Development of an immunogenomic landscape for the competing endogenous RNAs network of peri-implantitis

by Yang Li, Jina Zheng, Chanjuan Gong, Kengfu Lan, Yuqing Shen, Xiaojun Ding
Published 2020-10-01

Deep vein thrombosis inhibitor may play a therapeutic role in post-stroke patients

by Xixi Xiang, Di Yuan, Peiyan Kong, Ting Chen, Han Yao, Shijia Lin, Xi Zhang, Hongbao Cao
Published 2020-10-01

Association of soluble endothelial protein C receptor plasma levels and <it>PROCR</it> rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery diseas...

by Kallel Choumous, Cohen William, Saut Noémie, Blankenberg Stefan, Schnabel Renate, Rupprecht Hans J, Bickel Christoph, Munzel Thomas, Tregouet David-Alexandre, Morange Pierre-Emmanuel
Published 2012-11-01

<it>FTO </it>gene variation and measures of body mass in an African population

by Hattersley Andrew T, Rayco-Solon Pura, Sirugo Giorgio, Fulford Anthony J, Hennig Branwen J, Frayling Timothy M, Prentice Andrew M
Published 2009-03-01

The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA

by James Jiqi Wang, Bo Yu, Zongzhe Li
Published 2019-05-01

Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy

by Patricia S. Graham, Georgia Kaidonis, Sotoodeh Abhary, Mark C. Gillies, Mark Daniell, Rohan W. Essex, John H. Chang, Stewart R. Lake, Bishwanath Pal, Alicia J. Jenkins, Alex W. Hewitt, Ecosse L. Lamoureux, Philip G. Hykin, Nikolai Petrovsky, Matthew A. Brown, Jamie E. Craig, Kathryn P. Burdon
Published 2018-05-01

Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family

by Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed, Mustafa A. M. Salih, Ashraf Yahia, Rayan A. Siddig, Mutaz Amin, Mahmoud Koko, Mustafa I. Elbashir, Muntaser E. Ibrahim, Alexis Brice, Ammar E. Ahmed, Giovanni Stevanin
Published 2018-05-01

Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population

by Godwill Azeh Engwa, Friday Nweke Nwalo, Claribel Chidimma Chikezie, Christie Oby Onyia, Opeolu Oyejide Ojo, Wilfred Fon Mbacham, Benjamin Ewa Ubi
Published 2018-05-01

Interaction between obesity and the Hypoxia Inducible Factor 3 Alpha Subunit rs3826795 polymorphism in relation with plasma alanine aminotransferase

by Shuo Wang, Jieyun Song, Yide Yang, Yining Zhang, Nitesh V. Chawla, Jun Ma, Haijun Wang
Published 2017-07-01

Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family

by Vito Guarnieri, Raewyn M. Seaberg, Catherine Kelly, M. Jean Davidson, Simon Raphael, Andrew Y. Shuen, Filomena Baorda, Orazio Palumbo, Alfredo Scillitani, Geoffrey N. Hendy, David E. C. Cole
Published 2017-08-01

Polymorphism rs189037C > T in the promoter region of the ATM gene may associate with reduced risk of T2DM in older adults in China: a case control study

by Xiang Ding, Qiukui Hao, Ming Yang, Tie Chen, Shanping Chen, Jirong Yue, Sean X. Leng, Birong Dong
Published 2017-08-01

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

by Annika Winbo, Eva-Lena Stattin, Ida Maria Westin, Anna Norberg, Johan Persson, Steen M. Jensen, Annika Rydberg
Published 2017-07-01

Identification of a novel CTCF mutation responsible for syndromic intellectual disability – a case report

by Fatma Bastaki, Pratibha Nair, Madiha Mohamed, Ethar Mustafa Malik, Mustafa Helmi, Mahmoud Taleb Al-Ali, Abdul Rezzak Hamzeh
Published 2017-06-01

Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects

by Renata Watanabe Nonose, Karina Lezirovitz, Maria Teresa Balester de Mello Auricchio, Ana Carla Batissoco, Guilherme Lopes Yamamoto, Regina Célia Mingroni-Netto
Published 2018-05-01

Association between 28 single nucleotide polymorphisms and type 2 diabetes mellitus in the Kazakh population: a case-control study

by Nurgul Sikhayeva, Aisha Iskakova, Nuria Saigi-Morgui, Elena Zholdybaeva, Chin-Bin Eap, Erlan Ramanculov
Published 2017-07-01

A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report

by Y. Watanabe, E. Sharwood, B. Goodwin, M. K. Creech, H. Y. Hassan, M. G. Netea, M. Jaeger, A. Dumitrescu, S. Refetoff, T. Huynh, R. E. Weiss
Published 2018-05-01

Genetic polymorphism of HLA-DRB1 alleles in Mexican mestizo patients with abdominal aortic aneurysms

by Javier E. Anaya-Ayala, Susana Hernandez-Doño, Monica Escamilla-Tilch, Jose Marquez-Garcia, Kemberly Hernandez-Sotelo, Rodrigo Lozano-Corona, Daniela Ruiz-Gomez, Julio Granados, Carlos A. Hinojosa
Published 2019-06-01

Lack of association between <it>PKLR </it>rs3020781 and <it>NOS1AP </it>rs7538490 and type 2 diabetes, overweight, obesity and related metabolic phenotypes in a Danish large-scale...

by Almind Katrine, Lauritzen Torsten, Sandbæk Annelli, Borch-Johnsen Knut, Mogensen Mette, Andreasen Camilla, Hansen Lars, Jørgensen Torben, Pedersen Oluf, Hansen Torben
Published 2008-12-01

A simple, fast and inexpensive method for mutation scanning of CFTR gene

by Juan Emilio Figueredo Lago, Anny Armas Cayarga, Yaimé Josefina González González, Teresa Collazo Mesa
Published 2017-05-01

Clinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian population

by Renato Assis Machado, Edimilson Martins de Freitas, Sibele Nascimento de Aquino, Daniella Reis B. Martelli, Mário Sérgio Oliveira Swerts, Silvia Regina de Almeida Reis, Darlene Camati Persuhn, Helenara Salvati Bertolossi Moreira, Verônica Oliveira Dias, Ricardo D. Coletta, Hercílio Martelli-Júnior
Published 2017-04-01