نتائج البحث - Constantin Polychronakos
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A Common Autoimmunity Predisposing Signal Peptide Variant of the Cytotoxic T-lymphocyte Antigen 4 Results in Inefficient Glycosylation of the Susceptibility Allele حسب Suzana M. Anjos, Audrey Nguyen, Houria Ounissi‐Benkalha, Marie-Catherine Tessier, Constantin Polychronakos
منشور في 2002Artigo -
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Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease حسب D.N. Cooper, Michael Krawczak, Constantin Polychronakos, Chris Tyler‐Smith, Hildegard Kehrer‐Sawatzki
منشور في 2013Revisão -
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Class III Alleles of the Variable Number of Tandem Repeat Insulin Polymorphism Associated with Silencing of Thymic Insulin Predispose to Type 1 Diabetes حسب Petros Vafiadis, Houria Ounissi‐Benkalha, Michael Palumbo, Rosemarie Grabs, Marylène Rousseau, Cynthia G. Goodyer, Constantin Polychronakos
منشور في 2001Artigo -
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Clinically Relevant Circulating Protein Biomarkers for Type 1 Diabetes: Evidence From a Two-Sample Mendelian Randomization Study حسب Nahid Yazdanpanah, Mojgan Yazdanpanah, Ye Wang, Vincenzo Forgetta, Michaël Pollak, Constantin Polychronakos, J. Brent Richards, Despoina Manousaki
منشور في 2021Artigo -
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Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study حسب Despoina Manousaki, Adil Harroud, Ruth E. Mitchell, Stephanie Ross, Vincenzo Forgetta, Nicholas J. Timpson, George Davey Smith, Constantin Polychronakos, J. Brent Richards
منشور في 2021Artigo -
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Guidelines for Growth Hormone and Insulin-Like Growth Factor-I Treatment in Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-Like... حسب Adda Grimberg, Sara A. DiVall, Constantin Polychronakos, David B. Allen, Laurie E. Cohen, Jose Bernardo Quintos, Wilma C. Rossi, Chris Feudtner, M. Hassan Murad
منشور في 2016Artigo -
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Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome حسب John J. Mitchell, Zubin Punthakee, Bernard Lo, C. Bernard, Karen Chong, Catherine E. Newman, Lola Cartier, Valérie Désilets, E. Cutz, Inger Lise Skog Hansen, P Riley, Constantin Polychronakos
منشور في 2004Artigo -
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From Disease Association to Risk Assessment: An Optimistic View from Genome-Wide Association Studies on Type 1 Diabetes حسب Zhi Wei, Kai Wang, Hui‐Qi Qu, Haitao Zhang, Jonathan P. Bradfield, Cecilia Kim, Edward Frackleton, Cuiping Hou, Joseph Glessner, Rosetta Chiavacci, Charles A. Stanley, Dimitri Monos, Struan F.A. Grant, Constantin Polychronakos, Hákon Hákonarson
منشور في 2009Artigo -
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Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes حسب Vincenzo Forgetta, Despoina Manousaki, Roman Istomine, Stephanie Ross, Marie-Catherine Tessier, Luc Marchand, Min Li, Hui‐Qi Qu, Jonathan P. Bradfield, Struan F.A. Grant, Hákon Hákonarson, Andrew D. Paterson, Ciriaco A. Piccirillo, Constantin Polychronakos, J. Brent Richards
منشور في 2020Artigo -
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Genome-wide profiling using single-nucleotide polymorphism arrays identifies novel chromosomal imbalances in pediatric glioblastomas حسب Hui‐Qi Qu, Karine Jacob, Sarah Fatet, Bing Ge, David W. Barnett, Olivier Delattre, Damien Faury, Alexandre Montpetit, Lauren A. Solomon, Péter Hauser, Miklós Garami, László Bognár, Zoltan Hansely, Robert Mio, Jean‐Pierre Farmer, Steffen Albrecht, Constantin Polychronakos, Cynthia Hawkins, Nada Jabado
منشور في 2010Artigo -
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A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci حسب Jonathan P. Bradfield, Hui‐Qi Qu, Kai Wang, Haitao Zhang, Patrick Sleiman, Chong Ae Kim, Frank Mentch, Haijun Qiu, Joseph Glessner, Kelly Thomas, Edward C. Frackelton, Rosetta Chiavacci, Marcin Imieliński, Dimitri Monos, Rahul Pandey, Marina Bakay, Struan F.A. Grant, Constantin Polychronakos, Hákon Hákonarson
منشور في 2011Revisão -
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Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic risk حسب Jennie G. Pouget, Buhm Han, Yang Wu, Emmanuel Mignot, Hanna M. Ollila, Juliet N. Barker, Sarah L. Spain, Nick Dand, Richard C. Trembath, Javier Martı́n, Maureen D. Mayes, Lara Bossini‐Castillo, Elena López‐Isac, Ying Jin, Stephanie A. Santorico, Richard A. Spritz, Hákon Hákonarson, Constantin Polychronakos, Soumya Raychaudhuri, Jo Knight
منشور في 2019Artigo -
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A Polymorphism Within the <i>G6PC2</i> Gene Is Associated with Fasting Plasma Glucose Levels حسب Nabila Bouatia‐Naji, Ghislain Rocheleau, Leentje Van Lommel, Katleen Lemaire, Frans Schuit, Christine Cavalcanti-Proença, Marion Marchand, Anna‐Liisa Hartikainen, Ulla Sovio, Franck De Graeve, Johan Rung, Martine Vaxillaire, Jean Tichet, Michel Marre, Beverley Balkau, Jacques Weill, Paul Elliott, Marjo‐Riitta Järvelin, Stephen Eyre, Constantin Polychronakos, Christian Dina, Robert Sladek, Philippe Froguel
منشور في 2008Artigo -
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Rfx6 directs islet formation and insulin production in mice and humans حسب Stuart B. Smith, Hui‐Qi Qu, Nadine Taleb, Nina Kishimoto, David Scheel, Yang Lü, Ann‐Marie Patch, R. Grabs, Juehu Wang, Francis C. Lynn, Takeshi Miyatsuka, John J. Mitchell, Rina Seerke, Julie Désir, Serge Vanden Eijnden, Marc Abramowicz, N. Kacet, Jacques Weill, Marie-Ève Renard, Mattia Gentile, Inger Marie Jensen Hansen, Ken Dewar, Andrew T. Hattersley, Rennian Wang, Maria E. Wilson, Jeffrey D. Johnson, Constantin Polychronakos, Michael S. German
منشور في 2010Artigo -
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A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study حسب Hákon Hákonarson, Hui‐Qi Qu, Jonathan P. Bradfield, Luc Marchand, Cecilia E. Kim, Joseph Glessner, Rosemarie Grabs, Tracy Casalunovo, Shayne Taback, Edward C. Frackelton, Andrew W. Eckert, Kiran Annaiah, Margaret L. Lawson, F. George Otieno, Erin Santa, Julie L. Shaner, Ryan M. Smith, Chioma C. Onyiah, Robert Skraban, Rosetta Chiavacci, Luke J. Robinson, Charles A. Stanley, Susan Kirsch, Marcella Devoto, Dimitri Monos, Struan F.A. Grant, Constantin Polychronakos
منشور في 2008Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Medicine
Genotype
Endocrinology
Internal medicine
Single-nucleotide polymorphism
Diabetes mellitus
Genome-wide association study
Genetic association
Allele
Pathology
Type 2 diabetes
Computational biology
Genome
Immunology
Disease
Genetic variants
Locus (genetics)
Mendelian randomization
Odds ratio
Psychiatry
SNP
Bioinformatics
Computer science
Environmental health
Mutation
Phenotype
Population