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Cathy Barr

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Dempster Emma L; Burcescu Irina; Wigg Karen; Kiss Eniko; Baji Ildiko; Gadoros Julia; Tamás Zsuzsanna; Kapornai Krisztina; Daróczy Gabriella; Kennedy James L; Vetró Agnes; Kovacs Maria; Barr Cathy L;
Further genetic evidence implicates the vasopressin system in childhood-onset mood disorders.
Gomez Lissette; Wigg Karen; Feng Yu; Kiss Eniko; Kapornai Krisztina; Tamás Zsuzsa; Mayer László; Baji Ildikó; Daróczi Gabriella; Benák István; Kothencné Viola Osváth; Dombovári Edit; Kaczvinszk Emília; Besnyo Márta; Gádoros Julia; King Nicole; Székely Judit; Kovacs Maria; Vetró Agnes; Kennedy James L; Barr Cathy L
G72/G30 (DAOA) and juvenile-onset mood disorders.
Mill J; Wigg K; Burcescu I; Vetró A; Kiss E; Kapornai K; Tamás Z; Baji I; Gádoros J; Kennedy J L; Kovacs M; Barr C L;
Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD).

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All Publications

2009: Dempster Emma L; Burcescu Irina; Wigg Karen; Kiss Eniko; Baji Ildiko; Gadoros Julia; Tamás Zsuzsanna; Kapornai Krisztina; Daróczy Gabriella; Kennedy James L; Vetró Agnes; Kovacs Maria; Barr Cathy L;
Further genetic evidence implicates the vasopressin system in childhood-onset mood disorders.
The European journal of neuroscience 2009;30(8):1615-9.
2009: Gomez Lissette; Wigg Karen; Feng Yu; Kiss Eniko; Kapornai Krisztina; Tamás Zsuzsa; Mayer László; Baji Ildikó; Daróczi Gabriella; Benák István; Kothencné Viola Osváth; Dombovári Edit; Kaczvinszk Emília; Besnyo Márta; Gádoros Julia; King Nicole; Székely Judit; Kovacs Maria; Vetró Agnes; Kennedy James L; Barr Cathy L
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 2009;150B(7):1007-12.
2009: Mill J; Wigg K; Burcescu I; Vetró A; Kiss E; Kapornai K; Tamás Z; Baji I; Gádoros J; Kennedy J L; Kovacs M; Barr C L;
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 2009;150B(6):866-73.
2009: Couto Jillian M; Gomez Lissette; Wigg Karen; Ickowicz Abel; Pathare Tejaswee; Malone Molly; Kennedy James L; Schachar Russell; Barr Cathy L
Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p.
Biological psychiatry 2009;66(4):368-75.
2009: Wigg Karen; Feng Yu; Gomez Lissette; Kiss Eniko; Kapornai Krisztina; Tamás Zsuzsa; Mayer László; Baji Ildikó; Daróczi Gabriella; Benák István; Osváth Viola Kothencné; Dombovári Edit; Kaczvinszk Emília; Besnyõ Márta; Gádoros Julia; King Nicole; Székely Judit; Kovacs Maria; Vetró Agnes; Kennedy James L; Barr Cathy L
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 2009;150B(5):638-46.
2009: Misener Virginia L; Gomez Lissette; Wigg Karen G; King Nicole; Kiss Enikõ; Daróczi Gabriella; Kapornai Krisztina; Tamás Zsuzsanna; Mayer László; Gádoros Júlia; Baji Ildikó; Kennedy James L; Kovacs Maria; Vetró Agnes; Barr Cathy L;
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 2009;150B(5):653-9.
2009: Dorval Kimberley M; Burcescu Irina; Adams Jennifer; Wigg Karen G; King Nicole; Kiss Eniko; Kapornai Krisztina; Gádoros Julia; Tamás Zsuzsanna; Daróczi Gabriella; Baji Ildikó; Mayer László; Kennedy James L; Vetró Agnes; Kovacs Maria; Barr Cathy L
Association study of N-methyl-D-aspartate glutamate receptor subunit genes and childhood-onset mood disorders.
Psychiatric genetics 2009;19(3):156-7.
2009: Miranda Debora M; Wigg Karen; Kabia E Mameisia; Feng Yu; Sandor Paul; Barr Cathy L
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 2009;150B(4):483-6.
2009: Laurin Nancy; Wigg Karen G; Feng Yu; Sandor Paul; Barr Cathy L
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 2009;150B(1):95-103.
2008: Ouellet-Morin Isabelle; Wigg Karen G; Feng Yu; Dionne Ginette; Robaey Philippe; Brendgen Mara; Vitaro Frank; Simard Louise; Schachar Russell; Tremblay Richard E; Pérusse Daniel; Boivin Michel; Barr Cathy L
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 2008;147B(8):1442-9.
2008: Laurin Nancy; Lee Jonghun; Ickowicz Abel; Pathare Tejaswee; Malone Molly; Tannock Rosemary; Kennedy James L; Schachar Russell J; Barr Cathy L
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 2008;147B(5):600-5.
2008: Feng Yu; Vetró Agnes; Kiss Eniko; Kapornai Krisztina; Daróczi Gabriella; Mayer László; Tamás Zsuzsanna; Baji Ildikó; Gádoros Júlia; King Nicole; Kennedy James L; Wigg Karen; Kovacs Maria; Barr Cathy L;
Association of the neurotrophic tyrosine kinase receptor 3 (NTRK3) gene and childhood-onset mood disorders.
The American journal of psychiatry 2008;165(5):610-6.
2008: Shaikh Sajid A; Strauss John; King Nicole; Bulgin Natalie L; Vetró Agnes; Kiss Enikö; George Charles J; Kovacs Maria; Barr Cathy L; Kennedy James L;
Association study of serotonin system genes in childhood-onset mood disorder.
Psychiatric genetics 2008;18(2):47-52.
2008: Laurin Nancy; Ickowicz Abel; Pathare Tejaswee; Malone Molly; Tannock Rosemary; Schachar Russell; Kennedy James L; Barr Cathy L
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 2008;147(3):339-42.
2008: Lee J; Laurin N; Crosbie J; Ickowicz A; Pathare T; Malone M; Kennedy J L; Tannock R; Schachar R; Barr C L
Association study of the nicotinic acetylcholine receptor alpha4 subunit gene, CHRNA4, in attention-deficit hyperactivity disorder.
Genes, brain, and behavior 2008;7(1):53-60.
2008: Miranda D M; Wigg K; Feng Y; Sandor P; Barr C L
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 2008;147B(1):68-72.
2008: Laurin Nancy; Ickowicz Abel; Pathare Tejaswee; Malone Molly; Tannock Rosemary; Schachar Russell; Kennedy James L; Barr Cathy L
Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/hyperactivity disorder.
Journal of psychiatric research 2008;42(2):117-24.
2008: Misener V L; Gomez L; Wigg K G; Luca P; King N; Kiss E; Daróczi G; Kapornai K; Tamas Z; Mayer L; Gádoros J; Baji I; Kennedy J L; Kovacs M; Vetró A; Barr C L;
Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disorders.
Neuropsychobiology 2008;58(2):71-80.
2008: Bulgin Natalie L; Strauss John S; King Nicole A; Shaikh Sajid A; George Charles J; Fox Nathan A; Barr Cathy L; Kovacs Maria; Kennedy James L
Association study of theta EEG asymmetry and brain-derived neurotrophic factor gene variants in childhood-onset mood disorder.
Neuromolecular medicine 2008;10(4):343-55.
2008: Crosbie Jennifer; Pérusse Daniel; Barr Cathy L; Schachar Russell J
Validating psychiatric endophenotypes: inhibitory control and attention deficit hyperactivity disorder.
Neuroscience and biobehavioral reviews 2008;32(1):40-55.
2007: Feng Yu; Wigg Karen; King Nicole; Vetró Agnes; Kiss Eniko; Kapornai Krisztina; Mayer László; Gádoros Júlia; Kennedy James L; Kovacs Maria; Barr Cathy L;
GPR50 is not associated with childhood-onset mood disorders in a large sample of Hungarian families.
Psychiatric genetics 2007;17(6):347-50.
2007: Dempster E L; Kiss E; Kapornai K; Daróczy G; Mayer L; Baji I; Tamas Z; Gadoros J; Kennedy J L; Vetró A; Kovacs M; Barr C L
No evidence of association between a functional polymorphism in the MTHFR gene and childhood-onset mood disorders.
Molecular psychiatry 2007;12(12):1063-4.
2007: Lee Jonghun; Laurin Nancy; Crosbie Jennifer; Ickowicz Abel; Pathare Tejaswee; Malone Molly; Tannock Rosemary; Kennedy James L; Schachar Russell; Barr Cathy L
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 2007;144B(8):976-81.
2007: Dempster Emma L; Burcescu Irina; Wigg Karen; Kiss Eniko; Baji Ildiko; Gadoros Julia; Tamás Zsuzsanna; Kennedy James L; Vetró Agnes; Kovacs Maria; Barr Cathy L
Evidence of an association between the vasopressin V1b receptor gene (AVPR1B) and childhood-onset mood disorders.
Archives of general psychiatry 2007;64(10):1189-95.
2007: Luca P; Laurin N; Misener V L; Wigg K G; Anderson B; Cate-Carter T; Tannock R; Humphries T; Lovett M W; Barr C L
Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems.
Molecular psychiatry 2007;12(8):776-85.
2007: Dorval K M; Wigg K G; Crosbie J; Tannock R; Kennedy J L; Ickowicz A; Pathare T; Malone M; Schachar R; Barr C L
Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder.
Genes, brain, and behavior 2007;6(5):444-52.
2007: Makkar Rohit; Gomez Lissette; Wigg Karen G; Ickowicz Abel; Pathare Tejaswee; Tannock Rosemary; Malone Molly; Kennedy James L; Schachar Russell; Barr Cathy L
The gene for synapsin III and attention-deficit hyperactivity disorder.
Psychiatric genetics 2007;17(2):109-12.
2007: Laurin N; Feng Y; Ickowicz A; Pathare T; Malone M; Tannock R; Schachar R; Kennedy J L; Barr C L
No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder.
Molecular psychiatry 2007;12(3):226-9.
2007: Ickowicz Abel; Feng Yu; Wigg Karen; Quist Jennifer; Pathare Tejasawe; Roberts Wendy; Malone Molly; Schachar Russell; Tannock Rosemary; Kennedy James L; Barr Catyh L
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 2007;144B(1):121-5.
2006: Wigg Karen G; Takhar Amandeep; Ickowicz Abel; Tannock Rosemary; Kennedy James L; Pathare Tejaswee; Malone Molly; Schachar Russell; Barr Cathy L
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 2006;141B(6):566-70.
2006: Ozbay Fatih; Wigg Karen G; Turanli Eda Tahir; Asherson Phil; Yazgan Yanki; Sandor Paul; Barr Cathy L
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 2006;141B(6):673-7.
2006: Burcescu I; Wigg K; Gomez L; King N; Vetró A; Kiss E; Kapornai K; Gádoros J; Kennedy J L; Kovacs M; Barr C L;
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 2006;141B(3):227-33.
2005: Laurin N; Misener V L; Crosbie J; Ickowicz A; Pathare T; Roberts W; Malone M; Tannock R; Schachar R; Kennedy J L; Barr C L
Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder.
Molecular psychiatry 2005;10(12):1117-25.
2005: Feng Y; Crosbie J; Wigg K; Pathare T; Ickowicz A; Schachar R; Tannock R; Roberts W; Malone M; Swanson J; Kennedy J L; Barr C L
The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder.
Molecular psychiatry 2005;10(11):998-1005, 973.
2005: Feng Yu; Wigg Karen G; Makkar Rohit; Ickowicz Abel; Pathare Tejaswee; Tannock Rosemary; Roberts Wendy; Malone Molly; Kennedy James L; Schachar Russell; Barr Cathy L
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 2005;139B(1):1-6.
2005: Strauss J; Barr C L; George C J; Devlin B; Vetró A; Kiss E; Baji I; King N; Shaikh S; Lanktree M; Kovacs M; Kennedy J L
Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample.
Molecular psychiatry 2005;10(9):861-7.
2005: Burcescu I; Wigg K; King N; Vetró A; Kiss E; Katay L; Kennedy J L; Kovacs M; Barr C L
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 2005;137B(1):45-50.
2005: Schachar Russell J; Crosbie Jennifer; Barr Cathy L; Ornstein Tisha J; Kennedy James; Malone Molly; Roberts Wendy; Ickowicz Abel; Tannock Rosemary; Chen Shirley; Pathare Tejaswee
Inhibition of motor responses in siblings concordant and discordant for attention deficit hyperactivity disorder.
The American journal of psychiatry 2005;162(6):1076-82.
2005: Zai Gwyneth; King Nicole; Wong Gregory W H; Barr Cathy L; Kennedy James L
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 2005;15(3):347-52.
2005: Zai Gwyneth; Arnold Paul; Burroughs Eliza; Barr Cathy L; Richter Margaret A; Kennedy James L
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 2005;134B(1):25-9.
2005: Zai G; King N; Wigg K; Couto J; Wong G W H; Honer W G; Barr C L; Kennedy J L
Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia.
Genes, brain, and behavior 2005;4(1):2-9.
2005: Adams Jennifer H; Wigg Karen G; King Nicole; Burcescu Irina; Vetró Agnes; Kiss Eniko; Baji Ildikó; George Charles J; Kennedy James L; Kovacs Maria; Barr Cathy L
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 2005;132B(1):90-5.
2004: Wigg K G; Couto J M; Feng Y; Anderson B; Cate-Carter T D; Macciardi F; Tannock R; Lovett M W; Humphries T W; Barr C L
Support for EKN1 as the susceptibility locus for dyslexia on 15q21.
Molecular psychiatry 2004;9(12):1111-21.
2004: Strauss J; Barr C L; George C J; King N; Shaikh S; Devlin B; Kovacs M; Kennedy J L
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 2004;131B(1):16-9.
2004: Paschou P; Feng Y; Pakstis A J; Speed W C; DeMille M M; Kidd J R; Jaghori B; Kurlan R; Pauls D L; Sandor P; Barr C L; Kidd K K
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 2004;75(4):545-60.
2004: Zai Gwyneth; Bezchlibnyk Yarema B; Richter Margaret A; Arnold Paul; Burroughs Eliza; Barr Cathy L; Kennedy James L
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 2004;129B(1):64-8.
2004: Adams J; Crosbie J; Wigg K; Ickowicz A; Pathare T; Roberts W; Malone M; Schachar R; Tannock R; Kennedy J L; Barr C L
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 2004;9(5):494-9.
2004: Misener V L; Luca P; Azeke O; Crosbie J; Waldman I; Tannock R; Roberts W; Malone M; Schachar R; Ickowicz A; Kennedy J L; Barr C L
Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder.
Molecular psychiatry 2004;9(5):500-9.
2004: Strauss J; Barr C L; George C J; Ryan C M; King N; Shaikh S; Kovacs M; Kennedy J L
BDNF and COMT polymorphisms: relation to memory phenotypes in young adults with childhood-onset mood disorder.
Neuromolecular medicine 2004;5(3):181-92.
2004: Misener Virginia L; Schachar Russell; Ickowicz Abel; Malone Molly; Roberts Wendy; Tannock Rosemary; Kennedy James L; Pathare Tejaswee; Barr Cathy L
Replication test for association of the IL-1 receptor antagonist gene, IL1RN, with attention-deficit/hyperactivity disorder.
Neuropsychobiology 2004;50(3):231-4.
2003: Barr Cathy L; Levin Alex V; Kovacs Ronald; Muller Werner; Barsoum-Homsy Magda; Zachary Dalila; Clark Rakia A; Tsilfidis Catherine
Linkage study between congenital cataracts and five crystallin loci.
American journal of medical genetics. Part A 2003;121A(1):15-9.
2003: Xu Chun; Ozbay Fatih; Wigg Karen; Shulman Rayzie; Tahir Eda; Yazgan Yanki; Sandor Paul; Barr Cathy L;
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 2003;119B(1):54-9.
2003: Quist J F; Barr C L; Schachar R; Roberts W; Malone M; Tannock R; Basile V S; Beitchman J; Kennedy J L
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.
Molecular psychiatry 2003;8(1):98-102.
2002: Wigg Karen; Zai Gwyneth; Schachar Russell; Tannock Rosemary; Roberts Wendy; Malone Molly; Kennedy James L; Barr Cathy L
Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase.
The American journal of psychiatry 2002;159(6):1046-8.
2002: Barr Cathy L; Kroft Jamie; Feng Yu; Wigg Karen; Roberts Wendy; Malone Molly; Ickowicz Abel; Schachar Russell; Tannock Rosemary; Kennedy James L
The norepinephrine transporter gene and attention-deficit hyperactivity disorder.
American journal of medical genetics 2002;114(3):255-9.
2001: Barr C L; Best L; Weksberg R
Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.
American journal of medical genetics 2001;104(2):120-6.
2001: Barr C L; Wigg K; Zai G; Roberts W; Malone M; Schachar R; Tannock R; Kennedy J L
Attention-deficit hyperactivity disorder and the adrenergic receptors alpha 1C and alpha 2C.
Molecular psychiatry 2001;6(3):334-7.
2001: Barr C L; Shulman R; Wigg K; Schachar R; Tannock R; Roberts W; Malone M; Kennedy J L
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 2001;105(3):250-4.
2001: Barr C L; Xu C; Kroft J; Feng Y; Wigg K; Zai G; Tannock R; Schachar R; Malone M; Roberts W; Nöthen M M; Grünhage F; Vandenbergh D J; Uhl G; Sunohara G; King N; Kennedy J L
Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.
Biological psychiatry 2001;49(4):333-9.
2001: Barr C L; Feng Y; Wigg K G; Schachar R; Tannock R; Roberts W; Malone M; Kennedy J L
5'-untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder.
American journal of medical genetics 2001;105(1):84-90.
2001: Barr C L
Genetics of childhood disorders: XXII. ADHD, Part 6: The dopamine D4 receptor gene.
Journal of the American Academy of Child and Adolescent Psychiatry 2001;40(1):118-21.
2000: Sunohara G A; Roberts W; Malone M; Schachar R J; Tannock R; Basile V S; Wigal T; Wigal S B; Schuck S; Moriarty J; Swanson J M; Kennedy J L; Barr C L
Linkage of the dopamine D4 receptor gene and attention-deficit/hyperactivity disorder.
Journal of the American Academy of Child and Adolescent Psychiatry 2000;39(12):1537-42.
2000: Barr C L; Wigg K G; Feng Y; Zai G; Malone M; Roberts W; Schachar R; Tannock R; Kennedy J L
Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor.
Molecular psychiatry 2000;5(5):548-51.
2000: Quist J F; Barr C L; Schachar R; Roberts W; Malone M; Tannock R; Basile V S; Beitchman J; Kennedy J L
Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder (ADHD).
Molecular psychiatry 2000;5(5):537-41.
2000: Barr C L; Feng Y; Wigg K; Bloom S; Roberts W; Malone M; Schachar R; Tannock R; Kennedy J L
Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder.
Molecular psychiatry 2000;5(4):405-9.
2000: Barr C L; Wigg K G; Bloom S; Schachar R; Tannock R; Roberts W; Malone M; Kennedy J L
Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder.
American journal of medical genetics 2000;96(3):262-7.
2000: Barr C L; Wigg K G; Wu J; Zai C; Bloom S; Tannock R; Roberts W; Malone M; Schachar R; Kennedy J L
Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder.
American journal of medical genetics 2000;96(1):114-7.
2000: Zai C; Wigg K G; Barr C L
Genetics and sleep disorders.
Seminars in clinical neuropsychiatry 2000;5(1):33-43.
1999: Barr C L; Wigg K; Malone M; Schachar R; Tannock R; Roberts W; Kennedy J L
Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.
American journal of medical genetics 1999;88(6):710-3.
1999: Barr C L; Wigg K G; Sandor P
Catechol-O-methyltransferase and Gilles de la Tourette syndrome.
Molecular psychiatry 1999;4(5):492-5.
1999: Barr C L; Wigg K G; Pakstis A J; Kurlan R; Pauls D; Kidd K K; Tsui L C; Sandor P
Genome scan for linkage to Gilles de la Tourette syndrome.
American journal of medical genetics 1999;88(4):437-45.
1998: Barr C L; Sandor P
Current status of genetic studies of Gilles de la Tourette syndrome.
Canadian journal of psychiatry. Revue canadienne de psychiatrie 1998;43(4):351-7.
1997: Barr C L; Wigg K G; Zovko E; Sandor P; Tsui L C
Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome.
American journal of medical genetics 1997;74(1):58-61.
1996: Barr C L; Wigg K G; Zovko E; Sandor P; Tsui L C
No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families.
American journal of medical genetics 1996;67(3):301-5.
1994: Petronis A; O'Hara K; Barr C L; Kennedy J L; Van Tol H H
(G)n-mononucleotide polymorphism in the human D4 dopamine receptor (DRD4) gene.
Human genetics 1994;93(6):719.
1994: Barr C L; Kennedy J L; Pakstis A J; Wetterberg L; Sjögren B; Bierut L; Wadelius C; Wahlström J; Martinsson T; Giuffra L
Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred.
American journal of medical genetics 1994;54(1):51-8.
1994: Barr C L; Kennedy J L; Pakstis A J; Castiglione C M; Kidd J R; Wetterberg L; Kidd K K
Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region.
Schizophrenia bulletin 1994;20(2):277-86.
1993: Barr C L; Kennedy J L; Lichter J B; Van Tol H H; Wetterberg L; Livak K J; Kidd K K
Alleles at the dopamine D4 receptor locus do not contribute to the genetic susceptibility to schizophrenia in a large Swedish kindred.
American journal of medical genetics 1993;48(4):218-22.
1993: Barr C L; Kidd K K
Population frequencies of the A1 allele at the dopamine D2 receptor locus.
Biological psychiatry 1993;34(4):204-9.
1993: Lichter J B; Barr C L; Kennedy J L; Van Tol H H; Kidd K K; Livak K J
A hypervariable segment in the human dopamine receptor D4 (DRD4) gene.
Human molecular genetics 1993;2(6):767-73.

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