ANNALS OF HUMAN GENETICS

Association of polymorphisms in genes coding for antioxidant enzymes and human male infertility

The role of genetics and epigenetics in the pathogenesis of gestational diabetes mellitus

Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4‐subunit SCN4B with atrial fibrillation

DYNC1H1 gene methylation correlates with severity of spinal muscular atrophy

Expression patterns common and unique to ulcerative colitis and celiac disease

Argentinian clinical genomics in a leukodystrophies and genetic leukoencephalopathies cohort: Diagnostic yield in our first 9 years

Consanguinity: A blessing or menace at population level?

A novel heterozygous variant p.(Trp538Arg) of SYNM is identified by whole‐exome sequencing in a Chinese family with dilated cardiomyopathy

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella

A novel nonsense variant in PLS3 causes X‐linked osteoporosis in a Chinese family

Population genetics of 15 autosomal STR loci in the Han population of Ili Kazakh Autonomous Prefecture, Northwestern China

Ancestry informative SNP panels for discriminating the major East Asian populations: Han Chinese, Japanese and Korean

Association of rs10490924 in ARMS2/HTRA1 with age‐related macular degeneration in the Pakistani population

Association of MIR146A rs2910164 variation with a predisposition to sporadic breast cancer in a Pakistani cohort

Genetic model of MS severity predicts future accumulation of disability

A PEAR1 polymorphism (rs12041331) is associated with risk of coronary artery aneurysm in Kawasaki disease

Evaluation of methods for adjusting population stratification in genome‐wide association studies: Standard versus categorical principal component analysis

Associations of the melanocortin 3 receptor C17A + G241A haplotype with body composition and inflammation in African‐American adults

The rs2516839 variation of USF1 gene is associated with 4‐year mortality of nonagenarian women: The Vitality 90+ study

Intrauterine phenotype features of fetuses with Williams–Beuren syndrome and literature review

SIRT1 gene polymorphisms are associated with nondiabetic type 1 cardiorenal syndrome

Congenital microcephaly‐linked CDK5RAP2 affects eye development

Application of targeted exome and whole‐exome sequencing for Chinese families with Stargardt disease

Measuring gene–gene interaction using Kullback–Leibler divergence

Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations

A novel mutation of MSX1 inherited from maternal mosaicism causes a severely affected child with nonsyndromic oligodontia

A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh family

N‐acetyltransferase 2 polymorphism and acetylation profiles in Buginese ethnics of Indonesia

FAAH levels and its genetic polymorphism association with susceptibility to methamphetamine dependence

BBS5 and INPP5E mutations associated with ciliopathy disorders in families from Pakistan

Association between the BHMT gene rs3733890 polymorphism and the efficacy of oral folate therapy in patients with hyperhomocysteinemia

Differential gene expression analysis of sickle cell anemia in steady and crisis state

Type 2 diabetes–associated polymorphisms correlate with SIRT1 and TGF‐β1 gene expression

Association of interleukin‐10‐1082 (‐1087) A > G polymorphisms and periodontitis risk: An updated meta‐analysis based on 26 case‐control studies

Shared gene signature between pterygium and meibomian gland dysfunction uncovered through gene‐expression meta‐analysis

Novel mutation in the DSG1 gene causes autosomal‐dominant striate palmoplantar keratoderma in a large Syrian family

The association of the UHRF1BP1 gene with systemic lupus erythematosus was replicated in a Han Chinese population from mainland China

5α‐Reductase type 2 deficiency in families from an isolated Andean population in Venezuela

Chorionic villus sampling experience of a reference perinatal medicine center

Analysis of 15q11.2 CNVs in an Indian population with schizophrenia

Using microarray analysis to identify genes and pathways that regulate fetal hemoglobin levels

Genetic history of the population of Crete

General regression model: A “model‐free” association test for quantitative traits allowing to test for the underlying genetic model

Association study of M235T and A‐6G polymorphisms in angiotensinogen gene with risk of developing preeclampsia in Iranian population

Assessment of candidate folate sensitive‐differentially methylated regions in a randomised controlled trial of continued folic acid supplementation during the second and third trimesters of pregnancy

Genetic variations and population data on five supplementary STR markers in Lebanon

Classic galactosaemia in the Greek Cypriot population: An epidemiological and molecular study