Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease Susceptibility and MAF[original query] |
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| Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases. BMC medical genetics 2006 7 (): 20. Smyth Deborah J, Howson Joanna M M, Payne Felicity, Maier Lisa M, Bailey Rebecca, Holland Kieran, Lowe Christopher E, Cooper Jason D, Hulme John S, Vella Adrian, Dahlman Ingrid, Lam Alex C, Nutland Sarah, Walker Neil M, Twells Rebecca C J, Todd John |
| Interaction analysis of the CBLB and CTLA4 genes in type 1 diabetes. Journal of leukocyte biology 2007 Mar 81 (3): 581-3. Payne Felicity, Cooper Jason D, Walker Neil M, Lam Alex C, Smink Luc J, Nutland Sarah, Stevens Helen E, Hutchings Jayne, Todd John |
| Identification of genetic variants that influence circulating IGF1 levels: a targeted search strategy. Human molecular genetics 2008 May 17 (10): 1457-64. Palles Claire, Johnson Nichola, Coupland Ben, Taylor Claire, Carvajal Jaime, Holly Jeff, Fentiman Ian S, Silva Isabel dos Santos, Ashworth Alan, Peto Julian, Fletcher Oliv |
| Rare variation at the TNFAIP3 locus and susceptibility to rheumatoid arthritis. Human genetics 2010 Dec 128 (6): 627-33. Bowes John, Lawrence Robert, Eyre Stephen, Panoutsopoulou Kalliope, Orozco Gisela, Elliott Katherine S, Ke Xiayi, Morris Andrew P, , Thomson Wendy, Worthington Jane, Barton Anne, Zeggini Elefther |
| Investigation of Caucasian rheumatoid arthritis susceptibility loci in African patients with the same disease. Arthritis research & therapy 2012 14 (6): R239. Viatte Sebastien, Flynn Edward, Lunt Mark, Barnes Joanne, Singwe-Ngandeu Madeleine, Bas Sylvette, Barton Anne, Gabay C |
| Estimating the contributions of rare and common genetic variations and clinical measures to a model trait: adiponectin. Genetic epidemiology 2012 Oct . An SS, Palmer ND, Hanley AJ, Ziegler JT, Brown WM, Haffner SM, Norris JM, Rotter JI, Guo X, Chen YD, Wagenknecht LE, Langefeld CD, Bowden DW |
| IL-10 gene promoter and intron polymorphisms and changes in IL-10 secretion in women with idiopathic recurrent miscarriage. Human reproduction (Oxford, England) 2014 May 29 (5): 1025-34. Qaddourah R H, Magdoud K, Saldanha F L, Mahmood N, Mustafa F E, Mahjoub T, Almawi W |
| Multiple rare genetic variants co-segregating with familial IgA nephropathy all act within a single immune-related network. Journal of internal medicine 2016 Oct . Cox S N, Pesce F, El-Sayed Moustafa J S, Sallustio F, Serino G, Kkoufou C, Giampetruzzi A, Ancona N, Falchi M, Schena F P, |
| Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population. Human molecular genetics 2016 Nov 25 (22): 5027-5034. Momozawa Yukihide, Akiyama Masato, Kamatani Yoichiro, Arakawa Satoshi, Yasuda Miho, Yoshida Shigeo, Oshima Yuji, Mori Ryusaburo, Tanaka Koji, Mori Keisuke, Inoue Satoshi, Terasaki Hiroko, Yasuma Tetsuhiro, Honda Shigeru, Miki Akiko, Inoue Maiko, Fujisawa Kimihiko, Takahashi Kanji, Yasukawa Tsutomu, Yanagi Yasuo, Kadonosono Kazuaki, Sonoda Koh-Hei, Ishibashi Tatsuro, Takahashi Atsushi, Kubo Michia |
| Association of Genetic Variants in NF-kB with Susceptibility to Breast Cancer: a Case Control Study. Pathology oncology research : POR 2018 Jul . Ghali Rabeb M, Mahjoub Sana, Zaied Sonia, Bhiri Hanen, Bahia Wael, Mahjoub Touhami, Almawi Wassim |
Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.
Nature communications 2018 11 9 (1): 5101. Ferkingstad Egil, Oddsson Asmundur, Gretarsdottir Solveig, Benonisdottir Stefania, Thorleifsson Gudmar, Deaton Aimee M, Jonsson Stefan, Stefansson Olafur A, Norddahl Gudmundur L, Zink Florian, Arnadottir Gudny A, Gunnarsson Bjarni, Halldorsson Gisli H, Helgadottir Anna, Jensson Brynjar O, Kristjansson Ragnar P, Sveinbjornsson Gardar, Sverrisson David A, Masson Gisli, Olafsson Isleifur, Eyjolfsson Gudmundur I, Sigurdardottir Olof, Holm Hilma, Jonsdottir Ingileif, Olafsson Sigurdur, Steingrimsdottir Thora, Rafnar Thorunn, Bjornsson Einar S, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Sulem Patrick, Stefansson Ka |
| Contribution of ADIPOQ Variants to the Genetic Susceptibility of Recurrent Pregnancy Loss. Reproductive sciences (Thousand Oaks, Calif.) 2020 Aug . Bahia Wael, Soltani Ismael, Haddad Anis, Radhouani Assala, Mahdhi Abdelkarim, Ferchichi Salima, Almawi Wassim |
| Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. medRxiv : the preprint server for health sciences 2023 7 . Frederik H Lassen, Samvida S Venkatesh, Nikolas Baya, Wei Zhou, Alex Bloemendal, Benjamin M Neale, Benedikt M Kessler, Nicola Whiffin, Cecilia M Lindgren, Duncan S Palm |
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