Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2040-2392
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders ; volume:5 ; number:1 ; day:10 ; month:1 ; year:2014 ; pages:1-10 ; date:12.2014
Molecular autism ; 5, Heft 1 (10.1.2014), 1-10, 12.2014
- Urheber
-
Cukier, Holly N.
Dueker, Nicole D.
Slifer, Susan H.
Lee, Joycelyn M.
Whitehead, Patrice L.
Lalanne, Eminisha
Leyva, Natalia
Konidari, Ioanna
Gentry, Ryan C.
Hulme, William F.
Booven, Derek Van
Mayo, Vera
Hofmann, Natalia K.
Schmidt, Michael A.
Martin, Eden R.
Haines, Jonathan L.
Cuccaro, Michael L.
Gilbert, John R.
Pericak-Vance, Margaret A.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/2040-2392-5-1
- URN
-
urn:nbn:de:101:1-2021082108063320042484
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:52 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Cukier, Holly N.
- Dueker, Nicole D.
- Slifer, Susan H.
- Lee, Joycelyn M.
- Whitehead, Patrice L.
- Lalanne, Eminisha
- Leyva, Natalia
- Konidari, Ioanna
- Gentry, Ryan C.
- Hulme, William F.
- Booven, Derek Van
- Mayo, Vera
- Hofmann, Natalia K.
- Schmidt, Michael A.
- Martin, Eden R.
- Haines, Jonathan L.
- Cuccaro, Michael L.
- Gilbert, John R.
- Pericak-Vance, Margaret A.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
Exome Pool-Seq in neurodevelopmental disorders
Mapping a shared genetic basis for neurodevelopmental disorders
Neurodevelopmental heterogeneity and computational approaches for understanding autism
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders
Autism and related neurodevelopmental disorders: the many genes involved
Whole exome screening of neurodevelopmental regression disorders in a cohort of Egyptian patients
Transcriptomic immaturity inducible by neural hyperexcitation is shared by multiple neuropsychiatric disorders
Efficacy of cannabinoids in neurodevelopmental and neuropsychiatric disorders among children and adolescents: a systematic review
Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
Exome Pool-Seq in neurodevelopmental disorders
Mapping a shared genetic basis for neurodevelopmental disorders
Neurodevelopmental heterogeneity and computational approaches for understanding autism
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders
Autism and related neurodevelopmental disorders: the many genes involved
Whole exome screening of neurodevelopmental regression disorders in a cohort of Egyptian patients
Transcriptomic immaturity inducible by neural hyperexcitation is shared by multiple neuropsychiatric disorders
Efficacy of cannabinoids in neurodevelopmental and neuropsychiatric disorders among children and adolescents: a systematic review
Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
Exome Pool-Seq in neurodevelopmental disorders
Mapping a shared genetic basis for neurodevelopmental disorders
Neurodevelopmental heterogeneity and computational approaches for understanding autism
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders
Autism and related neurodevelopmental disorders: the many genes involved
Whole exome screening of neurodevelopmental regression disorders in a cohort of Egyptian patients
Transcriptomic immaturity inducible by neural hyperexcitation is shared by multiple neuropsychiatric disorders
Efficacy of cannabinoids in neurodevelopmental and neuropsychiatric disorders among children and adolescents: a systematic review
Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders