Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: THEMIS[original query] |
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Portal vein thrombosis in children and adolescents: the low prevalence of hereditary thrombophilic disorders. Journal of pediatric surgery 2004 Sep 39 (9): 1356-61. Pinto Raquel B, Silveira Themis R, Bandinelli Eliane, Röhsig Lia |
The Ala54Thr polymorphism of the FABP2 gene influences the postprandial fatty acids in patients with type 2 diabetes. The Journal of clinical endocrinology and metabolism 2010 Aug 95 (8): 3909-17. Almeida Jussara C, Gross Jorge L, Canani Luis H, Zelmanovitz Themis, Perassolo Magda S, Azevedo Mirela |
Multiple common variants for celiac disease influencing immune gene expression.
Nature genetics 2010 Apr 42 (4): 295-302. Dubois Patrick C A, Trynka Gosia, Franke Lude, Hunt Karen A, Romanos Jihane, Curtotti Alessandra, Zhernakova Alexandra, Heap Graham A R, Adány Róza, Aromaa Arpo, Bardella Maria Teresa, van den Berg Leonard H, Bockett Nicholas A, de la Concha Emilio G, Dema Bárbara, Fehrmann Rudolf S N, Fernández-Arquero Miguel, Fiatal Szilvia, Grandone Elvira, Green Peter M, Groen Harry J M, Gwilliam Rhian, Houwen Roderick H J, Hunt Sarah E, Kaukinen Katri, Kelleher Dermot, Korponay-Szabo Ilma, Kurppa Kalle, MacMathuna Padraic, Mäki Markku, Mazzilli Maria Cristina, McCann Owen T, Mearin M Luisa, Mein Charles A, Mirza Muddassar M, Mistry Vanisha, Mora Barbara, Morley Katherine I, Mulder Chris J, Murray Joseph A, Núñez Concepción, Oosterom Elvira, Ophoff Roel A, Polanco Isabel, Peltonen Leena, Platteel Mathieu, Rybak Anna, Salomaa Veikko, Schweizer Joachim J, Sperandeo Maria Pia, Tack Greetje J, Turner Graham, Veldink Jan H, Verbeek Wieke H M, Weersma Rinse K, Wolters Victorien M, Urcelay Elena, Cukrowska Bozena, Greco Luigi, Neuhausen Susan L, McManus Ross, Barisani Donatella, Deloukas Panos, Barrett Jeffrey C, Saavalainen Paivi, Wijmenga Cisca, van Heel David |
Polymorphisms in ABLIM1 are associated with personality traits and alcohol dependence. Journal of molecular neuroscience : MN 2011 May . Wang KS, Liu X, Aragam N, Mullersman JE, Jian X, Pan Y, Liu Y |
UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association? Pediatric research 2012 Aug 72 (2): 169-73. Alencastro de Azevedo Laura, Reverbel da Silveira Themis, Carvalho Clarissa Gutierrez, Martins de Castro Simone, Giugliani Roberto, Matte Ursu |
Evaluation of European coeliac disease risk variants in a north Indian population. European journal of human genetics : EJHG 2015 Apr 23 (4): 530-5. Senapati Sabyasachi, Gutierrez-Achury Javier, Sood Ajit, Midha Vandana, Szperl Agata, Romanos Jihane, Zhernakova Alexandra, Franke Lude, Alonso Santos, Thelma B K, Wijmenga Cisca, Trynka Gos |
Genome-wide association study of recalcitrant atopic dermatitis in Korean children.
The Journal of allergy and clinical immunology 2015 Sep 136 (3): 678-684.e4. Kim Kyung Won, Myers Rachel A, Lee Ji Hyun, Igartua Catherine, Lee Kyung Eun, Kim Yoon Hee, Kim Eun-Jin, Yoon Dankyu, Lee Joo-Shil, Hirota Tomomitsu, Tamari Mayumi, Takahashi Atsushi, Kubo Michiaki, Choi Je-Min, Kim Kyu-Earn, Nicolae Dan L, Ober Carole, Sohn Myung Hy |
Increased THEMIS First Exon Usage in CD4+ T-Cells Is Associated with a Genotype that Is Protective against Multiple Sclerosis. PloS one 2016 11 (7): e0158327. Davies Jessica L, Thompson Sara, Kaur-Sandhu Harpreet, Sawcer Stephen, Coles Alasdair, Ban Maria, Jones Joan |
Effect of Vitamin D Serum Levels and GC Gene Polymorphisms in Liver Fibrosis Due to Chronic Hepatitis C. Annals of hepatology 2017 Aug 16 (5): 742-748. Azevedo Laura A, Matte Ursula, Silveira Themis R, Bonfanti Jacqueline W, Bruch Juliana P, Álvares-da-Silva Mário |
Search for DQ2.5 and DQ8 alleles using a lower cost technique in patients with type 1 diabetes and celiac disease in a population of southern Brazil. Archives of endocrinology and metabolism 2017 Jul 0. Bastos Marília D, Kowalski Thayne W, Puñales Márcia, Tschiedel Balduíno, Mariath Luiza M, Pires Ana Luiza G, Faccini Lavínia S, Silveira Themis |
Genetic variants underlying vitamin D metabolism and VDR-TGFß-1-SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C study. Journal of human genetics 2017 Nov 62 (11): 969-977. de Azevedo Laura A, Matte Ursula, da Silveira Themis R, Álvares-da-Silva Mário |
The chromosome 6q22.33 region is associated with age at diagnosis of type 1 diabetes and disease risk in those diagnosed under 5 years of age. Diabetologia 2017 Oct . Inshaw Jamie R J, Walker Neil M, Wallace Chris, Bottolo Leonardo, Todd John |
Low linolenic and linoleic acid consumption are associated with chronic kidney disease in patients with type 2 diabetes. PloS one 2018 8 13 (8): e0195249. Dos Santos Ana Luiza Teixeira, Duarte Camila Kummel, Santos Manoella, Zoldan Maira, Almeida Jussara Carnevalle, Gross Jorge Luiz, Azevedo Mirela Jobim, Lichtenstein Alice Hinda, Zelmanovitz Them |
The association between adult-type hypolactasia and symptoms of functional dyspepsia. Genetics and molecular biology 2018 Jan 0. Wortmann André Castagna, Simon Daniel, Mazzoleni Luiz Edmundo, Sander Guilherme Becker, Francesconi Carlos Fernando de Magalhães, Nabinger Débora Dreher, Grott Camila Schultz, Rech Tássia Flores, Mazzoleni Felipe, Lunge Vagner Ricardo, Bona Laura Renata de, Milbradt Tobias Cancian, Silveira Themis Reverbel |
Genetic Variants Predisposing Most Strongly to Type 1 Diabetes Diagnosed Under Age 7 Years Lie Near Candidate Genes That Function in the Immune System and in Pancreatic ?-Cells. Diabetes care 2019 Sep . Inshaw Jamie R J, Cutler Antony J, Crouch Daniel J M, Wicker Linda S, Todd John |
Uptake of genetic counseling among adult children of BRCA1/2 mutation carriers in France. Psycho-oncology 2019 7 28 (9): 1894-1900. Gauna Cristaldo Fatima Belén, Touzani Rajae, Apostolidis Thémis, Mouret-Fourme Emmanuelle, Stoppa-Lyonnet Dominique, Lasset Christine, Fricker Jean-Pierre, Berthet Pascaline, Julian-Reynier Claire, Mancini Julien, Noguès Catherine, Bouhnik Anne-Débor |
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- Page last updated:Apr 29, 2024
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