1 - 25 of 32 results for author:"Ragoussis J." in Literature citations
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| Effect of IL12A and IL12B polymorphisms on the risk of Chlamydia trachomatis-induced tubal factor infertility and disease severity. Ohman H., Bailey R., Natividad A., Ragoussis J., Johnson L.L., Tiitinen A., Halttunen M., Paavonen J., Surcel H.M. Hum. Reprod. 27:2217-2223(2012) · Mapped (6) |
| Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. Vernes S.C., Oliver P.L., Spiteri E., Lockstone H.E., Puliyadi R., Taylor J.M., Ho J., Mombereau C., Brewer A., Lowy E. et al. PLoS Genet. 7:e1002145-e1002145(2011) · Mapped (45) |
| ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner. Law M.J., Lower K.M., Voon H.P., Hughes J.R., Garrick D., Viprakasit V., Mitson M., De Gobbi M., Marra M., Morris A. et al. Cell 143:367-378(2010) · Mapped (15) |
| The histone demethylase JMJD2B is regulated by estrogen receptor alpha and hypoxia, and is a key mediator of estrogen induced growth. Yang J., Jubb A.M., Pike L., Buffa F.M., Turley H., Baban D., Leek R., Gatter K.C., Ragoussis J., Harris A.L. Cancer Res. 70:6456-6466(2010) · Mapped (3) |
| A genome-wide scan for common alleles affecting risk for autism. Anney R., Klei L., Pinto D., Regan R., Conroy J., Magalhaes T.R., Correia C., Abrahams B.S., Sykes N., Pagnamenta A.T. et al. Hum. Mol. Genet. 19:4072-4082(2010) · Mapped (14) |
| Functional impact of global rare copy number variation in autism spectrum disorders. Pinto D., Pagnamenta A.T., Klei L., Anney R., Merico D., Regan R., Conroy J., Magalhaes T.R., Correia C., Abrahams B.S. et al. Nature 466:368-372(2010) · Mapped (7) |
| An oncogenic role of eIF3e/INT6 in human breast cancer. Grzmil M., Rzymski T., Milani M., Harris A.L., Capper R.G., Saunders N.J., Salhan A., Ragoussis J., Norbury C.J. Oncogene 29:4080-4089(2010) · Mapped (4) |
| MicroRNA-210 regulates mitochondrial free radical response to hypoxia and krebs cycle in cancer cells by targeting iron sulfur cluster protein ISCU. Favaro E., Ramachandran A., McCormick R., Gee H., Blancher C., Crosby M., Devlin C., Blick C., Buffa F., Li J.L. et al. PLoS ONE 5:e10345-e10345(2010) · Mapped (5) |
| Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. International Molecular Genetic Study Of Autism Consortium Biol. Psychiatry 68:320-328(2010) · Mapped (8) |
| Identification and characterization of enhancers controlling the inflammatory gene expression program in macrophages. Ghisletti S., Barozzi I., Mietton F., Polletti S., De Santa F., Venturini E., Gregory L., Lonie L., Chew A., Wei C.L. et al. Immunity 32:317-328(2010) · Mapped (4) |
| Association of the aromatase gene with Alzheimer's disease in women. Butler H.T., Warden D.R., Hogervorst E., Ragoussis J., Smith A.D., Lehmann D.J. Neurosci. Lett. 468:202-206(2010) · Mapped (9) |
| Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies. Iseri S.U., Osborne R.J., Farrall M., Wyatt A.W., Mirza G., Nurnberg G., Kluck C., Herbert H., Martin A., Hussain M.S. et al. Hum. Mutat. 30:1378-1386(2009) · UniProtKB (1) |
| CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Newbury D.F., Winchester L., Addis L., Paracchini S., Buckingham L.L., Clark A., Cohen W., Cowie H., Dworzynski K., Everitt A. et al. Am. J. Hum. Genet. 85:264-272(2009) · Mapped (6) |
| Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies. Kaur K., Ragge N.K., Ragoussis J. Mol. Vis. 15:1366-1373(2009) · Mapped (5) |
| Genome-wide and fine-resolution association analysis of malaria in West Africa. Wellcome Trust Case Control Consortium Nat. Genet. 41:657-665(2009) · Mapped (46) |
| Genome-wide association of hypoxia-inducible factor (HIF)-1alpha and HIF-2alpha DNA binding with expression profiling of hypoxia-inducible transcripts. Mole D.R., Blancher C., Copley R.R., Pollard P.J., Gleadle J.M., Ragoussis J., Ratcliffe P.J. J. Biol. Chem. 284:16767-16775(2009) · Mapped (13) |
| Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Paracchini S., Steer C.D., Buckingham L.L., Morris A.P., Ring S., Scerri T., Stein J., Pembrey M.E., Ragoussis J., Golding J. et al. Am J Psychiatry 165:1576-1584(2008) · Mapped (1) |
| VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5. Szumska D., Pieles G., Essalmani R., Bilski M., Mesnard D., Kaur K., Franklyn A., El Omari K., Jefferis J., Bentham J. et al. Genes Dev. 22:1465-1477(2008) · Mapped (23) |
| A commonly occurring polymorphism upstream of the estrogen receptor alpha alters transcription and is associated with increased HDL. Figtree G.A., Grieve S.M., Speller B., Geiger M.J., Robinson B.G., Channon K.M., Ragoussis J., Collins P., Watkins H. Atherosclerosis 199:354-361(2008) · Mapped (58) |
| Functional conservation of Rel binding sites in drosophilid genomes. Copley R.R., Totrov M., Linnell J., Field S., Ragoussis J., Udalova I.A. Genome Res. 17:1327-1335(2007) · Mapped (39) |
| LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Francks C., Maegawa S., Lauren J., Abrahams B.S., Velayos-Baeza A., Medland S.E., Colella S., Groszer M., McAuley E.Z., Caffrey T.M. et al. Mol. Psychiatry 12:1129-1139(2007) · UniProtKB (2) |
| TUCAN (CARD8) genetic variants and inflammatory bowel disease. McGovern D.P., Butler H., Ahmad T., Paolucci M., van Heel D.A., Negoro K., Hysi P., Ragoussis J., Travis S.P., Cardon L.R. et al. Gastroenterology 131:1190-1196(2006) · Mapped (23) |
| Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. Yamazaki K., McGovern D., Ragoussis J., Paolucci M., Butler H., Jewell D., Cardon L., Takazoe M., Tanaka T., Ichimori T. et al. Hum. Mol. Genet. 14:3499-3506(2005) · Mapped (1) |
| Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Bogani D., Willoughby C., Davies J., Kaur K., Mirza G., Paudyal A., Haines H., McKeone R., Cadman M., Pieles G. et al. Proc. Natl. Acad. Sci. U.S.A. 102:12477-12482(2005) · Mapped (5) |
| Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region. Davies S.J., Wise C., Venkatesh B., Mirza G., Jefferson A., Volpi E.V., Ragoussis J. Cytogenet. Genome Res. 105:47-53(2004) · UniProtKB (2) |