{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,8]],"date-time":"2026-01-08T03:16:19Z","timestamp":1767842179971,"version":"3.49.0"},"reference-count":6,"publisher":"Public Library of Science (PLoS)","issue":"2","license":[{"start":{"date-parts":[[2012,2,16]],"date-time":"2012-02-16T00:00:00Z","timestamp":1329350400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["www.plosgenetics.org"],"crossmark-restriction":false},"short-container-title":["PLoS Genet"],"DOI":"10.1371\/journal.pgen.1002535","type":"journal-article","created":{"date-parts":[[2012,2,16]],"date-time":"2012-02-16T21:51:53Z","timestamp":1329429113000},"page":"e1002535","update-policy":"https:\/\/doi.org\/10.1371\/journal.pgen.corrections_policy","source":"Crossref","is-referenced-by-count":17,"title":["Upsetting the Dogma: Germline Selection in Human Males"],"prefix":"10.1371","volume":"8","author":[{"given":"James F.","family":"Crow","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"340","published-online":{"date-parts":[[2012,2,16]]},"reference":[{"key":"ref1","first-page":"710","article-title":"Zur vererbung des zwergwuchses.","volume":"9","author":"W Weinberg","year":"1912","journal-title":"Arch Rassen-u Gesell Biolog"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"40","DOI":"10.1038\/35049558","article-title":"The origins, patterns and implications of human spontaneous mutation.","volume":"1","author":"JF Crow","year":"2000","journal-title":"Nat Rev Genet"},{"key":"ref3","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1126\/science.1085710","article-title":"Evidence for selective advantage of pathogenic FGFR2 mutations in the male germ line.","volume":"301","author":"A Goriely","year":"2003","journal-title":"Science"},{"key":"ref4","doi-asserted-by":"crossref","first-page":"10143","DOI":"10.1073\/pnas.0801267105","article-title":"A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations.","volume":"105","author":"S-K Choi","year":"2008","journal-title":"Proc Nat Acad Sci USA"},{"key":"ref5","doi-asserted-by":"crossref","first-page":"e1002420","DOI":"10.1371\/journal.pgen.1002420","article-title":"Positive selection for new disease mutations in the human germline: evidence from the heritable cancer syndrome multiple endocrine neoplasia type 2B.","volume":"8","author":"S-K Choi","year":"2012","journal-title":"PLoS Genet"},{"key":"ref6","article-title":"The causes of evolution","author":"JBS Haldane","year":"1931"}],"container-title":["PLoS Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/dx.plos.org\/10.1371\/journal.pgen.1002535","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2018,10,19]],"date-time":"2018-10-19T20:08:02Z","timestamp":1539979682000},"score":1,"resource":{"primary":{"URL":"https:\/\/dx.plos.org\/10.1371\/journal.pgen.1002535"}},"subtitle":[],"editor":[{"given":"Bret A.","family":"Payseur","sequence":"first","affiliation":[],"role":[{"role":"editor","vocabulary":"crossref"}]}],"short-title":[],"issued":{"date-parts":[[2012,2,16]]},"references-count":6,"journal-issue":{"issue":"2","published-online":{"date-parts":[[2012,2,16]]}},"URL":"https:\/\/doi.org\/10.1371\/journal.pgen.1002535","relation":{},"ISSN":["1553-7404"],"issn-type":[{"value":"1553-7404","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,2,16]]}}}