Skip to main content
padlock icon - secure page this page is secure

Publisher: Wiley-Blackwell

Volume 82, Number 4, 1 July 2018

The rs75932628 and rs2234253 polymorphisms of the TREM2 gene were associated with susceptibility to frontotemporal lobar degeneration in Caucasian populations
pp. 177-185(9)
Authors: Su, Wen‐Hua; Shi, Zhi‐Hong; Liu, Shu‐Ling; Wang, Xiao‐Dan; Liu, Shuai; Ji, Yong

Favourites:
ADD

In silico characterization of functional single nucleotide polymorphisms of folate pathway genes
pp. 186-199(14)
Authors: Vohra, Manik; Sharma, Anu Radha; Paul, Bobby; Bhat, Manoj K; Satyamoorthy, Kapaettu; Rai, Padmalatha S.

Favourites:
ADD

Increased expression of PRKCB mRNA in peripheral blood mononuclear cells from patients with systemic lupus erythematosus
pp. 200-205(6)
Authors: Zhu, Zhengwei; Yang, Lulu; Zhang, Yaohua; Liu, Lu; Huang, Yan; Wen, Leilei; Yang, Chao; Chen, Liyun; Wang, Wenjun; Zuo, Xianbo; Zhou, Fusheng; Wang, Hongyan; Tang, Huayang; Zhang, Xuejun; Yang, Sen; Sheng, Yujun; Cui, Yong

Favourites:
ADD

Gene‐based evaluation of low‐frequency variation and genetically‐predicted gene expression impacting risk of keloid formation
pp. 206-215(10)
Authors: Hellwege, Jacklyn N.; Russell, Shirley B.; Williams, Scott M.; Edwards, Todd L.; Velez Edwards, Digna R.

Favourites:
ADD

Genetic relatedness of indigenous ethnic groups in northern Borneo to neighboring populations from Southeast Asia, as inferred from genome‐wide SNP data
pp. 216-226(11)
Authors: Yew, Chee Wei; Hoque, Mohd Zahirul; Pugh‐Kitingan, Jacqueline; Minsong, Alexander; Voo, Christopher Lok Yung; Ransangan, Julian; Lau, Sophia Tiek Ying; Wang, Xu; Saw, Woei Yuh; Ong, Rick Twee‐Hee; Teo, Yik‐Ying; Xu, Shuhua; Hoh, Boon‐Peng; Phipps, Maude E.; Kumar, S. Vijay

Favourites:
ADD

Association between GOLGB1 tag‐polymorphisms and nonsyndromic cleft palate only in the Brazilian population
pp. 227-231(5)
Authors: Machado, Renato Assis; Martelli‐Júnior, Hercílio; Almeida Reis, Silvia Regina; Persuhn, Darlene Camati; Coletta, Ricardo D.

Favourites:
ADD

A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndrome
pp. 232-238(7)
Authors: Ahmad, Farooq; Nasir, Abdul; Thiele, Holger; Umair, Muhammad; Borck, Guntram; Ahmad, Wasim

Favourites:
ADD

  • Access Key
  • Free content
  • Partial Free content
  • New content
  • Open access content
  • Partial Open access content
  • Subscribed content
  • Partial Subscribed content
  • Free trial content
Cookie Policy
X
Cookie Policy
Ingenta Connect website makes use of cookies so as to keep track of data that you have filled in. I am Happy with this Find out more