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Refinado por: Nome da Publicação: American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics remover
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1
Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers
Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers
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Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers

Kraan, Claudine M. ; Hocking, Darren R. ; Georgiou-Karistianis, Nellie ; Metcalfe, Sylvia A. ; Archibald, Alison D. ; Fielding, Joanne ; Trollor, Julian ; Bradshaw, John L. ; Cohen, Jonathan ; Cornish, Kim M.

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2014-01, Vol.165B (1), p.41-51 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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2
Association of genetic risk severity with ADHD clinical characteristics
Association of genetic risk severity with ADHD clinical characteristics
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Association of genetic risk severity with ADHD clinical characteristics

Kotte, Amelia ; Faraone, Stephen V. ; Biederman, Joseph

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-10, Vol.162B (7), p.718-733 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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3
Association study of brain-derived neurotrophic factor (BDNF) and LIN-7 homolog (LIN-7) genes with adult attention-deficit/hyperactivity disorder
Association study of brain-derived neurotrophic factor (BDNF) and LIN-7 homolog (LIN-7) genes with adult attention-deficit/hyperactivity disorder
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Association study of brain-derived neurotrophic factor (BDNF) and LIN-7 homolog (LIN-7) genes with adult attention-deficit/hyperactivity disorder

Lanktree, Matthew ; Squassina, Alessio ; Krinsky, Marilee ; Strauss, John ; Jain, Umesh ; Macciardi, Fabio ; Kennedy, James L. ; Muglia, Pierandrea

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-09, Vol.147B (6), p.945-951 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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4
Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention-deficit/hyperactivity disorder
Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention-deficit/hyperactivity disorder
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Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention-deficit/hyperactivity disorder

Li, Jun ; Kang, Chuanyuan ; Zhang, Haobo ; Wang, Yufeng ; Zhou, Rulun ; Wang, Bing ; Guan, Lili ; Yang, Li ; Faraone, Stephen V.

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-06, Vol.144B (4), p.430-433 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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5
Family-based association study between brain-derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples
Family-based association study between brain-derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples
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Family-based association study between brain-derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples

Xu, Xiaohui ; Mill, Jonathan ; Zhou, Kaixin ; Brookes, Keeley ; Chen, Chih-Ken ; Asherson, Philip

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-01, Vol.144B (1), p.83-86 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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6
Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B
Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B
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Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B

Mill, Jonathan ; Xu, Xiaohui ; Ronald, Angelica ; Curran, Sarah ; Price, Tom ; Knight, Jo ; Craig, Ian ; Sham, Pak ; Plomin, Robert ; Asherson, Philip

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-02, Vol.133B (1), p.68-73 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Absence of association with DAT1 polymorphism and response to methylphenidate in a sample of adults with ADHD
Absence of association with DAT1 polymorphism and response to methylphenidate in a sample of adults with ADHD
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Absence of association with DAT1 polymorphism and response to methylphenidate in a sample of adults with ADHD

Mick, Eric ; Biederman, Joseph ; Spencer, Thomas ; Faraone, Stephen V. ; Sklar, Pamela

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2006-12, Vol.141B (8), p.890-894 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Association of dopamine transporter genotype with disruptive behavior disorders in an eight-year longitudinal study of children and adolescents
Association of dopamine transporter genotype with disruptive behavior disorders in an eight-year longitudinal study of children and adolescents
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Association of dopamine transporter genotype with disruptive behavior disorders in an eight-year longitudinal study of children and adolescents

Lee, Steve S. ; Lahey, Benjamin B. ; Waldman, Irwin ; Van Hulle, Carol A. ; Rathouz, Paul ; Pelham, William E. ; Loney, Jan ; Cook, Edwin H.

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-04, Vol.144B (3), p.310-317 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD)
A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD)
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A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD)

Banerjee, Emili ; Sinha, Swagata ; Chatterjee, Anindita ; Gangopadhyay, Prasanta Kumar ; Singh, Manoranjan ; Nandagopal, Krishnadas

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2006-06, Vol.141B (4), p.361-366 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Sequencing of sporadic Attention‐Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder
Sequencing of sporadic Attention‐Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder
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Sequencing of sporadic Attention‐Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder

Kim, Daniel Seung ; Burt, Amber A. ; Ranchalis, Jane E. ; Wilmot, Beth ; Smith, Joshua D. ; Patterson, Karynne E. ; Coe, Bradley P. ; Li, Yatong K. ; Bamshad, Michael J. ; Nikolas, Molly ; Eichler, Evan E. ; Swanson, James M. ; Nigg, Joel T. ; Nickerson, Deborah A. ; Jarvik, Gail P.

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-06, Vol.174 (4), p.381-389 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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