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1 in males than in females and increases with paternal age.
2 s were de novo and associated with increased paternal age.
3 proportion of mutants, which decreases with paternal age.
4 enetic alterations associated with advancing paternal age.
5 al evidence for an increase in mutation with paternal age.
6 Much less is known about the impact of paternal age.
7 of autism risk with increasing maternal and paternal age.
8 tism associated with increasing maternal and paternal age.
9 no association with ASD after adjusting for paternal age.
10 psychiatric disorder (lifetime PD); and (3) paternal age.
11 than female gametes and often increase with paternal age.
12 g habits, and they differed only slightly by paternal age.
13 no significant effects, after adjusting for paternal age.
14 n spectra between the sexes and at different paternal ages.
15 ce regarding the impact of both maternal and paternal ages.
16 DNMs in the offspring after controlling for paternal age (0.51 additional mutations per year, 95% CI
18 32; 95% CI: 0.11, 0.54; P < 0.01), and older paternal age (adjusted coefficient: 33.27; 95% CI: 4.10,
21 rved an inverse U-shaped association between paternal age and offspring AH4 score with the lowest sco
23 ant, monotonic association between advancing paternal age and risk of adult schizophrenia and schizop
26 xamined the association between maternal and paternal age and subgroups of trisomy 21 defined by pare
28 anation for the association between advanced paternal age and various neurodevelopmental disorders bu
29 story of psychiatric disorders, maternal and paternal age, and parental educational and employment st
32 es as well as additional reports of advanced paternal age associated with paternal origin of three sp
34 to better understand the association between paternal age at birth and hematological malignancies.
35 ication were verbal IQ for the ASD/ID genes, paternal age at birth for the DBE genes and adaptive fun
36 ippines, we first replicate the finding that paternal age at birth is associated with longer TL in of
38 (including sex, year of birth, maternal and paternal age at birth, and parity), for smoking 10 or mo
42 ial confounders (maternal age at conception, paternal age at conception, parental psychiatric history
44 9, 1.64, 1.42, 1.16, and 0.92; in women, for paternal age at MI of <50, 50 to 59, and >/=60 years, th
49 of DNMs in offspring increases not only with paternal age, but also with maternal age, and that some
50 2.32, and 2.74 among those of each increased paternal age category (27-<32, 32-<38, and > or =38 year
51 in (4:1 bias) and positively correlated with paternal age, consistent with the modest increased risk
53 n association with rare disorders related to paternal age (e.g., Apert syndrome, achondroplasia), thi
54 tant sperm over time-explaining the observed paternal age effect associated with these disorders-and
55 autosomal dominant disorders show a dramatic paternal age effect due to selfish mutations: substituti
56 ts age, and thus selection could explain the paternal age effect for Apert syndrome and other genetic
57 This identifies the biological basis of the paternal age effect for new mutations previously suggest
61 estes suggests that the common factor in the paternal age effect lies in the dysregulation of spermat
62 n seven to eight times that of females and a paternal age effect of three mutations per year of fathe
63 syndrome (HRAS), which we collectively term "paternal age effect" (PAE) disorders, provides a good mo
71 interval: 1.1, 1.6; adjusted odds ratio for paternal age > or =40 years vs. 25-29 years = 1.4, 95% c
72 n the second, third, and oldest quartiles of paternal age had 1.2, 1.3, and 1.7 times increased risk
73 comparison analyses indicated that advancing paternal age had a dose-response relationship with every
76 crease in autism risk with both maternal and paternal age has potential implications for public healt
77 schizophrenia was associated with advancing paternal age in a population-based birth cohort of 87 90
83 5.84) than did controls after adjustment for paternal age, low maternal education, race, residence, g
84 n-years among sons in the lowest quartile of paternal age (<27 years), to 2.00, 2.32, and 2.74 among
85 ma over time; a similar effect of increasing paternal age may be due to the same selection process.
87 age, maternal body mass index, maternal age, paternal age, newborn sex, newborn ethnicity, season of
94 ed for calendar year, age, sex, maternal and paternal age, place of residence at birth, and somatic c
95 observed to arise in fathers, and increasing paternal age positively correlates with the risk of new
96 d not differ in distributions of maternal or paternal age, previous livebirths, maternal smoking, or
97 c risk for schizophrenia was associated with paternal age (R(2) = 0.002; P = 1e-04), and offspring ed
98 nt with the clinical observation of advanced paternal age resulting in new cases of achondroplasia an
99 trend by adjusting for birth year, advanced paternal age showed no association with offspring IQ; ho
100 droplasia have been associated with advanced paternal age, suggesting that these mutations occur pref
101 ber of DNMs increases at a constant rate for paternal age, the contribution from the mother increases
102 academic morbidity associated with advancing paternal age using several quasi-experimental designs, i
103 oportional hazards regression, we found that paternal age was a strong and significant predictor of t
104 rval: 1.32, 1.44), and a 10-year increase in paternal age was associated with a 22% increase (odds ra
108 ternal age (> or =40 years) became null when paternal age was included in the statistical model.
110 mia and central nervous system tumors, older paternal age was not associated with risk of either type
115 radic AS births increases exponentially with paternal age, we hypothesized that the frequency of AS m
116 ion, and other covariates, both maternal and paternal age were independently associated with autism (
118 There was a joint effect of maternal and paternal age with increasing risk of ASD for couples wit
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