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1. Senior citizens behind bars
: challenges for the criminal justice system
by Jolley, Jennifer M and Kerbs, John J
2014, ISBN 1626370427, xi, 286
Criminal justice, Administration of | Services for | Older prisoners | Government policy | Corrections
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2. Full Text Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
by Burton, Paul R and Clayton, David G and Cardon, Lon R and Craddock, Nick and Deloukas, Panos and Duncanson, Audrey and Kwiatkowski, Dominic P and McCarthy, Mark I and Ouwehand, Willem H and Samani, Nilesh J and Todd, John A and Donnelly, Peter and Barrett, Jeffrey C and Davison, Dan and Easton, Doug and Evans, David M and Leung, Hin-Tak and Marchini, Jonathan L and Morris, Andrew P and Spencer, Chris C.A and Tobin, Martin D and Attwood, Antony P and Boorman, James P and Cant, Barbara and Everson, Ursula and Hussey, Judith M and Jolley, Jennifer D and Knight, Alexandra S and Koch, Kerstin and Meech, Elizabeth and Nutland, Sarah and Prowse, Christopher V and Stevens, Helen E and Taylor, Niall C and Walters, Graham R and Walker, Neil M and Watkins, Nicholas A and Winzer, Thilo and Jones, Richard W and McArdle, Wendy L and Ring, Susan M and Strachan, David P and Pembrey, Marcus and Breen, Gerome and Clair, David St and Caesar, Sian and Gordon-Smith, Katharine and Jones, Lisa and Fraser, Christine and Green, Elaine K and Grozeva, Detelina and Hamshere, Marian L and Holmans, Peter A and Jones, Ian R and Kirov, George and Moskivina, Valentina and Nikolov, Ivan and O'Donovan, Michael C and Owen, Michael J and Collier, David A and Elkin, Amanda and Farmer, Anne and Williamson, Richard and McGuffin, Peter and Young, Allan H and Ferrier, I. Nicol and Ball, Stephen G and Balmforth, Anthony J and Barrett, Jennifer H and Bishop, Timothy D and Iles, Mark M and Maqbool, Azhar and Yuldasheva, Nadira and Hall, Alistair S and Braund, Peter S and Dixon, Richard J and Mangino, Massimo and Stevens, Suzanne and Thompson, John R and Bredin, Francesca and Tremelling, Mark and Parkes, Miles and Drummond, Hazel and Lees, Charles W and Nimmo, Elaine R and Satsangi, Jack and Fisher, Sheila A and Forbes, Alastair and Lewis, Cathryn M and Onnie, Clive M and Prescott, Natalie J and Sanderson, Jeremy and Matthew, Christopher G and Barbour, Jamie and Mohiuddin, M. Khalid and Todhunter, Catherine E and Mansfield, John C and Ahmad, Tariq and Cummings, Fraser R and Jewell, Derek P and ... and Breast Cancer Susceptibility Collaboration (UK) and Wellcome Trust Case Control Consortium and Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering Committee and Australo-Anglo-American Spondylitis Consortium (TASC) and The Australo-Anglo-American Spondylitis Consortium (TASC)
Nature genetics, ISSN 1061-4036, 11/2007, Volume 39, Issue 11, pp. 1329 - 1337
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetics, Population | Aminopeptidases - genetics | Spondylitis, Ankylosing - genetics | Minor Histocompatibility Antigens | Thyroiditis, Autoimmune - epidemiology | Humans | Autoimmunity - genetics | Genotype | Multiple Sclerosis - genetics | Chromosome Mapping | Multiple Sclerosis - epidemiology | Receptors, Interleukin - genetics | Thyroiditis, Autoimmune - genetics | Case-Control Studies | Linkage Disequilibrium | Haplotypes - genetics | Breast Neoplasms - genetics | Polymerase Chain Reaction | Spondylitis, Ankylosing - epidemiology | Polymorphism, Single Nucleotide - genetics | North America - epidemiology | Receptors, Immunologic - genetics | Breast Neoplasms - epidemiology | Histocompatibility antigens | HLA histocompatibility antigens | Physiological aspects | Genetic aspects | Diagnosis | Research | Single nucleotide polymorphisms | Ankylosing spondylitis | Risk factors | Genotype & phenotype | Multiple sclerosis | Genetic research | Genetics | Arthritis | Breast cancer | Autoimmune diseases | Index Medicus
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3. Full Text Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
by Eleftheria Zeggini and Michael N. Weedon and Cecilia M. Lindgren and Timothy M. Frayling and Katherine S. Elliott and Hana Lango and Nicholas J. Timpson and John R. B. Perry and Nigel W. Rayner and Rachel M. Freathy and Jeffrey C. Barrett and Beverley Shields and Andrew P. Morris and Sian Ellard and Christopher J. Groves and Lorna W. Harries and Jonathan L. Marchini and Katharine R. Owen and Beatrice Knight and Lon R. Cardon and Mark Walker and Graham A. Hitman and Andrew D. Morris and Alex S. F. Doney and Mark I. McCarthy and Andrew T. Hattersley and WTCCC and Wellcome Trust Case Control Consortium (WTCCC) and The Wellcome Trust Case Control Consortium (WTCCC)
Science (American Association for the Advancement of Science), ISSN 0036-8075, 6/2007, Volume 316, Issue 5829, pp. 1336 - 1341
Medical research | Forestry research | Hospital buildings | Medical genetics | Genetic research | Hospital units | Genetic loci | Reports | Type 2 diabetes mellitus | Human genetics | Research universities | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Diabetes. Impaired glucose tolerance | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Insulin-Like Growth Factor Binding Proteins - genetics | Genetic Predisposition to Disease | Meta-Analysis as Topic | Oligonucleotide Array Sequence Analysis | Introns | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Male | United Kingdom | Chromosome Mapping | Transcription Factors - genetics | Genes, p16 | Case-Control Studies | Homeodomain Proteins - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome, Human | Type 2 diabetes | Genetic aspects | Research | Risk factors | Biomedical research | Cellular biology | Genomics | Diabetes | Molecular biology | Pancreas | Population genetics | Index Medicus
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4. Full Text Preterm neonatal morbidity and mortality by gestational age: a contemporary cohort
by Manuck, Tracy A., MD and Rice, Madeline Murguia, PhD and Bailit, Jennifer L., MD, MPH and Grobman, William A., MD and Reddy, Uma M., MD, MPH and Wapner, Ronald J., MD and Thorp, John M., MD and Caritis, Steve N., MD and Prasad, Mona, DO, MPH and Tita, Alan T.N., MD, PhD and Saade, George R., MD and Sorokin, Yoram, MD and Rouse, Dwight J., MD and Blackwell, Sean C., MD and Tolosa, Jorge E., MD and National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network and Eunice Kennedy Shriver Natl Inst C and Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network
American journal of obstetrics and gynecology, ISSN 0002-9378, 2016, Volume 215, Issue 1, pp. 103.e1 - 103.e14
Obstetrics and Gynecology | neonatal morbidity | prematurity | neonatal mortality | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Humans | Infant | Male | Gestational Age | Pregnancy Outcome - epidemiology | Pregnancy | Young Adult | Infant, Premature | Adult | Female | Infant, Premature, Diseases - epidemiology | Infant Mortality - trends | Infant, Newborn | Length of Stay - statistics & numerical data | Pregnancy Complications - epidemiology | Cohort Studies | Infants (Newborn) | Children | Health aspects | Patient outcomes | Mortality | Morbidity | Index Medicus | Abridged Index Medicus
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5. Full Text FTO genotype is associated with phenotypic variability of body mass index
by Yang, J and Loos, R.J and Powell, J.E and Medland, S.E and Speliotes, E.K and Chasman, D.I and Rose, L.M and Thorleifsson, G and Steinthorsdottir, V and Magi, R and Waite, L and Smith, A.V and Yerges-Armstrong, L.M and Monda, K.L and Hadley, D and Mahajan, A and Li, G and Kapur, K and Vitart, V and Huffman, J.E and Wang, S.R and Palmer, C and Esko, T and Fischer, K and Zhao, J.H and Demirkan, A and Isaacs, A and Feitosa, M.F and Luan, J and Heard-Costa, N.L and White, C and Jackson, A.U and Preuss, M and Ziegler, A and Eriksson, J and Kutalik, Z and Frau, F and Nolte, I.M and Van Vliet-Ostaptchouk, J.V and Hottenga, J.J and Jacobs, K.B and Verweij, N and Goel, A and Medina-Gomez, C and Estrada, K and Bragg-Gresham, J.L and Sanna, S and Sidore, C and Tyrer, J and Teumer, A and Prokopenko, I and Mangino, M and Lindgren, C.M and Assimes, T.L and Shuldiner, A.R and Hui, J and Beilby, J.P and McArdle, W.L and Hall, P and Haritunians, T and Zgaga, L and Kolcic, I and Polasek, O and Zemunik, T and Oostra, B.A and Junttila, M.J and Gronberg, H and Schreiber, S and Peters, A and Hicks, A.A and Stephens, J and Foad, N.S and Laitinen, J and Pouta, A and Kaakinen, M and Willemsen, G and Vink, J and Wild, S.H and Navis, G and Asselbergs, F.W and Homuth, G and John, U and Iribarren, C and Harris, T and Launer, L and Gudnason, V and O'Connell, J.R and Boerwinkle, E and Cadby, G and Palmer, L.J and James, A.L and Musk, A.W and Ingelsson, E and Psaty, B.M and Beckmann, J.S and Waeber, G and Vollenweider, P and Hayward, C and Wright, A.F and Rudan, I and ... and Göteborgs universitet and Gothenburg University and Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition and Sahlgrenska Academy and Centre for Bone and Arthritis Research and Sahlgrenska akademin and Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
Nature (London), ISSN 0028-0836, 2012, Volume 490, Issue 7419, pp. 267 - 272
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Analytical, structural and metabolic biochemistry | Molecular and cellular biology | Body Mass Index | Genome-Wide Association Study | Humans | Repressor Proteins - genetics | Alpha-Ketoglutarate-Dependent Dioxygenase FTO | Male | Nerve Tissue Proteins - genetics | Body Height - genetics | Genetic Variation | Proteins - genetics | Phenotype | Female | Polymorphism, Single Nucleotide | Co-Repressor Proteins | Body mass index | Physiological aspects | Phenotypic plasticity | Obesity gene | Genetic aspects | Single nucleotide polymorphisms | Methods | Studies | Genotype & phenotype | Genetics | Gene loci | Index Medicus | Clinical Medicine | Endokrinologi och diabetes | Klinisk medicin | Endocrinology and Diabetes
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6. Full Text Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
by Jostins, Luke and Ripke, Stephan and Weersma, Rinse K and Duerr, Richard H and McGovern, Dermot P and Hui, Ken Y and Lee, James C and Schumm, L. Philip and Sharma, Yashoda and Anderson, Carl A and Essers, Jonah and Mitrovic, Mitja and Ning, Kaida and Cleynen, Isabelle and Theatre, Emilie and Spain, Sarah L and Raychaudhuri, Soumya and Goyette, Philippe and Wei, Zhi and Abraham, Clara and Achkar, Jean-Paul and Ahmad, Tariq and Amininejad, Leila and Ananthakrishnan, Ashwin N and Andersen, Vibeke and Anews, Jane M and Baidoo, Leonard and Balschun, Tobias and Bampton, Peter A and Bitton, Alain and Boucher, Gabrielle and Brand, Stephan and Büning, Carsten and Cohain, Ariella and Cichon, Sven and D'Amato, Mauro and de Jong, Dirk and Devaney, Kathy L and Dubinsky, Marla and Edwards, Cathryn and Ellinghaus, David and Ferguson, Lynnette R and Franchimont, Denis and Fransen, Karin and Gearry, Richard and Georges, Michel and Gieger, Christian and Glas, Jürgen and Haritunians, Talin and Ponsioen, Cyriel Y and van Limbergen, Johan E and Int IBD Genetics Consortium IIBDGC and International IBD Genetics Consortium (IIBDGC) and The International IBD Genetics Consortium (IIBDGC)
Nature (London), ISSN 0028-0836, 2012, Volume 491, Issue 7422, pp. 119 - 124
no | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | Dermatology | Psoriasis. Parapsoriasis. Lichen | Diseases of the osteoarticular system | Inflammatory joint diseases | Biological and medical sciences | Medical sciences | Other diseases. Semiology | Crohn Disease - genetics | Humans | Inflammatory Bowel Diseases - immunology | Colitis, Ulcerative - genetics | Mycobacterium tuberculosis - immunology | Inflammatory Bowel Diseases - physiopathology | Colitis, Ulcerative - immunology | Host-Pathogen Interactions - immunology | Mycobacterium tuberculosis - pathogenicity | Haplotypes - genetics | Mycobacterium - pathogenicity | Mycobacterium Infections - genetics | Inflammatory Bowel Diseases - genetics | Crohn Disease - microbiology | Mycobacterium Infections - microbiology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Reproducibility of Results | Mycobacterium - immunology | Crohn Disease - immunology | Genome, Human - genetics | Phenotype | Colitis, Ulcerative - microbiology | Host-Pathogen Interactions - genetics | Polymorphism, Single Nucleotide - genetics | Inflammatory Bowel Diseases - microbiology | Crohn Disease - physiopathology | Colitis, Ulcerative - physiopathology | Inflammatory bowel disease | Candidates | Tuberculosis | Architecture | Genetics | Genomes | Diabetes | Gene expression | Health risk assessment | Immune system | Index Medicus | Medicin och hälsovetenskap
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7. Full Text Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome
by Albers, C.A and Paul, D.S and Schulze, H and Freson, K and Stephens, J.C and Smethurst, P.A and Jolley, J.D and Cvejic, A and Kostadima, M and Bertone, P and Breuning, M.H and Debili, N and Deloukas, P and Favier, R and Fiedler, J and Hobbs, C.M and Huang, N and Hurles, M.E and Kiddle, G and Krapels, I and Nurden, P and Ruivenkamp, C.A and Sambrook, J.G and Smith, K and Stemple, D.L and Strauss, G and Thys, C and van Geet, C and Newbury-Ecob, R and Ouwehand, W.H and Ghevaert, C
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 4, pp. 435 - 9, S1-2
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Complex syndromes | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Medical genetics | RNA-Binding Proteins - genetics | Humans | Child, Preschool | Infant | Male | 5' Untranslated Regions - genetics | Genetic Variation | Thrombocytopenia - genetics | Young Adult | Base Sequence | Adult | Female | Child | Infant, Newborn | Amino Acid Sequence | Genetic Predisposition to Disease | Thrombocytopenia - congenital | Radius - abnormalities | Upper Extremity Deformities, Congenital - genetics | Sequence Analysis, DNA | Zebrafish - genetics | Sequence Alignment | Animals | Platelet Count | Adolescent | Polymorphism, Single Nucleotide | Mutation | Physiological aspects | TAR syndrome | Research | Single nucleotide polymorphisms | RNA | Medical research | Genetics | Genes | Index Medicus
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