Kerr EN, Barr CL. Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia. Behavior Genetics. 41: 77-89. PMID 21207242 DOI: 10.1007/s10519-010-9434-1  0.52
2011 Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM. Family-based genetic association study of DLGAP3 in Tourette Syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 108-14. PMID 21184590 DOI: 10.1002/ajmg.b.31134  0.52
2010 Feng Y, Kapornai K, Kiss E, Tamás Z, Mayer L, Baji I, Daróczi G, Benák I, Kothencné VO, Dombovári E, Kaczvinszk E, Besnyo M, Gádoros J, Székely J, Kovacs M, ... ... Barr CL, et al. Association of the GABRD gene and childhood-onset mood disorders. Genes, Brain, and Behavior. 9: 668-72. PMID 20561060 DOI: 10.1111/j.1601-183X.2010.00598.x  0.52
2010 Strauss JS, Freeman NL, Shaikh SA, Vetró A, Kiss E, Kapornai K, Daróczi G, Rimay T, Kothencné VO, Dombovári E, Kaczvinszk E, Tamás Z, Baji I, Besny M, Gádoros J, ... ... Barr CL, et al. No association between oxytocin or prolactin gene variants and childhood-onset mood disorders. Psychoneuroendocrinology. 35: 1422-8. PMID 20547007 DOI: 10.1016/j.psyneuen.2010.04.008  0.52
2010 Knight S, Coon H, Johnson M, Leppert MF, Camp NJ, McMahon WM, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Santangelo S, Stewart SE, Scharf J, ... ... Barr CL, et al. Linkage analysis of Tourette syndrome in a large Utah pedigree American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 656-662. PMID 19777563 DOI: 10.1002/ajmg.b.31035  0.52
2010 Couto JM, Livne-Bar I, Huang K, Xu Z, Cate-Carter T, Feng Y, Wigg K, Humphries T, Tannock R, Kerr EN, Lovett MW, Bremner R, Barr CL. Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 447-62. PMID 19588467 DOI: 10.1002/ajmg.b.30999  0.52
2010 Dempster EL, Kiss E, Kapornai K, Daróczi G, Mayer L, Baji I, Tamas Z, Gadoros J, Kennedy JL, Vetró A, Kovacs M, Barr CL. No evidence of an association between two genes, EDN1 and ACE, and childhood-onset mood disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 341-6. PMID 19475602 DOI: 10.1002/ajmg.b.30983  0.52
2010 Barr CL, Sandor P. Adolescent brain development and behavior Pediatric Health. 4: 13-16. DOI: 10.2217/phe.09.66  0.52
2009 Dempster EL, Burcescu I, Wigg K, Kiss E, Baji I, Gadoros J, Tamás Z, Kapornai K, Daróczy G, Kennedy JL, Vetró A, Kovacs M, Barr CL. Further genetic evidence implicates the vasopressin system in childhood-onset mood disorders. The European Journal of Neuroscience. 30: 1615-9. PMID 19821843 DOI: 10.1111/j.1460-9568.2009.06930.x  0.52
2009 Couto JM, Gomez L, Wigg K, Ickowicz A, Pathare T, Malone M, Kennedy JL, Schachar R, Barr CL. Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biological Psychiatry. 66: 368-75. PMID 19362708 DOI: 10.1016/j.biopsych.2009.02.016  0.52
2009 Dorval KM, Burcescu I, Adams J, Wigg KG, King N, Kiss E, Kapornai K, Gádoros J, Tamás Z, Daróczi G, Baji I, Mayer L, Kennedy JL, Vetró A, Kovacs M, ... Barr CL, et al. Association study of N-methyl-D-aspartate glutamate receptor subunit genes and childhood-onset mood disorders. Psychiatric Genetics. 19: 156-7. PMID 19352217 DOI: 10.1097/YPG.0b013e32832a5097  0.52
2009 Gomez L, Wigg K, Feng Y, Kiss E, Kapornai K, Tamás Z, Mayer L, Baji I, Daróczi G, Benák I, Kothencné VO, Dombovári E, Kaczvinszk E, Besnyo M, Gádoros J, ... ... Barr CL, et al. G72/G30 (DAOA) and juvenile-onset mood disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 1007-12. PMID 19089835 DOI: 10.1002/ajmg.b.30904  0.52
2009 Mill J, Wigg K, Burcescu I, Vetró A, Kiss E, Kapornai K, Tamás Z, Baji I, Gádoros J, Kennedy JL, Kovacs M, Barr CL. Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 866-73. PMID 19089807 DOI: 10.1002/ajmg.b.30909  0.52
2009 Wigg K, Feng Y, Gomez L, Kiss E, Kapornai K, Tamás Z, Mayer L, Baji I, Daróczi G, Benák I, Osváth VK, Dombovári E, Kaczvinszk E, Besnyõ M, Gádoros J, ... ... Barr CL, et al. Genome scan in sibling pairs with juvenile-onset mood disorders: Evidence for linkage to 13q and Xq. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 638-46. PMID 19035515 DOI: 10.1002/ajmg.b.30883  0.52
2009 Misener VL, Gomez L, Wigg KG, King N, Kiss E, Daróczi G, Kapornai K, Tamás Z, Mayer L, Gádoros J, Baji I, Kennedy JL, Kovacs M, Vetró A, Barr CL, et al. Tagging SNP association study of the IL-1beta gene (IL1B) and childhood-onset mood disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 653-9. PMID 19016479 DOI: 10.1002/ajmg.b.30885  0.52
2009 Miranda DM, Wigg K, Kabia EM, Feng Y, Sandor P, Barr CL. Association of SLITRK1 to Gilles de la Tourette Syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 483-6. PMID 18698576 DOI: 10.1002/ajmg.b.30840  0.52
2009 Laurin N, Wigg KG, Feng Y, Sandor P, Barr CL. Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 95-103. PMID 18454440 DOI: 10.1002/ajmg.b.30779  0.52
2008 Couto JM, Gomez L, Wigg K, Cate-Carter T, Archibald J, Anderson B, Tannock R, Kerr EN, Lovett MW, Humphries T, Barr CL. The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities. Journal of Neurogenetics. 22: 295-313. PMID 19085271 DOI: 10.1080/01677060802354328  0.52
2008 Wigg KG, Feng Y, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Malone M, Schachar R, Barr CL. Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region. Genes, Brain, and Behavior. 7: 877-86. PMID 19076634 DOI: 10.1111/j.1601-183X.2008.00425.x  0.52
2008 Gizer IR, Waldman ID, Abramowitz A, Barr CL, Feng Y, Wigg KG, Misener VL, Rowe DC. Relations between multi-informant assessments of ADHD symptoms, DAT1, and DRD4. Journal of Abnormal Psychology. 117: 869-80. PMID 19025233 DOI: 10.1037/a0013297  0.52
2008 Misener VL, Gomez L, Wigg KG, Luca P, King N, Kiss E, Daróczi G, Kapornai K, Tamas Z, Mayer L, Gádoros J, Baji I, Kennedy JL, Kovacs M, Vetró A, ... Barr CL, et al. Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disorders. Neuropsychobiology. 58: 71-80. PMID 18832862 DOI: 10.1159/000159775  0.52
2008 Bulgin NL, Strauss JS, King NA, Shaikh SA, George CJ, Fox NA, Barr CL, Kovacs M, Kennedy JL. Association study of theta EEG asymmetry and brain-derived neurotrophic factor gene variants in childhood-onset mood disorder. Neuromolecular Medicine. 10: 343-55. PMID 18543122 DOI: 10.1007/s12017-008-8038-x  0.52
2008 Mill J, Kiss E, Baji I, Kapornai K, Daróczy G, Vetró A, Kennedy J, Kovacs M, Barr C. Association study of the estrogen receptor alpha gene (ESR1) and childhood-onset mood disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1323-6. PMID 18449864 DOI: 10.1002/ajmg.b.30751  0.52
2008 Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B, Jenike E, Stewart SE, Pauls DL. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample. Neurology. 70: 1495-6. PMID 18413575 DOI: 10.1212/01.wnl.0000296833.25484.bb  0.52
2008 Shaikh SA, Strauss J, King N, Bulgin NL, Vetró A, Kiss E, George CJ, Kovacs M, Barr CL, Kennedy JL. Association study of serotonin system genes in childhood-onset mood disorder. Psychiatric Genetics. 18: 47-52. PMID 18349694 DOI: 10.1097/YPG.0b013e3282f08ab8  0.52
2008 Feng Y, Vetró A, Kiss E, Kapornai K, Daróczi G, Mayer L, Tamás Z, Baji I, Gádoros J, King N, Kennedy JL, Wigg K, Kovacs M, Barr CL. Association of the neurotrophic tyrosine kinase receptor 3 (NTRK3) gene and childhood-onset mood disorders. The American Journal of Psychiatry. 165: 610-6. PMID 18347002 DOI: 10.1176/appi.ajp.2007.07050805  0.52
2008 Ouellet-Morin I, Wigg KG, Feng Y, Dionne G, Robaey P, Brendgen M, Vitaro F, Simard L, Schachar R, Tremblay RE, Pérusse D, Boivin M, Barr CL. Association of the dopamine transporter gene and ADHD symptoms in a Canadian population-based sample of same-age twins. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1442-9. PMID 18165969 DOI: 10.1002/ajmg.b.30677  0.52
2008 Laurin N, Lee J, Ickowicz A, Pathare T, Malone M, Tannock R, Kennedy JL, Schachar RJ, Barr CL. Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 600-5. PMID 18081024 DOI: 10.1002/ajmg.b.30654  0.52
2008 Lee SI, Schachar RJ, Chen SX, Ornstein TJ, Charach A, Barr C, Ickowicz A. Predictive validity of DSM-IV and ICD-10 criteria for ADHD and hyperkinetic disorder. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 49: 70-8. PMID 17979965 DOI: 10.1111/j.1469-7610.2007.01784.x  0.52
2008 Crosbie J, Pérusse D, Barr CL, Schachar RJ. Validating psychiatric endophenotypes: inhibitory control and attention deficit hyperactivity disorder. Neuroscience and Biobehavioral Reviews. 32: 40-55. PMID 17976721 DOI: 10.1016/j.neubiorev.2007.05.002  0.52
2008 Laurin N, Ickowicz A, Pathare T, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. No evidence for genetic association between DARPP-32 (PP1R1B) polymorphisms and attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 339-42. PMID 17948899 DOI: 10.1002/ajmg.b.30604  0.52
2008 Miranda DM, Wigg K, Feng Y, Sandor P, Barr CL. Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 68-72. PMID 17671968 DOI: 10.1002/ajmg.b.30580  0.52
2008 Lee J, Laurin N, Crosbie J, Ickowicz A, Pathare T, Malone M, Kennedy JL, Tannock R, Schachar R, Barr CL. Association study of the nicotinic acetylcholine receptor alpha4 subunit gene, CHRNA4, in attention-deficit hyperactivity disorder. Genes, Brain, and Behavior. 7: 53-60. PMID 17504247 DOI: 10.1111/j.1601-183X.2007.00325.x  0.52
2008 Laurin N, Ickowicz A, Pathare T, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/hyperactivity disorder. Journal of Psychiatric Research. 42: 117-24. PMID 17166517 DOI: 10.1016/j.jpsychires.2006.10.010  0.52
2008 Barr CL, Misener VL. Dopamine system genes and ADHD: A review of the evidence Future Neurology. 3: 705-728. DOI: 10.2217/14796708.3.6.705  0.52
2007 Feng Y, Wigg K, King N, Vetró A, Kiss E, Kapornai K, Mayer L, Gádoros J, Kennedy JL, Kovacs M, Barr CL. GPR50 is not associated with childhood-onset mood disorders in a large sample of Hungarian families. Psychiatric Genetics. 17: 347-50. PMID 18075476 DOI: 10.1097/YPG.0b013e3281ac232f  0.52
2007 Dempster EL, Kiss E, Kapornai K, Daróczy G, Mayer L, Baji I, Tamas Z, Gadoros J, Kennedy JL, Vetró A, Kovacs M, Barr CL. No evidence of association between a functional polymorphism in the MTHFR gene and childhood-onset mood disorders. Molecular Psychiatry. 12: 1063-4. PMID 18043712 DOI: 10.1038/sj.mp.4002071  0.52
2007 Lee J, Laurin N, Crosbie J, Ickowicz A, Pathare T, Malone M, Tannock R, Kennedy JL, Schachar R, Barr CL. Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 976-81. PMID 17918236 DOI: 10.1002/ajmg.b.30437  0.52
2007 Dempster EL, Burcescu I, Wigg K, Kiss E, Baji I, Gadoros J, Tamás Z, Kennedy JL, Vetró A, Kovacs M, Barr CL. Evidence of an association between the vasopressin V1b receptor gene (AVPR1B) and childhood-onset mood disorders. Archives of General Psychiatry. 64: 1189-95. PMID 17909131 DOI: 10.1001/archpsyc.64.10.1189  0.52
2007 Makkar R, Gomez L, Wigg KG, Ickowicz A, Pathare T, Tannock R, Malone M, Kennedy JL, Schachar R, Barr CL. The gene for synapsin III and attention-deficit hyperactivity disorder. Psychiatric Genetics. 17: 109-12. PMID 17413450 DOI: 10.1097/YPG.0b013e328012a0c6  0.52
2007 Schachar R, Logan GD, Robaey P, Chen S, Ickowicz A, Barr C. Restraint and cancellation: multiple inhibition deficits in attention deficit hyperactivity disorder. Journal of Abnormal Child Psychology. 35: 229-38. PMID 17351752 DOI: 10.1007/s10802-006-9075-2  0.52
2007 Laurin N, Feng Y, Ickowicz A, Pathare T, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder. Molecular Psychiatry. 12: 226-9. PMID 17325714 DOI: 10.1038/sj.mp.4001936  0.52
2007 Luca P, Laurin N, Misener VL, Wigg KG, Anderson B, Cate-Carter T, Tannock R, Humphries T, Lovett MW, Barr CL. Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems. Molecular Psychiatry. 12: 776-85. PMID 17310237 DOI: 10.1038/sj.mp.4001972  0.52
2007 Pauls D, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Scharf JM, Santangelo S, Stewart SE, Platko J, Pauls DL, Cox NJ, Robertson MM, Service S, ... ... Barr CL, et al. Genome scan for tourette disorder in affected-sibling-pair and multigenerational families American Journal of Human Genetics. 80: 265-272. PMID 17304708 DOI: 10.1086/511052  0.52
2007 Dorval KM, Wigg KG, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Pathare T, Malone M, Schachar R, Barr CL. Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder. Genes, Brain, and Behavior. 6: 444-52. PMID 17010153 DOI: 10.1111/j.1601-183X.2006.00273.x  0.52
2007 Ickowicz A, Feng Y, Wigg K, Quist J, Pathare T, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL, Barr CL. The serotonin receptor HTR1B: gene polymorphisms in attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 121-5. PMID 16958036 DOI: 10.1002/ajmg.b.30398  0.52
2006 Wigg KG, Takhar A, Ickowicz A, Tannock R, Kennedy JL, Pathare T, Malone M, Schachar R, Barr CL. Gene for the serotonin transporter and ADHD: no association with two functional polymorphisms. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 566-70. PMID 16856124 DOI: 10.1002/ajmg.b.30247  0.52
2006 Ozbay F, Wigg KG, Turanli ET, Asherson P, Yazgan Y, Sandor P, Barr CL. Analysis of the dopamine beta hydroxylase gene in Gilles de la Tourette syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 673-7. PMID 16838359 DOI: 10.1002/ajmg.b.30393  0.52
2006 Burcescu I, Wigg K, Gomez L, King N, Vetró A, Kiss E, Kapornai K, Gádoros J, Kennedy JL, Kovacs M, Barr CL. Association study of the adrenergic receptors and childhood-onset mood disorders in Hungarian families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 227-33. PMID 16526032 DOI: 10.1002/ajmg.b.30292  0.52
2005 Laurin N, Misener VL, Crosbie J, Ickowicz A, Pathare T, Roberts W, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder. Molecular Psychiatry. 10: 1117-25. PMID 16172615 DOI: 10.1038/sj.mp.4001737  0.52
2005 Feng Y, Crosbie J, Wigg K, Pathare T, Ickowicz A, Schachar R, Tannock R, Roberts W, Malone M, Swanson J, Kennedy JL, Barr CL. The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder. Molecular Psychiatry. 10: 998-1005, 973. PMID 16088329 DOI: 10.1038/sj.mp.4001722  0.52
2005 Feng Y, Wigg KG, Makkar R, Ickowicz A, Pathare T, Tannock R, Roberts W, Malone M, Kennedy JL, Schachar R, Barr CL. Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 139: 1-6. PMID 16082693 DOI: 10.1002/ajmg.b.30190  0.52
2005 Burcescu I, Wigg K, King N, Vetró A, Kiss E, Katay L, Kennedy JL, Kovacs M, Barr CL. Association study of CREB1 and childhood-onset mood disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 137: 45-50. PMID 15999345 DOI: 10.1002/ajmg.b.30201  0.52
2005 Strauss J, Barr CL, George CJ, Devlin B, Vetró A, Kiss E, Baji I, King N, Shaikh S, Lanktree M, Kovacs M, Kennedy JL. Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample. Molecular Psychiatry. 10: 861-7. PMID 15940299 DOI: 10.1038/sj.mp.4001685  0.52
2005 Schachar RJ, Crosbie J, Barr CL, Ornstein TJ, Kennedy J, Malone M, Roberts W, Ickowicz A, Tannock R, Chen S, Pathare T. Inhibition of motor responses in siblings concordant and discordant for attention deficit hyperactivity disorder. The American Journal of Psychiatry. 162: 1076-82. PMID 15930055 DOI: 10.1176/appi.ajp.162.6.1076  0.52
2005 Zai G, King N, Wong GW, Barr CL, Kennedy JL. Possible association between the gamma-aminobutyric acid type B receptor 1 (GABBR1) gene and schizophrenia. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 15: 347-52. PMID 15820424 DOI: 10.1016/j.euroneuro.2004.12.006  0.52
2005 Zai G, Arnold P, Burroughs E, Barr CL, Richter MA, Kennedy JL. Evidence for the gamma-amino-butyric acid type B receptor 1 (GABBR1) gene as a susceptibility factor in obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 134: 25-9. PMID 15685626 DOI: 10.1002/ajmg.b.30152  0.52
2005 Zai G, King N, Wigg K, Couto J, Wong GW, Honer WG, Barr CL, Kennedy JL. Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia. Genes, Brain, and Behavior. 4: 2-9. PMID 15660663 DOI: 10.1111/j.1601-183X.2004.00089.x  0.52
2005 Adams JH, Wigg KG, King N, Burcescu I, Vetró A, Kiss E, Baji I, George CJ, Kennedy JL, Kovacs M, Barr CL. Association study of neurotrophic tyrosine kinase receptor type 2 (NTRK2) and childhood-onset mood disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 132: 90-5. PMID 15389758 DOI: 10.1002/ajmg.b.30084  0.52
2005 Wigg KG, Couto JM, Feng Y, Crosbie J, Anderson B, Cate-Carter T, Tannock R, Lovett MW, Humphries T, Kennedy JL, Ickowicz A, Pathare T, Roberts W, Malone M, Schachar R, ... Barr CL, et al. Investigation of the relationship of attention deficit hyperactivity disorder to the EKN1 gene on chromosome 15q21 Scientific Studies of Reading. 9: 261-283. DOI: 10.1207/s1532799xssr0903_5  0.52
2004 Strauss J, Barr CL, George CJ, Ryan CM, King N, Shaikh S, Kovacs M, Kennedy JL. BDNF and COMT polymorphisms: relation to memory phenotypes in young adults with childhood-onset mood disorder. Neuromolecular Medicine. 5: 181-92. PMID 15626819 DOI: 10.1385/NMM:5:3:181  0.52
2004 Strauss J, Barr CL, George CJ, King N, Shaikh S, Devlin B, Kovacs M, Kennedy JL. Association study of brain-derived neurotrophic factor in adults with a history of childhood onset mood disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 131: 16-9. PMID 15384083 DOI: 10.1002/ajmg.b.30041  0.52
2004 Misener VL, Schachar R, Ickowicz A, Malone M, Roberts W, Tannock R, Kennedy JL, Pathare T, Barr CL. Replication test for association of the IL-1 receptor antagonist gene, IL1RN, with attention-deficit/hyperactivity disorder. Neuropsychobiology. 50: 231-4. PMID 15365221 DOI: 10.1159/000079976  0.52
2004 Paschou P, Feng Y, Pakstis AJ, Speed WC, DeMille MM, Kidd JR, Jaghori B, Kurlan R, Pauls DL, Sandor P, Barr CL, Kidd KK. Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region. American Journal of Human Genetics. 75: 545-60. PMID 15303240 DOI: 10.1086/424389  0.52
2004 Zai G, Bezchlibnyk YB, Richter MA, Arnold P, Burroughs E, Barr CL, Kennedy JL. Myelin oligodendrocyte glycoprotein (MOG) gene is associated with obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 129: 64-8. PMID 15274043 DOI: 10.1002/ajmg.b.30077  0.52
2004 Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, Macciardi F, Tannock R, Lovett MW, Humphries TW, Barr CL. Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Molecular Psychiatry. 9: 1111-21. PMID 15249932 DOI: 10.1038/sj.mp.4001543  0.52
2004 Ambrósio AM, Kennedy JL, Macciardi F, Barr C, Soares MJ, Oliveira CR, Pato CN. No evidence of association or linkage disequilibrium between polymorphisms in the 5' upstream and coding regions of the dopamine D4 receptor gene and schizophrenia in a Portuguese population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 20-4. PMID 14755438 DOI: 10.1002/ajmg.b.20084  0.52
2004 Lowe N, Kirley A, Hawi Z, Sham P, Wickham H, Kratochvil CJ, Smith SD, Lee SY, Levy F, Kent L, Middle F, Rohde LA, Roman T, Tahir E, Yazgan Y, ... ... Barr CL, et al. Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes. American Journal of Human Genetics. 74: 348-56. PMID 14732906 DOI: 10.1086/381561  0.52
2004 Adams J, Crosbie J, Wigg K, Ickowicz A, Pathare T, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL, Barr CL. Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region. Molecular Psychiatry. 9: 494-9. PMID 14699423 DOI: 10.1038/sj.mp.4001455  0.52
2004 Misener VL, Luca P, Azeke O, Crosbie J, Waldman I, Tannock R, Roberts W, Malone M, Schachar R, Ickowicz A, Kennedy JL, Barr CL. Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder. Molecular Psychiatry. 9: 500-9. PMID 14569274 DOI: 10.1038/sj.mp.4001440  0.52
2003 Barr CL, Levin AV, Kovacs R, Muller W, Barsoum-Homsy M, Zachary D, Clark RA, Tsilfidis C. Linkage study between congenital cataracts and five crystallin loci. American Journal of Medical Genetics. Part A. 121: 15-9. PMID 12900895 DOI: 10.1002/ajmg.a.20157  0.52
2003 Xu C, Ozbay F, Wigg K, Shulman R, Tahir E, Yazgan Y, Sandor P, Barr CL. Evaluation of the genes for the adrenergic receptors alpha 2A and alpha 1C and Gilles de la Tourette Syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 119: 54-9. PMID 12707939 DOI: 10.1002/ajmg.b.20001  0.52
2003 Wong AH, Macciardi F, Klempan T, Kawczynski W, Barr CL, Lakatoo S, Wong M, Buckle C, Trakalo J, Boffa E, Oak J, Azevedo MH, Dourado A, Coelho I, Macedo A, et al. Identification of candidate genes for psychosis in rat models, and possible association between schizophrenia and the 14-3-3eta gene. Molecular Psychiatry. 8: 156-66. PMID 12610648 DOI: 10.1038/sj.mp.4001237  0.52
2003 Quist JF, Barr CL, Schachar R, Roberts W, Malone M, Tannock R, Basile VS, Beitchman J, Kennedy JL. The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder. Molecular Psychiatry. 8: 98-102. PMID 12556913 DOI: 10.1038/sj.mp.4001244  0.52
2002 Wigg K, Zai G, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL, Barr CL. Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase. The American Journal of Psychiatry. 159: 1046-8. PMID 12042196 DOI: 10.1176/appi.ajp.159.6.1046  0.52
2002 Barr CL, Kroft J, Feng Y, Wigg K, Roberts W, Malone M, Ickowicz A, Schachar R, Tannock R, Kennedy JL. The norepinephrine transporter gene and attention-deficit hyperactivity disorder. American Journal of Medical Genetics. 114: 255-9. PMID 11920844 DOI: 10.1002/ajmg.10193  0.52
2001 Barr CL, Best L, Weksberg R. Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome. American Journal of Medical Genetics. 104: 120-6. PMID 11746041 DOI: 10.1002/ajmg.1587  0.52
2001 Barr CL, Feng Y, Wigg KG, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. 5'-untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder. American Journal of Medical Genetics. 105: 84-90. PMID 11425008 DOI: 10.1002/1096-8628(20010108)105:1<84::AID-AJMG1068>3.0.CO;2-Q  0.52
2001 Barr CL, Shulman R, Wigg K, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder. American Journal of Medical Genetics. 105: 250-4. PMID 11353444 DOI: 10.1002/ajmg.1302  0.52
2001 Barr CL, Wigg K, Zai G, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL. Attention-deficit hyperactivity disorder and the adrenergic receptors alpha 1C and alpha 2C. Molecular Psychiatry. 6: 334-7. PMID 11326305 DOI: 10.1038/sj.mp.4000863  0.52
2001 Xu C, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL, Barr CL. Linkage study of the alpha2A adrenergic receptor in attention-deficit hyperactivity disorder families. American Journal of Medical Genetics. 105: 159-62. PMID 11304829 DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1160>3.0.CO;2-B  0.52
2001 Barr CL, Xu C, Kroft J, Feng Y, Wigg K, Zai G, Tannock R, Schachar R, Malone M, Roberts W, Nöthen MM, Grünhage F, Vandenbergh DJ, Uhl G, Sunohara G, et al. Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder. Biological Psychiatry. 49: 333-9. PMID 11239904 DOI: 10.1016/S0006-3223(00)01053-2  0.52
2001 Barr CL. Genetics of childhood disorders: XXII. ADHD, Part 6: The dopamine D4 receptor gene. Journal of the American Academy of Child and Adolescent Psychiatry. 40: 118-21. PMID 11195554 DOI: 10.1097/00004583-200101000-00025  0.52
2001 Barr CL, Wigg KG, Ickowicz A, Roberts W, Malone M, Schachar R, Kennedy JL. Molecular genetic studies of attention-deficit hyperactivity disorder (ADHD) American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 573.  0.52
2000 Sunohara GA, Roberts W, Malone M, Schachar RJ, Tannock R, Basile VS, Wigal T, Wigal SB, Schuck S, Moriarty J, Swanson JM, Kennedy JL, Barr CL. Linkage of the dopamine D4 receptor gene and attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry. 39: 1537-42. PMID 11128331 DOI: 10.1097/00004583-200012000-00017  0.52
2000 Barr CL, Wigg KG, Feng Y, Zai G, Malone M, Roberts W, Schachar R, Tannock R, Kennedy JL. Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor. Molecular Psychiatry. 5: 548-51. PMID 11032390  0.52
2000 Quist JF, Barr CL, Schachar R, Roberts W, Malone M, Tannock R, Basile VS, Beitchman J, Kennedy JL. Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder (ADHD). Molecular Psychiatry. 5: 537-41. PMID 11032388  0.52
2000 Barr CL, Wigg KG, Bloom S, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder. American Journal of Medical Genetics. 96: 262-7. PMID 10898896 DOI: 10.1002/1096-8628(20000612)96:3<262::AID-AJMG5>3.0.CO;2-8  0.52
2000 Barr CL, Feng Y, Wigg K, Bloom S, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL. Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder. Molecular Psychiatry. 5: 405-9. PMID 10889551  0.52
2000 Zai C, Wigg KG, Barr CL. Genetics and sleep disorders. Seminars in Clinical Neuropsychiatry. 5: 33-43. PMID 10704536 DOI: 10.153/SCNP00500033  0.4
2000 Barr CL, Wigg KG, Wu J, Zai C, Bloom S, Tannock R, Roberts W, Malone M, Schachar R, Kennedy JL. Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder. American Journal of Medical Genetics. 96: 114-7. PMID 10686563 DOI: 10.1002/(SICI)1096-8628(20000207)96:1<114::AID-AJMG22>3.0.CO;2-R  0.52
1999 Barr CL, Wigg K, Malone M, Schachar R, Tannock R, Roberts W, Kennedy JL. Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder. American Journal of Medical Genetics. 88: 710-3. PMID 10581494 DOI: 10.1002/(SICI)1096-8628(19991215)88:6<710::AID-AJMG23>3.0.CO;2-Q  0.52
1999 Barr CL, Wigg KG, Sandor P. Catechol-O-methyltransferase and Gilles de la Tourette syndrome. Molecular Psychiatry. 4: 492-5. PMID 10523824  0.4
1999 Barr CL, Wigg KG, Pakstis AJ, Kurlan R, Pauls D, Kidd KK, Tsui LC, Sandor P. Genome scan for linkage to Gilles de la Tourette syndrome. American Journal of Medical Genetics. 88: 437-45. PMID 10402514 DOI: 10.1002/(SICI)1096-8628(19990820)88:4<437::AID-AJMG24>3.0.CO;2-E  0.4
1999 Vincent JB, Kovacs M, Krol R, Barr CL, Kennedy JL. Intergenerational CAG repeat expansion at ERDA1 in a family with childhood-onset depression, schizoaffective disorder, and recurrent major depression. American Journal of Medical Genetics. 88: 79-82. PMID 10050972 DOI: 10.1002/(SICI)1096-8628(19990205)88:1<79::AID-AJMG14>3.0.CO;2-N  0.52
1999 Minassian BA, Sainz J, Serratosa JM, Gee M, Sakamoto LM, Bohlega S, Geoffroy G, Barr C, Scherer SW, Tomiyasu U, Carpenter S, Wigg K, Sanghvi AV, Delgado-Escueta AV. Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy. Annals of Neurology. 45: 262-5. PMID 9989632 DOI: 10.1002/1531-8249(199902)45:2<262::AID-ANA20>3.0.CO;2-9  0.52
1997 Barr CL, Wigg KG, Zovko E, Sandor P, Tsui LC. Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome. American Journal of Medical Genetics. 74: 58-61. PMID 9034008 DOI: 10.1002/(SICI)1096-8628(19970221)74:1<58::AID-AJMG13>3.0.CO;2-Q  0.4
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