Male age and progeny

References

• Takizawa T, Hatakeyama S. Age associated changes in microvasculature of human adult testis. Acta Pathol Jpn 1978; 28: 541–54
   PubMedGoogle Scholar
• Auroux M, Nawar N NY, Rizkalla N. Testicular aging: vascularization and gametogenesis modifications in the Wistar rat. Arch Androl 1985; 14: 115–21
   PubMed Web of Science ®Google Scholar
• Johnson L. Spermatogenesis and aging in the human. J Androl 1986; 7: 331–54
   PubMedGoogle Scholar
• Lunenfeld B, Berezin M. L'insuffisance leydigienne liée au viellissement. Andrologie., G Arvis. Maloine, Paris 1989; 691–702
   Google Scholar
• Schwartz D, Mayaux M J, Spira A, Moscato M L, Jouannet P, Czyglik F, et al. Study of a group of 484 fertile men. II. Relation between age (20–59) and semen characteristics. Int J Androl 1981; 4: 450–6
   PubMedGoogle Scholar
• Haidl G, Jung A, Schill W B. Ageing and sperm function. Hum Reprod 1996; 11: 558–60
   PubMed Web of Science ®Google Scholar
• Anderson B A. Male age and infertility. Results from Ireland prior to 1911. Pop Index 1975; 41: 561–7
   Google Scholar
• Albert M, Roussel C. Strain differences in the concentration, mobility and morphology of epididymal sperm in relation to puberty in mice. Int J Androl 1984; 7: 334–47
   PubMedGoogle Scholar
• Lunstra D D, Echternkamp S E. Puberty in beef bulls: acrosome morphology and semen quality in bulls of different breeds. J Anim 1982; 55: 638–48, Sci;
   Google Scholar
• Burgoyne P S. Sperm phenotype and its relationship to somatic and germ line genotype: a study using mouse aggregation chimeras. Dev Biol 1975; 44: 63–76
   PubMed Web of Science ®Google Scholar
• Nantel F, Monaco L, Foulkes N S, Masquilier D, Le Meur M, Henricksen K, et al. Spermiogenesis deficiency and germ–cell apoptosis in CREM–mutant mice. Nature (London) 1996; 380: 159–62
   PubMed Web of Science ®Google Scholar
• Martin R H, Rademaker A W. The effect of age on the frequency of sperm chromosomal abnormalities in normal men. Am J Hum Genet 1987; 41: 484–92
   PubMed Web of Science ®Google Scholar
• Martin R H, Balkan W, Burns K, Rademaker A W, Lin C C, Rudd N L. The chromosome constitution of 1000 human spermatozoa. Hum Genet 1983; 63: 305–9
   PubMed Web of Science ®Google Scholar
• Brandriff B, Gordon L, Ashworth L, Watchmaker G, Moore D, II, Wyrobek A J, et al. Chromosomes of human sperm: variability among normal individuals. Hum Genet 1985; 70: 18–24
   PubMed Web of Science ®Google Scholar
• Sherman S L, Takaesu N, Freeman S, Philipps C, Blackston R D, Keats B J, et al. Trisomy 21: association between reduced recombination and nondisjunction. Am J Hum Genet 1990; 47: A97
   Google Scholar
• Stylianos E, Antonarakis M D. The Down syndrome collaborative group. Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. N Engl J Med 1991; 324: 872–6
   PubMed Web of Science ®Google Scholar
• Stene J, Fischer G, Stene E, Mikkelsen M, Petersen E. Paternal age effect in Down's syndrome. Ann Hum Genet 1977; 40: 299–306
   PubMed Web of Science ®Google Scholar
• Matsunaga E, Tonomura E, Oishi A, Kikuchi Y. Reexamination of paternal age effect in Down's syndrome. Hum Genet 1978; 40: 259–68
   PubMed Web of Science ®Google Scholar
• Thepot F, Wack T, Selva J, Czyglik F, Mayaux M J. Age paternal et issues de grossesses. Expérience des CECOS. Contracept Fertil Sex 1993; 21: 388–90
   PubMedGoogle Scholar
• Roth M P, Stoll C, Taillemite J L, Girard S, Boué A. Paternal age and Down's syndrome diagnosed pre–natally: no association in French data. Prenat Diagn 1983; 3: 327–35
   PubMed Web of Science ®Google Scholar
• Hook E B, Regal R R. A search for a paternal–age effect upon cases of 47,+21 in which the extra chromosome is of paternal origin. Am J Hum Genet 1984; 36: 413–21
   PubMed Web of Science ®Google Scholar
• Hassold T J, Sherman S L, Pettay D, Page D C, Jacobs P A. XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet 1991; 49: 255–60
   Web of Science ®Google Scholar
• Hook E B, Schreinemachers D M, Wiley A M, Cross P K. Inherited structural cytogenetic abnormalities detected incidentally in fetuses diagnosed prenatally: frequency, paternal age associations, sex–ratio trends, and comparisons with rates of mutants. Am J Hum Genet 1984; 36: 422–43
   PubMed Web of Science ®Google Scholar
• Penrose L S. Paternal age and mutation. Lancet 1955; 2: 312–13
   Web of Science ®Google Scholar
• Friedman J M. Genetic disease in the offspring of older fathers. Obstet Gynecol 1981; 57: 745–9
   PubMed Web of Science ®Google Scholar
• Vogel F, Motulsky A G. Human Genetics. Problems and Approaches, 3rd edn. Springer-Verlag, Paris 1997; 402–10
   Google Scholar
• Cohen F L. Paternal contribution to birth defects. Nurs Clin North Am 1986; 21: 49–64
   PubMed Web of Science ®Google Scholar
• Bordson B L, Leonardo V S. The appropriate upper age limit for semen donors: a review of the genetic effects of paternal age. Fertil Steril 1991; 56: 397–401
   PubMed Web of Science ®Google Scholar
• Lian Z H, Zack M M, Erickson J D. Paternal age and the occurrence of birth defects. Am J Hum Genet 1986; 39: 648–60
   PubMed Web of Science ®Google Scholar
• Riccardi V M, Dobson C E, II, Chakraborty R, Boutke C. The pathophysiology of neurofibromatosis. IX. Paternal age as a factor in the origin of new mutations. Am J Med Genet 1984; 18: 169–76
   PubMed Web of Science ®Google Scholar
• Jadayel D F, Fain P, Upadhyaya M, Ponder M A, Huson S M, Carey J, et al. Paternal origin of new mutations in Von Recklinghausen neurofibromatosis. Nature (London) 1990; 343: 558–9
   PubMed Web of Science ®Google Scholar
• Takano T, Kawashima T, Yamanonchi Y, Kitayama K, Baba T, Ueno K, et al. Genetics of neurofibromatis 1 in Japan: mutation rate and paternal age effect. Hum Genet 1992; 89: 281–6
   PubMed Web of Science ®Google Scholar
• Bunin G R, Needle M, Riccardi V M. Paternal age and sporadic neurofibromatosis 1: a case control study and consideration of the methodologic issues. Genet Epidemiol 1997; 14: 507–16
   PubMed Web of Science ®Google Scholar
• Auroux M. Decrease of learning capacity in offspring with increasing paternal age in the rat. Teratology 1983; 27: 141–8
   PubMedGoogle Scholar
• Anthenaise M, Salbreux R. Prévalence de la deficience mentale profonde chez l'enfant. Neuropsy Enfance Adolesc 1979; 27: 45–8
   PubMedGoogle Scholar
• Auroux M, Mayaux M J, Guihard-Moscato M L, Fromantin M, Barthe J, Schwartz D. Paternal age and mental functions of progeny in man. Hum Reprod 1989; 4: 794–7
   PubMed Web of Science ®Google Scholar
• Lee I P. Adaptive biochemical repair responses toward germ cell DNA damage. Am J Intern Med 1983; 4: 135–47
   Google Scholar
• Wallace D C. Mitochondrial genetics: a paradigm for aging and degenerative diseases?. Science 1992; 256: 628–32
   PubMed Web of Science ®Google Scholar
• Auroux M, Dulioust E, Selva J, Rince P. Cyclophosphamide in the Fo male rat: physical and behavioral changes in three successive adult generations. Mutat Res 1990; 229: 189–200
   PubMedGoogle Scholar
• Auroux M, Dulioust E M, Nawar N Y, Yacoub S G, Kempf E H, Ebel A B. Cyclophosphamide in the male rat: cerebral biochemical changes in progeny. Biomed Pharmacother 1990; 44: 519–23
   PubMed Web of Science ®Google Scholar
• Campbell J H, Zimmermann E G. Automodulation of genes: a proposed mechanism for persisting effects of drugs and hormones in mammals. Neurobehav Toxicol Teratol 1982; 4: 435–9
   PubMedGoogle Scholar
• Krumlauf R. Hox genes and pattern formation in the brachial region of the vertebrate head. Trends Genet 1993; 9: 106–12
   PubMed Web of Science ®Google Scholar
• Monk M. Variation in epigenetic inheritance. Trends Genet 1990; 6: 110–14
   PubMed Web of Science ®Google Scholar
• Surani M A, Kothary R, Allen N D, Singh P B, Fundele R, Ferguson-Smith A C, . Genome imprinting and development in the mouse. Genomics Imprinting. Development Supplement., M Monk, M A Surani, et al. The Company of Biologists Ltd., CambridgeUK 1990; 89–98
   Google Scholar
• Kafri T, Ariel M, Brandeis M, Shemer R, Urven L, McCarrey J, et al. Developmental pattern of genespecific DNA methylation in the mouse embryo and germ line. Genes Dev 1992; 6: 705–14
   PubMed Web of Science ®Google Scholar
• Ariel M, Cedar H, McCarrey J. Developmental changes in methylation of spermatogenesis–specific genes include reprogramming in the epididymis. Nature Genet 1994; 7: 59–63
   PubMed Web of Science ®Google Scholar
• Auroux M, Nawar N NY, Naguib M, Baud M, Lapaquellerie N. Post–pubescent to mature fathers: increase in progeny quality?. Hum Reprod 1998; 13: 55–9
   PubMed Web of Science ®Google Scholar
• Barton S C, Surani M AH, Norris M L. Role of paternal and maternal genome in mouse development. Nature (London) 1984; 311: 374–6
   PubMed Web of Science ®Google Scholar
• Sapienza C, Peterson A C, Rossant J, Balling R. Degree of methylation of transgenes is dependent on gamete of origin. Nature (London) 1987; 328: 251–4
   PubMed Web of Science ®Google Scholar