Published in J Pediatr Endocrinol Metab on January 01, 2012
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Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion. Nat Genet (2008) 4.84
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Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry. J Clin Endocrinol Metab (2012) 1.44
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A genetic basis for functional hypothalamic amenorrhea. N Engl J Med (2011) 1.24
Expanding the phenotype and genotype of female GnRH deficiency. J Clin Endocrinol Metab (2011) 1.16
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Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism. J Clin Endocrinol Metab (2011) 1.00
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Metformin improves glucose effectiveness, not insulin sensitivity: predicting treatment response in women with polycystic ovary syndrome in an open-label, interventional study. J Clin Endocrinol Metab (2014) 0.87
Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage. Stroke (2013) 0.86
Recombinant human prolactin for the treatment of lactation insufficiency. Clin Endocrinol (Oxf) (2010) 0.86
Isolated prolactin deficiency associated with serum autoantibodies against prolactin-secreting cells. J Clin Endocrinol Metab (2013) 0.85
The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people. Diabetes (2006) 0.85
Mutations in eIF4ENIF1 are associated with primary ovarian insufficiency. J Clin Endocrinol Metab (2013) 0.84
Cigarette smoking, nicotine levels and increased risk for metabolic syndrome in women with polycystic ovary syndrome. Gynecol Endocrinol (2013) 0.84
The male reproductive system in classic galactosemia: cryptorchidism and low semen volume. J Inherit Metab Dis (2012) 0.82
Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an American Indian population. PLoS One (2013) 0.82
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort. Circ Cardiovasc Genet (2014) 0.81
Fertility preservation in female classic galactosemia patients. Orphanet J Rare Dis (2013) 0.80
Effects of recombinant human prolactin on breast milk composition. Pediatrics (2011) 0.79
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Sleep duration does not mediate or modify association of common genetic variants with type 2 diabetes. Diabetologia (2013) 0.79
Common variants in CLOCK are not associated with measures of sleep duration in people of european ancestry from the sleep heart health study. Biol Psychiatry (2013) 0.78
Ovarian histopathological and ubiquitin-immunophenotypic features in fragile X-associated primary ovarian insufficiency: a study of five cases and selected controls. Histopathology (2011) 0.78
Variation in the human genome and risk to common disease. Keystone Symposium on 'Human Genome Sequence Variation and the Inherited Basis of Common Diseases'. January 8-13, Breckenridge, Colorado, USA. Pharmacogenomics (2004) 0.77
Evaluating reported candidate gene associations with polycystic ovary syndrome. Fertil Steril (2013) 0.77
Rv3080c regulates the rate of inhibition of mycobacteria by isoniazid through FabD. Mol Cell Biochem (2012) 0.76
Short-term prolactin administration causes expressible galactorrhea but does not affect bone turnover: pilot data for a new lactation agent. Int Breastfeed J (2007) 0.76
Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism. J Clin Endocrinol Metab (2013) 0.76
IBC CARe microarray allelic population prevalences in an American Indian population. PLoS One (2013) 0.75
Correction: Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population. PLoS One (2013) 0.75
Quantitative analysis of conjugated and free estrogens in swine manure: solutions to overcome analytical problems due to matrix effects. J Chromatogr A (2013) 0.75
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections. medRxiv (2022) 0.75
A patient's guide: polycystic ovary syndrome (PCOS). J Clin Endocrinol Metab (2014) 0.75
Corrigendum: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Nat Commun (2016) 0.75