Published in Eur J Endocrinol on May 01, 2008
Common variants in DGKK are strongly associated with risk of hypospadias. Nat Genet (2010) 1.23
Environmental and genetic contributors to hypospadias: a review of the epidemiologic evidence. Birth Defects Res A Clin Mol Teratol (2012) 1.17
The stress response mediator ATF3 represses androgen signaling by binding the androgen receptor. Mol Cell Biol (2012) 0.98
Distinct and competitive regulatory patterns of tumor suppressor genes and oncogenes in ovarian cancer. PLoS One (2012) 0.96
Molecular mechanisms of external genitalia development. Differentiation (2012) 0.94
Exploration of gene-environment interactions, maternal effects and parent of origin effects in the etiology of hypospadias. J Urol (2012) 0.84
Is activating transcription factor 3 up-regulated in patients with hypospadias? Korean J Urol (2010) 0.81
Increased gene copy number of VAMP7 disrupts human male urogenital development through altered estrogen action. Nat Med (2014) 0.81
The Genetic and Environmental Factors Underlying Hypospadias. Sex Dev (2015) 0.80
Twenty-Four Genes are Upregulated in Patients with Hypospadias. Balkan J Med Genet (2013) 0.80
A pilot study of the association between genetic polymorphisms involved in estrogen signaling and infant male genital phenotypes. Asian J Androl (2012) 0.79
Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias. Eur J Hum Genet (2014) 0.78
Regulatory SNPs and transcriptional factor binding sites in ADRBK1, AKT3, ATF3, DIO2, TBXA2R and VEGFA. Transcription (2014) 0.78
The power and perils of animal models with urogenital anomalies: handle with care. J Pediatr Urol (2014) 0.78
Clinical dilemmas and surgical treatment of penoscrotal, scrotal and perineal hypospadias. Bosn J Basic Med Sci (2009) 0.77
The common stress responsive transcription factor ATF3 binds genomic sites enriched with p300 and H3K27ac for transcriptional regulation. BMC Genomics (2016) 0.77
A new susceptibility locus for hypospadias on chromosome 7q32.2-q36.1. Hum Genet (2008) 0.76
Expression profiles of human epididymis epithelial cells reveal the functional diversity of caput, corpus and cauda regions. Mol Hum Reprod (2015) 0.76
Diagnostic Application of Targeted Next-Generation Sequencing of 80 Genes Associated with Disorders of Sexual Development. Sci Rep (2017) 0.75
A congenital anterior urethrocutaneous fistula in a boy whose mother was exposed to ionizing radiations: case report and literature review. Case Rep Urol (2013) 0.75
Genetic and environmental factors in the aetiology of hypospadias. Pediatr Surg Int (2015) 0.75
Polymorphism of 3' UTR of MAMLD1 gene is also associated with increased risk of isolated hypospadias in Indian children: a preliminary report. Pediatr Surg Int (2016) 0.75
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature (2011) 13.23
Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility. PLoS One (2012) 5.03
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet (2013) 4.62
Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis. Nat Genet (2007) 4.22
MMP12, lung function, and COPD in high-risk populations. N Engl J Med (2009) 3.96
Treatment with propiverine in children suffering from nonneurogenic overactive bladder and urinary incontinence: results of a randomized placebo-controlled phase 3 clinical trial. Eur Urol (2008) 2.85
AGC1 deficiency associated with global cerebral hypomyelination. N Engl J Med (2009) 2.43
Smoking and two human leukocyte antigen genes interact to increase the risk for multiple sclerosis. Brain (2011) 2.24
Optimizing the outcome of microsurgical subinguinal varicocelectomy using isosulfan blue: a prospective randomized trial. J Urol (2006) 2.15
Combination of lidocaine suppository and periprostatic nerve block during transrectal prostate biopsy: a prospective randomized trial. Int J Urol (2014) 1.98
Genetic effects on age-dependent onset and islet cell autoantibody markers in type 1 diabetes. Diabetes (2002) 1.89
EAU guidelines on vesicoureteral reflux in children. Eur Urol (2012) 1.76
Extracellular matrix degradation and reduced neural density in children with intrinsic ureteropelvic junction obstruction. Urology (2010) 1.75
Robotic-assisted laparoscopic partial nephrectomy: surgical technique and clinical outcomes at 1 year. BJU Int (2008) 1.68
Totally intracorporeal replacement of the ureter using whole-mount ileum. J Endourol (2014) 1.67
Changes to anti-JCV antibody levels in a Swedish national MS cohort. J Neurol Neurosurg Psychiatry (2013) 1.63
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nat Genet (2011) 1.60
Low serum levels of vitamin D in idiopathic inflammatory myopathies. Ann Rheum Dis (2012) 1.59
Interaction between adolescent obesity and HLA risk genes in the etiology of multiple sclerosis. Neurology (2014) 1.54
Y pouch neobladder-a simplified method of intracorporeal neobladder after robotic cystectomy. J Endourol (2014) 1.51
Urethral ultrasound as a screening tool for stricture recurrence after oral mucosa graft urethroplasty. Urology (2011) 1.50
Point-of-Care Tests for Bladder Cancer: The Influencing Role of Hematuria. Adv Urol (2011) 1.49
Influence of urinary tract instrumentation and inflammation on the performance of urine markers for the detection of bladder cancer. Urology (2012) 1.47
Cerebrospinal fluid CXCL13 in multiple sclerosis: a suggestive prognostic marker for the disease course. Mult Scler (2010) 1.46
Giant cystine stone in an infant bladder with no evidence of cystinuria--valence of possible pathomechanisms. Urol Int (2005) 1.44
Growth of spontaneously descended and surgically treated testes during early childhood. Pediatrics (2013) 1.42
Lack of replication of interaction between EBNA1 IgG and smoking in risk for multiple sclerosis. Neurology (2012) 1.42
Dorsal onlay skin graft urethroplasty in patients older than 65 years. Urology (2010) 1.41
PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome. Am J Hum Genet (2005) 1.41
Gender role behavior, sexuality, and psychosocial adaptation in women with congenital adrenal hyperplasia due to CYP21A2 deficiency. J Clin Endocrinol Metab (2009) 1.39
Lich-Gregoir reimplantation causes less discomfort than Politano-Leadbetter technique: Results of a prospective, randomized, pain scale-oriented study in a pediatric population. Eur Urol (2005) 1.39
The chitinase-like protein YKL-40: a possible biomarker of inflammation and airway remodeling in severe pediatric asthma. J Allergy Clin Immunol (2013) 1.25
Recombinant Fabs of human monoclonal antibodies specific to the middle epitope of GAD65 inhibit type 1 diabetes-specific GAD65Abs. Diabetes (2003) 1.23
Common variants in DGKK are strongly associated with risk of hypospadias. Nat Genet (2010) 1.23
CXorf6 is a causative gene for hypospadias. Nat Genet (2006) 1.21
Maternal and gestational risk factors for hypospadias. Environ Health Perspect (2008) 1.18
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nat Genet (2010) 1.16
The lack of anti-idiotypic antibodies, not the presence of the corresponding autoantibodies to glutamate decarboxylase, defines type 1 diabetes. Proc Natl Acad Sci U S A (2008) 1.15
Metabolic profile and body composition in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Endocrinol Metab (2006) 1.14
Heredity of hypospadias and the significance of low birth weight. J Urol (2002) 1.12
Anatomical radical retropubic prostatectomy: 'curtain dissection' of the neurovascular bundle. BJU Int (2005) 1.10
FGFR2, FGF8, FGF10 and BMP7 as candidate genes for hypospadias. Eur J Hum Genet (2007) 1.09
Fractures and bone mineral density in adult women with 21-hydroxylase deficiency. J Clin Endocrinol Metab (2007) 1.08
Soluble IL7Rα potentiates IL-7 bioactivity and promotes autoimmunity. Proc Natl Acad Sci U S A (2013) 1.07
Linkage between cryptorchidism, hypospadias, and GGN repeat length in the androgen receptor gene. J Clin Endocrinol Metab (2004) 1.07
Development and descent of the testis in relation to cryptorchidism. Acta Paediatr (2007) 1.06
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. Eur J Hum Genet (2009) 1.05
Nuclear matrix protein-22: a prospective evaluation in a population at risk for bladder cancer. Results from the UroScreen study. BJU Int (2012) 1.04
Transcriptome analysis reveals upregulation of bitter taste receptors in severe asthmatics. Eur Respir J (2012) 1.03
Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families. Acta Derm Venereol (2008) 1.03
The immunology of fibrosis: innate and adaptive responses. Trends Immunol (2010) 1.01
Optimizing the operative treatment of boys with varicocele: sequential comparison of 4 techniques. J Urol (2003) 1.00
The valine allele of the V89L polymorphism in the 5-alpha-reductase gene confers a reduced risk for hypospadias. J Clin Endocrinol Metab (2005) 1.00
Over-diagnosis and under-diagnosis of screen- vs non-screen-detected prostate cancers with in men with prostate-specific antigen levels of 2.0-10.0 ng/mL. BJU Int (2008) 1.00
Extracellular matrix degradation and reduced nerve supply in refluxing ureteral endings. J Urol (2004) 0.99
Assessment of the neuropeptide S system in anxiety disorders. Biol Psychiatry (2010) 0.99
Confirmation of association between multiple sclerosis and CYP27B1. Eur J Hum Genet (2010) 0.99
IL-22RA2 associates with multiple sclerosis and macrophage effector mechanisms in experimental neuroinflammation. J Immunol (2010) 0.99
Neoadjuvant gonadotropin-releasing hormone therapy before surgery may improve the fertility index in undescended testes: a prospective randomized trial. J Urol (2005) 0.98
Long-term outcome of laparoscopically managed nonpalpable testes. J Urol (2003) 0.98
Risk conferred by HLA-DR and DQ for type 1 diabetes in 0-35-year age group in Sweden. Ann N Y Acad Sci (2008) 0.98
Validation of the German Glasgow children's benefit inventory. J Eval Clin Pract (2007) 0.98
Current status of molecular markers for prognostication and outcome in invasive bladder cancer. BJU Int (2012) 0.97
SAMstrt: statistical test for differential expression in single-cell transcriptome with spike-in normalization. Bioinformatics (2013) 0.96
A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changes. PLoS One (2010) 0.95
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Hum Mol Genet (2013) 0.95
Loss of interstitial cells of Cajal and gap junction protein connexin 43 at the vesicoureteral junction in children with vesicoureteral reflux. J Urol (2005) 0.95
Single-stage dorsal inlay split-skin graft for salvage anterior urethral reconstruction. BJU Int (2008) 0.94
Chimerism resulting from parthenogenetic activation and dispermic fertilization. Am J Med Genet A (2010) 0.94
Multiple factors affect the loss of measurable C-peptide over 6 years in newly diagnosed 15- to 35-year-old diabetic subjects. J Diabetes Complications (2007) 0.93
Decline of C-peptide during the first year after diagnosis of Type 1 diabetes in children and adolescents. Diabetes Res Clin Pract (2013) 0.93
Embryology and anatomy of the vesicoureteric junction with special reference to the etiology of vesicoureteral reflux. Ther Adv Urol (2009) 0.93
Development of heart block in children of SSA/SSB-autoantibody-positive women is associated with maternal age and displays a season-of-birth pattern. Ann Rheum Dis (2011) 0.93
The intravesical ureter in children with vesicoureteral reflux: a morphological and immunohistochemical characterization. J Urol (2003) 0.93
Genetic and environmental origins of hypospadias. Curr Opin Endocrinol Diabetes Obes (2014) 0.92
Sexual function and surgical outcome in women with congenital adrenal hyperplasia due to CYP21A2 deficiency: clinical perspective and the patients' perception. J Clin Endocrinol Metab (2010) 0.92
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. PLoS One (2013) 0.92
Genetic influence on dystocia. Acta Obstet Gynecol Scand (2004) 0.92
Insulin receptor isoforms A and B as well as insulin receptor substrates-1 and -2 are differentially expressed in prostate cancer. PLoS One (2012) 0.92
Importance of human leukocyte antigen (HLA) class I and II alleles on the risk of multiple sclerosis. PLoS One (2012) 0.92
Single-stage dorsal inlay full-thickness genital skin grafts for hypospadias reoperations: extended follow up. J Pediatr Urol (2010) 0.92
Centrosomal localization of the psoriasis candidate gene product, CCHCR1, supports a role in cytoskeletal organization. PLoS One (2012) 0.91
A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb. Hum Mutat (2012) 0.90
GAD65 antibody epitope patterns of type 1.5 diabetic patients are consistent with slow-onset autoimmune diabetes. Diabetes Care (2002) 0.90
Preoperative C-reactive protein in the serum: a prognostic biomarker for upper urinary tract urothelial carcinoma treated with radical nephroureterectomy. Urol Int (2014) 0.90
A role for VAV1 in experimental autoimmune encephalomyelitis and multiple sclerosis. Sci Transl Med (2009) 0.90
Complex segregation analysis of hypospadias. Hum Genet (2002) 0.90
22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment. Eur J Med Genet (2010) 0.90
Anterior urethral reconstruction using the circular fasciocutaneous flap technique: long-term follow-up. World J Urol (2010) 0.89