Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission.

Al-Mubarak, Bashayer R; Omar, Aisha; Baz, Batoul; Al-Abdulaziz, Basma; Magrashi, Amna I; Al-Yemni, Eman; Jabaan, Amjad; Monies, Dorota; Abouelhoda, Mohamed; Abebe, Dejene; Ghaziuddin, Mohammad; Al-Tassan, Nada A

Al-Mubarak, Bashayer R; Omar, Aisha; Baz, Batoul; Al-Abdulaziz, Basma; Magrashi, Amna I; Al-Yemni, Eman; Jabaan, Amjad; Monies, Dorota; Abouelhoda, Mohamed; Abebe, Dejene; Ghaziuddin, Mohammad; Al-Tassan, Nada A.

Afiliación

Al-Mubarak BR; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia. BAl-Mubarak@kfshrc.edu.sa.
Omar A; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia. BAl-Mubarak@kfshrc.edu.sa.
Baz B; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
Al-Abdulaziz B; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
Magrashi AI; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Al-Yemni E; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
Jabaan A; National center for genomics technology, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Monies D; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
Abouelhoda M; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
Abebe D; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Ghaziuddin M; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Al-Tassan NA; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.

Eur J Hum Genet ; 28(8): 1098-1110, 2020 08.

Article en En | MEDLINE | ID: mdl-32238911

Asunto(s)

Trastorno por Déficit de Atención con Hiperactividad/genética; Sitios Genéticos; Herencia Multifactorial; Adolescente; Adulto; Niño; Exoma; Femenino; Predisposición Genética a la Enfermedad; Humanos; Masculino; Proteínas de la Membrana/genética; Quinasas Relacionadas con NIMA/genética; Proteínas de Neoplasias/genética; Linaje; Fosfoproteínas/genética; Polimorfismo Genético; Proteínas Tirosina Fosfatasas/genética

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Herencia Multifactorial / Sitios Genéticos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Arabia Saudita

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