An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples

Marta Ribases; Cristina Sanchez-Mora; Josep Antoni Ramos-Quiroga; Rosa Bosch; Nuria Gomez; Mariana Nogueira; Montse Corrales; Gloria Palomar; Christian P. Jacob; Silke Gross-Lesch; Susanne Kreiker; Andreas Reif; Klaus Peter Lesch; Bru Cormand; Miquel Casas; Monica Bayes

doi:10.1097/YPG.0b013e328353957e

An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples

Marta Ribases, Cristina Sanchez-Mora, Josep Antoni Ramos-Quiroga, Rosa Bosch, Nuria Gomez, Mariana Nogueira, Montse Corrales, Gloria Palomar, Christian P. Jacob, Silke Gross-Lesch, Susanne Kreiker, Andreas Reif, Klaus Peter Lesch, Bru Cormand, Miquel Casas, Monica Bayes

CARIM School for Cardiovascular Diseases

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	155-160
Journal	Psychiatric Genetics
Volume	22
Issue number	4
DOIs	https://doi.org/10.1097/YPG.0b013e328353957e
Publication status	Published - Aug 2012

Keywords

attention-deficit hyperactivity disorder
case-control association study
forkhead box P2
learning disability
single nucleotide polymorphism

Access to Document

10.1097/YPG.0b013e328353957e

Cite this

Ribases, M., Sanchez-Mora, C., Antoni Ramos-Quiroga, J., Bosch, R., Gomez, N., Nogueira, M., Corrales, M., Palomar, G., Jacob, C. P., Gross-Lesch, S., Kreiker, S., Reif, A., Lesch, K. P., Cormand, B., Casas, M., & Bayes, M. (2012). An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples. Psychiatric Genetics, 22(4), 155-160. https://doi.org/10.1097/YPG.0b013e328353957e

Ribases, Marta ; Sanchez-Mora, Cristina ; Antoni Ramos-Quiroga, Josep ; Bosch, Rosa ; Gomez, Nuria ; Nogueira, Mariana ; Corrales, Montse ; Palomar, Gloria ; Jacob, Christian P. ; Gross-Lesch, Silke ; Kreiker, Susanne ; Reif, Andreas ; Lesch, Klaus Peter ; Cormand, Bru ; Casas, Miquel ; Bayes, Monica. / An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples. In: Psychiatric Genetics. 2012 ; Vol. 22, No. 4. pp. 155-160.

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title = "An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples",

keywords = "attention-deficit hyperactivity disorder, case-control association study, forkhead box P2, learning disability, single nucleotide polymorphism",

author = "Marta Ribases and Cristina Sanchez-Mora and {Antoni Ramos-Quiroga}, Josep and Rosa Bosch and Nuria Gomez and Mariana Nogueira and Montse Corrales and Gloria Palomar and Jacob, {Christian P.} and Silke Gross-Lesch and Susanne Kreiker and Andreas Reif and Lesch, {Klaus Peter} and Bru Cormand and Miquel Casas and Monica Bayes",

year = "2012",

month = aug,

doi = "10.1097/YPG.0b013e328353957e",

language = "English",

volume = "22",

pages = "155--160",

journal = "Psychiatric Genetics",

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Ribases, M, Sanchez-Mora, C, Antoni Ramos-Quiroga, J, Bosch, R, Gomez, N, Nogueira, M, Corrales, M, Palomar, G, Jacob, CP, Gross-Lesch, S, Kreiker, S, Reif, A, Lesch, KP, Cormand, B, Casas, M & Bayes, M 2012, 'An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples', Psychiatric Genetics, vol. 22, no. 4, pp. 155-160. https://doi.org/10.1097/YPG.0b013e328353957e

An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples. / Ribases, Marta; Sanchez-Mora, Cristina; Antoni Ramos-Quiroga, Josep; Bosch, Rosa; Gomez, Nuria; Nogueira, Mariana; Corrales, Montse; Palomar, Gloria; Jacob, Christian P.; Gross-Lesch, Silke; Kreiker, Susanne; Reif, Andreas; Lesch, Klaus Peter; Cormand, Bru; Casas, Miquel; Bayes, Monica.

In: Psychiatric Genetics, Vol. 22, No. 4, 08.2012, p. 155-160.

Research output: Contribution to journal › Article › Academic › peer-review

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AU - Ribases, Marta

AU - Sanchez-Mora, Cristina

AU - Antoni Ramos-Quiroga, Josep

AU - Bosch, Rosa

AU - Gomez, Nuria

AU - Nogueira, Mariana

AU - Corrales, Montse

AU - Palomar, Gloria

AU - Jacob, Christian P.

AU - Gross-Lesch, Silke

AU - Kreiker, Susanne

AU - Reif, Andreas

AU - Lesch, Klaus Peter

AU - Cormand, Bru

AU - Casas, Miquel

AU - Bayes, Monica

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KW - case-control association study

KW - forkhead box P2

KW - learning disability

KW - single nucleotide polymorphism

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DO - 10.1097/YPG.0b013e328353957e

M3 - Article

VL - 22

SP - 155

EP - 160

JO - Psychiatric Genetics

JF - Psychiatric Genetics

SN - 0955-8829

IS - 4

ER -