These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 29983269)

  • 1. Schizophrenia and epilepsy as a result of maternally inherited CNTN6 copy number variant.
    Juan-Perez C; Farrand S; Velakoulis D
    Schizophr Res; 2018 Dec; 202():111-112. PubMed ID: 29983269
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations.
    Tassano E; Uccella S; Giacomini T; Severino M; Fiorio P; Gimelli G; Ronchetto P
    Cytogenet Genome Res; 2018; 156(3):144-149. PubMed ID: 30508811
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene.
    Gridina MM; Matveeva NM; Fishman VS; Menzorov AG; Kizilova HA; Beregovoy NA; Kovrigin II; Pristyazhnyuk IE; Oscorbin IP; Filipenko ML; Kashevarova AA; Skryabin NA; Nikitina TV; Sazhenova EA; Nazarenko LP; Lebedev IN; Serov OL
    Mol Neurobiol; 2018 Aug; 55(8):6533-6546. PubMed ID: 29327201
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Maternal transmission of CNTN6 copy number variation suggests mitochondrial disorder.
    Finsterer J; Scorza FA; Scorza CA
    Schizophr Res; 2019 Apr; 206():454-455. PubMed ID: 30473212
    [No Abstract]   [Full Text] [Related]  

  • 5. CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.
    Hu J; Liao J; Sathanoori M; Kochmar S; Sebastian J; Yatsenko SA; Surti U
    J Neurodev Disord; 2015; 7(1):26. PubMed ID: 26257835
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.
    Mullen SA; Carvill GL; Bellows S; Bayly MA; Trucks H; Lal D; Sander T; Berkovic SF; Dibbens LM; Scheffer IE; Mefford HC
    Neurology; 2013 Oct; 81(17):1507-14. PubMed ID: 24068782
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene.
    Gridina MM; Nikitina TV; Pristyazhnyuk IE; Kashevarova AA; Lopatkina ME; Vasilyev SA; Nazarenko LP; Lebedev IN; Serov OL
    Stem Cell Res; 2019 Oct; 40():101556. PubMed ID: 31518906
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
    Repnikova EA; Lyalin DA; McDonald K; Astbury C; Hansen-Kiss E; Cooley LD; Pfau R; Herman GE; Pyatt RE; Hickey SE
    Eur J Med Genet; 2020 Jan; 63(1):103636. PubMed ID: 30836150
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy.
    Damiano JA; Mullen SA; Hildebrand MS; Bellows ST; Lawrence KM; Arsov T; Dibbens L; Major H; Dahl HH; Mefford HC; Darbro BW; Scheffer IE; Berkovic SF
    Epilepsy Res; 2015 Nov; 117():70-3. PubMed ID: 26421493
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsy.
    Bassuk AG; Geraghty E; Wu S; Mullen SA; Berkovic SF; Scheffer IE; Mefford HC
    Am J Med Genet A; 2013 Jul; 161A(7):1722-5. PubMed ID: 23686817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review.
    Han JY; Park J
    Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34210021
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Estimation of association of CNTN6 copy number variation with idiopathic intellectual disability].
    Lopatkina ME; Kashevarova AA; Lebedev IN
    Genetika; 2016 Sep; 52(9):1109-12. PubMed ID: 29369566
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic components of microdeletion syndromes and their role in determining schizophrenia traits.
    Biswal SR; Kumar A; Muthuswamy S; Kumar S
    Mol Biol Rep; 2024 Jul; 51(1):804. PubMed ID: 39001960
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
    Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
    JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial inheritance of the 3q29 microdeletion syndrome: case report and review.
    Khan WA; Cohen N; Scott SA; Pereira EM
    BMC Med Genomics; 2019 Mar; 12(1):51. PubMed ID: 30885185
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations.
    Fejgin K; Nielsen J; Birknow MR; Bastlund JF; Nielsen V; Lauridsen JB; Stefansson H; Steinberg S; Sorensen HB; Mortensen TE; Larsen PH; Klewe IV; Rasmussen SV; Stefansson K; Werge TM; Kallunki P; Christensen KV; Didriksen M
    Biol Psychiatry; 2014 Jul; 76(2):128-37. PubMed ID: 24090792
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability.
    Heide S; Keren B; Billette de Villemeur T; Chantot-Bastaraud S; Depienne C; Nava C; Mignot C; Jacquette A; Fonteneau E; Lejeune E; Mach C; Marey I; Whalen S; Lacombe D; Naudion S; Rooryck C; Toutain A; Caignec CL; Haye D; Olivier-Faivre L; Masurel-Paulet A; Thauvin-Robinet C; Lesne F; Faudet A; Ville D; des Portes V; Sanlaville D; Siffroi JP; Moutard ML; Héron D
    J Pediatr; 2017 Jun; 185():160-166.e1. PubMed ID: 28284480
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case series.
    Malt EA; Juhasz K; Frengen A; Wangensteen T; Emilsen NM; Hansen B; Agafonov O; Nilsen HL
    Mol Genet Genomic Med; 2019 Sep; 7(9):e889. PubMed ID: 31347308
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.
    Rutkowski TP; Schroeder JP; Gafford GM; Warren ST; Weinshenker D; Caspary T; Mulle JG
    J Neurosci Res; 2017 May; 95(5):1144-1160. PubMed ID: 27859486
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
    Mercati O; Huguet G; Danckaert A; André-Leroux G; Maruani A; Bellinzoni M; Rolland T; Gouder L; Mathieu A; Buratti J; Amsellem F; Benabou M; Van-Gils J; Beggiato A; Konyukh M; Bourgeois JP; Gazzellone MJ; Yuen RK; Walker S; Delépine M; Boland A; Régnault B; Francois M; Van Den Abbeele T; Mosca-Boidron AL; Faivre L; Shimoda Y; Watanabe K; Bonneau D; Rastam M; Leboyer M; Scherer SW; Gillberg C; Delorme R; Cloëz-Tayarani I; Bourgeron T
    Mol Psychiatry; 2017 Apr; 22(4):625-633. PubMed ID: 27166760
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.