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Array Comparative Genomic Hybridization Profiling Analysis Reveals Deoxyribonucleic Acid Copy Number Variations Associated with Premature Ovarian Failure

https://doi.org/10.1210/jc.2009-0186
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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The humanFOXL2 mutation database
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Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure
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Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation
inferredcites →https://doi.org/10.1038/nature04489openalex-snapshot
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
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Global variation in copy number in the human genome
inferredcites →https://doi.org/10.1038/nature06862openalex-snapshot
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inferredcites →https://doi.org/10.1038/nbt.1509openalex-snapshot
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inferredcites →https://doi.org/10.1038/ng1985openalex-snapshot
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Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers
inferredcites →https://doi.org/10.1038/sj.onc.1210426openalex-snapshot
DUSP22/LMW-DSP2 regulates estrogen receptor-α-mediated signaling through dephosphorylation of Ser-118
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Mutations in NR5A1 Associated with Ovarian Insufficiency
inferredcites →https://doi.org/10.1073/pnas.0703834104openalex-snapshot
Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome
inferredcites →https://doi.org/10.1086/431652openalex-snapshot
Segmental Duplications and Copy-Number Variation in the Human Genome
inferredcites →https://doi.org/10.1086/505653openalex-snapshot
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inferredcites →https://doi.org/10.1086/510560openalex-snapshot
A Comprehensive Analysis of Common Copy-Number Variations in the Human Genome
inferredcites →https://doi.org/10.1086/519496openalex-snapshot
NOBOX Homeobox Mutation Causes Premature Ovarian Failure
inferredcites →https://doi.org/10.1093/hmg/ddl436openalex-snapshot
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals
inferredcites →https://doi.org/10.1093/hmg/ddm208openalex-snapshot
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases
inferredcites →https://doi.org/10.1093/hmg/ddn274openalex-snapshot
Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure
inferredcites →https://doi.org/10.1093/hmg/ddp011openalex-snapshot
Copy number variants, diseases and gene expression
inferredcites →https://doi.org/10.1093/humrep/deg046openalex-snapshot
A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics
inferredcites →https://doi.org/10.1093/humrep/del174openalex-snapshot
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients
inferredcites →https://doi.org/10.1093/humrep/dem358openalex-snapshot
Cryptic Xp duplication including the SHOX gene in a woman with 46,X, del(X)(q21.31) and premature ovarian failure
inferredcites →https://doi.org/10.1093/humrep/den086openalex-snapshot
Parathyroid hormone-responsive B1 gene is associated with premature ovarian failure
inferredcites →https://doi.org/10.1093/humrep/den193openalex-snapshot
Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia
inferredcites →https://doi.org/10.1093/humrep/den278openalex-snapshot
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus
inferredcites →https://doi.org/10.1093/humupd/dmi012openalex-snapshot
Premature ovarian failure
inferredcites →https://doi.org/10.1095/biolreprod.107.060152openalex-snapshot
Insulin Signaling in Mouse Oocytes1
inferredcites →https://doi.org/10.1097/01.gme.0000184424.96437.7aopenalex-snapshot
Mutational screening of the coding region of growth differentiation factor 9 gene in Indian women with ovarian failure
inferredcites →https://doi.org/10.1097/01.ogx.0000359268.91477.36openalex-snapshot
Mutations in NR5A1 Associated With Ovarian Insufficiency
inferredcites →https://doi.org/10.1126/science.1101160openalex-snapshot
The Influence of CCL3L1 Gene-Containing Segmental Duplications on HIV-1/AIDS Susceptibility
inferredcites →https://doi.org/10.1201/9780203021941.ch25openalex-snapshot
Premature Ovarian Failure
inferredcites →https://doi.org/10.1210/jc.2003-030217openalex-snapshot
Delayed Puberty and Primary Amenorrhea Associated with a Novel Mutation of the Human Follicle-Stimulating Hormone Receptor: Clinical, Histological, and Molecular Studies
inferredcites →https://doi.org/10.1210/jc.2005-2650openalex-snapshot
Identification of New Variants of Human BMP15 Gene in a Large Cohort of Women with Premature Ovarian Failure
inferredcites →https://doi.org/10.1210/jc.2008-0912openalex-snapshot
High Resolution Array-Comparative Genomic Hybridization Profiling Reveals Deoxyribonucleic Acid Copy Number Alterations Associated with Medullary Thyroid Carcinoma
inferredcites →https://doi.org/10.1371/journal.pgen.0030190openalex-snapshot
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
inferredcites →https://doi.org/10.1530/eje.1.02135openalex-snapshot
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure
inferredcites →https://doi.org/10.1684/vir.2011.1288openalex-snapshot
[The influence of CCL3L 1 gene-containing segmental duplications on HIV1 -Aids susceptibility].
inferredcites →https://doi.org/10.3346/jkms.2007.22.s.s17openalex-snapshot
Neuronal Apoptosis Inhibitory Protein is Overexpressed in Patients with Unfavorable Prognostic Factors in Breast Cancer

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Phenotypic and Evolutionary Consequences of Deletion, Duplication, and Triplication at 16p11.2
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Genetics of Female Infertility Due to Anomalies of the Ovary and Mullerian Ducts
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BCORL1, POF1B, and USP9X copy number variation in women with idiopathic diminished ovarian reserve
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Overexpressed miR-135b in the ovaries of PCOS promotes granulosa cell proliferation by inhibiting Hippo signaling pathway
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Copy number variants on the X chromosome in women with primary ovarian insufficiency
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A family with Xq22.3q25 interstitial deletion and normal ovarian function
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Identification of chromosomal copy number variations and novel candidate loci in hereditary nonpolyposis colorectal cancer with mismatch repair proficiency
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Next generation sequencing identifies abnormal Y chromosome and candidate causal variants in premature ovarian failure patients
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The effects of a heterochromatin polymorphism in chromosome 6 on premature ovarian failure
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Hippo signaling disruption and Akt stimulation of ovarian follicles for infertility treatment
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TBP2 gene may not be associated with primary ovarian insufficiency
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Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF)
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Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency
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Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform
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Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases
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High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function
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Variações no número de cópias cromossômicas submicroscópicas como causa de baixa estatura de início pré-natal
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Next Generation Sequencing Should Be Proposed to Every Woman With “Idiopathic” Primary Ovarian Insufficiency
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Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure
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Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways
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Insight into the Genomics of Premature Ovarian Failure
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Síndrome de Turner con mosaicismo 45,X/46Xdel(X)(q21). Comunicación de un caso
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Genetics of male infertility : genes implicated in non-obstructive azoospermia and severe oligozoospermia
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