Published in J Soc Biol on January 01, 2002
FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation. Am J Hum Genet (2003) 1.70
Cloacal exstrophy in an infant with 9q34.1-qter deletion resulting from a de novo unbalanced translocation between chromosome 9q and Yq. Am J Med Genet A (2004) 1.59
CATSPER2, a human autosomal nonsyndromic male infertility gene. Eur J Hum Genet (2003) 1.54
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. Eur J Endocrinol (2006) 1.36
Aetiological diagnosis of male sex ambiguity: a collaborative study. Eur J Pediatr (2002) 1.22
Molecular genetics of sex determination. Semin Reprod Med (2002) 1.18
The transcription factor Sox9 is degraded by the ubiquitin-proteasome system and stabilized by a mutation in a ubiquitin-target site. Matrix Biol (2004) 1.15
Genetic investigation of four meiotic genes in women with premature ovarian failure. Eur J Endocrinol (2008) 1.13
Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in children. J Urol (2008) 1.08
Familial occurrence of the IMAGe association: additional clinical variants and a proposed mode of inheritance. J Clin Endocrinol Metab (2005) 1.06
North African Jewish and non-Jewish populations form distinctive, orthogonal clusters. Proc Natl Acad Sci U S A (2012) 1.05
Disruption of the principal, progesterone-activated sperm Ca2+ channel in a CatSper2-deficient infertile patient. Proc Natl Acad Sci U S A (2013) 1.05
Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics. Proc Natl Acad Sci U S A (2007) 1.05
Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice. Mech Dev (2009) 1.05
An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation. J Mol Endocrinol (2004) 1.04
Genetic male infertility and mutation of CATSPER ion channels. Eur J Hum Genet (2010) 1.03
Extinction of FOXL2 expression in aggressive ovarian granulosa cell tumors in children. Fertil Steril (2007) 1.02
Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G). PLoS One (2010) 1.00
Novel paralogy relations among human chromosomes support a link between the phylogeny of doublesex-related genes and the evolution of sex determination. Genomics (2002) 0.99
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development. Hum Mol Genet (2007) 0.97
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles. Hum Mol Genet (2008) 0.96
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome. Hum Mutat (2008) 0.94
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure. PLoS One (2012) 0.91
Characterization of a putative type IV aminophospholipid transporter P-type ATPase. Mamm Genome (2003) 0.90
Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography. Int J Dev Biol (2009) 0.90
We request a serious reconsideration of the recent paper by Seralini et al. alleging tumorigenesis in rats resulting from consumption of corn derived from crops improved through biotechnology (Séralini et al., 2012). Food Chem Toxicol (2012) 0.89
The Human Y Chromosome: The Biological Role of a "Functional Wasteland" J Biomed Biotechnol (2001) 0.88
BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms? Clin Endocrinol (Oxf) (2009) 0.87
Sense and antisense Foxl2 transcripts in mouse. Genomics (2005) 0.87
Genetic structure of Mediterranean populations revealed by Y-chromosome haplotype analysis. Am J Phys Anthropol (2003) 0.87
Recent advances in the study of genes involved in non-syndromic premature ovarian failure. Mol Cell Endocrinol (2007) 0.86
Recovery of female fertility after chemotherapy, irradiation, and bone marrow allograft: further evidence against massive oocyte regeneration by bone marrow-derived germline stem cells. Stem Cells (2007) 0.85
Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation. Hum Mol Genet (2005) 0.83
Foxl2 gene and the development of the ovary: a story about goat, mouse, fish and woman. Reprod Nutr Dev (2005) 0.82
Does anonymous sperm donation increase the risk for unions between relatives and the incidence of autosomal recessive diseases due to consanguinity? Hum Reprod (2013) 0.82
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency. Hum Mol Genet (2011) 0.82
Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction. Pediatr Endocrinol Rev (2005) 0.81
FOXO3a variants in patients with premature ovarian failure. Clin Endocrinol (Oxf) (2007) 0.80
A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure. Clin Endocrinol (Oxf) (2009) 0.79
Interspecific chromosome-wide transcription profiles reveal the existence of mammalian-specific and species-specific chromosome domains. J Mol Evol (2004) 0.79
Male-specific protein (MSP): a new gene linked to sexual behavior and aggressiveness of tilapia males. Horm Behav (2008) 0.78
Gonad development in Drash and Frasier syndromes depends on WT1 mutations. Arkh Patol (2004) 0.77
Molecular aspects of female and male gonadal development in mammals. Pediatr Endocrinol Rev (2004) 0.77
CITED2 mutations potentially cause idiopathic premature ovarian failure. Transl Res (2012) 0.77
The transcription factor FOXL2 in ovarian function and dysfunction. Folia Histochem Cytobiol (2009) 0.76
Distribution of Y chromosome lineages in Jerba island population. Forensic Sci Int (2005) 0.76
Pillars article: A protein tyrosine kinase in the interferon α/β signaling pathway. Cell. 1992. 70: 313-322. J Immunol (2011) 0.76
Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood-onset adrenal hypoplasia congenita. Clin Endocrinol (Oxf) (2006) 0.76
Mutations in the NOG gene are not a common cause of nonsyndromic premature ovarian failure. Clin Endocrinol (Oxf) (2007) 0.76
[Discussion]. Med Sci (Paris) (2015) 0.75
MHC class II-deficient tumor cell lines with a defective expression of the class II transactivator. Int Immunol (2002) 0.75
[Hermaphroditism pathology]. Ann Pathol (2004) 0.75