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Annals of Human Genetics|July 31, 2008
A model incorporating potential skewed X-inactivation in MZ girls suggests that X-linked QTLs exist for several social behaviours including autism spectrum disorderC S Loat, C M A Haworth, R Plomin, et al.
Annals of Human Genetics|June 22, 2019
Association of interleukin-10-1082 (-1087) A > G polymorphisms and periodontitis risk: An updated meta-analysis based on 26 case-control studiesYao Li, Bo Hu, Ge Feng, et al.
Annals of Human Genetics|January 1, 1986
The gene for human muscle specific carbonic anhydrase (CAIII) is assigned to chromosome 8Y H Edwards, J Lloyd, M Parkar, et al.
Annals of Human Genetics|May 16, 2019
Association study of M235T and A-6G polymorphisms in angiotensinogen gene with risk of developing preeclampsia in Iranian populationEhsan Alaee, Maryam Mirahmadi, Masoumeh Ghasemi, et al.
Annals of Human Genetics|April 8, 2022
Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and H-type hypertension: A systematic review and meta-analysisShengyu Liao, Shuxia Guo, Rulin Ma, et al.
Annals of Human Genetics|April 19, 2022
No significant association between SNPs in the CLOCK and ADH4 genes and susceptibility to cluster headaches: A systematic review and meta-analysisJiarui Cui, Wei Peng, Ting Yi, et al.
Annals of Human Genetics|September 28, 2021
Genetics of ataxia telangiectasia in a highly consanguineous populationMohammed A Al-Muhaizea, Hanouf Aldeeb, Rawan Almass, et al.
Annals of Human Genetics|September 28, 2021
Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX ToolkitCynthia C Morton, Mary L Marazita, Beate Peter, et al.
Annals of Human Genetics|November 3, 2021
Clinical features of patients with Yin Yang 1 deficiency causing Gabriele-de Vries syndrome: A new case and review of the literatureHossein Jafari Khamirani, Sina Zoghi, Zahra Mehdipour Namdar, et al.
Annals of Human Genetics|May 9, 2019
Impact of next-generation sequencing panels in the evaluation of limb-girdle muscular dystrophiesBerk Özyilmaz, Özgür Kirbiyik, Taha R Özdemir, et al.
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