{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,8,21]],"date-time":"2023-08-21T17:50:47Z","timestamp":1692640247633},"reference-count":35,"publisher":"Public Library of Science (PLoS)","issue":"9","license":[{"start":{"date-parts":[[2017,9,21]],"date-time":"2017-09-21T00:00:00Z","timestamp":1505952000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"National Natural Science Foundation of China (CN)","award":["Grant No. 81571493"],"award-info":[{"award-number":["Grant No. 81571493"]}]}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS ONE"],"DOI":"10.1371\/journal.pone.0185084","type":"journal-article","created":{"date-parts":[[2017,9,21]],"date-time":"2017-09-21T17:47:22Z","timestamp":1506016042000},"page":"e0185084","update-policy":"http:\/\/dx.doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":2,"title":["Recurrent deletions of the X chromosome linked CNV64, CNV67, and CNV69 shows geographic differences across China and no association with idiopathic infertility in men"],"prefix":"10.1371","volume":"12","author":[{"given":"Xiulan","family":"Ma","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Martin","family":"Kuete","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiuli","family":"Gu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hui","family":"Zhou","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chengliang","family":"Xiong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Honggang","family":"Li","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"340","published-online":{"date-parts":[[2017,9,21]]},"reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1111\/j.2047-2927.2014.00188.x","article-title":"Genetic susceptibility to male infertility: news from genome-wide association studies","volume":"2","author":"KI Aston","year":"2014","journal-title":"Andrology"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"40","DOI":"10.1038\/aja.2011.67","article-title":"Genetic causes of spermatogenic failure","volume":"14","author":"A Massart","year":"2012","journal-title":"Asian J Androl"},{"key":"ref3","doi-asserted-by":"crossref","first-page":"324","DOI":"10.1016\/j.eururo.2012.04.048","article-title":"European Association of Urology Guidelines on Male Infertility: The 2012 Update","volume":"62","author":"A Jungwirth","year":"2012","journal-title":"European Urology"},{"key":"ref4","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1038\/ng.1040","article-title":"A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia","volume":"44","author":"Z Hu","year":"2011","journal-title":"Nat Genet"},{"key":"ref5","doi-asserted-by":"crossref","first-page":"3857","DOI":"10.1038\/ncomms4857","article-title":"Association analysis identifies new risk loci for non-obstructive azoospermia in Chinese men","volume":"5","author":"Z Hu","year":"2014","journal-title":"Nat Commun"},{"key":"ref6","doi-asserted-by":"crossref","first-page":"1510","DOI":"10.1093\/humrep\/dev088","article-title":"An association study of four candidate loci for human male fertility traits with male infertility","volume":"30","author":"Y Sato","year":"2015","journal-title":"Hum Reprod"},{"key":"ref7","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1038\/aja.2010.115","article-title":"Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies","volume":"13","author":"EB Trarbach","year":"2011","journal-title":"Asian J Androl"},{"key":"ref8","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pgen.1003349","article-title":"Human Spermatogenic Failure Purges Deleterious Mutation Load from the Autosomes and Both Sex Chromosomes, including the Gene DMRT1","volume":"9","author":"AM Lopes","year":"2013","journal-title":"Plos Genetics"},{"key":"ref9","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0044887","article-title":"High Resolution X Chromosome-Specific Array-CGH Detects New CNVs in Infertile Males","volume":"7","author":"C Krausz","year":"2012","journal-title":"Plos One"},{"key":"ref10","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0019426","article-title":"Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome","volume":"6","author":"F Tuttelmann","year":"2011","journal-title":"Plos One"},{"key":"ref11","article-title":"Genetic factors contributing to human primary ciliary dyskinesia and male infertility","author":"ZY Ji","year":"2016","journal-title":"Asian J Androl"},{"key":"ref12","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1146\/annurev-med-100708-204735","article-title":"Structural Variation in the Human Genome and its Role in Disease","volume":"61","author":"P Stankiewicz","year":"2010","journal-title":"Annual Review of Medicine"},{"key":"ref13","article-title":"The clinical context of copy number variation in the human genome","volume":"12","author":"C Lee","year":"2010","journal-title":"Expert Reviews In Molecular Medicine"},{"key":"ref14","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1080\/10495398.2014.887020","article-title":"Copy Number Differences of Y Chromosomal Genes Between Superior and Inferior Quality Semen Producing Crossbred (Bos taurus x Bos indicus) Bulls","volume":"26","author":"A Mukherjee","year":"2015","journal-title":"Animal Biotechnology"},{"key":"ref15","doi-asserted-by":"crossref","first-page":"1584","DOI":"10.1016\/j.fertnstert.2011.01.018","article-title":"Copy number variants on the X chromosome in women with primary ovarian insufficiency","volume":"95","author":"EAH Knauff","year":"2011","journal-title":"Fertility and Sterility"},{"key":"ref16","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1016\/j.ejogrb.2011.07.033","article-title":"DYZ1 copy number variation, Y chromosome polymorphism and early recurrent spontaneous abortion\/early embryo growth arrest","volume":"159","author":"JH Yan","year":"2011","journal-title":"European Journal of Obstetrics & Gynecology and Reproductive Biology"},{"key":"ref17","doi-asserted-by":"crossref","first-page":"4016","DOI":"10.1210\/jc.2009-1029","article-title":"TSPY1 Copy Number Variation Influences Spermatogenesis and Shows Differences among Y Lineages","volume":"94","author":"C Giachini","year":"2009","journal-title":"Journal of Clinical Endocrinology & Metabolism"},{"key":"ref18","doi-asserted-by":"crossref","first-page":"1864","DOI":"10.1016\/j.bbadis.2012.05.012","article-title":"X chromosomal mutations and spermatogenic failure","volume":"1822","author":"K Stouffs","year":"2012","journal-title":"Biochimica Et Biophysica Acta-Molecular Basis of Disease"},{"key":"ref19","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0097746","article-title":"X Chromosome-Linked CNVs in Male Infertility: Discovery of Overall Duplication Load and Recurrent, Patient-Specific Gains with Potential Clinical Relevance","volume":"9","author":"C Chianese","year":"2014","journal-title":"Plos One"},{"key":"ref20","doi-asserted-by":"crossref","first-page":"227","DOI":"10.5604\/12321966.1203881","article-title":"Infertility in the light of new scientific reports\u2014focus on male factor","volume":"23","author":"P Szkodziak","year":"2016","journal-title":"Ann Agric Environ Med"},{"key":"ref21","doi-asserted-by":"crossref","first-page":"1434","DOI":"10.1177\/1933719116641758","article-title":"A Novel Missense Mutation in USP26 Gene Is Associated with Nonobstructive Azoospermia","volume":"23","author":"Q Ma","year":"2016","journal-title":"Reprod Sci"},{"key":"ref22","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1016\/j.ajhg.2011.02.007","article-title":"A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation","volume":"88","author":"R Harbuz","year":"2011","journal-title":"American Journal of Human Genetics"},{"key":"ref23","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1016\/j.gene.2012.06.030","article-title":"Genome-wide screening of severe male factor infertile patients using BAC-array comparative genomic hybridization (CGH)","volume":"506","author":"SH Song","year":"2012","journal-title":"Gene"},{"key":"ref24","first-page":"90","article-title":"Identification of X-linked genetic factors involved in male infertility with a high resolution array-CGH","volume":"33","author":"C Giachini","year":"2010","journal-title":"International Journal of Andrology"},{"key":"ref25","doi-asserted-by":"crossref","first-page":"340","DOI":"10.1136\/jmedgenet-2013-101988","article-title":"Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility","volume":"51","author":"D Lo Giacco","year":"2014","journal-title":"Journal of Medical Genetics"},{"key":"ref26","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0156102","article-title":"Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population","volume":"11","author":"B Chylikova","year":"2016","journal-title":"Plos One"},{"key":"ref27","doi-asserted-by":"crossref","first-page":"19798","DOI":"10.1038\/srep19798","article-title":"Gr\/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analyses","volume":"6","author":"SK Bansal","year":"2016","journal-title":"Sci Rep"},{"key":"ref28","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1093\/humrep\/der377","article-title":"CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis","volume":"27","author":"J Yu","year":"2012","journal-title":"Hum Reprod"},{"key":"ref29","article-title":"WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction","year":"2010"},{"key":"ref30","doi-asserted-by":"crossref","first-page":"e0139485","DOI":"10.1371\/journal.pone.0139485","article-title":"High-Resolution Analyses of Human Leukocyte Antigens Allele and Haplotype Frequencies Based on 169,995 Volunteers from the China Bone Marrow Donor Registry Program","volume":"10","author":"XY Zhou","year":"2015","journal-title":"PLoS One"},{"key":"ref31","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1016\/j.beem.2010.08.006","article-title":"Male infertility: Pathogenesis and clinical diagnosis","volume":"25","author":"C Krausz","year":"2011","journal-title":"Best Practice & Research Clinical Endocrinology & Metabolism"},{"key":"ref32","doi-asserted-by":"crossref","first-page":"762","DOI":"10.1016\/j.ajhg.2009.10.015","article-title":"Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies","volume":"85","author":"SH Xu","year":"2009","journal-title":"American Journal of Human Genetics"},{"key":"ref33","doi-asserted-by":"crossref","first-page":"775","DOI":"10.1016\/j.ajhg.2009.10.016","article-title":"Genetic Structure of the Han Chinese Population Revealed by Genome-wide SNP Variation","volume":"85","author":"JM Chen","year":"2009","journal-title":"American Journal of Human Genetics"},{"key":"ref34","article-title":"High-Resolution Analyses of Human Leukocyte Antigens Allele and Haplotype Frequencies Based on 169,995 Volunteers from the China Bone Marrow Donor Registry Program","volume":"10","author":"XY Zhou","year":"2015","journal-title":"Plos One"},{"key":"ref35","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1038\/ejhg.2011.139","article-title":"Natural positive selection and north-south genetic diversity in East Asia","volume":"20","author":"C Suo","year":"2012","journal-title":"European Journal Of Human Genetics"}],"container-title":["PLOS ONE"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/dx.plos.org\/10.1371\/journal.pone.0185084","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,10,3]],"date-time":"2019-10-03T20:30:43Z","timestamp":1570134643000},"score":1,"resource":{"primary":{"URL":"https:\/\/dx.plos.org\/10.1371\/journal.pone.0185084"}},"subtitle":[],"editor":[{"given":"Xuejiang","family":"Guo","sequence":"first","affiliation":[],"role":[{"role":"editor","vocabulary":"crossref"}]}],"short-title":[],"issued":{"date-parts":[[2017,9,21]]},"references-count":35,"journal-issue":{"issue":"9","published-online":{"date-parts":[[2017,9,21]]}},"URL":"https:\/\/doi.org\/10.1371\/journal.pone.0185084","relation":{},"ISSN":["1932-6203"],"issn-type":[{"value":"1932-6203","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,9,21]]}}}