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

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Francks, C, Maegawa, S, McAuley, E, Richardson, A, Stein, J, Oshimura, M, Monaco, A
التنسيق:	Conference item
منشور في:	2004

مواد مشابهة

Handedness and schizophrenia susceptibility are paternally linked to a locus on chromosome 2p12-q11.
حسب: Francks, C, وآخرون
منشور في: (2003)

Confirmatory evidence for linkage of relative hand skill to 2p12-q11.
حسب: Francks, C, وآخرون
منشور في: (2003)

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.
حسب: Francks, C, وآخرون
منشور في: (2003)

Molecular genetic analysis of a quantitative measure of relative hand skill
حسب: Francks, C, وآخرون
منشور في: (2002)

A genomewide linkage screen for relative hand skill in sibling pairs.
حسب: Francks, C, وآخرون
منشور في: (2002)

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
حسب: Francks, C, وآخرون
منشور في: (2002)

Characterisation of a major locus for developmental dyslexia on 18p11.2.
حسب: MacPhie, I, وآخرون
منشور في: (2001)

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.
حسب: Fisher, S, وآخرون
منشور في: (1999)

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
حسب: L. Fontana, وآخرون
منشور في: (2018-09-01)

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
حسب: Francks, C, وآخرون
منشور في: (2007)

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
حسب: Fisher, S, وآخرون
منشور في: (2002)

A Susceptibility Locus on Chromosome 13 Profoundly Impacts the Stability of Genomic Imprinting in Mouse Pluripotent Stem Cells
حسب: Emily Swanzey, وآخرون
منشور في: (2020-03-01)

A non-coding RNA within the Rasgrf1 locus in mouse is imprinted and regulated by its homologous chromosome in trans.
حسب: Chelsea M Brideau, وآخرون
منشور في: (2010-11-01)

REX1 is the critical target of RNF12 in imprinted X chromosome inactivation in mice
حسب: Cristina Gontan, وآخرون
منشور في: (2018-11-01)

Microsatellite association mapping of a primary osteoarthritis susceptibility locus on chromosome 6p12.3-q13.
حسب: Southam, L, وآخرون
منشور في: (2004)

Three novel polymorphic microsatellite markers for the glaucoma locus GLC1B by datamining tetranucleotide repeats on chromosome 2p12-q12
حسب: Carlos Murga-Zamalloa, وآخرون
منشور في: (2009-01-01)

The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals
حسب: Dunham Ian, وآخرون
منشور في: (2007-09-01)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
حسب: Scerri, T, وآخرون
منشور في: (2012)

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
حسب: Francks, C, وآخرون
منشور في: (2004)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
حسب: Paracchini, S, وآخرون
منشور في: (2006)

Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12
حسب: Weeks Daniel E, وآخرون
منشور في: (2004-07-01)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
حسب: Paracchini, S, وآخرون
منشور في: (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.
حسب: Monk, S, وآخرون
منشور في: (1998)

Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation
حسب: Iromi Wanigasuriya, وآخرون
منشور في: (2022-07-01)

A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.
حسب: Francks, C, وآخرون
منشور في: (2000)

Evolutionary lineage-specific genomic imprinting at the ZNF791 locus.
حسب: Jinsoo Ahn, وآخرون
منشور في: (2025-01-01)

Genomic Imprinting at the Porcine <i>DIRAS3</i> Locus
حسب: Jinsoo Ahn, وآخرون
منشور في: (2021-05-01)

Trans-allelic mutational effects at the Peg3 imprinted locus.
حسب: Corey L Bretz, وآخرون
منشور في: (2018-01-01)

Linkage to the AUTS1 locus and analysis of candidate genes for autism on chromosome 7q.
حسب: Bonora, E, وآخرون
منشور في: (2003)

Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation.
حسب: Anupam Paliwal, وآخرون
منشور في: (2013-08-01)

Disruption of Imprinted Genes at Chromosome Region 11p15.5 in Paediatric Rhabdomyosarcoma
حسب: John Anderson, وآخرون
منشور في: (1999-10-01)

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.
حسب: Barnby, G, وآخرون
منشور في: (2005)

A novel quantitative trait locus controlling fetal haemoglobin on chromosome 2p15
حسب: Menzel, S, وآخرون
منشور في: (2008)

Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease.
حسب: Andrew, L, وآخرون
منشور في: (1999)

P2.38 THE ANRIL LOCUS ON CHROMOSOME 9P21 AFFECTS STIFFNESS OF THE ABDOMINAL AORTA
حسب: H.M. Bjorck, وآخرون
منشور في: (2008-09-01)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
حسب: Thomas S Scerri, وآخرون
منشور في: (2012-01-01)

A major susceptibility locus for leprosy in India maps to chromosome 10p13.
حسب: Siddiqui, MR, وآخرون
منشور في: (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.
حسب: Hovnanian, A, وآخرون
منشور في: (1998)

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
حسب: Tatsuki Urakawa, وآخرون
منشور في: (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
حسب: Rundek Tatjana, وآخرون
منشور في: (2009-07-01)