A novel imprinted locus on chromosome 2P12 associated with relative hand skill in humans

A novel imprinted locus on chromosome 2P12 associated with relative hand skill in humans

Bibliografiset tiedot
Päätekijät:	Francks, C, Maegawa, S, McAuley, E, Richardson, A, Stein, J, Oshimura, M, Monaco, A
Aineistotyyppi:	Conference item
Julkaistu:	2004

Samankaltaisia teoksia

Handedness and schizophrenia susceptibility are paternally linked to a locus on chromosome 2p12-q11.
Tekijä: Francks, C, et al.
Julkaistu: (2003)

Confirmatory evidence for linkage of relative hand skill to 2p12-q11.
Tekijä: Francks, C, et al.
Julkaistu: (2003)

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.
Tekijä: Francks, C, et al.
Julkaistu: (2003)

Molecular genetic analysis of a quantitative measure of relative hand skill
Tekijä: Francks, C, et al.
Julkaistu: (2002)

A genomewide linkage screen for relative hand skill in sibling pairs.
Tekijä: Francks, C, et al.
Julkaistu: (2002)

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
Tekijä: Francks, C, et al.
Julkaistu: (2002)

Characterisation of a major locus for developmental dyslexia on 18p11.2.
Tekijä: MacPhie, I, et al.
Julkaistu: (2001)

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.
Tekijä: Fisher, S, et al.
Julkaistu: (1999)

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
Tekijä: L. Fontana, et al.
Julkaistu: (2018-09-01)

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
Tekijä: Francks, C, et al.
Julkaistu: (2007)

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Tekijä: Fisher, S, et al.
Julkaistu: (2002)

A Susceptibility Locus on Chromosome 13 Profoundly Impacts the Stability of Genomic Imprinting in Mouse Pluripotent Stem Cells
Tekijä: Emily Swanzey, et al.
Julkaistu: (2020-03-01)

A non-coding RNA within the Rasgrf1 locus in mouse is imprinted and regulated by its homologous chromosome in trans.
Tekijä: Chelsea M Brideau, et al.
Julkaistu: (2010-11-01)

REX1 is the critical target of RNF12 in imprinted X chromosome inactivation in mice
Tekijä: Cristina Gontan, et al.
Julkaistu: (2018-11-01)

Microsatellite association mapping of a primary osteoarthritis susceptibility locus on chromosome 6p12.3-q13.
Tekijä: Southam, L, et al.
Julkaistu: (2004)

Three novel polymorphic microsatellite markers for the glaucoma locus GLC1B by datamining tetranucleotide repeats on chromosome 2p12-q12
Tekijä: Carlos Murga-Zamalloa, et al.
Julkaistu: (2009-01-01)

The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals
Tekijä: Dunham Ian, et al.
Julkaistu: (2007-09-01)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
Tekijä: Scerri, T, et al.
Julkaistu: (2012)

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
Tekijä: Francks, C, et al.
Julkaistu: (2004)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Tekijä: Paracchini, S, et al.
Julkaistu: (2006)

Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12
Tekijä: Weeks Daniel E, et al.
Julkaistu: (2004-07-01)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
Tekijä: Paracchini, S, et al.
Julkaistu: (2006)

Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region.
Tekijä: Monk, S, et al.
Julkaistu: (1998)

Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation
Tekijä: Iromi Wanigasuriya, et al.
Julkaistu: (2022-07-01)

A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.
Tekijä: Francks, C, et al.
Julkaistu: (2000)

Evolutionary lineage-specific genomic imprinting at the ZNF791 locus.
Tekijä: Jinsoo Ahn, et al.
Julkaistu: (2025-01-01)

Genomic Imprinting at the Porcine <i>DIRAS3</i> Locus
Tekijä: Jinsoo Ahn, et al.
Julkaistu: (2021-05-01)

Trans-allelic mutational effects at the Peg3 imprinted locus.
Tekijä: Corey L Bretz, et al.
Julkaistu: (2018-01-01)

Linkage to the AUTS1 locus and analysis of candidate genes for autism on chromosome 7q.
Tekijä: Bonora, E, et al.
Julkaistu: (2003)

Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation.
Tekijä: Anupam Paliwal, et al.
Julkaistu: (2013-08-01)

Disruption of Imprinted Genes at Chromosome Region 11p15.5 in Paediatric Rhabdomyosarcoma
Tekijä: John Anderson, et al.
Julkaistu: (1999-10-01)

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.
Tekijä: Barnby, G, et al.
Julkaistu: (2005)

A novel quantitative trait locus controlling fetal haemoglobin on chromosome 2p15
Tekijä: Menzel, S, et al.
Julkaistu: (2008)

Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease.
Tekijä: Andrew, L, et al.
Julkaistu: (1999)

P2.38 THE ANRIL LOCUS ON CHROMOSOME 9P21 AFFECTS STIFFNESS OF THE ABDOMINAL AORTA
Tekijä: H.M. Bjorck, et al.
Julkaistu: (2008-09-01)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
Tekijä: Thomas S Scerri, et al.
Julkaistu: (2012-01-01)

A major susceptibility locus for leprosy in India maps to chromosome 10p13.
Tekijä: Siddiqui, MR, et al.
Julkaistu: (2001)

The human 2',5'-oligoadenylate synthetase locus is composed of three distinct genes clustered on chromosome 12q24.2 encoding the 100-, 69-, and 40-kDa forms.
Tekijä: Hovnanian, A, et al.
Julkaistu: (1998)

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
Tekijä: Tatsuki Urakawa, et al.
Julkaistu: (2024-10-01)

Novel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis
Tekijä: Rundek Tatjana, et al.
Julkaistu: (2009-07-01)