{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T02:56:32Z","timestamp":1791860192802,"version":"4.3.4"},"reference-count":37,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"abstract":"<jats:p>\n                    Nonobstructive azoospermia (NOA) is a severe condition in infertile men, and increasing numbers of causative genes have been identified during the last few decades. Although certain causative genes can explain the presence of NOA in some patients, a proportion of NOA patients remain to be addressed. This study aimed to investigate potential high-risk genes associated with spermatogenesis in idiopathic NOA patients by whole-exome sequencing. Whole-exome sequencing was performed in 46 male patients diagnosed with NOA. First, screening was performed for 119 genes known to be related to male infertility. Next, further screening was performed to determine potential high-risk causative genes for NOA by comparisons with 68 healthy male controls. Finally, risk genes with high\/specific expression in the testes were selected and their expression fluctuations during spermatogenesis were graphed. The frequency of cystic fibrosis transmembrane conductance regulator (\n                    <jats:italic toggle=\"yes\">CFTR<\/jats:italic>\n                    ) gene pathogenic variant carriers was higher in the NOA patients compared with the healthy controls. Potential risk genes that may be causes of NOA were identified, including seven genes that were highly\/specifically expressed in the testes. Four risk genes previously reported to be involved in spermatogenesis (MutS homolog 5 [\n                    <jats:italic toggle=\"yes\">MSH5<\/jats:italic>\n                    ], cilia- and flagella-associated protein 54 [\n                    <jats:italic toggle=\"yes\">CFAP54<\/jats:italic>\n                    ], MAP7 domain containing 3 [\n                    <jats:italic toggle=\"yes\">MAP7D3<\/jats:italic>\n                    ], and coiled-coil domain containing 33 [\n                    <jats:italic toggle=\"yes\">CCDC33<\/jats:italic>\n                    ]) and three novel risk genes (coiled-coil domain containing 168 [\n                    <jats:italic toggle=\"yes\">CCDC168<\/jats:italic>\n                    ], chromosome 16 open reading frame 96 [\n                    <jats:italic toggle=\"yes\">C16orf96<\/jats:italic>\n                    ], and serine protease 48 [\n                    <jats:italic toggle=\"yes\">PRSS48<\/jats:italic>\n                    ]) were identified to be highly or specifically expressed in the testes and significantly different in the 46 NOA patients compared with 68 healthy controls. This study on clinical NOA patients provides further evidence for the four previously reported risk genes. The present findings pave the way for further functional investigations and provide candidate risk genes for genetic diagnosis of NOA.\n                  <\/jats:p>","DOI":"10.4103\/aja202275","type":"journal-article","created":{"date-parts":[[2022,10,18]],"date-time":"2022-10-18T09:30:42Z","timestamp":1666085442000},"page":"66-72","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":8,"title":["Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing"],"prefix":"10.4103","volume":"25","author":[{"given":"Yu-Jun","family":"Liu","sequence":"first","affiliation":[{"name":"Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China"},{"name":"National Clinical Research Center for Obstetrics and Gynecology, Beijing 100191, China"},{"name":"Key Laboratory of Assisted Reproduction, Peking University, Ministry of Education, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xin-Jie","family":"Zhuang","sequence":"additional","affiliation":[{"name":"Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China"},{"name":"National Clinical Research Center for Obstetrics and Gynecology, Beijing 100191, China"},{"name":"Key Laboratory of Assisted Reproduction, Peking University, Ministry of Education, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jian-Ting","family":"An","sequence":"additional","affiliation":[{"name":"Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China"},{"name":"National Clinical Research Center for Obstetrics and Gynecology, Beijing 100191, China"},{"name":"Key Laboratory of Assisted Reproduction, Peking University, Ministry of Education, Beijing 100191, China"},{"name":"Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hui","family":"Jiang","sequence":"additional","affiliation":[{"name":"Department of Urology, Peking University Third Hospital, Beijing 100191, China"},{"name":"Department of Andrology, Peking University Third Hospital, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rong","family":"Li","sequence":"additional","affiliation":[{"name":"Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China"},{"name":"National Clinical Research Center for Obstetrics and Gynecology, Beijing 100191, China"},{"name":"Key Laboratory of Assisted Reproduction, Peking University, Ministry of Education, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jie","family":"Qiao","sequence":"additional","affiliation":[{"name":"Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China"},{"name":"National Clinical Research Center for Obstetrics and Gynecology, Beijing 100191, China"},{"name":"Key Laboratory of Assisted Reproduction, Peking University, Ministry of Education, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Li-Ying","family":"Yan","sequence":"additional","affiliation":[{"name":"Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China"},{"name":"National Clinical Research Center for Obstetrics and Gynecology, Beijing 100191, China"},{"name":"Key Laboratory of Assisted Reproduction, Peking University, Ministry of Education, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xu","family":"Zhi","sequence":"additional","affiliation":[{"name":"Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China"},{"name":"National Clinical Research Center for Obstetrics and Gynecology, Beijing 100191, China"},{"name":"Key Laboratory of Assisted Reproduction, Peking University, Ministry of Education, Beijing 100191, China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2023,1]]},"reference":[{"key":"R1-20240829","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1186\/s12958-015-0032-1","article-title":"A unique view on male infertility around the globe","volume":"13","author":"Agarwal","year":"2015","journal-title":"Reprod Biol Endocrinol"},{"key":"R2-20240829","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1002\/j.1939-4640.2002.tb02231.x","article-title":"The evaluation and management of the azoospermic patient","volume":"23","author":"Kolettis","year":"2002","journal-title":"J Androl"},{"key":"R3-20240829","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1016\/S0022-5347(17)38662-7","article-title":"Evaluation of the azoospermic patient","volume":"142","author":"Jarow","year":"1989","journal-title":"J Urol"},{"key":"R4-20240829","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":"Yu","year":"2012","journal-title":"Hum Reprod"},{"key":"R5-20240829","doi-asserted-by":"crossref","first-page":"101479","DOI":"10.1016\/j.beem.2020.101479","article-title":"Genetic mutations contributing to non-obstructive azoospermia","volume":"34","author":"Pena","year":"2020","journal-title":"Best Pract Res Clin Endocrinol Metab"},{"key":"R6-20240829","doi-asserted-by":"crossref","first-page":"369","DOI":"10.1038\/s41585-018-0003-3","article-title":"Genetics of male infertility","volume":"15","author":"Krausz","year":"2018","journal-title":"Nat Rev Urol"},{"key":"R7-20240829","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1038\/ejhg.2008.206","article-title":"Kallmann syndrome","volume":"17","author":"Dode","year":"2009","journal-title":"Eur J Hum Genet"},{"key":"R8-20240829","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1016\/j.metabol.2017.10.012","article-title":"Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism","volume":"86","author":"Stamou","year":"2018","journal-title":"Metabolism"},{"key":"R9-20240829","doi-asserted-by":"crossref","first-page":"3421","DOI":"10.1093\/hmg\/ddu051","article-title":"STAG3 is a strong candidate gene for male infertility","volume":"23","author":"Llano","year":"2014","journal-title":"Hum Mol Genet"},{"key":"R10-20240829","doi-asserted-by":"crossref","first-page":"1376","DOI":"10.1101\/gad.329705","article-title":"Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation","volume":"19","author":"de Vries","year":"2005","journal-title":"Genes Dev"},{"key":"R11-20240829","doi-asserted-by":"crossref","first-page":"887","DOI":"10.1007\/s10815-015-0445-y","article-title":"Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia","volume":"32","author":"Maor-Sagie","year":"2015","journal-title":"J Assist Reprod Genet"},{"key":"R12-20240829","first-page":"2","article-title":"Testicular biopsy score count--a method for registration of spermatogenesis in human testes: normal values and results in 335 hypogonadal males","volume":"1","author":"Johnsen","year":"1970","journal-title":"Hormones"},{"key":"R13-20240829","doi-asserted-by":"crossref","first-page":"e164","DOI":"10.1093\/nar\/gkq603","article-title":"ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data","volume":"38","author":"Wang","year":"2010","journal-title":"Nucleic Acids Res"},{"key":"R14-20240829","doi-asserted-by":"crossref","first-page":"135","DOI":"10.1007\/s00439-020-02112-y","article-title":"Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives","volume":"140","author":"Kasak","year":"2021","journal-title":"Hum Genet"},{"key":"R15-20240829","doi-asserted-by":"crossref","first-page":"1592","DOI":"10.1002\/humu.23312","article-title":"Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia","volume":"38","author":"Oud","year":"2017","journal-title":"Hum Mutat"},{"key":"R16-20240829","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1093\/humupd\/dmab030","article-title":"A systematic review of the validated monogenic causes of human male infertility:2020 update and a discussion of emerging gene-disease relationships","volume":"28","author":"Houston","year":"2021","journal-title":"Hum Reprod Update"},{"key":"R17-20240829","doi-asserted-by":"crossref","first-page":"2451","DOI":"10.1093\/hmg\/ddaa101","article-title":"Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes","volume":"29","author":"Chen","year":"2020","journal-title":"Hum Mol Genet"},{"key":"R18-20240829","doi-asserted-by":"crossref","first-page":"1967","DOI":"10.1038\/s41436-020-0916-0","article-title":"A genomics approach to male infertility","volume":"22","author":"Alhathal","year":"2020","journal-title":"Genet Med"},{"key":"R19-20240829","doi-asserted-by":"crossref","first-page":"1365","DOI":"10.1038\/gim.2018.10","article-title":"Point-of-care whole-exome sequencing of idiopathic male infertility","volume":"20","author":"Fakhro","year":"2018","journal-title":"Genet Med"},{"key":"R20-20240829","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1007\/s00439-020-02147-1","article-title":"Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease","volume":"140","author":"Cangiano","year":"2021","journal-title":"Hum Genet"},{"key":"R21-20240829","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1093\/humupd\/dmh030","article-title":"Reproductive functions of the ageing male","volume":"10","author":"Kuhnert","year":"2004","journal-title":"Hum Reprod Update"},{"key":"R22-20240829","doi-asserted-by":"crossref","first-page":"1431","DOI":"10.1093\/humrep\/deh255","article-title":"Suppression of the high endogenous levels of plasma FSH in infertile men are associated with improved Sertoli cell function as reflected by elevated levels of plasma inhibin B","volume":"19","author":"Foresta","year":"2004","journal-title":"Hum Reprod"},{"key":"R23-20240829","first-page":"1940","article-title":"Increased follicle stimulating hormone in infertile men. Is increased plasma FSH always due to damaged germinal epithelium?","volume":"10","author":"Martin-du-Pan","year":"1995","journal-title":"Hum Reprod"},{"key":"R24-20240829","doi-asserted-by":"crossref","first-page":"107","DOI":"10.1093\/molehr\/4.2.107","article-title":"CFTR gene and male fertility","volume":"4","author":"Wong","year":"1998","journal-title":"Mol Hum Reprod"},{"key":"R25-20240829","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1111\/andr.12450","article-title":"Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling","volume":"6","author":"de Souza","year":"2018","journal-title":"Andrology"},{"key":"R26-20240829","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1016\/S1472-6483(10)60801-2","article-title":"Molecular pathology of the CFTR locus in male infertility","volume":"10","author":"Claustres","year":"2005","journal-title":"Reprod Biomed Online"},{"key":"R27-20240829","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1016\/j.molmed.2011.10.003","article-title":"CFTR: folding, misfolding and correcting the DeltaF508 conformational defect","volume":"18","author":"Lukacs","year":"2012","journal-title":"Trends Mol Med"},{"key":"R28-20240829","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1016\/S1472-6483(10)60289-1","article-title":"Molecular analysis of mutations and polymorphisms in the CFTR gene in male infertility","volume":"17","author":"Tamburino","year":"2008","journal-title":"Reprod Biomed Online"},{"key":"R29-20240829","doi-asserted-by":"crossref","first-page":"e13475","DOI":"10.1111\/and.13475","article-title":"The association between variants in the CFTR gene and nonobstructive male infertility: a meta-analysis","volume":"52","author":"Yang","year":"2020","journal-title":"Andrologia"},{"key":"R30-20240829","doi-asserted-by":"crossref","first-page":"529","DOI":"10.1038\/353529a0","article-title":"A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules","volume":"353","author":"Franco","year":"1991","journal-title":"Nature"},{"key":"R31-20240829","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1038\/ng1407","article-title":"Mutations in a new member of the chromodomain gene family cause CHARGE syndrome","volume":"36","author":"Vissers","year":"2004","journal-title":"Nat Genet"},{"key":"R32-20240829","doi-asserted-by":"crossref","first-page":"3339","DOI":"10.1111\/j.1460-9568.2007.05958.x","article-title":"Olfactory bulb hypoplasia in Prokr2 null mice stems from defective neuronal progenitor migration and differentiation","volume":"26","author":"Prosser","year":"2007","journal-title":"Eur J Neurosci"},{"key":"R33-20240829","first-page":"113","article-title":"Update on the genetics of idiopathic hypogonadotropic hypogonadism","volume":"9","author":"Topaloglu","year":"2017","journal-title":"J Clin Res Pediatr Endocrinol"},{"key":"R34-20240829","doi-asserted-by":"crossref","first-page":"523","DOI":"10.1101\/gad.13.5.523","article-title":"Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis","volume":"13","author":"de Vries","year":"1999","journal-title":"Genes Dev"},{"key":"R35-20240829","doi-asserted-by":"crossref","first-page":"3140","DOI":"10.1091\/mbc.e15-02-0121","article-title":"CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in mice","volume":"26","author":"McKenzie","year":"2015","journal-title":"Mol Biol Cell"},{"key":"R36-20240829","doi-asserted-by":"crossref","first-page":"56","DOI":"10.1136\/jmedgenet-2019-106598","article-title":"Human X chromosome exome sequencing identifies BCORL1 as contributor to spermatogenesis","volume":"58","author":"Lu","year":"2021","journal-title":"J Med Genet"},{"key":"R37-20240829","doi-asserted-by":"crossref","first-page":"243","DOI":"10.1159\/000251961","article-title":"Ccdc33, a predominantly testis-expressed gene, encodes a putative peroxisomal protein","volume":"126","author":"Kaczmarek","year":"2009","journal-title":"Cytogenet Genome Res"}],"container-title":["Asian Journal of Andrology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/aja202275","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T15:12:27Z","timestamp":1787757147000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/aja202275"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,10,18]]},"references-count":37,"journal-issue":{"issue":"1","published-online":{"date-parts":[[2023]]}},"URL":"https:\/\/doi.org\/10.4103\/aja202275","relation":{},"ISSN":["1745-7262","1008-682X"],"issn-type":[{"value":"1745-7262","type":"print"},{"value":"1008-682X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2022,10,18]]},"assertion":[{"value":"2022-03-20","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2022-08-31","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}