Association study of the three functional polymorphisms (TAS2R46G>A, OR4C16G>A, and OR4X1A>T) with recurrent pregnancy loss

Association analysis of the SNP (rs345476947) in the FUT2 gene with the production and reproductive traits in pigs

(2017) Haifei Wang et al.   Genes & Genomics

An efficient and tunable parameter to improve variant calling for whole genome and exome sequencing data

(2017) Yong Ju Ahn et al.   Genes & Genomics

Activation of intestinal olfactory receptor stimulates glucagon-like peptide-1 secretion in enteroendocrine cells and attenuates hyperglycemia in type 2 diabetic mice

(2017) Ki-Suk Kim et al.   Scientific Reports

A non-senseMCM9mutation in a familial case of primary ovarian insufficiency

(2016) F. Fauchereau et al.   CLINICAL GENETICS

Whole exome sequencing in recurrent early pregnancy loss

(2016) Ying Qiao et al.   MOLECULAR HUMAN REPRODUCTION

The Pharmacochaperone Activity of Quinine on Bitter Taste Receptors

(2016) Jasbir D. Upadhyaya et al.   PLoS One

Susceptibility to male infertility: replication study in Japanese men looking for an association with four GWAS-derived loci identified in European men

(2015) Makoto Chihara et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Denatonium induces secretion of glucagon-like peptide-1 through activation of bitter taste receptor pathways

(2014) Ki-Suk Kim et al.   DIABETOLOGIA

Genetic Variants in MicroRNA Machinery Genes Are Associate with Idiopathic Recurrent Pregnancy Loss Risk

(2014) Yong Wook Jung et al.   PLoS One

Analysis of Stop-Gain and Frameshift Variants in Human Innate Immunity Genes

(2014) Antonio Rausell et al.   PLoS Computational Biology

Association of methionine synthase and thymidylate synthase genetic polymorphisms with idiopathic recurrent pregnancy loss

(2013) Ji Hyang Kim et al.   FERTILITY AND STERILITY

Kallmann syndrome in women: from genes to diagnosis and treatment

(2013) Blazej Meczekalski et al.   GYNECOLOGICAL ENDOCRINOLOGY

Responsiveness to a Physiological Regimen of GnRH Therapy and Relation to Genotype in Women With Isolated Hypogonadotropic Hypogonadism

(2013) Brent S. Abel et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

(2012) Wenqing Fu et al.   NATURE

Haplotype-based association of ACE I/D, AT1R 1166A>C, and AGT M235T polymorphisms in renin–angiotensin–aldosterone system genes in Korean women with idiopathic recurrent spontaneous abortions

(2011) Yi Seul Choi et al.   European Journal of Obstetrics & Gynecology and Reproductive Biology

Loss-of-function variants in the genomes of healthy humans

(2010) D. G. MacArthur et al.   HUMAN MOLECULAR GENETICS

The Molecular Receptive Ranges of Human TAS2R Bitter Taste Receptors

(2009) Wolfgang Meyerhof et al.   CHEMICAL SENSES

CD56highCD16-CD62L- NK Cells Accumulate in Allergic Contact Dermatitis and Contribute to the Expression of Allergic Responses

(2009) T. Carbone et al.   JOURNAL OF IMMUNOLOGY

Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

(2008) Zahurul A. Bhuiyan et al.   HEART RHYTHM