Results 21 to 30 of about 583,132 (315)
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. [PDF]
, 2010 BACKGROUND: Autism spectrum disorders (ASDs) are a group of highly heritable neurodevelopmental disorders which are characteristically comprised of impairments in social interaction, communication and restricted interests/behaviours.Klauck, Sabine M., Mulder, EJ, Monaco, Anthony P, Klauck, Sabine M, Bailey, Anthony J., Bailey Anthony J, Poustka Fritz, Sousa, I, Bailey, Anthony J, Pagnamenta Alistair T, Fritz Poustka, Mulder, Erik J., Alistair T Pagnamenta, Battaglia Agatino, Taane G Clark, Clark, Taane Gregrory, Mulder Erik J, Clark, Taane G., Monaco, AP, Pagnamenta, Alistair T, Minderaa Ruud B, Klauck Sabine M, Sousa, Inês, Pagnamenta, AT, Anthony P Monaco, Monaco Anthony P, Erik J Mulder, null null, Clark, Taane G, Clark, TG, Klauck, SM, Monaco, Anthony P., Ruud B Minderaa, Pagnamenta, Alistair T., Minderaa, Ruud B., Inês Sousa, Holt, Richard, International Molecular Genetic Study of Autism Consortium (IMGS, Monaco, Anthony, Richard Holt, Anthony J Bailey, Clark Taane G, Minderaa, Ruud B, Battaglia, Agatino, Holt, R, Sabine M Klauck, Bailey, AJ, Agatino Battaglia, Holt Richard, Minderaa, RB, Mulder, Erik J, Sousa Inês, Poustka, F, Poustka, Fritz, Battaglia, A +54 morecore +1 more sourceThe genetics of infectious disease susceptibility: has the evidence for epistasis been overestimated? [PDF]
, 2013 Interactions amongst genes, known as epistasis, are assumed to make a substantial contribution to the genetic variation in infectious disease susceptibility, but this claim is controversial.Ebert, Dieter, Dieter Ebert, Hall, Matthew, Matthew D Hall, Hall, Matthew D. +4 morecore +1 more sourceIdentification of candidate genes for dyslexia susceptibility on chromosome 18 [PDF]
, 2010 Background: Six independent studies have identified linkage to chromosome 18 for developmental dyslexia or general reading ability. Until now, no candidate genes have been identified to explain this linkage.Olson, R K, Pennington Bruce F., Anthony P. Monaco, Pennington, B F, Scerri, TS, Alex J. Richardson, Smith, SD, Talcott, J, Richard K. Olson, Alex J Richardson, MacPhie, I L, Joel Talcott, Bruce F Pennington, Stein, J, Monaco, AP, Morris Andrew, Pennington, BF, Olson Richard K., Silvia Paracchini, Macphie, IL, DeFries, J C, Anthony P Monaco, Thomas S Scerri, Smith, Shelley D., Richardson, Alex J., Olson, RK, I Laurence MacPhie, Stein, John, Shelley D. Smith, Pennington, Bruce F., Monaco, Anthony P., Defries, JC, Paracchini, Silvia, John Stein, Stein, John F., Scerri Thomas S., MacPhie I. Laurence, Talcott, Joel B., I. Laurence MacPhie, Richardson, Alexandra, Monaco, Anthony, Andrew Morris, John C. DeFries, Talcott Joel, Morris, Andrew, Smith, S D, Smith Shelley D., Talcott, Joel, Bruce F. Pennington, Monaco Anthony P., Olson, Richard K., MacPhie, I. Laurence, Morris, A, Richardson, AJ, Paracchini, S, DeFries, John C., DeFries John C., Shelley D Smith, Stein John, John C DeFries, Monaco, A P, Richard K Olson, Paracchini Silvia, Thomas S. Scerri, Scerri, Thomas S., Scerri, T S +65 morecore +2 more sourcesConstruction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type I diabetes. [PDF]
, 2005 BACKGROUND: One strategy to help identify susceptibility genes for complex, multifactorial diseases is to map disease loci in a representative animal model of the disorder. The nonobese diabetic (NOD) mouse is a model for human type 1 diabetes.Undlien, Dag E, Lowe, C, Chamberlain, G, Savage, DA, Undlien, DE, Wicker, LS, Hunter, Kara M, Walker Neil, Wicker Linda S, Ionescu-Tîrgovişte, Constantin, Maier, Lisa M, Savage, David A, Fraser, H, Guja Cristian, Nutland Sarah, Vella, Adrian, Fraser, Heather, Nutland, Sarah, Moule, Carolyn, Payne, Felicity, Nutland, S, Maier, LM, Todd John A, Twells Rebecca C, Guja, Cristian, Twells, RC, Cooper, Jason D, Ionescu-Tîrgovişte Constantin, Maier Lisa M, Rønningen, Kjersti S, Payne Felicity, Moule Carolyn, Savage David A, Pask, Rebecca, Smyth Deborah J, Strachan, David P, Chamberlain Giselle, Twells, Rebecca C, Smink, LJ, Todd, John A, Hulme, J, Hunter Kara M, Vella, A, Hulme John, Hunter, KM, Lowe, Christopher, Wicker, Linda S, Walker, N, Lowe Christopher, Smyth, DJ, Peterson, LB, Smink, Luc J, Rønningen, KS, Smyth, Deborah J, Cooper Jason D, Strachan David P, Ionescu-Tîrgoviste, C, Payne, F, Pask Rebecca, Strachan, DP, Undlien Dag E, Hulme, John, Vella Adrian, Guja, C, Smink Luc J, Pask, R, Walker, Neil, Moule, C, Todd, JA, Fraser Heather, Rønningen Kjersti S, Chamberlain, Giselle, Peterson Laurence B, Cooper, JD, Peterson, Laurence B +74 morecore +2 more sourcesInfluence of Nitrogen on Grapevine Susceptibility to Downy Mildew
Plants, 2023 Downy mildew, caused by the obligate parasite Plasmopara viticola, is one of the most important threats to viticulture. The exploitation of resistant and susceptibility traits of grapevine is one of the most promising ways to increase the sustainability ...Demetrio Marcianò, Valentina Ricciardi, Giuliana Maddalena, Annamaria Massafra, Elena Marone Fassolo, Simona Masiero, Piero Attilio Bianco, Osvaldo Failla, Gabriella De Lorenzis, Silvia Laura Toffolatti +9 moredoaj +1 more sourceCircadian gene variants and susceptibility to type 2 diabetes : a pilot study [PDF]
, 2012 Background
Disruption of endogenous circadian rhythms has been shown to increase the risk of developing type 2 diabetes, suggesting that circadian genes might play a role in determining disease susceptibility.O’Hare J. Paul, Shahrad Taheri (57360), M. Ann Kelly (174447), Shera, A. Samad, Hydrie MZ, Barnett, Anthony H., Taheri, S., Anthony H Barnett, Kumar S, Shera, A.S., Rees, Simon D., Kelly, M. Ann, Kelly, Marilyn, Shera, AS, Raychaudhuri, Soumya, Sudhesh Kumar (89490), Abdul Basit (174463), Bellary, Srikanth, Rees, S.D., Kumar, S., Barnett AH, J Paul O'Hare, M. Zafar I. Hydrie (174450), Basit, A., Bellary Srikanth, O'Hare, JP, Bellary S, Shera, A Samad, Taheri S, DIAGRAM Consortium, Hydrie, MZ, Taheri, Shahrad, M Zafar I Hydrie, Bellary, S., Abdul Basit, Hydrie M. Zafar I., Shera A. Samad, Barnett, Anthony, Bellary, S, Basit Abdul, Basit, A, Rees SD, Kumar Sudhesh, Srikanth Bellary (89487), Rees, Simon D, Sudhesh Kumar, Shahrad Taheri, O'Hare, J Paul, Rees, Simon, Kelly, M Ann, SAT2D Consortium, Hydrie, M.Z.I., Kelly MA, A Samad Shera, Basit, Abdul, Barnett, A.H., Anthony H. Barnett (174467), Rees Simon D., Kelly, M.A., Srikanth Bellary, Shera AS, Basit A, Hydrie, M Zafar I, Hydriem, Zafar L., Kumar, Sudhesh, Barnett, Anthony H, O'Hare, J.P., Kelly M. Ann, Hydrie, M. Zafar I., Simon D Rees, Kumar, S, A. Samad Shera (174452), O'Hare, J. Paul, Taheri Shahrad, Barnett Anthony H., J. Paul O’Hare (174457), M Ann Kelly, Simon D. Rees (174448) +77 morecore +1 more sourceAssociation of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis [PDF]
, 2010 Recent genetic studies have led to identification of numerous loci that are associated with susceptibility to autoimmune diseases. The strategy of using information from these studies has facilitated the identification of novel juvenile idiopathic ...Martin, P., Barton, A., Gardner-Medwin, J. [CAPS and BSPAR study groups], UKRAG Consortium, Worthington, J., Thomson, W., Flynn, E., Packham, J., Hinks, A., British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group, Eyre, S., Ke, X., Childhood Arthritis Prospective Study (CAPS) +12 morecore +1 more source
