Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent (Q34109272)

31 July 2017

Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent (English)

1 reference

31 July 2017

Csilla Krausz

2

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author name string

Kenneth I Aston

1

1 reference

31 July 2017

Ilaria Laface

3

1 reference

31 July 2017

E Ruiz-Castané

4

1 reference

31 July 2017

Douglas T Carrell

5

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31 July 2017

language of work or name

English

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publication date

8 April 2010

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31 July 2017

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31 July 2017

25

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31 July 2017

1383-1397

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31 July 2017

6

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Understanding cardiovascular disease through the lens of genome-wide association studies

31 July 2017

1 reference

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The RsaI polymorphism in the estrogen receptor-beta gene is associated with male infertility

21 January 2018

1 reference

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Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia

21 January 2018

1 reference

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Genome-wide association studies in Alzheimer's disease

21 January 2018

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Homozygous methylenetetrahydrofolate reductase C677T mutation and male infertility

21 January 2018

1 reference

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The Mouse Genome Database (MGD): mouse biology and model systems

21 January 2018

1 reference

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Sequencing and haplotype analysis of the activator of CREM in the testis (ACT) gene in populations of fertile and infertile males

21 January 2018

1 reference

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Associations of MTHFR DNMT3b 4977 bp deletion in mtDNA and GSTM1 deletion, and aberrant CpG island hypermethylation of GSTM1 in non-obstructive infertility in Indian men.

21 January 2018

1 reference

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Genome-wide association studies in cancer.

21 January 2018

1 reference

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C677T methylenetetrahydrofolate reductase polymorphism interferes with the effects of folic acid and zinc sulfate on sperm concentration

21 January 2018

1 reference

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Review of recent genome-wide association scans in lupus

21 January 2018

1 reference

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Sequence alterations in the YBX2 gene are associated with male factor infertility

21 January 2018

1 reference

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

1 reference

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Genetic risk factors in male infertility

21 January 2018

1 reference

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Autoimmune diseases: insights from genome-wide association studies

21 January 2018

1 reference

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Is replication the gold standard for validating genome-wide association findings?

21 January 2018

1 reference

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Jmjd1a demethylase-regulated histone modification is essential for cAMP-response element modulator-regulated gene expression and spermatogenesis

21 January 2018

1 reference

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Finding the missing heritability of complex diseases

21 January 2018

1 reference

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New links to the pathogenesis of Crohn disease provided by genome-wide association scans

21 January 2018

1 reference

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The biology of infertility: research advances and clinical challenges

21 January 2018

1 reference

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Genome-wide association studies in type 2 diabetes

21 January 2018

1 reference

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Cooperative binding of two acetylation marks on a histone tail by a single bromodomain

21 January 2018

1 reference

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Finding common susceptibility variants for complex disease: past, present and future

21 January 2018

1 reference

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MTHFR C677T polymorphism associates with unexplained infertile male factors

21 January 2018

1 reference

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Acetylation-dependent chromatin reorganization by BRDT, a testis-specific bromodomain-containing protein

21 January 2018

1 reference

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Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.

21 January 2018

1 reference

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Genetic variations as cancer prognostic markers: review and update

21 January 2018

1 reference

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Genome-wide association studies in neurological disorders

21 January 2018

1 reference

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Mutation C677T in the methylenetetrahydrofolate reductase gene is associated with male infertility in an Indian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEQ081

A genome-wide association study identifies novel risk loci for type 2 diabetes

21 January 2018

1 reference

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The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy

21 January 2018

1 reference

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Mutation screening and association study of the TSSK4 Gene in Chinese infertile men with impaired spermatogenesis.

21 January 2018

1 reference

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Novel variants in UBE2B gene and idiopathic male infertility

21 January 2018

1 reference

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Y chromosome gr/gr deletions are a risk factor for low semen quality

21 January 2018

1 reference

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Genomic copy number variation, human health, and disease

21 January 2018

1 reference

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Mouse TEX15 is essential for DNA double-strand break repair and chromosomal synapsis during male meiosis

21 January 2018

1 reference

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Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.

21 January 2018

1 reference

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The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEQ081

Partial AZFc deletions and duplications: clinical correlates in the Italian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEQ081

21 January 2018

Identifiers

DOI

10.1093/HUMREP/DEQ081

1 reference

31 July 2017

1 reference