scholarly journals Fine Mapping and Functional Studies of Risk Variants for Type 1 Diabetes at Chromosome 16p13.13

Diabetes ◽  
2014 ◽  
Vol 63 (12) ◽  
pp. 4360-4368 ◽  
Author(s):  
M. J. Tomlinson ◽  
A. Pitsillides ◽  
R. Pickin ◽  
M. Mika ◽  
K. L. Keene ◽  
...  
2018 ◽  
Vol 50 (10) ◽  
pp. 1366-1374 ◽  
Author(s):  
Harm-Jan Westra ◽  
Marta Martínez-Bonet ◽  
Suna Onengut-Gumuscu ◽  
Annette Lee ◽  
Yang Luo ◽  
...  

Diabetes ◽  
2018 ◽  
Vol 67 (Supplement 1) ◽  
pp. 1702-P
Author(s):  
SUNA ONENGUT-GUMUSCU ◽  
NOAH VOGLER ◽  
MARIA FAIDAS ◽  
REBECCA R. PICKIN ◽  
ELAINE GERSZ ◽  
...  

Author(s):  
Melanie R Shapiro ◽  
Puchong Thirawatananond ◽  
Leeana Peters ◽  
Robert C Sharp ◽  
Similoluwa Ogundare ◽  
...  

Author(s):  
N. V Lagunova ◽  
T. F Golubova ◽  
Irina Anatol’evna Polenok ◽  
A. V Kurganova

The clinical, neurological, and functional studies in the children suffering from type 1 diabetes mellitus have demonstrated that practically every fourth patient presented with the complaints and symptoms of this pathology associated with the development of diabetic polyneuropathy, the reduced bioelectrical activity, and the changes of peripheral blood circulation strongly depending on the duration and the quality of compensation of the disease. Under the influence of the treatment under the conditions of a spa and health resort facility with the inclusion of hydrodynamic tablet therapy, the positive dynamics of the parameters of interest was documented in the form of the improvement of the state of carbohydrate metabolism, clinical and neurological characteristics, and the effectiveness of the functional methods for the examination of the children presenting with type 1 diabetes.


2020 ◽  
Author(s):  
Tatsuhiko Naito ◽  
Ken Suzuki ◽  
Jun Hirata ◽  
Yoichiro Kamatani ◽  
Koichi Matsuda ◽  
...  

Conventional HLA imputation methods drop their performance for infrequent alleles, which reduces reliability of trans-ethnic MHC fine-mapping due to inter-ethnic heterogeneity in allele frequency spectra. We developed DEEP*HLA, a deep learning method for imputing HLA genotypes. Through validation using the Japanese and European HLA reference panels (n = 1,118 and 5,112), DEEP*HLA achieved the highest accuracies in both datasets (0.987 and 0.976) especially for low-frequency and rare alleles. DEEP*HLA was less dependent of distance-dependent linkage disequilibrium decay of the target alleles and might capture the complicated region-wide information. We applied DEEP*HLA to type 1 diabetes GWAS data of BioBank Japan (n = 62,387) and UK Biobank (n = 356,855), and successfully disentangled independently associated class I and II HLA variants with shared risk between diverse populations (the top signal at HLA-DRβ1 amino acid position 71; P = 6.2 × 10-119). Our study illustrates a value of deep learning in genotype imputation and trans-ethnic MHC fine-mapping.


2015 ◽  
Vol 47 (4) ◽  
pp. 381-386 ◽  
Author(s):  
Suna Onengut-Gumuscu ◽  
◽  
Wei-Min Chen ◽  
Oliver Burren ◽  
Nick J Cooper ◽  
...  

2013 ◽  
Vol 24 (9-10) ◽  
pp. 358-375 ◽  
Author(s):  
Emma E. Hamilton-Williams ◽  
Daniel B. Rainbow ◽  
Jocelyn Cheung ◽  
Mikkel Christensen ◽  
Paul A. Lyons ◽  
...  

Diabetes ◽  
2019 ◽  
Vol 68 (Supplement 1) ◽  
pp. 1697-P
Author(s):  
SUNA ONENGUT ◽  
HANZHI YANG ◽  
REBECCA R. PICKIN ◽  
STEPHEN S. RICH

2021 ◽  
Author(s):  
Catherine C. Robertson ◽  
Jamie R. J. Inshaw ◽  
Suna Onengut-Gumuscu ◽  
Wei-Min Chen ◽  
David Flores Santa Cruz ◽  
...  

2012 ◽  
Vol 21 (12) ◽  
pp. 2815-2824 ◽  
Author(s):  
Chris Wallace ◽  
Maxime Rotival ◽  
Jason D. Cooper ◽  
Catherine M. Rice ◽  
Jennie H.M. Yang ◽  
...  

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